Age-associated B cells in autoimmune diseases

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

Longitudinal analysis reveals high prevalence of Epstein-Barr virus associated with multiple sclerosis

Bjornevik, K., Cortese, M., Healy, B. C., Kuhle, J., Mina, M. J., Leng, Y., Elledge, S. J., Niebuhr, D. W., Scher, A. I., Munger, K. L., et al. (2022) · Science · doi:10.1126/science.abj8222 · Cited by 2,049

Epidemiology and estimated population burden of selected autoimmune diseases in the United States

Jacobson, D. L., Gange, S. J., Rose, N. R., & Graham, N. M. H. (1997) · Clinical Immunology and Immunopathology · doi:10.1006/clin.1997.4412 · Cited by 1,667

B cells regulate autoimmunity by provision of IL-10

Fillatreau, S., Sweenie, C. H., McGeachy, M. J., Gray, D., & Anderton, S. M. (2002) · Nature Immunology · doi:10.1038/ni833 · Cited by 1,647

Distinct Effector B Cells Induced by Unregulated Toll-like Receptor 7 Contribute to Pathogenic Responses in Systemic Lupus Erythematosus

Jenks, S. A., Cashman, K. S., Zumaquero, E., Marigorta, U. M., Patel, A. V., Wang, X., Tomar, D., Woodruff, M. C., Simon, Z., Bugrovsky, R., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.08.015 · Cited by 1,078

IL-35-producing B cells are critical regulators of immunity during autoimmune and infectious diseases

Shen, P., Roch, T., Lampropoulou, V., O’Connor, R. A., Stervbo, U., Hilgenberg, E., Ries, S., Dang, V. D., Jaimes, Y., Daridon, C., et al. (2014) · Nature · doi:10.1038/nature12979 · Cited by 1,048

Rituximab (monoclonal anti-CD20 antibody): mechanisms of action and resistance

Smith, M. R. (2003) · Oncogene · doi:10.1038/sj.onc.1206939 · Cited by 835

Toll-like receptor 7 (TLR7)–driven accumulation of a novel CD11c+ B-cell population is important for the development of autoimmunity

Rubtsov, A. V., Rubtsova, K., Fischer, A., Meehan, R. T., Gillis, J. Z., Kappler, J. W., & Marrack, P. (2011) · Blood · doi:10.1182/blood-2011-01-331462 · Cited by 808

Extrafollicular B cell responses correlate with neutralizing antibodies and morbidity in COVID-19

Woodruff, M. C., Ramonell, R. P., Nguyen, D. C., Cashman, K. S., Saini, A. S., Haddad, N. S., Ley, A. M., Kyu, S., Howell, J. C., Ozturk, T., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-00814-z · Cited by 791

B cell depletion as a novel treatment for systemic lupus erythematosus: A phase I/II dose‐escalation trial of rituximab

Looney, R. J., Anolik, J. H., Campbell, D., Felgar, R. E., Young, F. M., Arend, L. J., Sloand, J. A., Rosenblatt, J. D., & Sanz, I. (2004) · Arthritis & Rheumatism · doi:10.1002/art.20430 · Cited by 779

A population-scale atlas of blood and tissue in lupus nephritisPreprint

Sugiarto, N. W., Gurajala, S., Curtis, M. L., Eisenhaure, T., Arazi, A., Fava, A., Xiao, Q., Mears, J., Rovin, B. H., Berthier, C. C., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.11.669754 · Cited by 4

Advanced strategies for targeting molecular pathways in Sjögren’s syndrome

Wang, D., Liu, Y., Lu, X., & Xu, F. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117116 · Cited by 3

Single-cell multi-omics analysis revealed the expansion of age-associated B cells in the pancreas of type 1 autoimmune pancreatitis patients

Wang, J., Liu, C., Zhang, X., Che, T., Zhao, Y., Yang, Q., Qin, X., Chen, Y., Ao, X., Shen, X., et al. (2025) · Genome Medicine · doi:10.1186/s13073-025-01567-w · Cited by 4

B cell-specific METTL3 depletion exacerbates experimental autoimmune encephalomyelitis

Pei, X., Wang, X., Ding, J., Yu, H., Xue, C., Xie, C., Chen, Y., Lin, X., Yang, H., & Guan, Y. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-06028-6 · Cited by 3

Presence of sputum IgG against eosinophilic inflammatory proteins in asthma

Qin, R., Long, F., Zhang, P., Huang, R., Hu, H., Guo, Y., Zheng, Z., Xiao, J., Li, H., Peng, T., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1423764 · Cited by 3

Novel model of multiple sclerosis induced by EBV-like virus generates a unique B cell population

Deffenbaugh, J. L., Jung, K.-J., Murphy, S. P., Liu, Y., Rau, C. N., Petersen‐Cherubini, C. L., Collins, P. L., Chung, D., & Lovett‐Racke, A. E. (2024) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2024.578408 · Cited by 3

Impact of Fli1 deletion on B cell populations: A focus on age-associated B cells and transcriptional dynamics

Awaji, K., Shibata, S., Koyama, A., Yamamoto, T., Fukui, Y., Toyama, S., Omatsu, J., Norimatsu, Y., Ikawa, T., Watanabe, Y., et al. (2024) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2024.12.003 · Cited by 3

Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system mice

Maharlooei, M. K., Vecchione, A., Danzl, N. M., Li, H. W., Nauman, G., Madley, R., Waffarn, E., WINCHESTER, R. J., Ruiz, A., Ding, X., et al. (2025) · eLife · doi:10.7554/elife.99389.3 · Cited by 3

Role of animal models in understanding the mechanisms of autoimmune diseases

Khan, W. N., Lacoume, G. M., & Greidinger, E. L. (2025) · Autoimmunity · doi:10.1080/08916934.2025.2531766 · Cited by 4

B-1a Cells, but Not Marginal Zone B Cells, Are Implicated in the Accumulation of Autoreactive Plasma Cells in Lyn−/− Mice

Ottens, K., Schneider, J., & Satterthwaite, A. B. (2024) · ImmunoHorizons · doi:10.4049/immunohorizons.2300089 · Cited by 3

Highlights of 2024: The rising role of age‐associated B cells in autoimmune diseases

Lee, A. Y. S., & Reed, J. H. (2025) · Immunology and Cell Biology · doi:10.1111/imcb.70023 · Cited by 3

Immune and molecular landscape behind non-response to Mycophenolate Mofetil and Azathioprine in lupus nephritis therapyPreprint

López-Domínguez, R., Villatoro-García, J. A., Marañón, C., GOLDMAN, D. W., Petri, M., Carmona‐Sáez, P., Alarcón-Riquelme, M. E., & Toro‐Domínguez, D. (2024) · Research Square · doi:10.21203/rs.3.rs-3783877/v1 · Cited by 5

Function and Regulation of Age‐Associated B Cells in Diseases

Geng, Z., Cao, Y., Zhao, L., Wang, L., Dong, Y., Bi, Y., & Liu, G. (2025) · Journal of Cellular Physiology · doi:10.1002/jcp.31522 · Cited by 4

B cell-intrinsic interleukin 17 receptor A signaling supports the establishment of chronic murine gammaherpesvirus 68 infection

Majeed, S. T., Huss, N. P., Bradford, S. M., & Jondle, C. N. (2025) · Journal of Virology · doi:10.1128/jvi.01842-25 · Cited by 1

ODC1 restricts meningeal B cell age-associated-like phenotype and function in multiple sclerosis: A human and experimental study

Zurawski, J. D., Tuncer, A., Profant, M. R., Wang, J., Green, M., Park, Y., Cao, K., Paris, S., Tauhid, S., Jalkh, Y., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2526147123 · Cited by 2

Tissue‐Specific Expansion of Age‐Associated B Cells via IFN‐γ and IL‐21 Within Salivary Glands in Sjögren Disease

Nishida, M., Otsuka, K., Nagao, R., Matsuzawa, S., Ushio, A., Tsunematsu, T., Aota, K., & Ishimaru, N. (2026) · Journal of Immunology Research · doi:10.1155/jimr/4221251 · Cited by 2

Age-associated B cells, key players in autoimmune pathogenesis

Hassani, S.-S., Ekrani, S. T., Rajabinejad, M., Faraj, T. A., Rezaiemanesh, A., & Esmaeili, S. (2026) · Immunity & Ageing · doi:10.1186/s12979-026-00564-w · Cited by 3

Biomarkers of Immune Dysregulation and What They Tell Us

Nguyen, T. H., & Chandrakasan, S. (2025) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2025.01.003 · Cited by 2

The impact of pre‐transplant anti‐HLA antibodies in transplants from HLA ‐identical sibling donors: A multicenter study

Wei, X., Chang, Y., Zhu, X., Hu, X., Guo, R., Zhang, Y., Ma, X., Han, Y., Wang, Y., Qiu, H., et al. (2023) · HLA · doi:10.1111/tan.15286 · Cited by 2

Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system micePreprint

Khosravi-Maharlooei, M., Vecchione, A., Danzl, N. M., Li, H. W., Nauman, G., Madley, R., Waffarn, E., WINCHESTER, R. J., Ruiz, A., Ding, X., et al. (2024) · eLife · doi:10.7554/elife.99389 · Cited by 2

Increased Fascin1 and Pak1 Expressions Enhance Age‐Associated B‐Cell Actin Cytoskeleton Remodeling and Motility

Fujiwara, M., Kondo, R., Sugiyama, Y., Maruyama, M., & Nishikimi, A. (2025) · Cell Biochemistry and Function · doi:10.1002/cbf.70090 · Cited by 1

CD19+CD11c+T-bet+ B cells in myasthenia gravis: a potential biomarker

Lu, Y., Shen, H., Wang, Y., Ma, K., Sun, R., Zhao, Y., Li, Y., Ma, Q., & Zhang, J. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2025.1623066 · Cited by 1

Oxidative Stress and Antioxidants in the Aging Brain

Pamu, S., Potdar, M. B., Parameshwar, K., Rajput, D., & Kaushik, M. (2025) · Nutritional neurosciences · doi:10.1007/978-981-95-2790-8_7 · Cited by 1

Temporal dynamics of IgG-mediated immunometabolic dysfunction: from acute obesity to chronic aging

Kim, S., Kim, J.-H., Lee, H.-L., & Kim, M. S. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1661391 · Cited by 1

Immunosenescence and Cancer: Cellular Aging Programs That Reshape Antitumor Immunity

Oh, S.-H., Kim, Y. W., Kim, S. H., & Chang, S.-Y. (2026) · Immune Network · doi:10.4110/in.2026.26.e15 · Cited by 2

Investigations of remibrutinib in models pertinent to multiple sclerosis

Jain, R. W., Rayatpour, A., Hagen, K. M., Mørch, M. T., Randhawa, G., Mobarakabadi, M., Zhang, X., Li, C., Nakhaei‐Nejad, M., Giuliani, F., et al. (2026) · Neurotherapeutics · doi:10.1016/j.neurot.2026.e00923 · Cited by 2

A population-scale transcriptional atlas of blood and tissue in lupus nephritis

Sugiarto, N. W., Gurajala, S., Curtis, M. L., Eisenhaure, T., Arazi, A., Fava, A., Xiao, Q., Mears, J., Rovin, B. H., Berthier, C. C., et al. (2026) · Science Translational Medicine · doi:10.1126/scitranslmed.aec0512 · Cited by 6

Cellular and humoral mechanisms of immune aging

Nesterova, I. V., Ковалева, С. В., Chudilova, G. A., Poezzhaev, E. A., Pirogova, A. I., Chapurina, V. N., Lomtatidze, L. V., Teterin, Y. V., Pikturno, S. N., & Safontseva, A. D. (2024) · Cytokines and inflammation · doi:10.17816/ci642739 · Cited by 1

Unveiling the differences: infection disorders associated with tumor necrosis factor α inhibitors in pediatric patients—a pharmacovigilance study (2004–2023)

Xu, X., Wang, L., Sun, Y., Yang, C., Wang, X., Guo, P., & Mei, D. (2025) · European Journal of Pediatrics · doi:10.1007/s00431-025-06152-2 · Cited by 1

Being old and female is an inflammatory combination

Norling, L. V., & Cooper, D. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiad077 · Cited by 1

Islet-antigen reactive B cells display a unique phenotype and BCR repertoire in autoantibody positive and recent-onset type 1 diabetes patientsPreprint

Nicholas, C. A., Tensun, F., Evans, S. A., Toole, K. P., BRONCUCIA, H. C., Hesselberth, J. R., Gottlieb, P. A., Wells, K. L., & Smith, M. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.20.599914 · Cited by 1

A multi-omics resource of B cell activation reveals genetic mechanisms for immune-mediated diseasesPreprint

Aguiar, V. R. C., Franco, M. E., Aziz, N. A., Fernandez‐Salinas, D., Chiñas, M., Colantuoni, M., Xiao, Q., Hackert, N. S., Liao, Y., Cervantes‐Díaz, R., et al. (2025) · medRxiv · doi:10.1101/2025.05.22.25328104 · Cited by 3

Editorial: Gender affirming hormone therapy and its immunological implications

Leffler, J., Holmberg, M., & Landegren, N. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1832442 · Cited by 1

PLCγ2 deficiency compromises systemic immune tolerance and erodes myelin homeostasis while enhancing oxidative metabolism in the mouse brain

Gutierrez-Kuri, E., Marie Garcia-Rogers, J. L., Perez, J., Smith, S., Kenwood, M. R., Archuleta, K. S., Xiao, Y., Campos, G., Barannikov, S., Wang, H., et al. (2026) · doi:10.64898/2026.07.13.738356

Autoimmune Hepatitis Following mRNA COVID-19 Vaccination in a Very Old Patient With Preexisting Sjögren’s Syndrome: A Case Report

Yoshida, Y., Iwata, N., Ishii, Y., Hinoda, Y., & Endo, T. (2022) · Cureus · doi:10.7759/cureus.30896

Increased of Fascin1 and Pak1 expression enhances age-associated B cell actin cytoskeleton remodelingPreprint

Fujiwara, M., Kondo, R., Sugiyama, Y., Maruyama, M., & Nishikimi, A. (2023) · Research Square · doi:10.21203/rs.3.rs-2659669/v1

Upregulated Fcrl5 disrupts B cell anergy and causes autoimmunityPreprint

Ono, C., Tanaka, S., Myouzen, K., Iwasaki, T., Ueda, M. T., Oda, Y., Yamamoto, K., Kochi, Y., & Baba, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.20.549843

The Effects of Aging on Solid Organ Transplantation—Characteristics and Consequences of Immunosenescence

Rollenhagen, C., & Maltzman, J. S. (2023) · Current Transplantation Reports · doi:10.1007/s40472-023-00405-5

Exploring the Dynamics of B Cell Subpopulations in Response to Immune Checkpoint Inhibitors: A Prospective Study

Pouliasi, F., Salamaliki, C., Kanaloupitis, S., Verigou, E., Liolis, E., Koutras, A. K., Makatsoris, T., Kalofonos, C. P., Liossis, S. C., & Solomou, E. E. (2024) · Applied Sciences · doi:10.3390/app14124990

Advanced treatments for autoimmune diseases

Singh, D. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-19085-8.00009-6

Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system micePreprint

Vecchione, A., Maharlooei, M. K., Danzl, N. M., Li, H. W., Nauman, G., Madley, R., Waffarn, E., WINCHESTER, R. J., Ruiz, A., Ding, X., et al. (2024) · eLife · doi:10.7554/elife.99389.1

Reviewer #2 (Public Review): Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system mice

(2024) · eLife · doi:10.7554/elife.99389.1.sa0

Reviewer #1 (Public Review): Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system mice

(2024) · eLife · doi:10.7554/elife.99389.1.sa1

eLife Assessment: Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system mice

Sakaguchi, S. (2024) · eLife · doi:10.7554/elife.99389.1.sa2

Neuromuscular Junction Disorders in the Elderly

Shanina, E., & Smith, R. G. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1007348

Memory B cells

Mensah, B. B., Stewart, A., & Dunn‐Walters, D. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-128-24465-4.00070-3

Research progress of immune cell senescence and anti-senescence strategy with exercise

Dong, X., & Cai, X.-X. (2024) · New cell · doi:10.61958/nchz1574

Follicular helper- and peripheral helper-like T cells drive autoimmune disease in human immune system micePreprint

Maharlooei, M. K., Vecchione, A., Danzl, N. M., Li, H. W., Nauman, G., Madley, R., Waffarn, E., WINCHESTER, R. J., Ruiz, A., Ding, X., et al. (2025) · eLife · doi:10.7554/elife.99389.2

Evolving Approach to Clinical Cytometry for Immunodeficiencies and Other Immune Disorders

Akha, A. A. S., Csomós, K., Ujházi, B., Walter, J. E., & Kumánovics, A. (2025) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2025.01.009

Assessing the Molecular Validity of Spontaneous Lupus Mouse Models and Its Implication for Human StudiesPreprint

Rivas-Torrubia, M., Morell, M. H., Makowska, Z., Kageyama, J., Bosshard, A., Lindblom, J., Borghi, M. O., Bettacchioli, É., Parodis, I., Beretta, L., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.15.654304

Immune dysregulation and lipid interactions in systemic lupus erythematosus-associated atherosclerosis: mechanisms and pathogenesis

Bilodeau, P., & Tselios, K. (2025) · Frontiers in Lupus · doi:10.3389/flupu.2025.1607792

CD11c+ Tbet+ B cells constrain obesity- and vaccination-induced germinal center B cells and T helper cellsPreprint

Vanz, C., Enslow, B. T., Collins, E., Dominguez-Lowry, M., Liendo, N. S., Dudley, E. A., & Leadbetter, E. A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.01.673552

Age-related alterations in the immune system of aging mice

С., М. К., & Shevyrev, D. (2025) · Bulletin of Russian State Medical University · doi:10.24075/brsmu.2025.043

Conventional and Alternative B Lymphopoiesis: Multiple Roads to Immunity

Chiron, A., Bessoles, S., Sarrabayrouse, G., Krzysiek, R., & Hacein‐Bey‐Abina, S. (2025) · Stem Cell Reviews and Reports · doi:10.1007/s12015-025-10999-1 · Cited by 1

Additional file 1 of Peripheral immune landscape for hypercytokinemia in myasthenic crisis utilizing single-cell transcriptomics

Zhong, H., Huan, X., Zhao, R., Su, M., Yan, C., Song, J., Xi, J., Zhao, C., Luo, F., & Luo, S. (2024) · Figshare · doi:10.6084/m9.figshare.26612603

Additional file 2 of Peripheral immune landscape for hypercytokinemia in myasthenic crisis utilizing single-cell transcriptomics

Zhong, H., Huan, X., Zhao, R., Su, M., Yan, C., Song, J., Xi, J., Zhao, C., Luo, F., & Luo, S. (2024) · Figshare · doi:10.6084/m9.figshare.26612606

Single-cell multiomics reveals epigenetic rewiring of splenic memory B cells in murine malaria reinfectionPreprint

Coronado, M., Vincelle-Nieto, Á., Azcárate, I. G., Pérez-Benavente, S., Puyet, A., Díez, A., Bautista, J. M., & Reyes‐Palomares, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.10.693423

Erythropoietin exposure disrupts B cell development and drives the emergence of myeloid-biased biphenotypic progenitors

Chiron, A., Bessoles, S., Sarrabayrouse, G., Hussen, K. A., Joulain, C., Darde, T., de la Grange, P., Abina, A. M., Canque, B., Krzysiek, R., et al. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.102795

Assessing the translational relevance of specific molecular pathways in spontaneous lupus mouse models

Rivas-Torrubia, M., Morell, M. H., Makowska, Z., Kageyama, J., Bosshard, A., Lindblom, J., Borghi, M. O., Bettacchioli, É., Parodis, I., Beretta, L., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1823650

The impact of aging on antitumor immunity and cancer immunotherapy

Cifuentes, C., Fontane, I. D., Hope, H. C., & Vannini, N. (2026) · Trends in cancer · doi:10.1016/j.trecan.2026.05.003

Female mice with a Xist deletion in B cells can develop lupus-associated phenotypes

Lovell, C. D., Jiwrajka, N., Toothacre, N. E., Amerman, H. K., Cancro, M. P., & Anguera, M. C. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117517

Aging-related autonomic nervous system imbalance and adrenergic regulation of immunity: Implications for inflammaging, autoimmunity, and long COVID

Giunta, S., Sabbatinelli, J., Olivieri, F., & Giuliani, A. (2026) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2026.101269

Age-associated B-cells across the rheumatoid arthritis continuum: from early immunopathogenesis to comorbidities

Miranda-Prieto, D., Suárez, A., & Rodríguez‐Carrio, J. (2026) · Frontiers in Aging · doi:10.3389/fragi.2026.1812225

Immunoglobulin G in aging and cancer

Bu, M., Li, Z., Jones, E., Lubaba, U., Liu, X., & Li, H. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1854902

Immunosenescence modulates radiation-induced anti-tumor immunity: implications for personalized immuno-oncology

Arnold, C. R., Mangesius, J., Weinberger, B., Portnaia, I., Santacroce, A., Ganswindt, U., & Muacevic, A. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1888282

BAFF and APRIL signaling in the B-cell lineage: implications for the pathogenesis of ANCA-associated vasculitis

Shimojima, Y., Yoshida, S., Matsumoto, H., Sumichika, Y., Asano, T., & Sato, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1890512

The liver-secreted protein FGL1 restrains a subset of innate-like B cell responses via the receptor TACI

Su, T. T., He, J., Wang, Y., Huang, J., Huang, B., Nassar, A. F., Willen, L., Eslami, M., Wu, C., Huang, M., et al. (2026) · Immunity · doi:10.1016/j.immuni.2026.07.005

Age‐Associated B Cells: Origins, Regulation, and Tissue‐Specific Pathogenic Contributions in Autoimmune, Metabolic, and Neurological Diseases

Rubtsova, K. (2026) · Immunological Reviews · doi:10.1111/imr.70144 · Cited by 1

m6A modification in immune-cell inflammatory fate: from RNA fate regulation to therapeutic translation in inflammatory diseases

Zhu, Y.-Z., Yang, S.-Y., Qin, L., Ding, D.-Y., & Gan, X.-J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1918662

The SLC15A4–TASL complex is essential for lupus development in mice

Drobek, A., Delacrétaz, M., Vasilakou, A., Tortajada, M., Bernaleau, L., Dubois, M., Sisirak, V., & Rebsamen, M. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2618215123

Pathogenic T-bet + memory B cells worsen multiple sclerosis through myeloid cell activationPreprint

Jain, R. W., Goiko, M., Mendes, A., Xue, S., Zein, S., Gorter, R. P., Mørch, M. T., Prat, A., Li, R., & Yong, V. W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.09.01.748682

The role of immune aging in rheumatoid arthritis and its clinical and therapeutic significance

Wei, Y., Qi, W., Li, P., Wang, T., Wang, Z., Liu, H., Zhang, Y., 田杰祥, & Wang, G. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.117531

Age-associated B cells, key players in autoimmune pathogenesis

Hassani, S.-S., Ekrani, S. T., Rajabinejad, M., Faraj, T. A., Rezaiemanesh, A., & Esmaeili, S. (2026) · Immunity & Ageing · doi:10.1186/s12979-026-00564-w · Cited by 3

Age‐Associated B Cells: Origins, Regulation, and Tissue‐Specific Pathogenic Contributions in Autoimmune, Metabolic, and Neurological Diseases

Rubtsova, K. (2026) · Immunological Reviews · doi:10.1111/imr.70144 · Cited by 1

Age-Associated B Cells in Autoimmune Diseases: Pathogenesis and Clinical Implications

Xie, G., Chen, X., Gao, Y., Yang, M., Zhou, S., Lu, L., Wu, H., & Lu, Q. (2025) · Clinical Reviews in Allergy & Immunology · doi:10.1007/s12016-025-09021-w · Cited by 55

The role of age-associated B cells in systemic lupus erythematosus

Su, Q. Y., Zheng, X., Han, X.-T., Li, Q., Gao, Y.-R., Zhang, S., & Li, X.-F. (2025) · Journal of Autoimmunity · doi:10.1016/j.jaut.2025.103433 · Cited by 12

Highlights of 2024: The rising role of age‐associated B cells in autoimmune diseases

Lee, A. Y. S., & Reed, J. H. (2025) · Immunology and Cell Biology · doi:10.1111/imcb.70023 · Cited by 3