Chronic intestinal inflammatory condition generates IL-10-producing regulatory B cell subset characterized by CD1d upregulation

被引:805
作者
Mizoguchi, A [1 ]
Mizoguchi, E
Takedatsu, H
Blumberg, RS
Bhan, AK
机构
[1] Massachusetts Gen Hosp, Dept Pathol, Immunopathol Unit, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Med, Div Gastroenterol, Boston, MA 02115 USA
[5] Massachusetts Gen Hosp, Ctr Stusy Inflammatory Bowel Dis, Boston, MA 02114 USA
关键词
D O I
10.1016/S1074-7613(02)00274-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cells possess a variety of immune functions that are involved in normal and abnormal immune responses, including autoimmune disorders. Through murine models of intestinal inflammation, we here demonstrate a B cell subset that is induced in gut-associated lymphoid tissues and is characterized by CD1d upregulation. This B cell subset appears under a chronic inflammatory environment, produces IL-10, and suppresses progression of intestinal inflammation by downregulating inflammatory cascades associated with IL-1 upregulation and STAT3 activation rather than by altering polarized T helper responses. This study indicates that B cells, by producing cytokines such as IL-10, can act as regulatory cells in immunologically mediated inflammatory reactions.
引用
收藏
页码:219 / 230
页数:12
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