Reduced Akkermansia muciniphila and Faecalibacterium prausnitzii levels in the gut microbiota of children with allergic asthma

Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells

Furusawa, Y., Obata, Y., Fukuda, S., Endo, T. A., Nakato, G., Takahashi, D., Nakanishi, Y., Uetake, C., Kato, K., Kato, T., et al. (2013) · Nature · doi:10.1038/nature12721 · Cited by 5,549 · see citing works

<i>Faecalibacterium prausnitzii</i> is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients

Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413 · see citing works

Interactions Between the Microbiota and the Immune System

Hooper, L. V., Littman, D. R., & Macpherson, A. J. (2012) · Science · doi:10.1126/science.1223490 · Cited by 4,173 · see citing works

Expert Panel Report 2: Guidelines for the Diagnosis and Management of Asthma

Program, P., & theDiagnosis, T. E. P. O. (1997) · Cited by 4,082 · see citing works

Inducible Foxp3 ⁺ regulatory T-cell development by a commensal bacterium of the intestinal microbiota

Round, J. L., & Mazmanian, S. K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909122107 · Cited by 2,233 · see citing works

Expert Panel Report 3 (EPR-3): Guidelines for the Diagnosis and Management of Asthma–Summary Report 2007

(2007) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2007.09.029 · Cited by 2,181 · see citing works

Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine

Louis, P., & Flint, H. J. (2009) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2009.01514.x · Cited by 2,179 · see citing works

Early infancy microbial and metabolic alterations affect risk of childhood asthma

Arrieta, M., Stiemsma, L. T., Dimitriu, P. A., Thorson, L., Russell, S., Yurist‐Doutsch, S., Kuzeljevic, B., Gold, M. J., Britton, H. M., Lefebvre, D. L., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aab2271 · Cited by 1,783 · see citing works

Mucolytic Bacteria With Increased Prevalence in IBD Mucosa Augment In Vitro Utilization of Mucin by Other Bacteria

Png, C. W., Lindén, S. K., Gilshenan, K. S., Zoetendal, E. G., McSweeney, C. S., Sly, L. I., McGuckin, M. A., & Florin, T. H. J. (2010) · American Journal of Gastroenterology · doi:10.1038/ajg.2010.281 · Cited by 1,364 · see citing works

Low counts of Faecalibacterium prausnitzii in colitis microbiota

Sokol, H., Seksik, P., Furet, J. P., Firmesse, O., Nion-Larmurier, I., Beaugerie, L., Cosnes, J., Corthier, G., Marteau, P., & Doré, J. (2009) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20903 · Cited by 1,275 · see citing works

Faecalibacterium prausnitzii and human intestinal health

Miquel, S., Martín, R., Rossi, O., Bermúdez‐Humarán, L. G., Chatel, J., Sokol, H., Thomas, M., Wells, J. M., & Langella, P. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.06.003 · Cited by 1,239 · see citing works

Family size, infection and atopy: the first decade of the 'hygiene hypothesis'

Strachan, D. (2000) · Thorax · doi:10.1136/thorax.55.suppl_1.s2 · Cited by 1,183 · see citing works

Neonatal gut microbiota associates with childhood multisensitized atopy and T cell differentiation

Fujimura, K. E., Sitarik, A. R., Havstad, S. L., Lin, D. L., Levan, S., Fadrosh, D. W., Panzer, A. R., LaMere, B. J., Rackaityte, E., Lukacs, N. W., et al. (2016) · Nature Medicine · doi:10.1038/nm.4176 · Cited by 1,168 · see citing works

Next-Generation Beneficial Microbes: The Case of Akkermansia muciniphila

Cani, P. D., & de Vos, W. M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01765 · Cited by 1,058 · see citing works

Identification of an anti-inflammatory protein from Faecalibacterium prausnitzii , a commensal bacterium deficient in Crohn’s disease

Quévrain, E., Maubert, M.-A., Michon, C., Chain, F., Marquant, R., Tailhades, J., Miquel, S., Carlier, L., Bermúdez‐Humarán, L. G., Pigneur, B., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-307649 · Cited by 861 · see citing works

Interleukin 10 acts on regulatory T cells to maintain expression of the transcription factor Foxp3 and suppressive function in mice with colitis

Murai, M., Turovskaya, O., Kim, G., Madan, R., Karp, C. L., Cheroutre, H., & Kronenberg, M. (2009) · Nature Immunology · doi:10.1038/ni.1791 · Cited by 851 · see citing works

Growth requirements and fermentation products of Fusobacterium prausnitzii, and a proposal to reclassify it as Faecalibacterium prausnitzii gen. nov., comb. nov

Duncan, S. H., Hold, G. L., Harmsen, H. J. M., Stewart, C. S., & Flint, H. J. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-6-2141 · Cited by 735 · see citing works

The genetics of asthma and allergic disease: a 21st century perspective

Ober, C., & Yao, T. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01029.x · Cited by 698 · see citing works

Pili-like proteins of Akkermansia muciniphila modulate host immune responses and gut barrier function

Ottman, N., Reunanen, J., Meijerink, M., Pietilä, T. E., Kainulainen, V., Klievink, J., Huuskonen, L., Aalvink, S., Skurnik, M., Boeren, S. A., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173004 · Cited by 522 · see citing works

Differential Modulation by Akkermansia muciniphila and Faecalibacterium prausnitzii of Host Peripheral Lipid Metabolism and Histone Acetylation in Mouse Gut Organoids

Lukovac, S., Belzer, C., Pellis, L., Keijser, B. J. F., de Vos, W. M., Montijn, R. C., & Roeselers, G. (2014) · mBio · doi:10.1128/mbio.01438-14 · Cited by 476 · see citing works

Akkermansia muciniphila in the Human Gastrointestinal Tract: When, Where, and How?

Geerlings, S. Y., Kostopoulos, I., de Vos, W. M., & Belzer, C. (2018) · Microorganisms · doi:10.3390/microorganisms6030075 · Cited by 452 · see citing works

Faecalibacterium prausnitzii subspecies-level dysbiosis in the human gut microbiome underlying atopic dermatitis

Song, H., Yoo, Y., Hwang, J., Na, Y.-C., & Kim, H. S. (2016) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.08.021 · Cited by 416 · see citing works

Role of commensal and probiotic bacteria in human health: a focus on inflammatory bowel disease

Martín, R., Miquel, S., Ulmer, J., Kechaou, N., Langella, P., & Bermúdez‐Humarán, L. G. (2013) · Microbial Cell Factories · doi:10.1186/1475-2859-12-71 · Cited by 269 · see citing works

The butyrate story: old wine in new bottles?

Scheppach, W. M., & Weiler, F. (2004) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/00075197-200409000-00009 · Cited by 246 · see citing works

Beyond diversity: functional microbiomics of the human colon

Egert, M., de Graaf, A. A., Smidt, H., de Vos, W. M., & Venema, K. (2006) · Trends in Microbiology · doi:10.1016/j.tim.2005.12.007 · Cited by 202 · see citing works

Altered Gut Microbiota Composition Associated with Eczema in Infants

Zheng, H., Liang, H., Wang, Y., Miao, M., Shi, T., Yang, F., Liu, E., Yuan, W., Ji, Z., & Li, D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166026 · Cited by 167 · see citing works

Unbalance of intestinal microbiota in atopic children

Candela, M., Rampelli, S., Turroni, S., Severgnini, M., Consolandi, C., Bellis, G. D., Masetti, R., Ricci, G., Pession, A., & Brigidi, P. (2012) · BMC Microbiology · doi:10.1186/1471-2180-12-95 · Cited by 166 · see citing works

Influence of Proton-Pump Inhibitors on the Luminal Microbiota in the Gastrointestinal Tract

Tsuda, A., Suda, W., Morita, H., Takanashi, K., Takagi, A., Koga, Y., & Hattori, M. (2015) · Clinical and Translational Gastroenterology · doi:10.1038/ctg.2015.20 · Cited by 164 · see citing works

Clostridium leptum group bacteria abundance and diversity in the fecal microbiota of patients with inflammatory bowel disease: a case–control study in India

Kabeerdoss, J., Vijayalakshmi, S. P., Pugazhendhi, S., & Ramakrishna, B. (2013) · BMC Gastroenterology · doi:10.1186/1471-230x-13-20 · Cited by 149 · see citing works

Fecal microbiota transplantation reverses antibiotic and chemotherapy-induced gut dysbiosis in mice

Le Bastard, Q., Ward, T., Sidiropoulos, D., Hillmann, B. M., Chun, C. L., Sadowsky, M. J., Knights, D., & Montassier, E. (2018) · Scientific Reports · doi:10.1038/s41598-018-24342-x · Cited by 134 · see citing works

Intestinal microbiota and allergic diseases: A systematic review

Melli, L. C. F. L., do Carmo-Rodrigues, M. S., Araújo-Filho, H. B., Solé, D., & de Morais, M. B. (2016) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2015.01.013 · Cited by 110 · see citing works

Fecal Microbiome and Food Allergy in Pediatric Atopic Dermatitis: A Cross-Sectional Pilot Study

Fieten, K. B., Totté, J. E. E., Levin, E., Reyman, M., Meijer, Y., Knulst, A. C., Schuren, F. H. J., & Pasmans, S. G. M. A. (2018) · International Archives of Allergy and Immunology · doi:10.1159/000484897 · Cited by 85 · see citing works

The Potential Link between Gut Microbiota and IgE-Mediated Food Allergy in Early Life

Molloy, J., Allen, K. J., Collier, F., Tang, M. L. K., Ward, A. C., & Vuillermin, P. (2013) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph10127235 · Cited by 69 · see citing works

Age-associated effect of kestose on Faecalibacterium prausnitzii and symptoms in the atopic dermatitis infants

Koga, Y., Tokunaga, S., Nagano, J., Sato, F., Konishi, K., Tochio, T., Murakami, Y., Masumoto, N., Tezuka, J.-I., Sudo, N., et al. (2016) · Pediatric Research · doi:10.1038/pr.2016.167 · Cited by 66 · see citing works

Association of altered gut microbiota composition with chronic urticaria

Nabizadeh, E., Jazani, N. H., Bagheri, M., & Shahabi, S. (2017) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2017.05.006 · Cited by 66 · see citing works

Comorbidities of Atopic Dermatitis: Beyond Rhinitis and Asthma

Andersen, Y. M. F., Egeberg, A., Skov, L., & Thyssen, J. P. (2017) · Current Dermatology Reports · doi:10.1007/s13671-017-0168-7 · Cited by 62 · see citing works

Faecalibacterium prausnitzii and Crohn’s Disease – is There any Connection?

Gałęcka, M., Szachta, P., Bartnicka, A., Łykowska‐Szuber, L., Eder, P., & Schwiertz, A. (2013) · Polish Journal of Microbiology · doi:10.33073/pjm-2013-013 · Cited by 24 · see citing works

Lack of association between GSTM1, GSTP1, and GSTT1 gene polymorphisms and asthma in adult patients from Rome, central Italy.

Piacentini, S., Polimanti, R. A., Moscatelli, B., Re, M. A., Manfellotto, D., & Fuciarelli, M. (2012) · PubMed · Cited by 22 · see citing works

The protective role of Helicobacter pylori neutrophil-activating protein in childhood asthma

Karakullukçu, A., Tokman, H. B., Nepesov, S., Demırci, M., Sarıbaş, S., Vehid, S., Caliskan, R., Taner, Z., Çokuğraş, H. C., Ziver, T., et al. (2017) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2017.01.008 · Cited by 10 · see citing works

Rola mikrobioty w zachowaniu zdrowego jelita

Szachta, P., Bartnicka, A., & Gałęcka, M. (2017) · Pomeranian Journal of Life Sciences · doi:10.21164/pomjlifesci.160 · Cited by 5 · see citing works

S1725 Interleukin 10 Acts on Regulatory T Cells to Maintain FOXP3 Expression and Suppressive Function in Mice With Colitis

Murai, M., Kim, G., Madan, R., Karp, C. L., Cheroutre, H., & Kronenberg, M. (2010) · Gastroenterology · doi:10.1016/s0016-5085(10)61195-x · Cited by 2 · see citing works

Faecalibacterium : a bacterial genus with promising human health applications

Martín, R., Ríos-Covián, D., Huillet, E., Auger, S., Khazaal, S., Bermúdez‐Humarán, L. G., Sokol, H., Chatel, J., & Langella, P. (2023) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuad039 · Cited by 583 · see citing works

The Cross-Talk Between Gut Microbiota and Lungs in Common Lung Diseases

Zhang, D., Li, S., Wang, N., Tan, H., Zhang, Z., & Feng, Y. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00301 · Cited by 437 · see citing works

Akkermansia muciniphila and Faecalibacterium prausnitzii in Immune-Related Diseases

Effendi, R. M. R. A., Anshory, M., Kalim, H., Dwiyana, R. F., Suwarsa, O., Pardo, L. M., Nijsten, T. E. C., & Thio, H. B. (2022) · Microorganisms · doi:10.3390/microorganisms10122382 · Cited by 190 · see citing works

Viral Infections, the Microbiome, and Probiotics

Harper, A., Vijayakumar, V., Ouwehand, A. C., ter Haar, J., Obis, D., Espadaler, J., Binda, S., Desiraju, S., & Day, R. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.596166 · Cited by 177 · see citing works

Microbiome dysbiosis in lung cancer: from composition to therapy

Liu, N., Ma, Q., Ge, Y., Yi, C., Wei, L., Tan, J.-C., Chu, Q., Li, J., Zhang, P., & Wang, H. (2020) · npj Precision Oncology · doi:10.1038/s41698-020-00138-z · Cited by 145 · see citing works

Revisiting the role of Akkermansia muciniphila as a therapeutic bacterium

Si, J., Kang, H., You, H. J., & Ko, G. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2078619 · Cited by 126 · see citing works

Faecalibacterium prausnitzii: A Next-Generation Probiotic in Gut Disease Improvement

He, X., Zhao, S., & Li, Y. (2021) · Canadian Journal of Infectious Diseases and Medical Microbiology · doi:10.1155/2021/6666114 · Cited by 117 · see citing works

Gut Microbiota, in the Halfway between Nutrition and Lung Function

Santo, C. E., Caseiro, C., Martins, M. J., Monteiro, R., & Brandão, I. (2021) · Nutrients · doi:10.3390/nu13051716 · Cited by 103 · see citing works

Capsaicin and Gut Microbiota in Health and Disease

Roşca, A. E., Ieșanu, M. I., Zahiu, C. D. M., Voiculescu, S. E., Paslaru, A. C., & Zăgrean, A. (2020) · Molecules · doi:10.3390/molecules25235681 · Cited by 102 · see citing works

The role of the probiotic Akkermansia muciniphila in brain functions: insights underpinning therapeutic potential

Xu, R., Zhang, Y., Chen, S., Zeng, Y., Fu, X., Chen, T., Luo, S., & Zhang, X. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2022.2044286 · Cited by 95 · see citing works

Prebiotics: Mechanisms and Preventive Effects in Allergy

Brosseau, C., Selle, A., Palmer, D. J., Prescott, S. L., Barbarot, S., & Bodinier, M. (2019) · Nutrients · doi:10.3390/nu11081841 · Cited by 88 · see citing works

Microbiome changes: an indicator of Parkinson’s disease?

Haikal, C., Chen, Q., & Li, J. (2019) · Translational Neurodegeneration · doi:10.1186/s40035-019-0175-7 · Cited by 84 · see citing works

Gut Microbiota: the Emerging Link to Lung Homeostasis and Disease

Zhou, A., Lei, Y., Tang, L., Hu, S., Yang, M., Wu, L., Yang, S., & Tang, B. (2020) · Journal of Bacteriology · doi:10.1128/jb.00454-20 · Cited by 78 · see citing works

Gut‐lung axis and asthma: A historical review on mechanism and future perspective

Song, X., Liang, J., Lin, S., Xie, Y., Ke, C., Ao, D., Lü, J., Chen, X., He, Y., Liu, X., et al. (2024) · Clinical and Translational Allergy · doi:10.1002/clt2.12356 · Cited by 71 · see citing works

Mode of action of Akkermansia muciniphila in the intestinal dialogue: role of extracellular proteins, metabolites and cell envelope components

Segers, A., & de Vos, W. M. (2023) · Microbiome Research Reports · doi:10.20517/mrr.2023.05 · Cited by 67 · see citing works

Microbiota Biomarkers for Lung Cancer

Leng, Q., Holden, V. K., Deepak, J., Todd, N. W., & Jiang, F. (2021) · Diagnostics · doi:10.3390/diagnostics11030407 · Cited by 66 · see citing works

Respiratory tract infections and gut microbiome modifications: A systematic review

Woodall, C. A., McGeoch, L. J., Hay, A. D., & Hammond, A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0262057 · Cited by 64 · see citing works

Disease-associated dysbiosis and potential therapeutic role of Akkermansia muciniphila, a mucus degrading bacteria of gut microbiome

Aggarwal, V., Sunder, S., & Verma, S. R. (2022) · Folia Microbiologica · doi:10.1007/s12223-022-00973-6 · Cited by 63 · see citing works

The role of gut microbiota in atopic asthma and allergy, implications in the understanding of disease pathogenesis

Salameh, M. A., Burney, Z. A., Mhaimeed, N., Laswi, I., Yousri, N. A., Bendriss, G., & Zakaria, D. (2019) · Scandinavian Journal of Immunology · doi:10.1111/sji.12855 · Cited by 62 · see citing works

The Association Between Intestinal Bacteria and Allergic Diseases—Cause or Consequence?

Han, P., Gu, J., Li, L., Wang, X., Wang, H., Wang, Y., Chang, C. C.-C., & Sun, J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.650893 · Cited by 62 · see citing works

Impact of Phlorotannin Extracts from Fucus vesiculosus on Human Gut Microbiota

Catarino, M. D., Marçal, C., Bonifácio-Lopes, T., Campos, D. A., Mateus, N. F. D. C. B., Silva, A. M. S., Pintado, M. M., & Cardoso, S. M. (2021) · Marine Drugs · doi:10.3390/md19070375 · Cited by 62 · see citing works

Probiotics in the prophylaxis of COVID-19: something is better than nothing

Gohil, K. N., Samson, R., Dastager, S. G., & Dharne, M. S. (2020) · 3 Biotech · doi:10.1007/s13205-020-02554-1 · Cited by 57 · see citing works

The abundance of Ruminococcus bromii is associated with faecal butyrate levels and atopic dermatitis in infancy

Sasaki, M., Schwab, C., Garcia, A. R., Li, Q., Ferstl, R., Bersuch, E., Akdiş, C. A., Lauener, R. P., CK‐CARE study group, Frei, R., et al. (2022) · Allergy · doi:10.1111/all.15440 · Cited by 57 · see citing works

Cross-talk between airway and gut microbiome links to IgE responses to house dust mites in childhood airway allergies

Chiu, C., Chan, Y., Tsai, M., Wang, C., Chiang, M., Chiu, C., & Su, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-70528-7 · Cited by 52 · see citing works

Cross-talk between immune system and microbiota in COVID-19

Ghavami, S. B., Pourhamzeh, M., Farmani, M., Raftar, S. K. A., Shahrokh, S., Shpichka, A. I., Aghdaei, H. A., Hakemi-Vala, M., Hossein‐Khannazer, N., Timashev, P. S., et al. (2021) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2021.1991311 · Cited by 49 · see citing works

The Role of CD4+ T Cells and Microbiota in the Pathogenesis of Asthma

Jeong, J., & Lee, H. K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111822 · Cited by 52 · see citing works

Salinity significantly affects intestinal microbiota and gene expression in striped catfish juveniles

Hieu, D. Q., Hằng, B. T. B., Lokesh, J., Garigliany, M.-M., Huong, D. T. T., Yên, D. T., Liêm, P. T., Tâm, B. M., Hai, D. M., Sơn, V. N., et al. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-11895-1 · Cited by 49 · see citing works

Probiotics Prevents Sensitization to Oral Antigen and Subsequent Increases in Intestinal Tight Junction Permeability in Juvenile–Young Adult Rats

Tulyeu, J., Kumagai, H., Jimbo, E. F., Watanabe, S., Yokoyama, K., Cui, L., Osaka, H., Mieno, M., & Yamagata, T. (2019) · Microorganisms · doi:10.3390/microorganisms7100463 · Cited by 49 · see citing works

The Role of Short-Chain Fatty Acids in the Interplay between a Very Low-Calorie Ketogenic Diet and the Infant Gut Microbiota and Its Therapeutic Implications for Reducing Asthma

Alsharairi, N. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249580 · Cited by 46 · see citing works

Goat Milk Consumption Enhances Innate and Adaptive Immunities and Alleviates Allergen-Induced Airway Inflammation in Offspring Mice

Kao, H.-F., Wang, Y.-C., Tseng, H.-Y., Wu, L. S.-H., Tsai, H., Hsieh, M.-H., Chen, P., Kuo, W.-S., Liu, L., Liu, Z.-G., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00184 · Cited by 44 · see citing works

Health and Disease:Akkermansia muciniphila, the Shining Star of the Gut Flora

Xue, C., Li, G., Gu, X., Su, Y., Zheng, Q., Yuan, X. H., Bao, Z., Lu, J., & Li, L. (2023) · Research · doi:10.34133/research.0107 · Cited by 43 · see citing works

Gut Microbiota-Derived Tryptophan Metabolites Alleviate Allergic Asthma Inflammation in Ovalbumin-Induced Mice

Wang, H., He, Y., Dang, D., Zhao, Y., Zhao, J., & Lu, W. (2024) · Foods · doi:10.3390/foods13091336 · Cited by 39 · see citing works

Gut Microbiota in Bone Health and Diabetes

Knudsen, J. K., Leutscher, P., & Sørensen, S. (2021) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00629-9 · Cited by 38 · see citing works

Paradoxical Reactions to Anti-TNFα and Anti-IL-17 Treatment in Psoriasis Patients: Are Skin and/or Gut Microbiota Involved?

Zakostelska, Z. J., Reiss, Z., Tlaskalová‐Hogenová, H., & Rob, F. (2023) · Dermatology and Therapy · doi:10.1007/s13555-023-00904-4 · Cited by 40 · see citing works

Oral administration of Faecalibacterium prausnitzii and Akkermansia muciniphila strains from humans improves atopic dermatitis symptoms in DNCB induced NC/Nga mice

Lee, Y., Byeon, H. R., Jang, S.-Y., Hong, M.-G., Kim, D., Lee, D., Shin, J., Kim, Y., Kang, S. G., & Seo, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-11048-4 · Cited by 38 · see citing works

The establishment of the gut microbiota in 1-year-aged infants: from birth to family food

Vacca, M., Raspini, B., Calabrese, F. M., Porri, D., Giuseppe, R. D., Chieppa, M., Liso, M., Cerbo, R. M., Civardi, E., Garofoli, F., et al. (2022) · European Journal of Nutrition · doi:10.1007/s00394-022-02822-1 · Cited by 35 · see citing works

Human Breast Milk: The Role of Its Microbiota and Metabolites in Infant Health

Zhang, M., Qiao, H., Yang, S., Kwok, L., Zhang, H., & Zhang, W. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c07690 · Cited by 34 · see citing works

The Influence of the Gut Microbiota on Host Health: A Focus on the Gut–Lung Axis and Therapeutic Approaches

Alswat, A. S. (2024) · Life · doi:10.3390/life14101279 · Cited by 35 · see citing works

The role of Akkermansia muciniphila in maintaining health: a bibliometric study

Gao, F., Cheng, C., Li, R., Chen, Z., Tang, K., & Du, G. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1484656 · Cited by 38 · see citing works

Gu-Ben-Fang-Xiao Decoction Ameliorated Murine Asthma in Remission Stage by Modulating Microbiota-Acetate-Tregs Axis

Dong, Y., Yan, H., Zhao, X., Lin, R., Lin, L., Ding, Y., Liu, L., Ren, L., Xing, Q.-Q., & Ji, J. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00549 · Cited by 34 · see citing works

KGNMDA: A Knowledge Graph Neural Network Method for Predicting Microbe-Disease Associations

Jiang, C., Tang, M., Jin, S., Huang, W., & Liu, X. (2022) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2022.3184362 · Cited by 32 · see citing works

Role of gut-lung microbiome crosstalk in COVID-19

Srinath, B. S., Shastry, R. P., & Bajire, S. K. (2020) · Research on Biomedical Engineering · doi:10.1007/s42600-020-00113-4 · Cited by 29 · see citing works

Gut-lung axis in allergic asthma: microbiota-driven immune dysregulation and therapeutic strategies

Lv, J., Zhang, Y., Liu, S., Wang, R., & Zhao, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1617546 · Cited by 29 · see citing works

Gut microbiota dysbiosis and its impact on asthma and other lung diseases: potential therapeutic approaches

Kim, Y., Sohn, K., & Kang, H. (2024) · The Korean Journal of Internal Medicine · doi:10.3904/kjim.2023.451 · Cited by 28 · see citing works

Health Impact and Therapeutic Manipulation of the Gut Microbiome

Daliri, E. B., Ofosu, F. K., Chelliah, R., Lee, B. H., & Oh, D. (2020) · Microarrays · doi:10.3390/ht9030017 · Cited by 28 · see citing works

Akkermansia muciniphila: The state of the art, 18 years after its first discovery

Iwaza, R., Wasfy, R. M., Dubourg, G., Raoult, D., & Lagier, J. (2022) · Frontiers in Gastroenterology · doi:10.3389/fgstr.2022.1024393 · Cited by 30 · see citing works

A Next-Generation Bacteria (Akkermansia muciniphila BAA-835) Presents Probiotic Potential Against Ovalbumin-Induced Food Allergy in Mice

Miranda, V. C., Souza, R. O., Quintanilha, M. F., Gallotti, B., de Assis, H. C., Faria, A. M. C., Nicoli, J. R., Cara, D. C., & Martins, F. S. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10076-4 · Cited by 27 · see citing works

From anaerobes to aerointolerant prokaryotes

Ndongo, S., Khelaifia, S., Lagier, J., & Raoult, D. (2020) · Human Microbiome Journal · doi:10.1016/j.humic.2019.100068 · Cited by 15 · see citing works

Gut microbiota comparison of vaginally and cesarean born infants exclusively breastfed by mothers secreting α1–2 fucosylated oligosaccharides in breast milk

Tonon, K. M., Morais, T. B., Taddei, C. R., Filho, H. B. D. A., Abrão, A. C. F. V., Miranda, A., & de Morais, M. B. (2021) · PLoS ONE · doi:10.1371/journal.pone.0246839 · Cited by 26 · see citing works

Heat-killed Akkermansia muciniphila ameliorates allergic airway inflammation in mice

Yoon, S. A., Lim, Y., Byeon, H. R., Jung, J.-Y., Ma, S., Hong, M.-G., Kim, D., Song, E., Nam, Y., Seo, J., et al. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1386428 · Cited by 25 · see citing works

Maternal supplementation with Bifidobacterium breve M-16V prevents their offspring from allergic airway inflammation accelerated by the prenatal exposure to an air pollutant aerosol

Terada-Ikeda, C., Kitabatake, M., Hiraku, A., Kato, K., Yasui, S., Imakita, N., Ouji-Sageshima, N., Iwabuchi, N., Hamada, K., & Ito, T. (2020) · PLoS ONE · doi:10.1371/journal.pone.0238923 · Cited by 25 · see citing works

A probiotic has differential effects on allergic airway inflammation in A/J and C57BL/6 mice and is correlated with the gut microbiome

Casaro, M. B., Thomas, A. M., Mendes, E., Fukumori, C., Ribeiro, W. R., Oliveira, F. A., Crisma, A. R., Murata, G. M., Bizzarro, B., Sá-Nunes, A., et al. (2021) · Microbiome · doi:10.1186/s40168-021-01081-2 · Cited by 24 · see citing works

Type 3 resistant starch from Canna edulis reduce lipid levels in patients with mild hyperlipidemia through altering gut microbiome: A double- blind randomized controlled trial

Miao, T., Zhang, X., Zhang, C., Wu, J., Zhu, Y., Xiao, M., Zhang, N., Zhong, Y., Liu, Y., Lin, Y., et al. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107232 · Cited by 26 · see citing works

Immunomodulatory Roles of Faecalibacterium prausnitzii and Akkermansia muciniphila in Autoimmune Diseases: Mechanistic Insights and Therapeutic Potential

Han, E. J., Ahn, J., Chae, Y. J., & Chung, H. (2025) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-025-09093-8 · Cited by 27 · see citing works

A. muciniphila Supplementation in Mice during Pregnancy and Lactation Affects the Maternal Intestinal Microenvironment

Qi, Y., Yu, L., Tian, F., Zhao, J., Zhang, H., Chen, W., & Zhai, Q. (2022) · Nutrients · doi:10.3390/nu14020390 · Cited by 21 · see citing works

Microbial Reprogramming in Obsessive–Compulsive Disorders: A Review of Gut–Brain Communication and Emerging Evidence

Bendriss, G., MacDonald, R. S., & McVeigh, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241511978 · Cited by 25 · see citing works

Predicting potential microbe-disease associations with graph attention autoencoder, positive-unlabeled learning, and deep neural network

Peng, L., Huang, L., Tian, G., Wu, Y., Li, G., Cao, J., Wang, P., Li, Z., & Duan, L. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1244527 · Cited by 21 · see citing works

The human microbiome in space: parallels between Earth-based dysbiosis, implications for long-duration spaceflight, and possible mitigation strategies

Etlin, S. M., Rose, J. K., Bielski, L., Walter, C. E., Kleinman, A. S., & Mason, C. E. (2024) · Clinical Microbiology Reviews · doi:10.1128/cmr.00163-22 · Cited by 23 · see citing works

Microbiota associations with inflammatory pathways in asthma

Wang, J., Chai, J., Zhang, L., Zhang, L., Yan, W., Sun, L., Chen, Y., Sun, Y., Zhao, J., & Chang, C. H. (2021) · Clinical & Experimental Allergy · doi:10.1111/cea.14089 · Cited by 20 · see citing works

Uncovering the core principles of the gut-lung axis to enhance innate immunity in the chicken

Saint-Martin, V., Quéré, P., Trapp, S., & Guabiraba, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.956670 · Cited by 22 · see citing works

Does “all disease begin in the gut”? The gut-organ cross talk in the microbiome

Chaudhary, P. P., Kaur, M., & Myles, I. A. (2024) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-024-13180-9 · Cited by 26 · see citing works

The Impact of Diet on Gut Microbiome Composition: Implications for Immune-Mediated Diseases - Clinical Immunology Communications

Rondinella, D., Margarita, E., Raoul, P., Galli, F. S., Severino, A., Porcari, S., Mele, M. C., Gasbarrini, A., Cammarota, G., Rinninella, E., et al. (2025) · Clinical Immunology Communications · doi:10.1016/j.clicom.2025.12.001 · Cited by 17 · see citing works

Similar bacterial signatures in the gut microbiota of type 1 and type 2 diabetes patients and its association with G protein-coupled receptor 41 and 43 gene expression

Demırci, M., Taner, Z., Keskin, F. E., Özyazar, M., Kiraz, N., Kocazeybek, B. S., & Tokman, H. B. (2022) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-022-01068-2 · Cited by 18 · see citing works

Respiratory tract microbiome and pneumonia

Narendrakumar, L., & Ray, A. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.07.002 · Cited by 18 · see citing works

Probiotics in Infancy and Childhood for Food Allergy Prevention and Treatment

Costanzo, M. D., Vella, A., Infantino, C., Morini, R., Bruni, S., Esposito, S., & Biasucci, G. (2024) · Nutrients · doi:10.3390/nu16020297 · Cited by 18 · see citing works

Predicting potential microbe-disease associations based on heterogeneous graph attention network and deep sparse autoencoder

Wang, B., Zhao, W., Du, X., Zhang, J., Zhang, C., Wang, L., & He, Y. (2025) · Engineering Applications of Artificial Intelligence · doi:10.1016/j.engappai.2025.110301 · Cited by 16 · see citing works

Leonurine protects against ulcerative colitis by alleviating inflammation and modulating intestinal microflora in mouse models

Zheng, S., Zhuang, T., Tang, Y., Wu, R., Xu, T., Leng, T., Wang, Y., Lin, Z., & Ji, M. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10633 · Cited by 16 · see citing works

Dietary Boswellia serrata Acid Alters the Gut Microbiome and Blood Metabolites in Experimental Models

Suther, C., Daddi, L., Bokoliya, S. C., Panier, H. A., Liu, Z., Lin, Q., Han, Y., Chen, K., Moore, M. D., & Zhou, Y. (2022) · Nutrients · doi:10.3390/nu14040814 · Cited by 16 · see citing works

The Role of the Gallbladder, the Intestinal Barrier and the Gut Microbiota in the Development of Food Allergies and Other Disorders

Abril, A. G., Villa, T., Sánchez-Pérez, Á., Notario, V., & Carrera, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214333 · Cited by 16 · see citing works

[Computer-assisted cognitive training of schizophrenic patients. Use of evaluation outcome for developing an individualized training method].

Geibel-Jakobs, M., & Olbrich, R. (1998) · PubMed · Cited by 15 · see citing works

Traditional Chinese medicine to improve immune imbalance of asthma: focus on the adjustment of gut microbiota

Ke, L., Li, C., Men, J., Xu, B., Yang, C., Yan, P., Gai, Z., Zhang, Q., & Zhang, L. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1409128 · Cited by 14 · see citing works

Causal associations between gut microbiota, metabolites and asthma: a two-sample Mendelian randomization study

Li, J., Zhang, C., Tang, J., He, M., He, C., Pu, G., Liu, L., & Sun, J. (2024) · BMC Pulmonary Medicine · doi:10.1186/s12890-024-02898-x · Cited by 14 · see citing works

No effects of a 4-week post-exercise sauna bathing on targeted gut microbiota and intestinal barrier function, and hsCRP in healthy men: a pilot randomized controlled trial

Karolkiewicz, J., Nieman, D. C., Cisoń, T., Szurkowska, J., Gałęcka, M., Sitkowski, D., & Szyguła, Z. (2022) · BMC Sports Science Medicine and Rehabilitation · doi:10.1186/s13102-022-00497-z · Cited by 13 · see citing works

Prevention and alleviation of allergic rhinitis by oral administration of Lacticaseibacillus paracasei GOLDGUT-Lpc969

Zhou, X., Song, X., Shu, T., Zhang, S., Zhang, Z., Hu, C., Pan, J., Dai, X., Hao, H., Xiao, G., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1444778 · Cited by 14 · see citing works

Water extract of Pingchuan formula ameliorated murine asthma through modulating metabolites and gut microbiota

Liu, F., Duan, W., Guan, T., Zhou, Q., Yan, W., & Geng, Y. (2023) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2023.115728 · Cited by 12 · see citing works

Bacteria and fungi of the lung: allies or enemies?

Garaci, E., Pariano, M., Nunzi, E., Costantini, C., Bellet, M. M., Antognelli, C., Russo, M. A., & Romani, L. R. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1497173 · Cited by 12 · see citing works

Efficacy of ETB-F01, Heat-Killed Akkermansia muciniphila Strain EB-AMDK19, in Patients with Respiratory Symptoms: A Multicenter Clinical Trial

Lee, H. W., Lee, S., Seo, J., Koo, Y., Kang, S., Choi, C. W., Park, S., Lee, S., Kim, S., Kim, J. H., et al. (2024) · Nutrients · doi:10.3390/nu16234113 · Cited by 12 · see citing works

Extremely small and incredibly close: Gut microbes as modulators of inflammation and targets for therapeutic intervention

Piazzesi, A., & Putignani, L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.958346 · Cited by 12 · see citing works

The Role of Gut Bacteriome in Asthma, Chronic Obstructive Pulmonary Disease and Obstructive Sleep Apnoea

Bikov, A., Dragonieri, S., Csoma, B., Mazzuca, C., Finamore, P., Rocchi, G., Putignani, L., Guarino, M. P. L., & Scarlata, S. (2022) · Microorganisms · doi:10.3390/microorganisms10122457 · Cited by 11 · see citing works

SAELGMDA: Identifying human microbe–disease associations based on sparse autoencoder and LightGBM

Wang, F., Yang, H., Wu, Y., Peng, L., & Li, X.-L. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1207209 · Cited by 11 · see citing works

The Microbiota and Equine Asthma: An Integrative View of the Gut–Lung Axis

Leduc, L., Costa, M., & Leclère, M. (2024) · Animals · doi:10.3390/ani14020253 · Cited by 10 · see citing works

The association of infant and mother gut microbiomes with development of allergic diseases in children: a systematic review

Mousavian, A.-H., Garizi, F. Z., Ghoreshi, B., Ketabi, S., Eslami, S., Ejtahed, H., & Qorbani, M. (2024) · Journal of Asthma · doi:10.1080/02770903.2024.2332921 · Cited by 11 · see citing works

Lactobacillus reuteri CCFM1175 and Lactobacillus paracasei CCFM1176 Could Prevent Capsaicin-Induced Ileal and Colonic Injuries

Mao, B., Xiang, Q., Tang, X., Zhang, Q., Liu, X., Zhao, J., Cui, S., & Zhang, H. (2023) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-023-10106-1 · Cited by 9 · see citing works

State of the art: Alternative overlap syndrome—asthma and obstructive sleep apnea

Ioachimescu, O. C. (2024) · Journal of Investigative Medicine · doi:10.1177/10815589241249993 · Cited by 11 · see citing works

Characteristics of gut microbiota and serum metabolism in patients with atopic dermatitis

Zeng, Y., Fan, N., Gu, X., Zhang, Y., Wei, M., Mao, Q., & Qian, Q. (2024) · Skin Research and Technology · doi:10.1111/srt.13792 · Cited by 9 · see citing works

Isolation, probiotic characterization and whole-genome sequencing of gut Faecalibacterium prausnitzii

Sun, X., Zhang, Z., & Hu, J. (2025) · Human Nutrition & Metabolism · doi:10.1016/j.hnm.2025.200315 · Cited by 9 · see citing works

Modulation of Gut Microbiota by Traditional Chinese Medicine: A Novel Therapeutic Approach for Chronic Inflammatory Airway Diseases

Zheng, L., Fu, Y., Jiawang, W., Liu, T., Zhang, X., Qu, C., Zeng, B., Zhang, N., Xu, S., Yang, J., et al. (2025) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x25500764 · Cited by 9 · see citing works

Application of PCR-Based Techniques for the Identification of Genetic Fingerprint Diversity of Dominant Bacteria in Fecal Samples of Children with Diarrhea in Vietnam

Nguyen, T. Q., Dao, T. K., Nguyen, H. D., Phung, T. B. T., Pham, T. T. N., Nguyen, T. V. H., Trinh, T. H., Le, H. C., Le, T. T. H., & Huyen, T. (2024) · Infectious Disease Reports · doi:10.3390/idr16050075 · Cited by 9 · see citing works

The Changes in Bacterial Microbiome Associated with Immune Disorder in Allergic Respiratory Disease

Lyu, J., Kou, F., Men, X., Liu, Y., Tang, L., & Shu, W. (2022) · Microorganisms · doi:10.3390/microorganisms10102066 · Cited by 9 · see citing works

The worldview of Akkermansia muciniphila, a bibliometric analysis

Zhang, Z., Wang, J., Dang, S., Liu, X., Zhang, Y., & Zhang, H. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1500893 · Cited by 9 · see citing works

Response of Akkermansia muciniphila to Bioactive Compounds: Effects on Its Abundance and Activity

Temis-Cortina, J. A., Prada-Ramírez, H. A., Ríos-Guerra, H., Espinosa‐Raya, J., & Gómez‐Pliego, R. (2025) · Fermentation · doi:10.3390/fermentation11080427 · Cited by 8 · see citing works

Advances in the Gut‐Lung Axis and Bronchial Asthma: From Mechanisms to Therapeutic Potential

Zheng, T., Huang, Y., & Yao, H. (2025) · Clinical and Translational Allergy · doi:10.1002/clt2.70128 · Cited by 8 · see citing works

Oral Microbiota Signatures in the Pathogenesis of Euthyroid Hashimoto’s Thyroiditis

Erdem, M. G., Ünlü, Ö., Ates, F., Karış, D., & Demırci, M. (2023) · Biomedicines · doi:10.3390/biomedicines11041012 · Cited by 8 · see citing works

Akkermansia muciniphila and herbal medicine in immune-related diseases: current evidence and future perspectives

Ding, X., Meng, P., Ma, X., Yue, J.-Y., Li, L., & Xu, L. (2024) · Frontiers in Microbiomes · doi:10.3389/frmbi.2024.1276015 · Cited by 9 · see citing works

Causal associations among gut microbiota, 1400 plasma metabolites, and asthma: a two-sample Mendelian randomization study

Wang, L., & Lv, Z. (2024) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2024.1370919 · Cited by 7 · see citing works

Harnessing Next‐Generation 3D Cancer Models to Elucidate Tumor‐Microbiome Crosstalk

Buzhor, M. G., Longobardi, G., Kandli, O., Krinsky, A., Avramoff, O., Katyal, A., Salomon, K., Miari, A., Venkert, D., Barnatan, T. T., et al. (2025) · Advanced Healthcare Materials · doi:10.1002/adhm.202503198 · Cited by 7 · see citing works

A Comparative Pilot Study of Bacterial and Fungal Dysbiosis in Neurodevelopmental Disorders and Gastrointestinal Disorders: Commonalities, Specificities and Correlations with Lifestyle

Laswi, I., Shafiq, A., Al‐Ali, D., Burney, Z. A., Pillai, K. V., Salameh, M. A., Mhaimeed, N., Zakaria, D., Châari, A., Yousri, N. A., et al. (2021) · Microorganisms · doi:10.3390/microorganisms9040741 · Cited by 8 · see citing works

Prophylactic treatment of Lacticaseibacillus paracasei K56 ameliorates asthma by regulating short-chain fatty acid production and Treg differentiation

Cui, J., Hong, Y., Liu, W., Zhao, W., Nan, X., Shang, X., Li, Y., Feng, H., Jiang, Q., Hung, W., et al. (2024) · Food Science and Human Wellness · doi:10.26599/fshw.2024.9250036 · Cited by 6 · see citing works

The advantages of Faecalibacterium prasnitzii in gestational diabetes mellitus

Safarzadeh, H., Aliramezani, A., Rahimi, A., Yousefi, B., & Heidarzadeh, S. (2025) · Future Microbiology · doi:10.1080/17460913.2025.2520699 · Cited by 6 · see citing works

Exploring clade differentiation of the Faecalibacterium prausnitzii complex

Fabbrini, M., Candela, M., Turroni, S., Brigidi, P., & Rampelli, S. (2022) · iScience · doi:10.1016/j.isci.2022.105533 · Cited by 6 · see citing works

Both living and dead Faecalibacterium prausnitzii alleviate house dust mite‐induced allergic asthma through the modulation of gut microbiota and short‐chain fatty acid production

Hu, W., Lu, W., Li, L., Zhang, H., Lee, Y., Chen, W., & Zhao, J. (2021) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.11207 · Cited by 63 · see citing works

Microbiota and Potential Asthma Markers: A Case Control Study in a Sample of Egyptian Children

Abdelhamid, E. R., Refay, A. S. E., Elkhatib, A. A., Armaneous, A. F., Sherif, L. S., Hussien, S. M., Hashish, A. F., & Mehanna, N. S. (2022) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/2560

Allergic Patients with Long-Term Asthma Display Low Levels of Bifidobacterium adolescentis

Hevia, A., Milani, C., López, P., Donado, C. D., Cuervo, A., González, S., Suárez, A., Turroni, F., Gueimonde, M., Ventura, M., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147809 · Cited by 109 · see citing works

Intestinal Microbes-based Analysis of Immune Mechanism of Childhood Asthma

Mo, M., Wang, J., Gu, H., Zhou, J., Zheng, C., Zheng, Q., & Chen, H. (2022) · Cellular and Molecular Biology · doi:10.14715/cmb/2022.68.2.11 · Cited by 6 · see citing works

Altered IgA Response to Gut Bacteria Is Associated with Childhood Asthma in Peru

Hsieh, C., Rengarajan, S., Kau, A. L., Tarazona-Meza, C. E., Nicholson, A., Checkley, W., Romero, K. M., & Hansel, N. N. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2001296 · Cited by 17 · see citing works