Marginal zone B cells exacerbate endotoxic shock via interleukin-6 secretion induced by Fcα/μR-coupled TLR4 signalling
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M. Fujimoto | S. Honda | K. Miyake | A. Shibuya | K. Shibuya | S. Tahara-Hanaoka | C. Nakahashi-Oda | Satoshi Fujiyama | Kazuki Sato | N. Totsuka
[1] M. Hudson. Human , 2018, Critical Theory and the Classical World.
[2] Amit Bar-Or,et al. IL-35-producing B cells are critical regulators of immunity during autoimmune and infectious diseases , 2014, Nature.
[3] S. Honda,et al. Molecular characterization of the dimer formation of Fcα/μ receptor (CD351). , 2013, Molecular immunology.
[4] S. Fujieda,et al. Expression and Function of Allergin-1 on Human Primary Mast Cells , 2013, PloS one.
[5] D. Tsiantoulas,et al. B lymphocytes trigger monocyte mobilization and impair heart function after acute myocardial infarction , 2013, Nature Medicine.
[6] P. Ward,et al. The inflammatory response in sepsis. , 2013, Trends in immunology.
[7] M. Heise,et al. Regulatory B Cell (B10 Cell) Expansion during Listeria Infection Governs Innate and Cellular Immune Responses in Mice , 2013, The Journal of Immunology.
[8] Irene Puga,et al. Marginal zone B cells: virtues of innate-like antibody-producing lymphocytes , 2013, Nature Reviews Immunology.
[9] L. Moldawer,et al. DAMPs, PAMPs, and the origins of SIRS in bacterial sepsis. , 2013, Shock.
[10] Chen-Cheng Lee,et al. Marginal Zone B Cell Is a Major Source of Il-10 in Listeria monocytogenes Susceptibility , 2012, The Journal of Immunology.
[11] W. Leonard,et al. Regulatory B Cells Control T Cell Autoimmunity Through IL-21-Dependent Cognate Interactions , 2012, Nature.
[12] R. Weissleder,et al. Innate Response Activator B Cells Protect Against Microbial Sepsis , 2012, Science.
[13] S. Serrano,et al. B–helper neutrophils stimulate immunoglobulin diversification and production in the marginal zone of the spleen , 2011, Nature Immunology.
[14] S. Akira,et al. B cells enhance early innate immune responses during bacterial sepsis , 2011, The Journal of experimental medicine.
[15] C. Libert,et al. Cecal ligation and puncture: the gold standard model for polymicrobial sepsis? , 2011, Trends in microbiology.
[16] M. Ehrenstein,et al. The importance of natural IgM: scavenger, protector and regulator , 2010, Nature Reviews Immunology.
[17] A. Shibuya,et al. An immunoglobulin-like receptor, Allergin-1, inhibits immunoglobulin E–mediated immediate hypersensitivity reactions , 2010, Nature Immunology.
[18] T. Tedder,et al. B10 cells and regulatory B cells balance immune responses during inflammation, autoimmunity, and cancer , 2010, Annals of the New York Academy of Sciences.
[19] S. Honda,et al. Requirement of the cytoplasmic portion for dimer formation of Fcalpha/micro receptor expressed on cell surface. , 2010, Molecular immunology.
[20] T. Fujita,et al. Enhanced humoral immune responses against T-independent antigens in Fcα/μR-deficient mice , 2009, Proceedings of the National Academy of Sciences.
[21] J. Weill,et al. Human marginal zone B cells. , 2009, Annual review of immunology.
[22] M. Fujimoto,et al. Regulatory B cells inhibit EAE initiation in mice while other B cells promote disease progression. , 2008, The Journal of clinical investigation.
[23] M. Fujimoto,et al. A regulatory B cell subset with a unique CD1dhiCD5+ phenotype controls T cell-dependent inflammatory responses. , 2008, Immunity.
[24] M. Zachariah,et al. Follicular shuttling of marginal zone B cells facilitates antigen transport , 2008, Nature Immunology.
[25] S. Honda,et al. Molecular and functional characteristics of the Fcα/μR, a novel Fc receptor for IgM and IgA , 2006, Springer Seminars in Immunopathology.
[26] S. Honda,et al. Molecular and functional characteristics of the Fcalpha/muR, a novel Fc receptor for IgM and IgA. , 2006, Springer seminars in immunopathology.
[27] Jiancheng Hu,et al. Lsc regulates marginal-zone B cell migration and adhesion and is required for the IgM T-dependent antibody response. , 2005, Immunity.
[28] C. Kaetzel. The polymeric immunoglobulin receptor: bridging innate and adaptive immune responses at mucosal surfaces , 2005, Immunological reviews.
[29] R. Steinman,et al. Association of SIGNR1 with TLR4-MD-2 enhances signal transduction by recognition of LPS in gram-negative bacteria. , 2005, International immunology.
[30] S. Pillai,et al. Marginal zone B cells. , 2005, Annual review of immunology.
[31] L. Staudt,et al. Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire. , 2004, Blood.
[32] Makiko Kobayashi,et al. Lipid A antagonist, lipid IVa, is distinct from lipid A in interaction with Toll-like receptor 4 (TLR4)-MD-2 and ligand-induced TLR4 oligomerization. , 2004, International immunology.
[33] R. Steinman,et al. The C-type lectin SIGN-R1 mediates uptake of the capsular polysaccharide of Streptococcus pneumoniae in the marginal zone of mouse spleen , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[34] B. Beutler,et al. Innate immune sensing and its roots: the story of endotoxin , 2003, Nature Reviews Immunology.
[35] M. Nolte,et al. Marginal zone macrophages express a murine homologue of DC-SIGN that captures blood-borne antigens in vivo. , 2002, Blood.
[36] J. Kearney,et al. Blood dendritic cells interact with splenic marginal zone B cells to initiate T-independent immune responses. , 2002, Immunity.
[37] T. Takai. Roles of Fc receptors in autoimmunity , 2002, Nature Reviews Immunology.
[38] T. Honjo,et al. Notch–RBP-J signaling is involved in cell fate determination of marginal zone B cells , 2002, Nature Immunology.
[39] W. Timens,et al. CD27 expression in the human splenic marginal zone: the infant marginal zone is populated by naive B cells. , 2001, Tissue antigens.
[40] H. Nakauchi,et al. Fcα/µ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1 , 2001, Immunogenetics.
[41] K. Tedford,et al. Lsc is required for marginal zone B cells, regulation of lymphocyte motility and immune responses , 2001, Nature Immunology.
[42] J. Kearney,et al. Marginal zone and B1 B cells unite in the early response against T-independent blood-borne particulate antigens. , 2001, Immunity.
[43] H. Nakauchi,et al. A novel Fc receptor for IgA and IgM is expressed on both hematopoietic and non‐hematopoietic tissues , 2001, European journal of immunology.
[44] H. Nakauchi,et al. Fc(alpha)/mu receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1. , 2001, Immunogenetics.
[45] J. Schlessinger,et al. Absence of marginal zone B cells in Pyk-2–deficient mice defines their role in the humoral response , 2000, Nature Immunology.
[46] H. Nakauchi,et al. Fc alpha/mu receptor mediates endocytosis of IgM-coated microbes. , 2000, Nature immunology.
[47] T. Kishimoto,et al. Blockage of interleukin-6 receptor ameliorates joint disease in murine collagen-induced arthritis. , 1998, Arthritis and rheumatism.
[48] M. Jordana,et al. IL-6 is an antiinflammatory cytokine required for controlling local or systemic acute inflammatory responses. , 1998, The Journal of clinical investigation.
[49] J. Ravetch,et al. Divergent roles for Fc receptors and complement in vivo. , 1998, Annual review of immunology.
[50] F. Rosen,et al. Endotoxin shock in antibody-deficient mice: unraveling the role of natural antibody and complement in the clearance of lipopolysaccharide. , 1997, Journal of immunology.
[51] B. Koller,et al. Abnormal B lymphocyte development, activation, and differentiation in mice that lack or overexpress the CD19 signal transduction molecule. , 1995, Immunity.