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10.1016/j.immuni.2018.06.007

http://scihub22266oqcxt.onion/10.1016/j.immuni.2018.06.007
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C6057275!6057275!30005826
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suck abstract from ncbi


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pmid30005826      Immunity 2018 ; 49 (1): 120-133.e9
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  • LAG-3 Inhibitory Receptor Expression Identifies Immunosuppressive Natural Regulatory Plasma Cells #MMPMID30005826
  • Lino AC; Dang VD; Lampropoulou V; Welle A; Joedicke J; Pohar J; Simon Q; Thalmensi J; Baures A; Flühler V; Sakwa I; Stervbo U; Ries S; Jouneau L; Boudinot P; Tsubata T; Adachi T; Hutloff A; Dörner T; Zimber-Strobl U; de Vos AF; Dahlke K; Loh G; Korniotis S; Goosmann C; Weill JC; Reynaud CA; Kaufmann SH; Walter J; Fillatreau S
  • Immunity 2018[Jul]; 49 (1): 120-133.e9 PMID30005826show ga
  • B lymphocytes can suppress immunity through interleukin (IL)-10 production in infectious, autoimmune, and malignant diseases. Here, we have identified a natural plasma cell subset that distinctively expresses the inhibitory receptor LAG-3 and mediates this function in vivo. These plasma cells also express the inhibitory receptors CD200, PD-L1, and PD-L2. They develop from various B cell subsets in a B cell receptor (BCR)-dependent manner independently of microbiota in naive mice. After challenge they upregulate IL-10 expression via a Toll-like receptor-driven mechanism within hours and without proliferating. This function is associated with a unique transcriptome and epigenome, including the lowest amount of DNA methylation at the Il10 locus compared to other B cell subsets. Their augmented accumulation in naive mutant mice with increased BCR signaling correlates with the inhibition of memory T cell formation and vaccine efficacy after challenge. These natural regulatory plasma cells may be of broad relevance for disease intervention.
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