Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Kenyan blood donors
Open accessPublished version of a preprint
Abstract
Pandemic progress in Kenya: By the end of July 2020, Kenya had reported only 341 deaths and ∼20,000 cases of COVID-19. This is in marked contrast to the tens of thousands of deaths reported in many higher-income countries. The true extent of COVID-19 in the community was unknown and likely to be higher than reports indicated. Uyoga et al. found an overall seroprevalence among blood donors of 4.3%, peaking in 35- to 44-year-old individuals (see the Perspective by Maeda and Nkengasong). The low mortality can be partly explained by the steep demographics in Kenya, where less than 4% of the population is 65 or older. These circumstances combine to result in Kenyan hospitals not currently being overwhelmed by patients with respiratory distress. However, the imposition of a strict lockdown in this country has shifted the disease burden to maternal and child deaths as a result of disruption to essential medical services. Science , this issue p. 79 ; see also p. 27
AI snapshot
Written from the paper’s full text.
TL;DR
In a national serosurvey of Kenyan blood transfusion donors from 30 April to 16 June 2020, anti–SARS-CoV-2 spike IgG seroprevalence was 5.6% crude and 4.3% after population weighting and test-performance adjustment. The authors conclude that SARS-CoV-2 exposure was considerably more widespread than reported case counts suggested, with higher seroprevalence in urban counties and younger/middle-aged adults.
Key findings
- Among 3098 blood donor samples, 174 were seropositive, giving a crude seroprevalence of 5.6% (95% CI, 4.8 to 6.5%); the Bayesian population-weighted, test-adjusted seroprevalence was 4.3% (95% CI, 2.9 to 5.8%).
- Crude seroprevalence varied by age (P = 0.046), ranging from 3.4 to 7.0% among adults 15 to 54 years, with all 71 donors aged 55 to 64 years seronegative; it did not vary by sex (P = 0.50) but varied geographically from 1.9% in Rift Valley to 10.0% in Western (P = 0.002).
- County-level seroprevalence was 8.0% (95% CI, 5.5 to 11.1%) in Mombasa, 7.3% (95% CI, 4.2 to 11.4%) in Nairobi, and 5.5% (95% CI, 2.8 to 9.6%) in Kisumu.
- The authors note that Kenya’s younger population structure, with only 3.9% aged ≥65 years, may partly explain lower severe outcomes, and estimate that applying 4.3% seroprevalence to all 15- to 64-year-olds would suggest approximately 1.3 million infections.
Methods
- Residual blood samples from transfusion donors were collected from four Kenya National Blood Transfusion Service regional centers and satellites/hospitals between 30 April and 16 June 2020; after excluding duplicates, missing age/date records, and donors aged ≥65 years, 3098 samples from individuals aged 15 to 66 years were analyzed.
- A validated ELISA for anti–SARS-CoV-2 spike IgG was used, with seropositivity defined as an optical density ratio >2; validation used 910 prepandemic serum samples, 174 sera from PCR-defined SARS-CoV-2 cases, and a five-sera NIBSC panel, yielding sensitivity 92.7% (95% CI, 87.9 to 96.1%) and specificity 99.0% (95% CI, 98.1 to 99.5%).
- Prevalence was estimated using Bayesian multilevel regression and poststratification to reweight to the 2019 Kenya Population and Housing Census age, sex, and regional distribution, then adjusted for assay sensitivity and specificity.
Limitations
- The paper states that blood donors are not representative of the Kenyan population; although estimates were standardized to age, sex, and region, 43% of Kenya’s population is outside the sampled 15- to 64-year age range, and seroprevalence in children <15 years and adults >65 years is often lower, so the donor estimate may be higher than the population-wide estimate.
- The paper states that donor selection may bias estimates in both directions: potential donors are excluded if ill in the past 6 months, which may underestimate population prevalence, while people shielding at home are unlikely to be captured, which may overestimate seroprevalence; donor type also varied, with voluntary nonremunerated donors at 8.5% crude seroprevalence versus 5.4% for family replacement donors, though 92% of the sample came from the lower-seroprevalence group.
- The paper states that it did not adjust for sample date because sampling periods varied by county; more broadly, the cross-sectional residual-sample design cannot establish incidence timing or individual exposure risk.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 34 cited sources checked · 0 supported · 0 flagged
- Findingown data
Crude seroprevalence varied by age (P = 0.046).
“Crude seroprevalence varied by age (P = 0.046), ranging between 3.4 to 7.0% among adults 15 to 54 years; all 71 donors aged 55 to 64 years were seronegative (Table 1).”
Quote in the paperNot a substantial claim - Findingown data
Using OD ratios, both RBD and spike ELISAs correctly classified 901 of 910 prepandemic samples as seronegative.
“By using OD ratios, both RBD and spike ELISAs correctly classified 901 of 910 prepandemic samples as seronegative (table S1).”
Quote in the paperSubstantial claim - Findingown data
For either RBD or whole spike, specificity was higher when using a ratio of sample OD/negative control OD than when using raw sample OD plus 3 standard deviations to define seropositivity.
“For either receptor-binding domain (RBD) or whole spike, specificity was higher when using a ratio of the sample optical density (OD)/negative control OD than when using the raw sample OD plus 3 standard deviations to define seropositivity (table S1).”
Quote in the paperSubstantial claim - Findingown data
The spike ELISA detected more seropositives (166 of 179) than the RBD ELISA (145 of 179) among sera from SARS-CoV-2 PCR-positive individuals.
“However, the spike ELISA detected more seropositives (166 of 179 compared with 145 of 179 for RBD ELISA) among sera from SARS-CoV-2 PCR-positive individuals (fig. S2, A and B).”
Quote in the paperSubstantial claim - Findingown data
All 71 donors aged 55 to 64 years were seronegative.
“all 71 donors aged 55 to 64 years were seronegative (Table 1).”
Quote in the paperNot a substantial claim
- Findingown data
The study did not identify evidence of cross-reactive antibodies to endemic coronaviruses in the validation study.
“Despite our prior work showing that HCoVs circulate in Kenya (24), we did not identify evidence of cross-reactive antibodies to endemic coronaviruses in our validation study.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [24] 24. Otieno G. P., Murunga N., Agoti C. N., Gallagher K. E., Awori J. O., Nokes D. J., Surveillance of endemic human coronaviruses (HCoV-NL63, OC43 and 229E) associated with childhood pneumonia in Kilifi, Kenya. Wellcome Open Res. 5, 150 (2020). 10.12688/wellcomeopenres.16037.2 source
Not checked in the free run.
- Findingown data
Crude seroprevalence varied geographically, from 1.9% in the Rift Valley region to 10.0% in the Western region (P = 0.002).
“but did vary geographically, from 1.9% in the Rift Valley region to 10.0% in the Western region (P = 0.002) (Table 1).”
Quote in the paperNot a substantial claim - Findingown data
The Bayesian population-weighted and test-adjusted seroprevalence for Kenya was 4.3% (95% CI, 2.9 to 5.8%).
“The Bayesian population-weighted and test-adjusted seroprevalence for Kenya was 4.3% (95% CI, 2.9 to 5.8%) (Table 1)”
Quote in the paperSubstantial claim - Findingown data
Crude seroprevalence did not vary by sex (P = 0.50).
“Crude seroprevalence did not vary by sex (P = 0.50) but did vary geographically, from 1.9% in the Rift Valley region to 10.0% in the Western region (P = 0.002) (Table 1).”
Quote in the paperNot a substantial claim - Findingown data
Exclusion of VNRDs reduced little the crude seroprevalence in the study, from 5.6% to 5.4%.
“exclusion of VNRDs reduced little the crude seroprevalence in our study, from 5.6 to 5.4%.”
Quote in the paperNot a substantial claim - Findingown data
Seroprevalence was similar for both sexes.
“but was similar for both sexes.”
Quote in the paperNot a substantial claim - Premisecitation
Currently, there are few estimates of SARS-CoV-2 seroprevalence in Africa in the literature.
“Currently, there are few estimates of SARS-CoV-2 seroprevalence in Africa in the literature (11).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [11] 11. Chibwana M. G., Jere K. C., Kamng’ona R., Mandolo J., Katunga-Phiri V., Tembo D., Mitole N., Musasa S., Sichone S., Lakudzala A., Sibale L., Matambo P., Kadwala I., Byrne R. L., Mbewe A., Morton B., Phiri C., Mallewa J., Mwandumba H. C., Adams E. R., Gordon S. B., Jambo K. C., High SARS-CoV-2 seroprevalence in Health Care Workers but relatively low numbers of deaths in urban Malawi. Wellcome Open Res. 5, 199 (2020). 10.12688/wellcomeopenres.16188.132766597
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
The low COVID-19 mortality in Kenya can be partly explained by the steep demographic age-pyramid, with less than 4% of the population aged 65 or older.
“The low mortality can be partly explained by the steep demographics in Kenya, where less than 4% of the population is 65 or older.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [4] 4. Dowd J. B., Andriano L., Brazel D. M., Rotondi V., Block P., Ding X., Liu Y., Mills M. C., Demographic science aids in understanding the spread and fatality rates of COVID-19. Proc. Natl. Acad. Sci. U.S.A. 117, 9696–9698 (2020). 10.1073/pnas.2004911117 source
Not checked in the free run.
- Study design and conductown data
The ELISA was validated with 910 prepandemic serum samples, 174 PCR-defined SARS-CoV-2 case sera, and a five-sera NIBSC panel.
“We validated a widely used enzyme-linked immunosorbent assay (ELISA) for SARS-CoV-2 IgG (15) with 910 serum samples from the prepandemic period and 174 sera from polymerase chain reaction (PCR)–defined SARS-CoV-2 cases, and a well-characterized five-sera panel from the National Institute of Biological Standards and Control (NIBSC) in the UK.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [15] 15. Amanat F., Stadlbauer D., Strohmeier S., Nguyen T. H. O., Chromikova V., McMahon M., Jiang K., Arunkumar G. A., Jurczyszak D., Polanco J., Bermudez-Gonzalez M., Kleiner G., Aydillo T., Miorin L., Fierer D. S., Lugo L. A., Kojic E. M., Stoever J., Liu S. T. H., Cunningham-Rundles C., Felgner P. L., Moran T., García-Sastre A., Caplivski D., Cheng A. C., Kedzierska K., Vapalahti O., Hepojoki J. M., Simon V., Krammer F., A serological assay to detect SARS-CoV-2 seroconversion in humans. Nat. Med. 26, 1033–1036 (2020). 10.1038/s41591-020-0913-5 source
Not checked in the free run.
- Interpretationcitation
SARS-CoV-2 seroprevalence in this study is comparable with estimates from large population-based serosurveys in China, Switzerland, Spain, and the United States after the initial epidemic peak and after many tens of thousands of deaths.
“SARS-CoV-2 seroprevalence in our study is comparable with estimates from large population-based serosurveys in China, Switzerland, Spain, and the United States after the initial epidemic peak and after many tens of thousands of deaths (9, 10, 17, 18).”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [9] 9. Pollán M., Pérez-Gómez B., Pastor-Barriuso R., Oteo J., Hernán M. A., Pérez-Olmeda M., Sanmartín J. L., Fernández-García A., Cruz I., Fernández de Larrea N., Molina M., Rodríguez-Cabrera F., Martín M., Merino-Amador P., León Paniagua J., Muñoz-Montalvo J. F., Blanco F., Yotti R., ENE-COVID Study Group, Prevalence of SARS-CoV-2 in Spain (ENE-COVID): A nationwide, population-based seroepidemiological study. Lancet 396, 535–544 (2020). 10.1016/S0140-6736(20)31483-5 source
Not checked in the free run.
- cites [10] 10. Stringhini S., Wisniak A., Piumatti G., Azman A. S., Lauer S. A., Baysson H., De Ridder D., Petrovic D., Schrempft S., Marcus K., Yerly S., Arm Vernez I., Keiser O., Hurst S., Posfay-Barbe K. M., Trono D., Pittet D., Gétaz L., Chappuis F., Eckerle I., Vuilleumier N., Meyer B., Flahault A., Kaiser L., Guessous I., Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): A population-based study. Lancet 396, 313–319 (2020). 10.1016/S0140-6736(20)31304-0 source
Not checked in the free run.
- cites [17] 17. Xu X., Sun J., Nie S., Li H., Kong Y., Liang M., Hou J., Huang X., Li D., Ma T., Peng J., Gao S., Shao Y., Zhu H., Lau J. Y.-N., Wang G., Xie C., Jiang L., Huang A., Yang Z., Zhang K., Hou F. F., Seroprevalence of immunoglobulin M and G antibodies against SARS-CoV-2 in China. Nat. Med. 26, 1193–1195 (2020). 10.1038/s41591-020-0949-6 source
Not checked in the free run.
- cites [18] 18. F. P. Havers et al, Seroprevalence of antibodies to SARS-CoV-2 in 10 sites in the United States, March 23-May 12, 2020. JAMA Intern Med, 10.1001/jamainternmed.2020.4130 (2020).
Not checked in the free run.
- Interpretationreasoning
If the transfusion donor seroprevalence of 4.3% was applied to all 15- to 64-year-olds, it would suggest approximately 1.3 million infections.
“If the transfusion donor seroprevalence of 4.3% was applied to all 15- to 64-year-olds, it would suggest approximately 1.3 million infections.”
Quote in the paperSubstantial claim - Interpretationcitation
Our results are also comparable with those of other surveys of blood donors in Brazil, Italy, and many parts of England.
“Our results are also comparable with those of other surveys of blood donors in Brazil (13), Italy (12), and many parts of England (19).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [13] 13. Amorim Filho L., Szwarcwald C. L., Mateos S. O. G., Leon A. C. M. P., Medronho R. A., Veloso V. G., Lopes J. I. F., Porto L. C. M. S., Chieppe A., Werneck G. L.; Grupo Hemorio de Pesquisa em Covid-19, Seroprevalence of anti–SARS-CoV-2 among blood donors in Rio de Janeiro, Brazil. Rev. Saude Publica 54, 69 (2020). 10.11606/s1518-8787.2020054002643 source
Not checked in the free run.
- cites [12] 12. L. Valenti et al., SARS-CoV-2 seroprevalence trends in healthy blood donors during the COVID-19 Milan outbreak. medRxiv 2020.2005.2011.20098442 [Preprint] 31 May 2020. 10.1101/2020.05.11.20098442 source
Not checked in the free run.
- cites [19] 19. Public Health England, “Sero-prevalence epidemiology, England. in Weekly Coronavirus Disease 2019 (COVID-19) Surveillance Report 2020 Week 28” (2020); https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/899301/Weekly_COVID19_Surveillance_Report_week_28.pdf.
Not checked in the free run.
- Interpretationown data
The infection is more widespread in Kenya than the current PCR test results suggest.
“they do strongly suggest that the infection is more widespread in Kenya than the current PCR test results suggest and indicate a need for more systematic testing.”
Quote in the paperSubstantial claim- Rests on an assumption: Kenyan hospitals were not overwhelmed by patients with respiratory distress.
- Rests on an assumption: The current PCR testing strategy in Kenya targets symptomatic individuals, health care workers, contacts of confirmed cases, international travelers, cross-border truck drivers, and residents of areas identified as hotspots.
- May combine two claims. 27
- Classified as probably not a substantial claim. 13
May combine two claims.
FindingcitationThe RBD and whole-spike ELISA responses were highly correlated, with very little interassay variation.
“As previously noted (15), the RBD and whole-spike ELISA responses were highly correlated (fig. S3C), with very little interassay variation (fig. S4).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [15] 15. Amanat F., Stadlbauer D., Strohmeier S., Nguyen T. H. O., Chromikova V., McMahon M., Jiang K., Arunkumar G. A., Jurczyszak D., Polanco J., Bermudez-Gonzalez M., Kleiner G., Aydillo T., Miorin L., Fierer D. S., Lugo L. A., Kojic E. M., Stoever J., Liu S. T. H., Cunningham-Rundles C., Felgner P. L., Moran T., García-Sastre A., Caplivski D., Cheng A. C., Kedzierska K., Vapalahti O., Hepojoki J. M., Simon V., Krammer F., A serological assay to detect SARS-CoV-2 seroconversion in humans. Nat. Med. 26, 1033–1036 (2020). 10.1038/s41591-020-0913-5 source
Not checked in the free run.
May combine two claims.
Findingown dataOf the 3098 samples, 174 were positive for anti-SARS-CoV-2 spike IgG, giving a crude seroprevalence of 5.6% (95% CI, 4.8 to 6.5%).
“Of the 3098 samples, 174 were positive for anti–SARS-CoV-2 spike IgG, giving a crude seroprevalence of 5.6% (95% CI, 4.8 to 6.5%).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataAt the OD ratio >2 threshold, the sensitivity was 92.7% (95% CI, 87.9 to 96.1%) and specificity was 99.0% (95% CI, 98.1 to 99.5%).
“The sensitivity and specificity, at this threshold, were 92.7% [95% confidence interval (CI), 87.9 to 96.1%] and 99.0% [95% CI, 98.1 to 99.5%], respectively”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe median sample date for VNRDs (14 June 2020) was 2 weeks later than that for FRDs (29 May 2020).
“The median sample date for VNRDs (14 June 2020) was 2 weeks later than that for FRDs (29 May 2020).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataSeroprevalence was higher (4.2 to 5.2%) in the younger age groups (15 to 44 years) and declined in the older age groups (45 to 64 years).
“Seroprevalence was higher (4.2 to 5.2%) in the younger age groups (15 to 44 years) and declined in the older age groups (45 to 64 years) but was similar for both sexes.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe three largest urban counties of Mombasa, Nairobi, and Kisumu had SARS-CoV-2 seroprevalence of 8.0% (95% CI, 5.5 to 11.1%), 7.3% (95% CI, 4.2 to 11.4%), and 5.5% (95% CI, 2.8 to 9.6%), respectively.
“The three largest urban counties of Mombasa, Nairobi, and Kisumu had SARS-CoV-2 seroprevalence of 8.0% (95% CI, 5.5 to 11.1%), 7.3% (95% CI, 4.2 to 11.4%), and 5.5% (95% CI, 2.8 to 9.6%), respectively (table S4).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataCompared with the 2019 Kenya Population and Housing Census, the study participants were more commonly male (82.0% vs 49.3%), had more persons aged 25 to 34 years (40.1% vs 27.3%), and more residents of coastal counties (49.2% vs 9.1%).
“Compared with the 2019 Kenya Population and Housing Census, our participants were more commonly male (82.0% in our study versus 49.3% in the census), had more persons aged 25 to 34 years (40.1 versus 27.3%), and more residents of coastal counties (49.2 versus 9.1%) (Table 2).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe VNRD and FRD groups did not differ significantly by age (P = 0.15) or sex (P = 0.51).
“The two groups did not differ significantly by age (P = 0.15) or sex (P = 0.51) (table S5).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe frequency of blood donor sampling and crude seroprevalence estimates increased with time over the 7-week study period.
“The frequency of blood donor sampling and crude seroprevalence estimates increased with time over the 7-week study period (Fig. 2).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataSeroprevalence was highest for those living in Mombasa, Nairobi, and the Western region, although the number of observations for the Western region was small.
“Seroprevalence was highest for those living in Mombasa, Nairobi, and the Western region, although the number of observations for the Western region was small.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe posterior sensitivity and specificity estimates were 92.4% (95% CI, 88.0 to 95.6%) and 98.9% (95% CI, 98.2 to 99.5%), respectively.
“the posterior sensitivity and specificity estimates were 92.4% (95% CI, 88.0 to 95.6%) and 98.9 (95% CI, 98.2 to 99.5%), respectively.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataVoluntary nonremunerated donors (VNRDs) made up 7.6% (236 of 3098) of the sample; the remainder were family replacement donors (FRDs).
“Voluntary nonremunerated donors (VNRDs), who donate blood at community-based “blood drives,” made up only 7.6% (236 of 3098) of our sample of donors; the remainder were family replacement donors (FRDs) who provide a unit of blood in compensation for a transfusion received by a sick relative.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataCrude seroprevalence was 8.5% (20 of 236) for VNRDs and 5.4% (154 of 2862) for FRDs.
“Crude seroprevalence was 8.5% (20 of 236) for VNRDs and 5.4% (154 of 2862) for FRDs.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSeveral countries have monitored seroprevalence in blood transfusion donors or expectant mothers attending antenatal clinics.
“Several countries have monitored seroprevalence in blood transfusion donors (12, 13) or expectant mothers attending antenatal clinics (14).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [12] 12. L. Valenti et al., SARS-CoV-2 seroprevalence trends in healthy blood donors during the COVID-19 Milan outbreak. medRxiv 2020.2005.2011.20098442 [Preprint] 31 May 2020. 10.1101/2020.05.11.20098442 source
Not checked in the free run.
- cites [13] 13. Amorim Filho L., Szwarcwald C. L., Mateos S. O. G., Leon A. C. M. P., Medronho R. A., Veloso V. G., Lopes J. I. F., Porto L. C. M. S., Chieppe A., Werneck G. L.; Grupo Hemorio de Pesquisa em Covid-19, Seroprevalence of anti–SARS-CoV-2 among blood donors in Rio de Janeiro, Brazil. Rev. Saude Publica 54, 69 (2020). 10.11606/s1518-8787.2020054002643 source
Not checked in the free run.
- cites [14] 14. Flannery D. D., Gouma S., Dhudasia M. B., Mukhopadhyay S., Pfeifer M. R., Woodford E. C., Gerber J. S., Arevalo C. P., Bolton M. J., Weirick M. E., Goodwin E. C., Anderson E. M., Greenplate A. R., Kim J., Han N., Pattekar A., Dougherty J., Kuthuru O., Mathew D., Baxter A. E., Vella L. A., Weaver J., Verma A., Leite R., Morris J. S., Rader D. J., Elovitz M. A., Wherry E. J., Puopolo K. M., Hensley S. E., SARS-CoV-2 seroprevalence among parturient women in Philadelphia. Sci. Immunol. 5, eabd5709 (2020). 10.1126/sciimmunol.abd5709 source
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Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAs the epidemic curve declined in Geneva, seroprevalence rose over 3 weeks from 4.8 to 10.9%.
“As the epidemic curve declined in Geneva, seroprevalence rose over 3 weeks from 4.8 to 10.9% (10).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] 10. Stringhini S., Wisniak A., Piumatti G., Azman A. S., Lauer S. A., Baysson H., De Ridder D., Petrovic D., Schrempft S., Marcus K., Yerly S., Arm Vernez I., Keiser O., Hurst S., Posfay-Barbe K. M., Trono D., Pittet D., Gétaz L., Chappuis F., Eckerle I., Vuilleumier N., Meyer B., Flahault A., Kaiser L., Guessous I., Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): A population-based study. Lancet 396, 313–319 (2020). 10.1016/S0140-6736(20)31304-0 source
Not checked in the free run.
Classified as probably not a substantial claim. May combine two claims.
Interpretationnone givenThe true extent of COVID-19 in the community was unknown and likely to be higher than reports indicated.
“The true extent of COVID-19 in the community was unknown and likely to be higher than reports indicated.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationThe disparity in COVID-19 burden between Africa and the rest of the world has been attributed to limited capacity for diagnosis, timely implementation of stringent containment measures, a younger population structure, and a predominance of asymptomatic and mild infections.
“This disparity has been attributed to limited capacity for diagnosis, timely implementation of stringent containment measures, a younger population structure, and a predominance of asymptomatic and mild infections (3, 4).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [3] 3. Diop B. Z., Ngom M., Pougué Biyong C., Pougué Biyong J. N., The relatively young and rural population may limit the spread and severity of COVID-19 in Africa: A modelling study. BMJ Glob. Health 5, e002699 (2020). 10.1136/bmjgh-2020-002699 source
Not checked in the free run.
- cites [4] 4. Dowd J. B., Andriano L., Brazel D. M., Rotondi V., Block P., Ding X., Liu Y., Mills M. C., Demographic science aids in understanding the spread and fatality rates of COVID-19. Proc. Natl. Acad. Sci. U.S.A. 117, 9696–9698 (2020). 10.1073/pnas.2004911117 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAt the end of the epidemic wave in Spain, seropositivity was 5.0% in a random population sample of 60,897.
“At the end of the epidemic wave in Spain, seropositivity was 5.0% in a random population sample of 60,897 (9).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [9] 9. Pollán M., Pérez-Gómez B., Pastor-Barriuso R., Oteo J., Hernán M. A., Pérez-Olmeda M., Sanmartín J. L., Fernández-García A., Cruz I., Fernández de Larrea N., Molina M., Rodríguez-Cabrera F., Martín M., Merino-Amador P., León Paniagua J., Muñoz-Montalvo J. F., Blanco F., Yotti R., ENE-COVID Study Group, Prevalence of SARS-CoV-2 in Spain (ENE-COVID): A nationwide, population-based seroepidemiological study. Lancet 396, 535–544 (2020). 10.1016/S0140-6736(20)31483-5 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBy 31 July 2020, national surveillance in Kenya recorded 20,636 cases and 341 deaths.
“By 31 July national surveillance recorded 20,636 cases and 341 deaths (6).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [6] 6. Ministry of Health Kenya, “COVID-19 Situation Reports (SITREP)” (2020); www.health.go.ke/#1591180376422-52af4c1e-256b.
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAt the release of lockdown in Wuhan, 9.6% of staff resuming work were found to have antibodies to SARS-CoV-2.
“For example, at the release of lockdown in Wuhan, 9.6% of staff resuming work were found to have antibodies to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (8).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] 8. Wu X., Fu B., Chen L., Feng Y., Serological tests facilitate identification of asymptomatic SARS-CoV-2 infection in Wuhan, China. J. Med. Virol. 92, 1795–1796 (2020). 10.1002/jmv.25904 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationAfrica accounts for 17% of the global population but by late July 2020 accounted for only 5% of global COVID-19 cases and 3% of global COVID-19 deaths reported.
“Africa accounts for 17% of the global population (1) but by late July 2020 accounted for only 5% of the global COVID-19 cases and 3% of global COVID-19 deaths reported (2).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] 1. United Nations Department of Economic and Social Affairs Population Division, “World Urbanization Prospects: The 2018 Revision,” custom data acquired via (2018); https://population.un.org/wup/DataQuery.
Not checked in the free run.
- cites [2] 2. Africa Centres for Diseases Control and Prevention, “Coronavirus Disease 2019 (COVID-19)” (2020); https://africacdc.org/covid-19[accessed 21 July 2020].
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataThe study did not adjust for sample date because the period of sampling varied for residents of different counties; instead, it shows the variation in crude prevalence over time.
“We did not adjust for sample date because the period of sampling varied for residents of different counties (Fig. 2C); instead, we show the variation in crude prevalence over time (Fig. 2A).”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningPeople who are shielding at home are unlikely to be captured in the sample, leading to an overestimate of seroprevalence.
“however, people who are shielding at home are unlikely to be captured in our sample, leading to an overestimate of seroprevalence.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataSeroprevalence did not vary significantly by sex, consistent with other studies.
“Consistent with other studies, seroprevalence did not vary significantly by sex (9, 10, 16); however, it peaked in 35- to 44-year-olds and was lowest for those ≥45 years, which is also consistent with existing reports in which seroprevalence was found to be lower in older adults (9, 10).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [9] 9. Pollán M., Pérez-Gómez B., Pastor-Barriuso R., Oteo J., Hernán M. A., Pérez-Olmeda M., Sanmartín J. L., Fernández-García A., Cruz I., Fernández de Larrea N., Molina M., Rodríguez-Cabrera F., Martín M., Merino-Amador P., León Paniagua J., Muñoz-Montalvo J. F., Blanco F., Yotti R., ENE-COVID Study Group, Prevalence of SARS-CoV-2 in Spain (ENE-COVID): A nationwide, population-based seroepidemiological study. Lancet 396, 535–544 (2020). 10.1016/S0140-6736(20)31483-5 source
Not checked in the free run.
- cites [10] 10. Stringhini S., Wisniak A., Piumatti G., Azman A. S., Lauer S. A., Baysson H., De Ridder D., Petrovic D., Schrempft S., Marcus K., Yerly S., Arm Vernez I., Keiser O., Hurst S., Posfay-Barbe K. M., Trono D., Pittet D., Gétaz L., Chappuis F., Eckerle I., Vuilleumier N., Meyer B., Flahault A., Kaiser L., Guessous I., Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): A population-based study. Lancet 396, 313–319 (2020). 10.1016/S0140-6736(20)31304-0 source
Not checked in the free run.
- cites [16] 16. Huang A. T., Garcia-Carreras B., Hitchings M. D. T., Yang B., Katzelnick L. C., Rattigan S. M., Borgert B. A., Moreno C. A., Solomon B. D., Trimmer-Smith L., Etienne V., Rodriguez-Barraquer I., Lessler J., Salje H., Burke D. S., Wesolowski A., Cummings D. A. T., A systematic review of antibody mediated immunity to coronaviruses: Kinetics, correlates of protection, and association with severity. Nat. Commun. 11, 4704 (2020). 10.1038/s41467-020-18450-4 source
Not checked in the free run.
May combine two claims.
Interpretationown dataPopulation exposure across Kenya, with a population-weighted test-adjusted seroprevalence of 4.3%, is considerably higher than was previously thought, on the basis of the cases and deaths reported to date.
“Population exposure across Kenya, with a population-weighted test-adjusted seroprevalence of 4.3%, is considerably higher than was previously thought, on the basis of the cases and deaths reported to date.”
Quote in the paperSubstantial claimMay combine two claims.
Study design and conductnone givenAlthough blood donors are not representative of the Kenyan population as a whole, the study adjusted for demographic bias in the sample structure by standardization against the age, sex, and regional distribution of the Kenyan population.
“Although blood donors are not representative of the Kenyan population as a whole, we adjusted for demographic bias in the sample structure by standardization against the age, sex, and regional distribution of the Kenyan population.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningPotential donors are excluded from giving blood if they have been ill during the past 6 months, so the sample may underestimate the population prevalence of SARS-CoV-2 antibodies.
“For example, potential donors are excluded from giving blood if they have been ill during the past 6 months, so the sample may underestimate the population prevalence of SARS-CoV-2 antibodies”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationA substantial proportion (43%) of the Kenyan population is outside the age range (15 to 64 years) sampled in this study, and the seroprevalence in children <15 years and adults >65 years is often lower; thus the blood donor estimate may be higher than the estimate for the population as a whole.
“A substantial proportion (43%) of the population of Kenya is outside the age range (15 to 64 years) sampled in this study, and the seroprevalence in children <15 years and adults >65 years is often lower (9, 10); our estimate for blood donors may be higher than the estimate for the population as a whole.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [9] 9. Pollán M., Pérez-Gómez B., Pastor-Barriuso R., Oteo J., Hernán M. A., Pérez-Olmeda M., Sanmartín J. L., Fernández-García A., Cruz I., Fernández de Larrea N., Molina M., Rodríguez-Cabrera F., Martín M., Merino-Amador P., León Paniagua J., Muñoz-Montalvo J. F., Blanco F., Yotti R., ENE-COVID Study Group, Prevalence of SARS-CoV-2 in Spain (ENE-COVID): A nationwide, population-based seroepidemiological study. Lancet 396, 535–544 (2020). 10.1016/S0140-6736(20)31483-5 source
Not checked in the free run.
- cites [10] 10. Stringhini S., Wisniak A., Piumatti G., Azman A. S., Lauer S. A., Baysson H., De Ridder D., Petrovic D., Schrempft S., Marcus K., Yerly S., Arm Vernez I., Keiser O., Hurst S., Posfay-Barbe K. M., Trono D., Pittet D., Gétaz L., Chappuis F., Eckerle I., Vuilleumier N., Meyer B., Flahault A., Kaiser L., Guessous I., Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): A population-based study. Lancet 396, 313–319 (2020). 10.1016/S0140-6736(20)31304-0 source
Not checked in the free run.
May combine two claims.
Study design and conductreasoningThe study adjusted the prevalence estimate for the demographics of the sample using poststratification, and for the sensitivity and specificity of the test.
“We therefore adjusted the prevalence estimate for the demographics of the sample using poststratification, and for the sensitivity and specificity of the test.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim. May combine two claims.
PremisecitationBy the median sample date, 30 May 2020, only 2093 cases had been detected (of which approximately 90% were asymptomatic), and there were 71 deaths among all ages.
“However, by the median sample date, 30 May 2020, only 2093 cases had been detected (of which approximately 90% were asymptomatic), and there were 71 deaths among all ages (6).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [6] 6. Ministry of Health Kenya, “COVID-19 Situation Reports (SITREP)” (2020); www.health.go.ke/#1591180376422-52af4c1e-256b.
Not checked in the free run.
May combine two claims.
InterpretationcitationThe 4.3% prevalence in blood transfusion donors is in sharp contrast with the reported COVID-19 cases and deaths and supports the impression that disease may be attenuated in Africa.
“The 4.3% prevalence in blood transfusion donors is in sharp contrast with the reported COVID-19 cases and deaths and supports the impression that disease may be attenuated in Africa (7).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [7] 7. Mbow M., Lell B., Jochems S. P., Cisse B., Mboup S., Dewals B. G., Jaye A., Dieye A., Yazdanbakhsh M., COVID-19 in Africa: Dampening the storm? Science 369, 624–626 (2020). 10.1126/science.abd3902 source
Not checked in the free run.
- Rests on an assumption: Kenyan hospitals were not overwhelmed by patients with respiratory distress.
Classified as probably not a substantial claim.
Study design and conductnone givenThe study adopted a conservative seropositivity threshold to optimize assay specificity and sensitivity for the setting.
“In addition, we adopted a conservative seropositivity threshold to optimize assay specificity and sensitivity for our setting.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationSeroprevalence peaked in 35- to 44-year-olds and was lowest for those ≥45 years, consistent with existing reports of lower seroprevalence in older adults.
“it peaked in 35- to 44-year-olds and was lowest for those ≥45 years, which is also consistent with existing reports in which seroprevalence was found to be lower in older adults (9, 10).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [9] 9. Pollán M., Pérez-Gómez B., Pastor-Barriuso R., Oteo J., Hernán M. A., Pérez-Olmeda M., Sanmartín J. L., Fernández-García A., Cruz I., Fernández de Larrea N., Molina M., Rodríguez-Cabrera F., Martín M., Merino-Amador P., León Paniagua J., Muñoz-Montalvo J. F., Blanco F., Yotti R., ENE-COVID Study Group, Prevalence of SARS-CoV-2 in Spain (ENE-COVID): A nationwide, population-based seroepidemiological study. Lancet 396, 535–544 (2020). 10.1016/S0140-6736(20)31483-5 source
Not checked in the free run.
- cites [10] 10. Stringhini S., Wisniak A., Piumatti G., Azman A. S., Lauer S. A., Baysson H., De Ridder D., Petrovic D., Schrempft S., Marcus K., Yerly S., Arm Vernez I., Keiser O., Hurst S., Posfay-Barbe K. M., Trono D., Pittet D., Gétaz L., Chappuis F., Eckerle I., Vuilleumier N., Meyer B., Flahault A., Kaiser L., Guessous I., Seroprevalence of anti–SARS-CoV-2 IgG antibodies in Geneva, Switzerland (SEROCoV-POP): A population-based study. Lancet 396, 313–319 (2020). 10.1016/S0140-6736(20)31304-0 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenA key strength of this study is the rigorous validation that included testing positive and negative control samples from the target population, as well as reference plasma from the UK NIBSC as part of a WHO-coordinated effort on SARS-CoV-2 seroepidemiology.
“A key strength of this study is the rigorous validation that included testing positive and negative control samples from the target population, as well as reference plasma from the UK NIBSC as part of a World Health Organization (WHO)–coordinated effort on SARS-CoV-2 seroepidemiology.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationOther countries have relied on blood transfusion donors for an early estimate of seroprevalence, but later estimates from random population samples have not been substantially different.
“Against these considerations, other countries have relied on blood transfusion donors for an early estimate of seroprevalence, but later estimates from random population samples have not been substantially different (25, 26).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [25] 25. H. Ward et al., Antibody prevalence for SARS-CoV-2 following the peak of the pandemic in England: REACT2 study in 100,000 adults. medRxiv 2020.2008.2012.20173690v20173692 [Preprint] 21 August 2020. 10.1101/2020.08.12.20173690
Not checked in the free run.
- cites [26] 26. Public Health England, National COVID-19 surveillance report week 40 (2020); https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/923668/Weekly_COVID19_Surveillance_Report_week_40.pdf.
Not checked in the free run.
The paper relies on this without support.
Movement restrictions in response to COVID-19 limited the conduct of fieldwork for population-based serosurveys.
“Movement restrictions, in response to COVID-19, have limited the conduct of fieldwork for population-based serosurveys.”
The paper relies on this without support.
Kenyan hospitals were not overwhelmed by patients with respiratory distress.
“These circumstances combine to result in Kenyan hospitals not currently being overwhelmed by patients with respiratory distress.”
“hospitals in Kenya were not overwhelmed by admissions with respiratory illness.”
The paper relies on this without support.
The increase in COVID-19 cases in Kenya is notably slower than the epidemic in Wuhan, Europe, or the United States.
“This increase in cases is notably slower than the epidemic in Wuhan, Europe, or the United States.”
The paper relies on this without support.
The current PCR testing strategy in Kenya targets symptomatic individuals, health care workers, contacts of confirmed cases, international travelers, cross-border truck drivers, and residents of areas identified as hotspots.
“The current PCR testing strategy targets symptomatic individuals, health care workers, contacts of confirmed cases, international travelers, cross-border truck drivers, and residents of areas identified as “hotspots.””
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Reliance on healthy blood donors and voluntary child participants did not result in a material underestimate of COVID-19 seroprevalence in the general population.
“These independent estimates provide confidence that our reliance on healthy blood donors and voluntary child participants did not result in a material underestimate of COVID-19 seroprevalence in the general population.”
From Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population (2023) · cites this paper as [49]
The passage on sample representativeness (indexed under Abstract; page unavailable) says that random-population estimates in other countries were not substantially different from blood-donor estimates. It also says Kenyan donors may underestimate or overestimate population seroprevalence. The paper did not study voluntary child participants, so it does not establish the sentence’s conclusion for both participant groups. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rift Valley crude seroprevalence differs from Table 1
MinorThe text gives Rift Valley's crude seroprevalence as 1.9%, but Table 1 reports 1.7% (8 positives among 481 samples).
“from 1.9% in the Rift Valley region to 10.0% in the Western region”
“| Rift Valley | 481 | 8 | 1.7 | 0.7 to 3.3 |”
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BackgroundDemographic science aids in understanding the spread and fatality rates of COVID-19
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“Our results are also comparable with those of other surveys of blood donors in Brazil (13), Italy (12), andmany parts of England (19).”
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Pre-existing and de novo humoral immunity to SARS-CoV-2 in humansPreprint
Ng, K. W., Faulkner, N., Cornish, G. H., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.14.095414 · Cited by 85 · see citing works
Humoral Response Dynamics Following Infection with SARS-CoV-2Preprint
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SARS-CoV-2 Seroprevalence Among Parturient Women
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Replication Data for: Seroprevalence of anti-SARS-CoV-2 IgG antibodies in Kenyan blood donors
Uyoga, S. M., Adetifa, I., Karanja, H., et al. (2020) · Harvard Dataverse · doi:10.7910/dvn/renvc9
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- Ministry of Health Kenya “Press Statement on the update of the coronavirus in the country and response measures” (2020); www.health.go.ke/wp-content/uploads/2020/03/Coronavirus-Press-Statement-March-17-2020.pdf.
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Infection fatality rate of COVID-19 inferred from seroprevalence data
Ioannidis, J. P. A. (2021) · Bulletin of the World Health Organization · doi:10.2471/blt.20.265892 · Cited by 684 · see citing works
Buss, L. F., Prete, C. A., Abrahim, C. M. M., Mendrone, A., Salomon, T., de Almeida-Neto, C., França, R. F. O., Belotti, M. C., Carvalho, M. P. S. S., Costa, A. G., et al. (2021) · Science · doi:10.1126/science.abe9728 · Cited by 488 · see citing works
Looking beyond COVID-19 vaccine phase 3 trials
Kim, J. H., Marks, F., & Clemens, J. D. (2021) · Nature Medicine · doi:10.1038/s41591-021-01230-y · Cited by 586 · see citing works
Serological evidence of human infection with SARS-CoV-2: a systematic review and meta-analysis
Chen, X., Chen, Z., Azman, A. S., Deng, X., Sun, R., Zhao, Z., Zheng, N., Chen, X., Lu, W., Zhuang, T., et al. (2021) · The Lancet Global Health · doi:10.1016/s2214-109x(21)00026-7 · Cited by 239 · see citing works
Lau, J. J., Cheng, S. M. S., Leung, K., Lee, C. K., Hachim, A., Tsang, L. C. H., Yam, K. W. H., Chaothai, S., Kwan, K. K. H., Chai, Z. Y. H., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02219-5 · Cited by 198 · see citing works
A year of genomic surveillance reveals how the SARS-CoV-2 pandemic unfolded in Africa
Wilkinson, E., Giovanetti, M., Tegally, H., San, J. E., Lessells, R. J., Cuadros, D. F., Martin, D. P., Rasmussen, D. A., Zekri, A. N., Sangaré, A. K., et al. (2021) · Science · doi:10.1126/science.abj4336 · Cited by 213 · see citing works
“and deaths may be several fold higher than reported (3, 4).”
BackgroundOn the Effect of Age on the Transmission of SARS-CoV-2 in Households, Schools, and the Community
Goldstein, E., Lipsitch, M., & Çevik, M. (2020) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaa691 · Cited by 355 · see citing works
Mulenga, L. B., Hines, J. Z., Fwoloshi, S., Chirwa, L., Siwingwa, M., Yingst, S., Wolkon, A., Barradas, D. T., Favaloro, J., Zulu, J. E., et al. (2021) · The Lancet Global Health · doi:10.1016/s2214-109x(21)00053-x · Cited by 149 · see citing works
Point-of-care COVID-19 diagnostics powered by lateral flow assay
Zhou, Y., Wu, Y., Ding, L., Huang, X., & Xiong, Y. (2021) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2021.116452 · Cited by 182 · see citing works
Acheampong, T., Akorsikumah, E. A., Osae-Kwapong, J., Khalid, M., Appiah, A., & Amuasi, J. (2021) · Vaccines · doi:10.3390/vaccines9080814 · Cited by 141 · see citing works
“3% population-weighted and test performance-adjusted national seroprevalence rate [86].”
BackgroundThe puzzle of the COVID-19 pandemic in Africa
Maeda, J. M., & Nkengasong, J. N. (2020) · Science · doi:10.1126/science.abf8832 · Cited by 135 · see citing works
Artemisia annua L. extracts inhibit the in vitro replication of SARS-CoV-2 and two of its variants
Nair, M. S., Huang, Y., Fidock, D. A., Polyak, S. J., Wagoner, J., Towler, M. J., & Weathers, P. J. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114016 · Cited by 122 · see citing works
The Conundrum of Low COVID-19 Mortality Burden in sub-Saharan Africa: Myth or Reality?
Adams, J. A., MacKenzie, M. J., Amegah, A. K., Ezeh, A., Gadanya, M. A., Omigbodun, A. O., Sarki, A. M., Thistle, P., Ziraba, A. K., Stranges, S., et al. (2021) · Global Health Science and Practice · doi:10.9745/ghsp-d-21-00172 · Cited by 150 · see citing works
“Furthermore, a recent study by Uyoga et al.62 observed increased rates of antibody prevalence to SARS-CoV-2 among Kenyan blood donors between April 30–June 16, 2020, that are higher than case counts would predict.”
BackgroundArtemisia annua L. extracts inhibit the in vitro replication of SARS-CoV-2 and two of its variantsPreprint
Nair, M. S., Huang, Y., Fidock, D. A., Polyak, S. J., Wagoner, J., Towler, M. J., & Weathers, P. J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.08.425825 · Cited by 8 · see citing works
Ioannidis, J. P. A. (2021) · European Journal of Clinical Investigation · doi:10.1111/eci.13554 · Cited by 116 · see citing works
The COVID-19 pandemic in the African continent
Bwire, G., Ario, A. R., Eyu, P., Ocom, F., Wamala, J. F., Kusi, K. A., Ndeketa, L., Jambo, K., Wanyenze, R. K., & Talisuna, A. O. (2022) · BMC Medicine · doi:10.1186/s12916-022-02367-4 · Cited by 123 · see citing works
Variation in SARS-CoV-2 outbreaks across sub-Saharan Africa
Rice, B. L., Annapragada, A. V., Baker, R. E., Bruijning, M., Dotse‐Gborgbortsi, W., Mensah, K., Miller, I. F., Motaze, N. V., Raherinandrasana, A. H., Rajeev, M., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01234-8 · Cited by 101 · see citing works
Kleynhans, J., Tempia, S., Wolter, N., von Gottberg, A., Bhiman, J. N., Buys, A., Moyes, J., McMorrow, M. L., Kahn, K., Gómez-Olivé, F. X., et al. (2021) · Emerging Infectious Diseases · doi:10.3201/eid2712.211465 · Cited by 97 · see citing works
“In Kenya, the seroprevalence in blood donors during the country’s first wave of infections was 4% and was also higher in urban communities (17).”
BackgroundIndirect health effects of the COVID-19 pandemic in Kenya: a mixed methods assessment
(2021) · doi:10.1186/s12913-021-06726-4 · Cited by 85
“According to official case data, and model predictions that incorporate both case data and serology surveys [3], the country has had three waves of the pandemic, with the first peaking in July/August 2020, the second peaking in October/November 2020, and the third one peaking in March/April 2021.”
MethodCOVID-19 transmission dynamics underlying epidemic waves in Kenya
Brand, S. P. C., Ojal, J., Aziza, R., Were, V. O., Okiro, E. A., Kombe, I. K., Mburu, C., Ogero, M. O., Agweyu, A., Warimwe, G. M., et al. (2021) · Science · doi:10.1126/science.abk0414 · Cited by 83 · see citing works
The European Medicines Agency's EU conditional marketing authorisations for COVID-19 vaccines
Cavaleri, M., Enzmann, H., Straus, S., & Cooke, E. (2021) · The Lancet · doi:10.1016/s0140-6736(21)00085-4 · Cited by 98 · see citing works
Development and deployment of COVID-19 vaccines for those most vulnerable
Koff, W. C., Schenkelberg, T., Williams, T. M., Baric, R. S., McDermott, A. B., Cameron, C., Cameron, M. J., Frieman, M. B., Neumann, G., Kawaoka, Y., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abd1525 · Cited by 78 · see citing works
“The current low level of COVID-19 cases in some LMICs is likely masked by low surveillance capacity (27).”
BackgroundWamai, R. G., Hirsch, J. L., Damme, W. V., Alnwick, D. J., Bailey, R. C., Hodgins, S., Alam, U., & Anyona, R. M. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18168638 · Cited by 107 · see citing works
“5% nationally [17] and 60% among South African black populations, seven times that of in-country white populations [18].”
BackgroundSeroprevalence of anti‐SARS‐CoV‐2 antibodies in Africa: A systematic review and meta‐analysis
Chisale, M., Ramazanu, S., Mwale, S. E., Kumwenda, P., Chipeta, M. C., Kaminga, A. C., Nkhata, O., Nyambalo, B. W., Chavura, E., & Mbakaya, B. C. (2021) · Reviews in Medical Virology · doi:10.1002/rmv.2271 · Cited by 81 · see citing works
“High anti‐SARS‐CoV‐2 antibody seroprevalence was reported among those aged 50 years or less.(17,22,26,27,30,33,36,39) Five of these studies(17,20,27,30,39) showed high anti‐SARS‐CoV‐2 antibody seroprevalence among participants with ages between 30 and 50 years.”
BackgroundResultMasood, K., Yameen, M., Ashraf, J., Shahid, S., Mahmood, S., Nasir, A., Nasir, N., Jamil, B., Ghanchi, N., Khanum, I., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-02489-4 · Cited by 71 · see citing works
Musa, H. H., Musa, T. H., Musa, I. H., Musa, I. H., Ranciaro, A., & Campbell, M. C. (2020) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2020.09.1456 · Cited by 87 · see citing works
The coronavirus pandemic and food security: Evidence from Mali
Adjognon, G. S., Bloem, J. R., & Sanoh, A. (2021) · Food Policy · doi:10.1016/j.foodpol.2021.102050 · Cited by 68 · see citing works
“…3,000 blood donors in Kenya find that one in 20 Kenyans aged 15–64, representing roughly 1.6 million people, have antibodies to the COVID-19 virus (Uyoga et al., 2020).11 If this estimate is correct, then the spread of the virus in Kenya is roughly equivalent to Spain in midMay 2020 which had…”
InfluentialChallenges in interpreting SARS-CoV-2 serological results in African countries
Nkuba-Ndaye, A., Hoxha, A., Madinga, J. N., Mariën, J., Peeters, M., Leendertz, F. H., Mundeke, S. A., Ariën, K. K., Tanfumu, J.-J. M., Kingebeni, P. M., et al. (2021) · The Lancet Global Health · doi:10.1016/s2214-109x(21)00060-7 · Cited by 55 · see citing works
Mandolo, J., Msefula, J., Henrion, M. Y. R., Brown, C., Moyo, B., Samon, A., Moyo-Gwete, T., Makhado, Z., Ayres, F., Motlou, T., et al. (2021) · BMC Medicine · doi:10.1186/s12916-021-02187-y · Cited by 61 · see citing works
COVID-19 surveillance systems in 13 African countries
Adebisi, Y. A., Rabe, A. P. J., & Lucero‐Prisno, D. E. (2021) · Health Promotion Perspectives · doi:10.34172/hpp.2021.49 · Cited by 76 · see citing works
Nkuba, A. N., Makiala, S. M., Guichet, E., Tshiminyi, P. M., Bazitama, Y. M., Yambayamba, M. K., Kazenza, B. M., Kabeya, T. M., Matungulu, E. B., Baketana, L. K., et al. (2022) · Clinical Infectious Diseases · doi:10.1093/cid/ciab515 · Cited by 51 · see citing works
“This variability could be explained, first, by the fact that most of these studies were carried out in specific populations and, second, apart from the Malawi study, all the other studies reported a seroprevalence using positivity against a single antigen (SP or NC).”
Shaw, J. A., Meiring, M., Cummins, T., Chegou, N. N., Claassen, C., du Plessis, N., Flinn, M., Hiemstra, A. M., Kleynhans, L., Leukes, V., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0247852 · Cited by 64 · see citing works
SARS-CoV-2 Antibody Seroprevalence and Associated Risk Factors in an Urban District in Cameroon
Nwosu, K. O. S., Fokam, J., Wanda, F., Mama, L., Orel, E., Ray, N., Meke, J., Tassegning, A., Takou, D., Mimbe, E., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25946-0 · Cited by 59 · see citing works
Seroprevalence surveys in sub-Saharan Africa: what do they tell us?
Usuf, E., & Roca, A. (2021) · The Lancet Global Health · doi:10.1016/s2214-109x(21)00092-9 · Cited by 43 · see citing works
Temporal trends of SARS-CoV-2 seroprevalence during the first wave of the COVID-19 epidemic in Kenya
Adetifa, I. M. O., Uyoga, S., Gitonga, J. N., Mugo, D., Otiende, M., Nyagwange, J., Karanja, H. K., Tuju, J., Wanjiku, P., Aman, R., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24062-3 · Cited by 67 · see citing works
“3,5 .”
Snyman, J., Hwa, S.-H., Krause, R. G. E., Muema, D., Reddy, T., Ganga, Y., Karim, F., Leslie, A. J., Sigal, A., Ndung’u, T., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab758 · Cited by 43 · see citing works
“Antibodies are also important diagnostic and surveillance tools [18, 19] and understanding whether there are differences in responses between PLWH and the HIV uninfected population may have implications for the development of diagnostic and surveillance algorithms particularly in regions with high HIV burden.”
Etyang, A. O., Lucinde, R. K., Karanja, H., Kalu, C., Mugo, D., Nyagwange, J., Gitonga, J. N., Tuju, J., Wanjiku, P., Karani, A., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab346 · Cited by 42 · see citing works
Barrie, M. B., Lakoh, S., Kelly, J. D., Kanu, J. S., Squire, J. S., Koroma, Z., Bah, S., Sankoh, O. A., Brima, A. S., Ansumana, R., et al. (2021) · BMJ Global Health · doi:10.1136/bmjgh-2021-007271 · Cited by 59 · see citing works
Ngere, I., Dawa, J., Hunsperger, E., Otieno, N. A., Masika, M., Amoth, P., Makayotto, L., Nasimiyu, C., Gunn, B. M., Nyawanda, B. O., et al. (2021) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2021.08.062 · Cited by 57 · see citing works
Examining unit costs for COVID-19 case management in Kenya
Barasa, E., Kairu, A., Ng’ang’a, W., Maritim, M. C., Were, V. O., Akech, S., & Mwangangi, M. (2021) · BMJ Global Health · doi:10.1136/bmjgh-2020-004159 · Cited by 58 · see citing works
Seroepidemiological study of SARS-CoV-2 infection in East Java, Indonesia
(2021) · doi:10.1371/journal.pone.0251234 · Cited by 43
“, healthcare workers [12–14], blood donors [15, 16], or dialysis patients [17, 18].”
BackgroundCOVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy
Novelli, G., Biancolella, M., Mehrian-Shai, R., Colona, V., Brito, A., Grubaugh, N., Vasiliou, V., Luzzatto, L., & Reichardt, J. (2021) · Human Genomics · doi:10.1186/s40246-021-00326-3 · Cited by 42 · see citing works
“Third, a significant fraction of people (perhaps up to 30%) [64] may have antibodies against other corona viruses that cross-react with SARS-CoV2 (even though only 2-8% have specific anti-SARSCoV2 antibodies suggesting there may be, like in Europe, a large number of asymptomatic infections) [65].”
BackgroundCherrie, M. P. C., Clemens, T. L., Colandrea, C., Feng, Z., Webb, D. J., Dibben, C. J. L., & Weller, R. (2021) · British Journal of Dermatology · doi:10.1111/bjd.20093 · Cited by 53 · see citing works
Tracking the introduction and spread of SARS-CoV-2 in coastal Kenya
Githinji, G., de Laurent, Z. R., Mohammed, K. S., Omuoyo, D. O., Macharia, P. M., Morobe, J. M., Otieno, E. G., Kinyanjui, S., Agweyu, A., Maitha, E. K., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25137-x · Cited by 40 · see citing works
SARS-CoV-2 antibody prevalence in health care workers: Preliminary report of a single center study
Brant-Zawadzki, M. N., Fridman, D., Robinson, P. A., Zahn, M., Chau, C., German, R., Breit, M., Bock, J. R., & Hara, J. (2020) · PLoS ONE · doi:10.1371/journal.pone.0240006 · Cited by 43 · see citing works
COVID-19 spread, detection, and dynamics in Bogota, Colombia
Laajaj, R., De Los Rios, C., Sarmiento-Barbieri, I., Aristizabal, D., Behrentz, E., Bernal, R., Buitrago, G., Cucunubá, Z., de la Hoz, F., Gaviria, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25038-z · Cited by 38 · see citing works
Seroprevalence of Severe Acute Respiratory Syndrome Coronavirus 2 IgG in Juba, South Sudan, 20201
Wiens, K. E., Mawien, P. N., Rumunu, J. P., Slater, D., Jones, F. K., Moheed, S., Caflisch, A. C., Bior, B. K., Jacob, I. A., Lako, R. L. L., et al. (2021) · Emerging infectious diseases · doi:10.3201/eid2706.210568 · Cited by 74 · see citing works
“3% in blood donors in Kenya in June 2020 (7), increasing to 9.”
BackgroundSaalim, K., Sakyi, K. S., Fatema-Tuz-Zohra, Morrison, E., Owusu, P. G., Dalglish, S. L., & Kanyangarara, M. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252890 · Cited by 47 · see citing works
“The relatively lower spread and severity of the disease in Africa have been presumably attributed to the relatively younger population with lower rates of chronic disease [3], limited testing and surveillance capacities resulting in an underestimation of the true burden of the coronavirus [4], milder symptoms in these…”
Backgrounddu Bruyn, E., Stek, C., Daroowala, R., Said-Hartley, Q., Hsiao, M., Schafer, G., Goliath, R., Abrahams, F., Jackson, A., Wasserman, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-022-35689-1 · Cited by 36 · see citing works
Epidemiological impact and cost-effectiveness analysis of COVID-19 vaccination in Kenya
Orangi, S., Ojal, J., Brand, S. P. C., Orlendo, C., Kairu, A., Aziza, R., Ogero, M. O., Agweyu, A., Warimwe, G. M., Uyoga, S. M., et al. (2022) · BMJ Global Health · doi:10.1136/bmjgh-2022-009430 · Cited by 38 · see citing works
Seroprevalence of anti-SARS-CoV-2 IgG antibodies in Juba, South Sudan: a population-based study
(2021) · doi:10.1101/2021.03.08.21253009 · Cited by 33
“Seroprevalence was lower at 4.3% (2.9 - 5.8) in blood donors in Kenya in June [7], increasing to 9.1% (7.6 - 10.8) by September [17].”
InfluentialMutevedzi, P. C., Kawonga, M., Kwatra, G., Moultrie, A., Baillie, V. L., Mabena, N., Mathibe, M. N., Rafuma, M. M., Maposa, I., Abbott, G., et al. (2021) · International Journal of Epidemiology · doi:10.1093/ije/dyab217 · Cited by 46 · see citing works
“25,26 The mortality risk in our study varied by 2.39-fold when calculated using reported COVID-19 deaths (0.28”
InfluentialAbdella, S., Riou, S., Tessema, M., Assefa, A., Seifu, A., Blachman, A., Abera, A., Moreno, N., Irarrazaval, F., Tollera, G., et al. (2021) · EClinicalMedicine · doi:10.1016/j.eclinm.2021.100880 · Cited by 35 · see citing works
“While one study has recently reported important seroprevalence estimates for Kenya, these were based on a population of volunteer blood donors [20].”
ResultWambua, S., Malla, L., Mbevi, G., Nwosu, A.-P., Tuti, T., Paton, C., Cheburet, S., Manya, A. S., English, M., & Okiro, E. A. (2021) · PLOS Global Public Health · doi:10.1371/journal.pgph.0000029 · Cited by 36 · see citing works
“This wave peaked in July/August 2020, and cases started to drop gradually [2].”
BackgroundSARS-CoV-2 Infection in Ivory Coast: A Serosurveillance Survey among Gold Mine Workers
Milleliri, J., Coulibaly, D., Nyobe, B., Rey, J., Lamontagne, F., Hocqueloux, L., Giachè, S., Valéry, A., & Prazuck, T. (2021) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.21-0081 · Cited by 28 · see citing works
“1%).(7) In two small populations of household contacts and healthcare workers in Nigeria, seroprevalence rates were to 25.”
BackgroundThe Heterogeneous Severity of COVID-19 in African Countries: A Modeling Approach
Musa, S. S., Wang, X., Zhao, S., Li, S., Hussaini, N., Wang, W., & He, D. (2022) · Bulletin of Mathematical Biology · doi:10.1007/s11538-022-00992-x · Cited by 32 · see citing works
“In particular, Uyoga et al. (2021) examined the seroprevalence of anti-SARS-CoV-2 immunoglobulin G antibodies among Kenyan blood donors to determine the extent to which COVID-19 spread in the community.”
BackgroundResultInfluentialWambua, S., Malla, L., Mbevi, G., Kandiah, J., Nwosu, A.-P., Tuti, T., Paton, C., Wambu, B., English, M., & Okiro, E. A. (2022) · BMJ Open · doi:10.1136/bmjopen-2021-055815 · Cited by 36 · see citing works
Antibody response and therapy in COVID-19 patients: what can be learned for vaccine development?
Lu, L., Zhang, H., Zhan, M., Jiang, J., Yin, H., Dauphars, D. J., Li, S.-Y., Li, Y., & He, Y.-W. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1859-y · Cited by 40 · see citing works
“6% (174/ 3,098) of blood donors had anti-SARS-CoV-2 IgG (Uyoga et al., 2020).”
BackgroundInfluentialLongitudinal Serology of SARS-CoV-2-Infected Individuals in India: A Prospective Cohort Study
Thiruvengadam, R., Chattopadhyay, S., Mehdi, F., Desiraju, B. K., Chaudhuri, S., Singh, S., Bhartia, V., Kshetrapal, P., Natchu, U. C. M., Wadhwa, N., et al. (2021) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.21-0164 · Cited by 19 · see citing works
“Results of seroprevalence studies performed in India and other South Asian countriesmay need to be adjusted after considering our findings.(18,19) The S/Co ratio for both assays reached the maxima between 15 and 28 days and plateaued, suggesting a stable IgG response during up to 10weeks of illness.”
BackgroundSeroprevalence of SARS-CoV-2 Antibodies in Africa: A Systematic Review and Meta-Analysis
Hajissa, K., Islam, M. A., Hassan, S. A., Zaidah, A. R., Ismail, N., & Mohamed, Z. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19127257 · Cited by 28 · see citing works
“Uyoga 2021 [51] Kenya April to June 2020 3098 Blood donors Blood transfusion centre ELISA IgG”
BackgroundKalungi, A., Kinyanda, E., Akena, D. H., Kaleebu, P., & Bisangwa, I. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.565625 · Cited by 40 · see citing works
“(9) has reported a SARS-CoV-2 seroprevalence of 5.”
BackgroundPedersen, J., Koumakpayi, I. H., Babuadze, G. G., Baz, M., Ndiaye, O., Faye, O., Diagne, C. T., Dia, N., Naghibosadat, M., McGeer, A., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-17241-9 · Cited by 30 · see citing works
(2021) · doi:10.1101/2021.04.26.21256016 · Cited by 24
“1% in households in Zambia in July, and up to 60% in blood donors in parts of South Africa in January 2021 [10-12].”
Attributed causes of excess mortality during the COVID-19 pandemic in a south Indian city
Lewnard, J. A., B, C. M., Kang, G., & Laxminarayan, R. (2023) · Nature Communications · doi:10.1038/s41467-023-39322-7 · Cited by 23 · see citing works
Etyang, A. O., Adetifa, I., Omore, R., Misore, T., Ziraba, A. K., Ng’oda, M., Gitau, E., Gitonga, J. N., Mugo, D., Kutima, B., et al. (2022) · PLOS Global Public Health · doi:10.1371/journal.pgph.0000883 · Cited by 28 · see citing works
“Validation of the assay was described previously [6].”
BackgroundMethodSARS-CoV-2 Seroprevalence in Tamil Nadu in October-November 2020Preprint
Malani, A., Ramachandran, S., Tandel, V., Parasa, R., Imad, S., Sudharshini, S., Prakash, V., Yogananth, Y., Raju, S., & Selvavinayagam, T. S. (2021) · medRxiv · doi:10.1101/2021.02.03.21250949 · Cited by 20 · see citing works
COVID-19 and beyond: Use of digital technology for pandemic response in Africa
Maharana, A., Amutorine, M., Sengeh, D. M., & Nsoesie, E. O. (2021) · Scientific African · doi:10.1016/j.sciaf.2021.e01041 · Cited by 28 · see citing works
“Seroprevalence surveys conducted in Kenya, Zambia and Mozambique reported rates higher than recorded infections at the time of the studies [ 2 , 4–6 ].”
(2021) · doi:10.1101/2021.03.02.21252448 · Cited by 22
“…blood donors (Sughayer et al., 2020, Slot et al., 2020, Nesbitt et al., 2021, Gallian et al., 2020, Olariu et al., 2021, Younas et al., 2020, Banjar et al., 2021, Uyoga et al., 2021, Busch and Stone, 2021, Martinez-Acuña et al., 2020, Saeed et al., 2021, Slot et al., 2020, Fiore et al., 2021).”
Sero-surveillance for IgG to SARS-CoV-2 at antenatal care clinics in two Kenyan referral hospitalsPreprint
Lucinde, R. K., Mugo, D., Bottomley, C., Aziza, R., Gitonga, J. N., Karanja, H., Nyagwange, J., Tuju, J., Wanjiku, P., Nzomo, E., et al. (2021) · medRxiv · doi:10.1101/2021.02.05.21250735 · Cited by 18 · see citing works
Schoenhals, M. J., Rabenindrina, N., Rakotondramanga, J. M., Dussart, P., Randremanana, R. V., Héraud, J., Andriamandimby, S. F., Sahondranirina, P. H., Vololoniaina, M. C., Randriatsarafara, F. M., et al. (2021) · EBioMedicine · doi:10.1016/j.ebiom.2021.103419 · Cited by 35 · see citing works
“We used vague or weakly informative priors for all parameters [4,10].”
Batchi-Bouyou, A. L., Ingoba, L. L., Ndounga, M., Vouvoungui, J. C., Mapanguy, C. C. M., Boumpoutou, R. K., & Ntoumi, F. (2020) · International Journal of Infectious Diseases · doi:10.1016/j.ijid.2020.12.065 · Cited by 25 · see citing works
Sagara, I., Woodford, J., Koné, M., Assadou, M. H., Katilé, A., Attaher, O., Zéguimé, A., Doucoure, M., Higbee, E., Lane, J., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab589 · Cited by 41 · see citing works
Nyagwange, J., Kutima, B., Mwai, K., Karanja, H., Gitonga, J. N., Mugo, D., Uyoga, S. M., Tuju, J., Ochola‐Oyier, L. I., Ndungu, F. M., et al. (2021) · Journal of Clinical Virology · doi:10.1016/j.jcv.2021.105061 · Cited by 24 · see citing works
“We have since used the KWTRP ELISA to estimate SARS-CoV-2 seroprevalence in several target groups [3 – 5].”
SARS CoV-2 Seroprevalence in Selected States of High and Low Disease Burden in Nigeria
Kolawole, O. M., Tomori, O., Agbonlahor, D. E., Ekanem, E., Bakare, R. A., Abdulsalam, N., Okojie, O. H., Braide, E. I., Uzochukwu, B. S. C., Rafindadi, A., et al. (2022) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.36053 · Cited by 26 · see citing works
Coyer, L., Boyd, A. C., Schinkel, J., Agyemang, C. O., Galenkamp, H., Koopman, A. D. M., Leenstra, T., van Charante, E. P. M., van den Born, B. H., Lok, A., et al. (2022) · BMJ Open · doi:10.1136/bmjopen-2021-052752 · Cited by 23 · see citing works
(2022) · doi:10.12688/wellcomeopenres.17661.1 · Cited by 20
“Spike antigen production and ELISA assay We have recently described the production and purification of full-length SARS-CoV-2 spike protein in mammalian expression system (Uyoga et al., 2021).”
BackgroundMethodInfluentialMolecular detection of SARS-CoV-2 being challenged by virus variation and asymptomatic infection
Jiang, C., Li, X., Ge, C., Ding, Y., Zhang, T., Cao, S., Meng, L., & Lu, S. (2021) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2021.03.006 · Cited by 21 · see citing works
Lapidus, S., Liu, F., Casanovas‐Massana, A., Dai, Y., Huck, J. D., Lucas, C. G. D. O., Klein, J., Filler, R. B., Strine, M. S., Sy, M., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-26709-7 · Cited by 48 · see citing works
COVID-19: Mechanistic Model of the African Paradox Supports the Central Role of the NF-κB Pathway
Kircheis, R., Schuster, M., & Planz, O. (2021) · Viruses · doi:10.3390/v13091887 · Cited by 18 · see citing works
“However, in the same period, only 2093 cases were detected (with 90% asymptomatic), and there were only 71 deaths among all ages, implicating an apparently much lower mortality and morbidity of COVID-19 in this African country compared to other parts of the world [51].”
BackgroundQuantifying previous SARS-CoV-2 infection through mixture modelling of antibody levels
Bottomley, C., Otiende, M., Uyoga, S. M., Gallagher, K. E., Kagucia, E. W., Etyang, A. O., Mugo, D., Gitonga, J. N., Karanja, H., Nyagwange, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26452-z · Cited by 24 · see citing works
SARS-CoV-2 seroprevalence around the world: an updated systematic review and meta-analysis
Azami, M., Moradi, Y., Moradkhani, A., & Aghaei, A. (2022) · European journal of medical research · doi:10.1186/s40001-022-00710-2 · Cited by 22 · see citing works
Intense and Mild First Epidemic Wave of Coronavirus Disease, The Gambia
Abatan, B. O., Agboghoroma, O., Akemoke, F., Antonio, M., Awokola, B. I., Bittaye, M., Bojang, A., Bojang, K., Brotherton, H., Cerami, C., et al. (2021) · Emerging infectious diseases · doi:10.3201/eid2708.204954 · Cited by 22 · see citing works
“In Kenya, a retrospective survey of blood donor samples collected during April–June 2020 found that 1 in 20 adults had SARS-CoV-2 antibodies (13).”
BackgroundRenzaho, A. M. N. (2020) · Risk Analysis · doi:10.1111/risa.13596 · Cited by 21 · see citing works
“The seroprevalence reported in Kenya was comparable to that reported in countries hard-hit by the pandemic such as China, Brazil, Switzerland, Spain, and the United States after the initial epidemic peak (Uyoga et al., 2020).”
ResultTalla, C., Loucoubar, C., Roka, J. L., Barry, M. A., Ndiaye, S., Diarra, M., Thiam, M. S., Faye, O., Dia, M., Diop, M. M., et al. (2021) · IJID Regions · doi:10.1016/j.ijregi.2022.02.007 · Cited by 22 · see citing works
“…healthcare workers, and COVID-19 exposed populations or the general population in some targeted districts/states ( Chibwana et al., 2020 ; Etyang et al., 2021 ; Halatoko et al., 2020 ; Kempen et al., 2020 ; Milleliri et al., 2021 ; Mulenga et al., 2021 ; Uyoga et al., 2021 Wiens et al., 2021 ).”
Tsinda, E. K., & Mmbando, G. S. (2021) · Bulletin of the National Research Centre/Bulletin of the National Research Center · doi:10.1186/s42269-021-00589-9 · Cited by 21 · see citing works
The Missing Millions: Uncovering the Burden of Covid‐19 Cases and Deaths in the African Region
McKay, T., Robinson, R. S., Musungu, S., Padi‐Adjirackor, N. A., & Angotti, N. (2024) · Population and Development Review · doi:10.1111/padr.12608 · Cited by 21 · see citing works
Individual’s daily behaviour and intergenerational mixing in different social contexts of Kenya
Fava, E. D., Adema, I. W., Kiti, M. C., Poletti, P., Merler, S., Nokes, D. J., Manfredi, P., & Melegaro, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-00799-1 · Cited by 19 · see citing works
Cost-effectiveness of COVID-19 vaccination in low- and middle-income countries
Siedner, M., Alba, C., Fitzmaurice, K., Gilbert, R., Scott, J. A., Shebl, F. M., Ciaranello, A. L., Reddy, K. P., & Freedberg, K. (2021) · medRxiv · doi:10.1101/2021.04.28.21256237 · Cited by 18 · see citing works
Quantitative serology for SARS-CoV-2 using self-collected saliva and finger-stick blood
Campbell, C., Padmanabhan, N., Romero, D., Joe, J., Gebremeskel, M., Manjula, N., Wohlstadter, N., Wohlstadter, R., Goodwin, P., Quintero, L., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-10484-6 · Cited by 14 · see citing works
Tapela, K., Oyawoye, F. O., Olwal, C. O., Opurum, P. C., Amponsah, J. A., Segbedzi, K. A. L., Tetteh, B. E., Kumi-Ansah, F., Mutungi, J. K., Obodai, E., et al. (2022) · BMC Medicine · doi:10.1186/s12916-022-02571-2 · Cited by 18 · see citing works
Carcelen, A. C., Winter, A. K., Moss, W. J., Chilumba, I., Mutale, I., Chongwe, G., Monze, M., Mulundu, G., Nkamba, H., Mwansa, F. D., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-14493-3 · Cited by 19 · see citing works
Arnold, C., Srinivasan, S., Rodriguez, S., Rydzak, N., Herzog, C. M., Gontu, A., Bharti, N., Small, M. L., Rogers, C. J., Schade, M. M., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-12499-5 · Cited by 29 · see citing works
Kagucia, E. W., Ziraba, A. K., Nyagwange, J., Kutima, B., Kimani, M., Akech, D. O., Ng’oda, M. A., Sigilai, A. K., Mugo, D., Karanja, H., et al. (2023) · Influenza and Other Respiratory Viruses · doi:10.1111/irv.13173 · Cited by 25 · see citing works
- Authors
- Uyoga, S., Adetifa, I. M. O., Karanja, H. K., Nyagwange, J., Tuju, J., Wanjiku, P., Aman, R., Mwangangi, M., Amoth, P., Kasera, K., Ng’ang’a, W., Rombo, C., Yegon, C., Kithi, K., Odhiambo, E., Rotich, T., Orgut, I., Kihara, S., Otiende, M., Bottomley, C., Mupe, Z. N., Kagucia, E. W., Gallagher, K. E., Etyang, A., Voller, S., Gitonga, J. N., Mugo, D., Agoti, C. N., Otieno, E., Ndwiga, L., Lambe, T., Wright, D., Barasa, E., Tsofa, B., Bejon, P., Ochola-Oyier, L. I., Agweyu, A., Scott, J. A. G., & Warimwe, G. M.
- Affiliations
- Kenya Medical Research Institute (KE)
- Ministry of Health (KE)
- Government of Kenya (KE)
- Kenya National Blood Transfusion Services (KE)
- London School of Hygiene & Tropical Medicine (GB)
- University of Oxford (GB)
- KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
- Corresponding author
- Uyoga, Sophie
- ORCID
- Uyoga, Sophie
- Adetifa, Ifedayo M. O.
- Karanja, Henry K.
- Nyagwange, James
- Tuju, James
- Wanjiku, Perpetual
- Aman, Rashid
- Amoth, Patrick
- Kasera, Kadondi
- Ng’ang’a, Wangari
- Rotich, Thomas
- Otiende, Mark
- Bottomley, Christian
- Mupe, Zonia N.
- Kagucia, Eunice W.
- Gallagher, Katherine E.
- Etyang, Anthony
- Voller, Shirine
- Gitonga, John N.
- Mugo, Daisy
- Agoti, Charles N.
- Otieno, Edward
- Ndwiga, Leonard
- Lambe, Teresa
- Wright, Daniel
- Barasa, Edwine
- Tsofa, Benjamin
- Bejon, Philip
- Agweyu, Ambrose
- Scott, J. Anthony G.
- Warimwe, George M.
- Venue
- Science
- Published
- 2021-01
- Volume
- 371
- Issue
- 6524
- Pages
- 79-82
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC7877494
- OpenAlex
- W3104471981
- Cited by
- 328
- References
- 38
- Citations by year
- 2026: 13 · 2025: 26 · 2024: 23 · 2023: 39 · 2022: 84 · 2021: 122 · 2020: 20 · 2012: 1
- FWCI
- 8.69
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Science (publishedVersion, cc-by)
- medRxiv (acceptedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion, cc-by)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (submittedVersion, cc-by)
- Greater South Information System
- Funders
- Oak Foundation
- Wellcome (220991/Z/20/Z, 203077/Z/16/Z, 107568/Z/15/Z, 214320)
- Medical Research Council (MR/S005293/1)
- African Academy of Sciences (DEL-15-003)
- DFID and Wellcome (220985/Z/20/Z)
- NIHR MPRU (2268427)
- Department for International Development (MR/R006083/1)
- NIHR Health Protection Research Unit in Immunisation
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Physical Sciences › Mathematics › Modeling and Simulation › COVID-19 epidemiological studies
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 detection and testing
- Keywords
- SARS-CoV-2, COVID-19 pandemic, seroprevalence, anti-SARS-CoV-2 IgG, blood donors, Kenya, SARS-CoV-2 exposure, urban-rural differences, pandemic response
- MeSH terms
- COVID-19, SARS-CoV-2, Adolescent, Adult, Aged, Antibodies, Viral, Blood Donors, Communicable Disease Control, Humans, Immunoglobulin G, Kenya, Middle Aged, Seroepidemiologic Studies, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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