Duration of Humoral Immunity to Common Viral and Vaccine Antigens

Adjusting for multiple testing—when and how?

Bender, R., & Lange, S. (2001) · Journal of Clinical Epidemiology · doi:10.1016/s0895-4356(00)00314-0 · Cited by 3,168

Efficacy of B-cell-targeted therapy with rituximab in patients with rheumatoid arthritis

Edwards, J. C. W., Szczepański, L., Szechiński, J., Filipowicz-Sosnowska, A., Emery, P., Close, D. R., Stevens, R. M., & Shaw, T. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa032534 · Cited by 2,623

Immunological memory and protective immunity: understanding their relation

Ahmed, R., & Gray, D. (1996) · Science · doi:10.1126/science.272.5258.54 · Cited by 1,775

Maintenance of Serological Memory by Polyclonal Activation of Human Memory B Cells

Bernasconi, N. L., Traggiai, E., & Lanzavecchia, A. (2002) · Science · doi:10.1126/science.1076071 · Cited by 1,304

Humoral Immunity Due to Long-Lived Plasma Cells

Slifka, M. K., Antia, R., Whitmire, J. K., & Ahmed, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80541-5 · Cited by 1,249

Competence and competition: the challenge of becoming a long-lived plasma cell

Radbruch, A., Muehlinghaus, G., Luger, E., Inamine, A., Smith, K. G. C., Dörner, T., & Hiepe, F. (2006) · Nature reviews. Immunology · doi:10.1038/nri1886 · Cited by 1,033

Duration of antiviral immunity after smallpox vaccination

Hammarlund, E., Lewis, M. W., Hansen, S. G., Strelow, L. I., Nelson, J. A., Sexton, G. J., Hanifin, J. M., & Slifka, M. K. (2003) · Nature Medicine · doi:10.1038/nm917 · Cited by 946

Lifetime of plasma cells in the bone marrow

Manz, R. A., Thiel, A., & Radbruch, A. (1997) · Nature · doi:10.1038/40540 · Cited by 866

Cutting edge: long-term B cell memory in humans after smallpox vaccination

Crotty, S., Felgner, P., Davies, H., Glidewell, J., Villarreal, L., & Ahmed, R. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.10.4969 · Cited by 695

Measles Antibody: Reevaluation of Protective Titers

Chen, R. T., Markowitz, L. E., Albrecht, P. G., Stewart, J. A., MOFENSON, L. M., Preblud, S. R., & Orenstein, W. A. (1990) · The Journal of Infectious Diseases · doi:10.1093/infdis/162.5.1036 · Cited by 606

Ongoing activation of autoantigen-specific B cells in primary biliary cirrhosis

Zhang, J., Zhang, W., Leung, P. S. C., Bowlus, C. L., Dhaliwal, S. S., Coppel, R. L., Ansari, A. A., Yang, G., Wang, J., Kenny, T. P., et al. (2014) · Hepatology · doi:10.1002/hep.27313 · Cited by 86

Rituximab-induced hypogammaglobulinemia in patients with neuromyelitis optica spectrum disorders

Marcinnò, A., Marnetto, F., Valentino, P., Martire, S., Balbo, A., Drago, A., Leto, M., Capobianco, M. A. N., Panzica, G., & Bertolotto, A. (2018) · Neurology Neuroimmunology & Neuroinflammation · doi:10.1212/nxi.0000000000000498 · Cited by 86

Raising Expectations For Subunit Vaccine

Schiller, J. T., & Lowy, D. R. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu648 · Cited by 85

Immune recall improves antibody durability and breadth to SARS-CoV-2 variants

Chen, Y., Tong, P., Whiteman, N. B., Moghaddam, A. S., Zarghami, M., Zuiani, A., Habibi, S., Gautam, A. K., Keerti, K., Bi, C., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abp8328 · Cited by 89

Intrinsically determined turnover underlies broad heterogeneity in plasma-cell lifespan

Robinson, M. J., Ding, Z., Dowling, M. R., Hill, D. L., Webster, R. H., McKenzie, C. I., Pitt, C., O’Donnell, K., Mulder, J., Brodie, E. J., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.04.015 · Cited by 87

Immunization delivered by lentiviral vectors for cancer and infectious diseases

Hu, B., Tai, A., & Wang, P. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00967.x · Cited by 88

Impact of age and pre-existing influenza immune responses in humans receiving split inactivated influenza vaccine on the induction of the breadth of antibodies to influenza A strains

Nuñez, I. A., Carlock, M. A., Allen, J. D., Owino, S. O., Geffel, K. M., Nowalk, M. P., Susick, M., Diagle, K., Sweeney, K., Mundle, S. T., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0185666 · Cited by 85

A vaccinia-based single vector construct multi-pathogen vaccine protects against both Zika and chikungunya viruses

Prow, N. A., Liu, L., Nakayama, E., Cooper, T. H., Yan, K., Eldi, P., Hazlewood, J. E., Tang, B., Le, T. T., Setoh, Y. X., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03662-6 · Cited by 85

Antibody Responses to SARS-CoV-2: Let’s Stick to Known Knowns

Baumgarth, N., Nikolich-Žugich, J., Lee, F. E.-H., & Bhattacharya, D. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000839 · Cited by 84

Measles immunity and immunosuppression

Griffin, D. E. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.08.002 · Cited by 84

Antibodies against vaccine-preventable infections after CAR-T cell therapy for B cell malignancies

Walti, C. S., Krantz, E. M., Maalouf, J., Boonyaratanakornkit, J. B., Keane-Candib, J., Joncas-Schronce, L., Stevens‐Ayers, T., Dasgupta, S., Taylor, J. J., Hirayama, A. V. V., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.146743 · Cited by 86

A replication-competent adenovirus-vectored influenza vaccine induces durable systemic and mucosal immunity

Matsuda, K., Migueles, S. A., Huang, J., Bolkhovitinov, L., Stuccio, S., Griesman, T., Pullano, A. A., Kang, B. H., Ishida, E., Zimmerman, M. G., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci140794 · Cited by 86

Circulating Human Antibody-Secreting Cells during Vaccinations and Respiratory Viral Infections Are Characterized by High Specificity and Lack of Bystander Effect

Lee, F. E.-H., Halliley, J. L., Walsh, E. E., Moscatiello, A. P., Kmush, B. L., Falsey, A. R., Randall, T. D., Kaminiski, D. A., Miller, R. K., & Sanz, I. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002932 · Cited by 83

Differential regulation of self-reactivity discriminates between IgG + human circulating memory B cells and bone marrow plasma cells

Scheid, J. F., Mouquet, H., Kofer, J., Yurasov, S., Nussenzweig, M. C., & Wardemann, H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113395108 · Cited by 83

IgM memory B cells: a mouse/human paradox

Reynaud, C., Descatoire, M., Dogan, I., Huetz, F., Weller, S., & Weill, J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0971-z · Cited by 86

Masking of antigenic epitopes by antibodies shapes the humoral immune response to influenza

Zarnitsyna, V. I., Ellebedy, A. H., Davis, C. W., Jacob, J., Ahmed, R., & Antia, R. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2014.0248 · Cited by 82

Measles, mumps, and rubella in Finland: 25 years of a nationwide elimination programme

Peltola, H., Jokinen, S., Paunio, M., Hovi, T., & Davidkin, I. (2008) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(08)70282-2 · Cited by 82

BAFF and CD4+ T cells are major survival factors for long-lived splenic plasma cells in a B-cell–depletion context

Thai, L.-H., Gallou, S. L., Robbins, A., Crickx, É., Fadeev, T., Zhou, Z., Cagnard, N., Megret, J., Bôle‐Feysot, C., Weill, J., et al. (2018) · Blood · doi:10.1182/blood-2017-06-789578 · Cited by 82

Age-Related Seroprevalence of Antibodies Against AAV-LK03 in a UK Population Cohort

Perocheau, D. P., Cunningham, S. C., Lee, J., Antinao Diaz, J., Waddington, S. N., Gilmour, K., Eaglestone, S., Lisowski, L., Thrasher, A. J., Alexander, I. E., et al. (2019) · Human Gene Therapy · doi:10.1089/hum.2018.098 · Cited by 81

SARS-CoV-2-specific plasma cells are not durably established in the bone marrow long-lived compartment after mRNA vaccination

Nguyen, D. C., Hentenaar, I., Morrison-Porter, A., Solano, D., Haddad, N. S., Castrillon, C. E., Runnstrom, M. C., Lamothe, P. A., Andrews, J., Roberts, D., et al. (2024) · Nature Medicine · doi:10.1038/s41591-024-03278-y · Cited by 81

A Positive Correlation between Atypical Memory B Cells and Plasmodium falciparum Transmission Intensity in Cross-Sectional Studies in Peru and Mali

Weiss, G. E., Clark, E. H., Li, S., Traoré, B., Kayentao, K., Ongoïba, A., Hernandez, J. N., Doumbo, O. K., Pierce, S. K., Branch, O. H., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015983 · Cited by 81

Long-lived plasma cells accumulate in the bone marrow at a constant rate from early in an immune response

Robinson, M. J., Dowling, M. R., Pitt, C., O’Donnell, K., Webster, R. H., Hill, D. L., Ding, Z., Dvorscek, A. R., Brodie, E. J., Hodgkin, P. D., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abm8389 · Cited by 80

Perspectives on the Impact of Varicella Immunization on Herpes Zoster. A Model-Based Evaluation from Three European Countries

Poletti, P., Melegaro, A., Ajelli, M., Fava, E. D., Guzzetta, G., Faustini, L., Scalia‐Tomba, G., Lopalco, P. L., Rizzo, C., Merler, S., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060732 · Cited by 79

Long-term immunogenicity after measles vaccine vs. wild infection: an Italian retrospective cohort study

Bianchi, F. P., Mascipinto, S., Stefanizzi, P., Nitto, S. D., Germinario, C. A., & Tafuri, S. (2021) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2020.1871296 · Cited by 79

T cells control the generation of nanomolar-affinity anti-glycan antibodies

Polonskaya, Z., Deng, S., Sarkar, A., Kain, L., Comellas-Aragonès, M., McKay, C. S., Kaczanowska, K., Holt, M., McBride, R., Palomo, V., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci91192 · Cited by 79

A highly immunogenic and effective measles virus-based Th1-biased COVID-19 vaccine

Hörner, C., Schürmann, C., Auste, A., Ebenig, A., Muraleedharan, S., Dinnon, K. H., Scholz, T., Herrmann, M., Schnierle, B. S., Baric, R. S., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2014468117 · Cited by 80

Transforming vaccinology

Rappuoli, R., Alter, G., & Pulendran, B. (2024) · Cell · doi:10.1016/j.cell.2024.07.021 · Cited by 87

Distinction of the memory B cell response to cognate antigen versus bystander inflammatory signals

Benson, M. J., Elgueta, R., Schpero, W. L., Molloy, M. J., Zhang, W., Usherwood, E. J., & Noelle, R. J. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20090667 · Cited by 78

Adjuvant-specific regulation of long-term antibody responses by ZBTB20

Wang, Y., & Bhattacharya, D. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20131821 · Cited by 80

Preterm Birth Affects the Risk of Developing Immune-Mediated Diseases

Goedicke‐Fritz, S., Härtel, C., Krasteva‐Christ, G., Kopp, M., Meyer, S., & Zemlin, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01266 · Cited by 77

The TLR9 Ligand CpG Promotes the Acquisition of Plasmodium falciparum -Specific Memory B Cells in Malaria-Naive Individuals

Crompton, P. D., Mircetic, M., Weiss, G. E., Baughman, A., Huang, C., Topham, D. J., Treanor, J. J., Sanz, I., Lee, F. E.-H., Durbin, A. P., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803596 · Cited by 77

Safety and Immunogenicity of a Single Administration of Live-attenuated Japanese Encephalitis Vaccine in Previously Primed 2- to 5-year-olds and Naive 12- to 24-month-olds

Chokephaibulkit, K., Sirivichayakul, C., Thisyakorn, U., Sabchareon, A., Pancharoen, C., Bouckenooghe, A. R., Gailhardou, S., Boaz, M. J., & Feroldi, E. (2010) · The Pediatric Infectious Disease Journal · doi:10.1097/inf.0b013e3181f68e9c · Cited by 76

Bone marrow of NZB/W mice is the major site for plasma cells resistant to dexamethasone and cyclophosphamide: Implications for the treatment of autoimmunity

Mumtaz, I. M., Hoyer, B. F., Panne, D., Moser, K., Winter, O., Cheng, Q., Yoshida, T., Burmester, G. R., Radbruch, A., Manz, R. A., et al. (2012) · Journal of Autoimmunity · doi:10.1016/j.jaut.2012.05.010 · Cited by 76

Antibody responses to merozoite antigens after natural Plasmodium falciparum infection: kinetics and longevity in absence of re-exposure

Yman, V., White, M. T., Asghar, M., Sundling, C., Sondén, K., Draper, S. J., Osier, F. H. A., & Färnert, A. (2019) · BMC Medicine · doi:10.1186/s12916-019-1255-3 · Cited by 75

Living on Three Time Scales: The Dynamics of Plasma Cell and Antibody Populations Illustrated for Hepatitis A Virus

Andraud, M., Lejeune, O., Musoro, J. Z., Ogunjimi, B., Beutels, P., & Hens, N. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002418 · Cited by 75

Discordant memory B cell and circulating anti-Env antibody responses in HIV-1 infection

Guan, Y., Sajadi, M. M., Kamin‐Lewis, R., FOUTS, T. R., Dimitrov, A., Zhang, Z., Redfield, R. R., DeVico, A. L., Gallo, R. C., & Lewis, G. K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813392106 · Cited by 75

Durability of Antibody Response Against Hepatitis B Virus in Healthcare Workers Vaccinated as Adults

Gara, N., Abdalla, A., Rivera, E., Zhao, X., Werner, J. M., Liang, T. J., Hoofnagle, J. H., Rehermann, B., & Ghany, M. G. (2014) · Clinical Infectious Diseases · doi:10.1093/cid/ciu867 · Cited by 75

Progressive differentiation toward the long-lived plasma cell compartment in the bone marrow

Koike, T., Fujii, K., Kometani, K., Butler, N. S., Funakoshi, K., Yari, S., Kikuta, J., Ishii, M., Kurosaki, T., & Ise, W. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20221717 · Cited by 74

World Malaria Day 2009: What Malaria Knows about the Immune System That Immunologists Still Do Not

Pierce, S. K., & Miller, L. H. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0804153 · Cited by 77

Neutralizing antibodies against West Nile virus identified directly from human B cells by single-cell analysis and next generation sequencing

Tsioris, K., Gupta, N. T., Ogunniyi, A. O., Zimnisky, R. M., Qian, F., Yao, Y., Wang, X., Stern, J. N. H., Chari, R., Briggs, A. W., et al. (2015) · Integrative Biology · doi:10.1039/c5ib00169b · Cited by 74

Serology in the 21st century: the molecular-level analysis of the serum antibody repertoire

Wine, Y., Horton, A. P., Ippolito, G. C., & Georgiou, G. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.06.009 · Cited by 74

TLR-adjuvanted nanoparticle vaccines differentially influence the quality and longevity of responses to malaria antigen Pfs25

Thompson, E. A., Ols, S., Miura, K., Rausch, K. M., Narum, D. L., Spångberg, M., Juraska, M., Wille-Reece, U., Weiner, A. J., Howard, R. F., et al. (2018) · JCI Insight · doi:10.1172/jci.insight.120692 · Cited by 73

Waning immunity and re-emergence of measles and mumps in the vaccine era

Yang, L., Grenfell, B. T., & Mina, M. J. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.05.009 · Cited by 73

HIV-1 Envelope Induces Memory B Cell Responses That Correlate with Plasma Antibody Levels after Envelope gp120 Protein Vaccination or HIV-1 Infection

Bonsignori, M., Moody, M. A., Parks, R., Holl, T. M., Kelsoe, G. H., Hicks, C. B., Vandergrift, N., Tomaras, G. D., & Haynes, B. F. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901068 · Cited by 73

Durable preservation of antiviral antibodies after CD19-directed chimeric antigen receptor T-cell immunotherapy

Hill, J. A., Krantz, E. M., Hay, K. A., Dasgupta, S., Stevens‐Ayers, T., Ignacio, R. B., Bar, M., Maalouf, J., Cherian, S., Chen, X., et al. (2019) · Blood Advances · doi:10.1182/bloodadvances.2019000717 · Cited by 75

Mumps Outbreaks in Vaccinated Populations—Is It Time to Re-assess the Clinical Efficacy of Vaccines?

Connell, A. R., Connell, J., Leahy, T. R., & Hassan, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02089 · Cited by 73

Mucosal adjuvants and long-term memory development with special focus on CTA1-DD and other ADP-ribosylating toxins

Lycke, N. Y., & Bemark, M. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.54 · Cited by 74

Metformin improves in vivo and in vitro B cell function in individuals with obesity and Type-2 Diabetes

Diaz, A., Romero, M., Vazquez, T., Lechner, S. C., Blomberg, B. B., & Frasca, D. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.03.078 · Cited by 71

How Can HIV-Type-1-Env Immunogenicity Be Improved to Facilitate Antibody-Based Vaccine Development?

Klasse, P. J., Sanders, R. W., Cerutti, A., & Moore, J. P. (2011) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2011.0053 · Cited by 75

Transcriptional and Metabolic Control of Memory B Cells and Plasma Cells

Ripperger, T. J., & Bhattacharya, D. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-093019-125603 · Cited by 72

Long-term persistence of SARS-CoV-2 neutralizing antibody responses after infection and estimates of the duration of protection

Lau, E. H. Y., Hui, D. S. C., Tsang, O. T., Chan, W. H., Kwan, M. Y. W., Chiu, S. S. S., Cheng, S. M. S., Ko, R. L., Li, J. K., Chaothai, S., et al. (2021) · EClinicalMedicine · doi:10.1016/j.eclinm.2021.101174 · Cited by 71

New insights into the ontogeny, diversity, maturation and survival of long-lived plasma cells

Fooksman, D., Jing, Z., & Park, R. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-00991-0 · Cited by 70

Intranasal vaccination with an adjuvanted Norwalk virus-like particle vaccine elicits antigen-specific B memory responses in human adult volunteers

Ramírez, K., Wahid, R., Richardson, C., Bargatze, R. F., El‐Kamary, S. S., Sztein, M. B., & Pasetti, M. F. (2012) · Clinical Immunology · doi:10.1016/j.clim.2012.05.006 · Cited by 70

Predicting vaccine effectiveness for mpox

Berry, M. T., Khan, S. R., Schlub, T. E., Notaras, A., Kunasekaran, M. P., Grulich, A. E., MacIntyre, C. R., Davenport, M. P., & Khoury, D. S. (2024) · Nature Communications · doi:10.1038/s41467-024-48180-w · Cited by 69

Characteristics of Memory B Cells Elicited by a Highly Efficacious HPV Vaccine in Subjects with No Pre-existing Immunity

Scherer, E. M., Smith, R. A. J., Simonich, C. A. L., Niyonzima, N., Carter, J. J., & Galloway, D. A. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004461 · Cited by 68

Yellow fever revaccination during infliximab therapy

Scheinberg, M. A., Guedes-Barbosa, L. S., Mangueira, C. L. P., Rosseto, E. A., da Mota, L. M. H., Oliveira, A., & Lima, R. A. C. (2010) · Arthritis Care & Research · doi:10.1002/acr.20045 · Cited by 68

Comparative Study of Immune Status to Infectious Agents in Elderly Patients with Multiple Myeloma, Waldenstrom's Macroglobulinemia, and Monoclonal Gammopathy of Undetermined Significance

Karlsson, J., Andréasson, B., Kondori, N., Erman, E., Riesbeck, K., Hogevik, H., & Wennerås, C. (2011) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00021-11 · Cited by 68

Successful Vaccines

Amanna, I. J., & Slifka, M. K. (2018) · Current topics in microbiology and immunology · doi:10.1007/82_2018_102 · Cited by 68

The durability of vaccine-induced protection: an overview

Vashishtha, V. M., & Kumar, P. (2024) · Expert Review of Vaccines · doi:10.1080/14760584.2024.2331065 · Cited by 70

System vaccinology analysis of predictors and mechanisms of antibody response durability to multiple vaccines in humans

Cortese, M., Hagan, T., Rouphael, N., Wu, S.-Y., Xie, X., Kazmin, D. A., Wimmers, F., Gupta, S., der Most, R. G. V., Coccia, M., et al. (2025) · Nature Immunology · doi:10.1038/s41590-024-02036-z · Cited by 71

No pain no gain? Adjuvant effects of alum and monophosphoryl lipid A in pertussis and HPV vaccines

Mitchell, T. C., & Casella, C. R. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.06.009 · Cited by 66

Measles virus persistence and its consequences

Griffin, D. E. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.03.003 · Cited by 68

Waning antibody responses in COVID-19: what can we learn from the analysis of other coronaviruses?

Hamady, A., Lee, J., & Loboda, Z. (2021) · Infection · doi:10.1007/s15010-021-01664-z · Cited by 66

Potential mechanisms for HPV vaccine-induced long-term protection

Stanley, M. (2010) · Gynecologic Oncology · doi:10.1016/j.ygyno.2010.04.002 · Cited by 66

The Antibody-Secreting Cell Response to Infection: Kinetics and Clinical Applications

Carter, M. J., Mitchell, R. M., Sauteur, P. M. M., Kelly, D. F., & Trück, J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00630 · Cited by 70

Quantitative assessment of the robustness of next-generation sequencing of antibody variable gene repertoires from immunized mice

Greiff, V., Menzel, U., Haessler, U., Cook, S. C., Friedensohn, S., Khan, T. A., Pogson, M., Hellmann, I., & Reddy, S. T. (2014) · BMC Immunology · doi:10.1186/s12865-014-0040-5 · Cited by 64

Risk factors for West Nile virus infection and disease in populations and individuals

Montgomery, R. R., & Murray, K. O. (2015) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.2015.1007043 · Cited by 66

Desensitization strategies in adult heart transplantation—Will persistence pay off?

Chih, S., & Patel, J. K. (2016) · The Journal of Heart and Lung Transplantation · doi:10.1016/j.healun.2016.03.021 · Cited by 64

How malaria modulates memory: activation and dysregulation of B cells in Plasmodium infection

Scholzen, A., & Sauerwein, R. W. (2013) · Trends in Parasitology · doi:10.1016/j.pt.2013.03.002 · Cited by 69

Questions regarding the safety and duration of immunity following live yellow fever vaccination

Amanna, I. J., & Slifka, M. K. (2016) · Expert Review of Vaccines · doi:10.1080/14760584.2016.1198259 · Cited by 69

Instructing durable humoral immunity for COVID-19 and other vaccinable diseases

Bhattacharya, D. (2022) · Immunity · doi:10.1016/j.immuni.2022.05.004 · Cited by 64

Proteasome Inhibition with Bortezomib Depletes Plasma Cells and Specific Autoantibody Production in Primary Thymic Cell Cultures from Early-Onset Myasthenia Gravis Patients

Gomez, A. M., Willcox, N., Vrolix, K., Hummel, J. F., Nogales‐Gadea, G., Saxena, A., Duimel, H., Verheyen, F., Molenaar, P. C., Buurman, W. A., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1301555 · Cited by 64

TLR4 Ligands Lipopolysaccharide and Monophosphoryl Lipid A Differentially Regulate Effector and Memory CD8+ T Cell Differentiation

Cui, W., Joshi, N. S., Liu, Y., Meng, H., Kleinstein, S. H., & Kaech, S. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302569 · Cited by 63

Backward bifurcations and multiple equilibria in epidemic models with structured immunity

Reluga, T. C., Medlock, J., & Perelson, A. S. (2008) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2008.01.014 · Cited by 63

Changes to anti-JCV antibody levels in a Swedish national MS cohort

Warnke, C., Ramanujam, R., Plavina, T., Bergström, T. B., Goelz, S. E., Subramanyam, M., Kockum, I. S., Rahbar, A., Kieseier, B. C., Holmén, C., et al. (2013) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-304332 · Cited by 63

Bacterial superglue generates a full-length circumsporozoite protein virus-like particle vaccine capable of inducing high and durable antibody responses

Janitzek, C. M., Matondo, S., Thrane, S., Nielsen, M. A., Kavishe, R. A., Mwakalinga, S., Theander, T. G., Salanti, A., & Sander, A. F. (2016) · Malaria Journal · doi:10.1186/s12936-016-1574-1 · Cited by 64

Here, There, and Anywhere? Arguments for and against the Physical Plasma Cell Survival Niche

Wilmore, J. R., & Allman, D. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700461 · Cited by 63

Humoral immune responses to infection: common mechanisms and unique strategies to combat pathogen immune evasion tactics

Sebina, I., & Pepper, M. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.02.001 · Cited by 66

Decreased humoral immunity to mumps in young adults immunized with MMR vaccine in childhood

Rasheed, M. A. U., Hickman, C. J., McGrew, M., Sowers, S. B., Mercader, S., Hopkins, A., Grimes, V., Yu, T., Wrammert, J., Mulligan, M. J., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905570116 · Cited by 62

Vaccination and immunotherapies in neuroimmunological diseases

Winkelmann, A., Loebermann, M., Barnett, M. H., Hartung, H., & Zettl, U. K. (2022) · Nature Reviews Neurology · doi:10.1038/s41582-022-00646-5 · Cited by 64

Translating transitions - how to decipher peripheral human B cell development

Bemark, M. (2015) · Journal of Biomedical Research · doi:10.7555/jbr.29.20150035 · Cited by 65

Generating memory with vaccination

Castellino, F., Galli, G., Giudice, G. D., & Rappuoli, R. (2009) · European Journal of Immunology · doi:10.1002/eji.200939550 · Cited by 64

Dengue and Zika virus infections in children elicit cross-reactive protective and enhancing antibodies that persist long term

Katzelnick, L. C., Zambrana, J. V., Elizondo, D., Collado, D., García, N., Arguello, S., Mercado, J. C., Miranda, T., Ampie, O., Mercado, B. L., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abg9478 · Cited by 61

Wanted, dead or alive: New viral vaccines

Amanna, I. J., & Slifka, M. K. (2009) · Antiviral Research · doi:10.1016/j.antiviral.2009.08.008 · Cited by 61

Protective antiviral antibody responses in a mouse model of influenza virus infection require TACI

Wolf, A. I., Mozdzanowska, K., Quinn, W. J., Metzgar, M. H., Williams, K. L., Caton, A. J., Meffre, E., Bram, R. J., Erickson, L. D., Allman, D., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci57362 · Cited by 61

CD28 Promotes Plasma Cell Survival, Sustained Antibody Responses, and BLIMP-1 Upregulation through Its Distal PYAP Proline Motif

Rozanski, C. H., Utley, A. T., Carlson, L. M., Farren, M. R., Murray, M. E., Russell, L., Nair, J. R., Yang, Z., Brady, W., Garrett‐Sinha, L. A., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402260 · Cited by 63

EXPRESSION OF CONCERN: COVID‐19 re‐infection

Brouqui, P., Colson, P., Melenotte, C., Houhamdi, L., Bedotto, M., Devaux, C. A., Gautret, P., Million, M., Parola, P., Stoupan, D., et al. (2021) · European Journal of Clinical Investigation · doi:10.1111/eci.13537 · Cited by 63

Vaccines for preventing herpes zoster in older adults

Gagliardi, A. M., Andriolo, B. N., Torloni, M. R., Soares, B. G., Gomes, J. D. O., Andriolo, R. B., & Cruz, E. C. (2019) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd008858.pub4 · Cited by 60

Frequencies of human influenza-specific antibody secreting cells or plasmablasts post vaccination from fresh and frozen peripheral blood mononuclear cells

Kyu, S. Y., Kobie, J. J., Yang, H., Zand, M. S., Topham, D. J., Quataert, S. A., Sanz, I., & Lee, F. E.-H. (2008) · Journal of Immunological Methods · doi:10.1016/j.jim.2008.09.025 · Cited by 60

Antiviral Immunity following Smallpox Virus Infection: a Case-Control Study

Hammarlund, E., Lewis, M. W., Hanifin, J. M., Mori, M., Koudelka, C. W., & Slifka, M. K. (2010) · Journal of Virology · doi:10.1128/jvi.01763-10 · Cited by 62

Adjuvant and carrier protein-dependent T-cell priming promotes a robust antibody response against the Plasmodium falciparum Pfs25 vaccine candidate

Radtke, A. J., Anderson, C. F., Riteau, N., Rausch, K. M., Scaria, P. V., Kelnhofer, E., Howard, R. F., Sher, A., Germain, R. N., & Duffy, P. E. (2017) · Scientific Reports · doi:10.1038/srep40312 · Cited by 62

Supplying the trip to antibody production—nutrients, signaling, and the programming of cellular metabolism in the mature B lineage

Boothby, M. R., Brookens, S. K., Raybuck, A. L., & Cho, S. H. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00782-w · Cited by 60

Immune Regulation of Human Herpesviruses and Its Implications for Human Transplantation

Smith, C., & Khanna, R. (2013) · American Journal of Transplantation · doi:10.1111/ajt.12005 · Cited by 59

A Unique Role of the Cholera Toxin A1-DD Adjuvant for Long-Term Plasma and Memory B Cell Development

Bemark, M., Bergqvist, P. J., Stensson, A., Holmberg, A. H., Mattsson, J., & Lycke, N. Y. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002881 · Cited by 59

Immuno-epidemiology of a population structured by immune status: a mathematical study of waning immunity and immune system boosting

Barbarossa, M. V., & Röst, G. (2015) · Journal of Mathematical Biology · doi:10.1007/s00285-015-0880-5 · Cited by 62

Vaccination Against Tuberculosis With Whole-Cell Mycobacterial Vaccines

Scriba, T. J., Kaufmann, S. H. E., Lambert, P. H., Sanicas, M., Martı́n, C., & Neyrolles, O. (2016) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiw228 · Cited by 59

Immune memory and aging: an infinite or finite resource?

Nikolich-Žugich, J., & Rudd, B. D. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.011 · Cited by 58

The Hepatitis B Vaccine Protects Re-Exposed Health Care Workers, But Does Not Provide Sterilizing Immunity

Werner, J. M., Abdalla, A., Gara, N., Ghany, M. G., & Rehermann, B. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.07.044 · Cited by 58

Current perspectives in assessing humoral immunity after measles vaccination

Haralambieva, I. H., Kennedy, R. B., Ovsyannikova, I. G., Schaid, D. J., & Poland, G. A. (2018) · Expert Review of Vaccines · doi:10.1080/14760584.2019.1559063 · Cited by 60

How intrinsic and extrinsic regulators of plasma cell survival might intersect for durable humoral immunity

Robinson, M. J., Webster, R. H., & Tarlinton, D. M. (2020) · Immunological Reviews · doi:10.1111/imr.12895 · Cited by 60

Heterogeneity and longevity of antibody memory to viruses and vaccines

Antia, A., Ahmed, H., Handel, A., Carlson, N. E., Amanna, I. J., Antia, R., & Slifka, M. (2018) · PLOS Biology · doi:10.1371/journal.pbio.2006601 · Cited by 123

Memory and Infection

Masopust, D., & Slifka, M. K. (2014) · ASM Press eBooks · doi:10.1128/9781555816872.ch9

Role of Multivalency and Antigenic Threshold in Generating Protective Antibody Responses

Slifka, M. K., & Amanna, I. J. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00956 · Cited by 138

Regulation of Memory Antibody Levels: The Role of Persisting Antigen versus Plasma Cell Life Span

Gatto, D., Martin, S. W., Bessa, J., Pellicioli, E. C., Saudan, P., Hinton, H. J., & Bachmann, M. F. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.1.67 · Cited by 56

Long-term presence of memory B-cells specific for different vaccine components

Buisman, A., de Rond, C. G. H., Öztürk, K., ten Hulscher, H. I., & van Binnendijk, R. S. (2009) · Vaccine · doi:10.1016/j.vaccine.2009.09.102 · Cited by 103