The double life of a B-1 cell: self-reactivity selects for protective effector functions

Predominant Autoantibody Production by Early Human B Cell Precursors

Wardemann, H., Yurasov, S., Schaefer, A., Young, J. W., Meffre, E., & Nussenzweig, M. C. (2003) · Science · doi:10.1126/science.1086907 · Cited by 2,088

Innate production of TH2 cytokines by adipose tissue-associated c-Kit+Sca-1+ lymphoid cells

Moro, K., Yamada, T., Tanabe, M., Takeuchi, T., Ikawa, T., Kawamoto, H., Furusawa, J.-I., Ohtani, M., Fujii, H., & Koyasu, S. (2009) · Nature · doi:10.1038/nature08636 · Cited by 1,994

CD19+CD24hiCD38hi B Cells Exhibit Regulatory Capacity in Healthy Individuals but Are Functionally Impaired in Systemic Lupus Erythematosus Patients

Blair, P. A., Noreña, L. Y., Flores-Borja, F., Rawlings, D. J., Isenberg, D. A., Ehrenstein, M. R., & Mauri, C. (2010) · Immunity · doi:10.1016/j.immuni.2009.11.009 · Cited by 1,574

MACROPHAGE RECEPTORS AND IMMUNE RECOGNITION

Taylor, P. R., Martínez‐Pomares, L., Stacey, M. A., Lin, H.-H., Brown, G. D., & Gordon, S. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.23.021704.115816 · Cited by 1,366

A Regulatory B Cell Subset with a Unique CD1dhiCD5+ Phenotype Controls T Cell-Dependent Inflammatory Responses

Yanaba, K., Bouaziz, J., Haas, K. M., Poe, J. C., Fujimoto, M., & Tedder, T. F. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.017 · Cited by 1,233

Marginal Zone and B1 B Cells Unite in the Early Response against T-Independent Blood-Borne Particulate Antigens

Martin, F., Oliver, A. M., & Kearney, J. F. (2001) · Immunity · doi:10.1016/s1074-7613(01)00129-7 · Cited by 987

Chronic Intestinal Inflammatory Condition Generates IL-10-Producing Regulatory B Cell Subset Characterized by CD1d Upregulation

Mizoguchi, A., Mizoguchi, E., Takedatsu, H., Blumberg, R. S., & Bhan, A. K. (2002) · Immunity · doi:10.1016/s1074-7613(02)00274-1 · Cited by 978

Control of Early Viral and Bacterial Distribution and Disease by Natural Antibodies

Ochsenbein, A. F., Fehr, T. H., Lutz, C., Suter, M., Brombacher, F., Hengartner, H., & Zinkernagel, R. M. (1999) · Science · doi:10.1126/science.286.5447.2156 · Cited by 911

Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals

Moir, S. L., Ho, J., Malaspina, A., Wang, W., DiPoto, A. C., O’Shea, M. A., Roby, G. A., Kottilil, S., Arthos, J. A., Proschan, M. A., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072683 · Cited by 894

Marginal-zone B cells

Martin, F., & Kearney, J. F. (2002) · Nature reviews. Immunology · doi:10.1038/nri799 · Cited by 867

Sex Influences Age-Related Changes in Natural Antibodies and CD5+ B-1 Cells

Webster, S. E., Ryali, B., Clemente, M. J., Tsuji, N. L., & Holodick, N. E. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2101150 · Cited by 15

Comparison patterns of 4 T1 antigens recognized by humoral immune response mediated by IgG and IgM antibodies in female and male mice with breast cancer using 2D-immnunoblots

Díaz-Zaragoza, M., Hernández-Ávila, R., Govezensky, T., Mendoza, L., Ruiz, D. M. M., & Ostoa‐Saloma, P. (2015) · Immunobiology · doi:10.1016/j.imbio.2015.05.012 · Cited by 15

Specificity, promiscuity, and precursor frequency in immunoreceptors

Venturi, V., Rudd, B. D., & Davenport, M. P. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.07.001 · Cited by 17

Central nervous system infiltrates are characterized by features of ongoing B cell-related immune activity in MP4-induced experimental autoimmune encephalomyelitis

Batoulis, H., Wunsch, M., Birkenheier, J., Rottlaender, A., Gorboulev, V., & Küerten, S. (2015) · Clinical Immunology · doi:10.1016/j.clim.2015.03.009 · Cited by 15

Control of lymphocyte homeostasis and effector function by the aryl hydrocarbon receptor

Wang, H., Wei, Y., & Yu, D. (2015) · International Immunopharmacology · doi:10.1016/j.intimp.2015.03.046 · Cited by 15

Endothelial Plasmalemma Vesicle–Associated Protein Regulates the Homeostasis of Splenic Immature B Cells and B-1 B Cells

Elgueta, R., Tse, D., Deharvengt, S. J., Luciano, M. R., Carrière, C., Noelle, R. J., & Stan, R. V. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501859 · Cited by 15

Effects of Simulated Smog Atmospheres in Rodent Models of Metabolic and Immunologic Dysfunction

McGee, M. A., Snow, S. J., Luebke, R. W., Wood, C. E., Krug, J. D., Krantz, Q. T., King, C. J., Copeland, C. B., McCullough, S. D., Gowdy, K. M., et al. (2018) · Environmental Science & Technology · doi:10.1021/acs.est.7b06534 · Cited by 15

Enhanced Antibody Production in Clever-1/Stabilin-1–Deficient Mice

Dunkel, J., Viitala, M., Karikoski, M., Rantakari, P., Virtakoivu, R., Elima, K., Hollmén, M., Jalkanen, S., & Salmi, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02257 · Cited by 15

Maternal Transfer of Natural (Auto-) Antibodies in Chickens

Ismiraj, M. R., Arts, J. A. J., & Parmentier, H. K. (2019) · Poultry Science · doi:10.3382/ps/pez017 · Cited by 15

Immunoglobulin M-degrading enzyme of Streptococcus suis (IdeSsuis) impairs porcine B cell signaling

Breitfelder, A. K., Schrödl, W., Rungelrath, V., Baums, C. G., Alber, G., Schütze, N., & Müller, U. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1122808 · Cited by 14

A genomic perspective of the aging human and mouse lung with a focus on immune response and cellular senescence

He, M., & Borlak, J. T. (2023) · Immunity & Ageing · doi:10.1186/s12979-023-00373-5 · Cited by 14

ω-3 polyunsaturated fatty acid alleviates systemic lupus erythematosus by suppressing autoimmunity in a murine model

Liu, A., Li, Z., Peng, Y., Peng, Y., Wang, S., Bi, X., Zhao, Z., Zhou, S., Zhao, A. Z., Mu, Y., et al. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.111299 · Cited by 14

Mast cells and the gut-liver Axis: Implications for liver disease progression and therapy

Nair, B., Kamath, A. J., Tergaonkar, V., Sethi, G., & Nath, L. R. (2024) · Life Sciences · doi:10.1016/j.lfs.2024.122818 · Cited by 14

Cmtm7 knockout inhibits B-1a cell development at transitional (TrB-1a) stage.

Liu, Z., Liu, Y., Li, T.-T., Wang, P.-Z., Mo, X.-N., Lv, P., Ge, Q., Ma, D., & Han, W. (2019) · International Immunology · doi:10.1093/intimm/dxz041 · Cited by 12

Regulation of B Cell Responses in SLE by Three Classes of Interferons

Domeier, P. P., & Rahman, Z. S. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910464 · Cited by 13

Postnatal regulation of B-1a cell development and survival by the CIC-PER2-BHLHE41 axis

Hong, H., Lee, J., Park, G.-Y., Kim, S., Park, J., Park, J. S., Song, Y., Lee, S., Kim, T. J., Lee, Y. J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110386 · Cited by 16

Peripheral CD 4+ T ‐cell tolerance is induced in vivo by rare antigen‐bearing B cells in follicular, marginal zone, and B ‐1 subsets

Murray, S., Toren, K. G., & Parker, D. C. (2013) · European Journal of Immunology · doi:10.1002/eji.201242784 · Cited by 14

Effects of Prunus mume Sieb. et Zucc. extract and its biopolymer encapsulation on a mouse model of colitis

Lee, S. Y., Lee, S., & Hur, S. J. (2016) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.7790 · Cited by 14

Role of Polycomb RYBP in Maintaining the B-1-to-B-2 B-Cell Lineage Switch in Adult Hematopoiesis

Calés, C., Pavón, L., Starowicz, K., Pérez‐Martínez, C., Bravo, M., Ikawa, T., Koseki, H., & Vidal, M. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00869-15 · Cited by 17

Innate immune response to peritoneal bacterial infection

Català, C., Andrés, M. V., Casadó‐Llombart, S., Leyton-Pereira, A., Carrillo‐Serradell, L., Isamat, M., & Lozano, F. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.04.014 · Cited by 13

Development and organization of omental milky spots

Okabe, Y. (2024) · Immunological Reviews · doi:10.1111/imr.13337 · Cited by 14

Need for a paradigm shift in therapeutic approaches to CNS injury

Wootla, B., Đenić, A., Warrington, A. E., & Rodriguez, M. (2012) · Expert Review of Neurotherapeutics · doi:10.1586/ern.12.24 · Cited by 13

Dysregulation of peritoneal cavity B1a cells and murine primary biliary cholangitis

Yang, Y., Yang, W., Yao, Y., Ma, H.-D., Wang, Y., Li, L., Wu, Q., Gershwin, M. E., & Lian, Z. (2016) · Oncotarget · doi:10.18632/oncotarget.8853 · Cited by 13

Immune Niche Within the Peritoneal Cavity

Okabe, Y. (2021) · Current topics in microbiology and immunology · doi:10.1007/978-3-030-86016-5_6 · Cited by 13

Immunoglobulin M as a vaccine adjuvant

Ilag, L. L. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.06.013 · Cited by 13

Presence of Rheumatoid Factor during Chronic HCV Infection Is Associated with Expansion of Mature Activated Memory B-Cells that Are Hypo-Responsive to B-Cell Receptor Stimulation and Persist during the Early Stage of IFN Free Therapy

Reyes-Avilés, E., Kostadinova, L., Rusterholtz, A., Cruz-Lebrón, A., Falck-Ytter, Y. T., & Anthony, D. D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144629 · Cited by 13

Autoimmunity and Traumatic Brain Injury

Yang, Z., Zhu, T., Weissman, A. S., Jaalouk, E., Rathore, D. S., Romo, P., Shi, Y., Wagner, A. K., & Wang, K. (2017) · Current Physical Medicine and Rehabilitation Reports · doi:10.1007/s40141-017-0146-9 · Cited by 13

Sialic Acid Ligand Binding of CD22 and Siglec-G Determines Distinct B Cell Functions but Is Dispensable for B Cell Tolerance Induction

Özgör, L., Meyer, S. J., Korn, M. A., Terörde, K., & Nitschke, L. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800296 · Cited by 13

Humoral autoimmunity after solid organ transplantation: Germinal ideas may not be natural

Siu, J. H. Y., Motallebzadeh, R., & Pettigrew, G. J. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104131 · Cited by 13

Relevance of PSGL-1 Expression in B Cell Development and Activation

Rafael, G.-T., González‐Sánchez, E., Silván, J., Muñoz‐Callejas, A., Vicente‐Rabaneda, E. F., García-Pérez, J., Castañeda, S., & Urzainqui, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.588212 · Cited by 13

Developmental changes in the rules for B cell selection

Vergani, S., & Yuan, J. (2021) · Immunological Reviews · doi:10.1111/imr.12949 · Cited by 13

Ferroptosis contributes to immunosuppression

He, N., Yuan, D., Luo, M., Xu, Q., Wen, Z., Wang, Z., Zhao, J., & Liu, Y. (2024) · Frontiers of Medicine · doi:10.1007/s11684-024-1080-8 · Cited by 13

B cell receptor-induced IL-10 production from neonatal mouse CD19+CD43- cells depends on STAT5-mediated IL-6 secretion

Sakai, J., Yang, J., Chou, C., Wu, W. W., & Akkoyunlu, M. (2023) · eLife · doi:10.7554/elife.83561 · Cited by 11

Development of systemic and mucosal immune responses against gut microbiota in early life and implications for the onset of allergies

Pirker, A.-L., & Vogl, T. J. (2024) · Frontiers in Allergy · doi:10.3389/falgy.2024.1439303 · Cited by 15

Group 2 innate lymphoid cells are a non-redundant source of interleukin-5 required for development and function of murine B1 cells

Troch, K. F., Jakob, M. O., Forster, P. M., Jarick, K. J., Schreiber, J., Preußer, A., Guerra, G. M., Durek, P., Tizian, C., Sterczyk, N., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54780-3 · Cited by 12

Age-related immune response to pneumococcal polysaccharide vaccination: lessons for the clinic

Iyer, A. S., Ohtola, J. A., & Westerink, M. A. J. (2014) · Expert Review of Vaccines · doi:10.1586/14760584.2015.963058 · Cited by 12

Syndrome of selective IgM deficiency with severe T cell deficiency associated with disseminated cutaneous mycobacterium avium intracellulaire infection.

Gharib, A., Louis, A. G., Agrawal, S., & Gupta, S. (2015) · Europe PMC (PubMed Central) · Cited by 12

B cells and atherosclerosis in systemic lupus erythematosus

Koulouri, V., Koutsilieris, M., & Mavragani, C. P. (2019) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2019.1571411 · Cited by 12

Noncanonical B Cells: Characteristics of Uncharacteristic B Cells

Haas, K. M. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200944 · Cited by 12

An Apoptosis-Associated Mammary Protein Deficiency Leads to Enhanced Production of IgM Antibodies against Multiple Damage-Associated Molecules

Chikazawa, M., Otaki, N., Shibata, T., Yasueda, T., Matsuda, T., & Uchida, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068468 · Cited by 12

Differences in multiple immune parameters between Indian and U.S. infants

Rathore, D. K., Holmes, T. H., Nadeau, K. C., Mittal, P., Batra, A., Rosenberg‐Hasson, Y., Sopory, S., Gupta, R. K., Chellani, H. K., Aggarwal, K. C., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207297 · Cited by 12

The novel multiple sclerosis susceptibility gene ATXN1 regulates B cell receptor signaling in B-1a cells

Ma, Q., & Didonna, A. (2021) · Molecular Brain · doi:10.1186/s13041-020-00715-0 · Cited by 12

The roles of immune cells in atherosclerotic calcification

Cao, J., Zu, X., & Liu, J. (2021) · Vascular · doi:10.1177/17085381211032756 · Cited by 12

Regeneration of immunocompetent B lymphopoiesis from pluripotent stem cells guided by transcription factors

Zhang, Q., Wu, B., Weng, Q., Hu, F., Lin, Y., Xia, C., Peng, H., Wang, Y., Liu, X., Liu, L., et al. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00805-6 · Cited by 12

Editorial: Natural Antibodies in Health and Disease

Hernández, A., & Holodick, N. E. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01795 · Cited by 12

Sex Differences in the Frequencies of B and T Cell Subpopulations of Human Cord Blood

Bous, M., Schmitt, C., Hans, M. C., Weber, R., Nourkami‐Tutdibi, N., Tenbruck, S., Hamoud, B. H., Wagenpfeil, G., Kaiser, E., Solomayer, E., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411511 · Cited by 10

Role of canonical and noncanonical autophagy pathways in shaping the life journey of B cells

Wang, Y., Wu, L., & Kaer, L. V. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1426204 · Cited by 13

Fc Receptor-Like 6 (FCRL6) Discloses Progenitor B Cell Heterogeneity That Correlates With Pre-BCR Dependent and Independent Pathways of Natural Antibody Selection

Honjo, K., Won, W.-J., King, R. G., Ianov, L., Crossman, D. K., Easlick, J. L., Shakhmatov, M. A., Khass, M., Vale, A. M., Stephan, R. P., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00082 · Cited by 11

Evaluation of dietary Pancreatin as an exogenous enzyme on growth performance, gene expression, immunological responses, serum immunoglobins, and intestinal morphology in cockerels

Asare, E., Yang, Z., Yang, H., & Wang, Z. (2022) · Journal of Applied Animal Research · doi:10.1080/09712119.2021.2019044 · Cited by 11

The Forgotten Brother: The Innate-like B1 Cell in Multiple Sclerosis

Halperin, S. T., Hart, B. A. ‘., Luchicchi, A., & Schenk, G. J. (2022) · Biomedicines · doi:10.3390/biomedicines10030606 · Cited by 12

Single‐Cell Transcriptomics Reveals the Difference of Aortic Atherosclerosis Response to Phytosterols and Oxidation Products of Sterols

Wang, Z., Wang, M., Lu, Y., Ji, Y., Simal‐Gándara, J., Xiao, F., Liu, Y., Zhang, L., Battino, M. A., Li, P., et al. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200811 · Cited by 11

Insights into B‐cell ontogeny inferred from human immunology

Dirks, J., Viemann, D., Beyersdorf, N., Härtel, C., & Morbach, H. (2023) · European Journal of Immunology · doi:10.1002/eji.202250116 · Cited by 11

NF‐κB2/p100 deficiency impairs immune responses to T‐cell‐independent type 2 antigens

Krljanac, B., Weih, D., Jacobsen, I. D., Hu, D., Koliesnik, I. O., Reppe, K., Witzenrath, M., & Weih, F. (2013) · European Journal of Immunology · doi:10.1002/eji.201343484 · Cited by 11

Analysis of IgM antibody production and repertoire in a mouse model of Sjögren’s syndrome

Kramer, J. M., Holodick, N. E., Vizconde, T., Raman, I., Yan, M., Li, Q., Gaile, D. P., & Rothstein, T. L. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.2a0715-297r · Cited by 11

Heterozygous Mutation in IκBNS Leads to Reduced Levels of Natural IgM Antibodies and Impaired Responses to T-Independent Type 2 Antigens

Pedersen, G. K., Ádori, M., Stark, J. M., Khoenkhoen, S., Arnold, C., Beutler, B., & Hedestam, G. B. K. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00065 · Cited by 11

FcμR in human B cell subsets in primary selective IgM deficiency, and regulation of FcμR and production of natural IgM antibodies by IGIV

Gupta, S., Agrawal, S., Gollapudi, S. V. S., & Kubagawa, H. (2016) · Human Immunology · doi:10.1016/j.humimm.2016.10.003 · Cited by 11

Potential Relevance of B-cell Maturation Pathways in Defining the Cell(s) of Origin for Chronic Lymphocytic Leukemia

Ng, A. K. Y., & Chiorazzi, N. (2021) · Hematology/Oncology Clinics of North America · doi:10.1016/j.hoc.2021.03.002 · Cited by 12

X-linked immunodeficient (XID) mice exhibit high susceptibility to Cryptococcus gattii infection

Diniz-Lima, I., da Rosa, P. R., da Silva-Júnior, E. B., Guimarães-de-Oliveira, J. C., de Freitas, E. O., Nascimento, D. D. O., Morrot, A., Nimrichter, L., Previato, J. O., Mendonça‐Previato, L., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-97041-9 · Cited by 12

A nasal double DNA adjuvant system induces atheroprotective IgM antibodies via dendritic cell-B-1a B cell interactions

Yoshimatsu, H., Kataoka, K., Fujihashi, K., Miyake, T., & Ono, Y. (2022) · Vaccine · doi:10.1016/j.vaccine.2022.01.027 · Cited by 11

Stimulation of naïve B cells with a fusion protein consisting of FlaA and Bet v 1 induces regulatory B cells ex vivo

Goretzki, A., Lin, Y., Meier, C., Dorn, B., Wolfheimer, S., Jamin, A., Schott, M., Wangorsch, A., Vieths, S., Jakob, T., et al. (2022) · Allergy · doi:10.1111/all.15542 · Cited by 11

Characterization of human B cells in umbilical cord blood-transplanted NOD/SCID mice.

Wang, X., Qi, Z., Wei, H.-M., Tian, Z., & Sun, R. (2012) · Transplant Immunology · doi:10.1016/j.trim.2011.12.003 · Cited by 11

Cutting Edge: Krüppel-like Factor 2 Is Required for Phenotypic Maintenance but Not Development of B1 B Cells

Hart, G. T., Peery, S. L., Hamilton, S. E., & Jameson, S. C. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201439 · Cited by 11

Siglec‐G is a B‐1 cell inhibitory receptor and also controls B cell tolerance

Nitschke, L. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12826 · Cited by 11

Selective breeding on natural antibodies in chickens

Berghof, T. V. L. (2018) · doi:10.18174/426278 · Cited by 12

Butyrate in broiler diets : impact of butyrate presence in distinct gastrointestinal tract segments on digestive function, microbiota composition and immune responses

Moquet, P. C. A. (2018) · doi:10.18174/449961 · Cited by 11

Immuno-regulatory malignant B cells contribute to Chronic Lymphocytic Leukemia progression

MEKINIAN, A., Quinquenel, A., Belkacem, K. A., Kanoun, F., Dondi, E., Franck, E., Boubaya, M., Mhibik, M., Baran‐Marszak, F., Letestu, R., et al. (2023) · Cancer Gene Therapy · doi:10.1038/s41417-023-00602-5 · Cited by 10

Reduced Number of Transitional and Naive B Cells in Addition to Decreased BAFF Levels in Response to the T Cell Independent Immunogen Pneumovax®23

Roth, A., Glaesener, S., Schütz, K., & Meyer‐Bahlburg, A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152215 · Cited by 10

Evidence for a Mesothelial Origin of Body Cavity Effusion Lymphomas

Sánchez‐Martín, D., Uldrick, T. S., Kwak, H., Ohnuki, H., Polizzotto, M. N., Annunziata, C. M., Raffeld, M. A., Wyvill, K. M., Aleman, K. O., Wang, V., et al. (2017) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djx016 · Cited by 11

Heartbreakers or Healers? Innate Lymphoid Cells in Cardiovascular Disease and Obesity

Roberts, L. B., Lord, G. M., & Howard, J. K. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.903678 · Cited by 10

Beyond Adaptive Alloreactivity: Contribution of Innate B Cells to Allograft Inflammation and Rejection

Sayin, I., & Chong, A. S. (2022) · Transplantation · doi:10.1097/tp.0000000000004377 · Cited by 10

DNAJA3 regulates B cell development and immune function

Sayson, S. L., Fan, J.-N., Ku, C.-L., Lo, J., & Chou, S.-H. (2023) · Biomedical Journal · doi:10.1016/j.bj.2023.100628 · Cited by 10

Involvement of Zizimin2/3 in the age-related defect of peritoneal B-1a cells as a source of anti-bacterial IgM

Sakamoto, A., Matsuda, T., Kawaguchi, K., Takaoka, A., & Maruyama, M. (2017) · International Immunology · doi:10.1093/intimm/dxx054 · Cited by 10

Critical roles of the E3 ubiquitin ligase FBW7 in B‐cell response and the pathogenesis of experimental autoimmune arthritis

Feng, C., Li, L., Zhou, L., Li, D., Liu, M., Han, S., & Zheng, B. Q. (2021) · Immunology · doi:10.1111/imm.13398 · Cited by 10

Mouse innate-like B-1 lymphocytes promote inhaled particle-induced in vitro granuloma formation and inflammation in conjunction with macrophages

Hiéronimus, L., Demazy, R., Christiaens, L., Uwambayinema, F., Geuens, J.-F., Yacoub, Y., & Huaux, F. (2021) · Archives of Toxicology · doi:10.1007/s00204-021-03200-2 · Cited by 10

Innate Response Activator (IRA) B Cells Reside in Human Tonsils and Internalize Bacteria In Vitro

Chiappini, N., Cantisani, R., Pancotto, L., Ruggiero, P., Rosa, D., Manetti, A. G. O., Romano, A., Montagnani, F., Bertholet, S., Castellino, F., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129879 · Cited by 10

Detection of bacterial-reactive natural IgM antibodies in desert bighorn sheep populations

Dugovich, B. S., Peel, M. J., Palmer, A. L., Zielke, R. A., Sikora, A. E., Beechler, B. R., Jolles, A. E., Epps, C. W., & Dolan, B. P. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180415 · Cited by 10

Naegleria fowleri immunization modifies lymphocytes and APC of nasal mucosa

Carrasco‐Yépez, M. M., Campos-Rodrı́guez, R., Reséndiz‐Albor, A. A., Peña‐Juárez, C., de Oca, A. C.-M., Arciniega-Martínez, I. M., Bonilla‐Lemus, P., & Hernández, S. R. (2017) · Parasite Immunology · doi:10.1111/pim.12508 · Cited by 10

B-1a Cell Development in Splenectomized Neonatal Mice

Pedersen, G. K., Li, X., Khoenkhoen, S., Ádori, M., Beutler, B., & Hedestam, G. B. K. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01738 · Cited by 10

Murine Leukemia Virus Exploits Innate Sensing by Toll-Like Receptor 7 in B-1 Cells To Establish Infection and Locally Spread in Mice

Pi, R., Iwasaki, A., Sewald, X., Mothes, W., & Uchil, P. D. (2019) · Journal of Virology · doi:10.1128/jvi.00930-19 · Cited by 11

B-1a cells acquire their unique characteristics by bypassing the pre-BCR selection stagePreprint

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