Department of Medicine, Park-Klinik Weissensee, Berlin, Germany.
Autoimmun Rev. 2010 Jul;9(9):600-3. doi: 10.1016/j.autrev.2010.05.005. Epub 2010 May 7.
Abnormalities of memory B cells seem to be closely involved in the pathogenesis of primary Sjögrens Syndrome (pSS) and its malignant complication, B cell lymphoma. Recent studies on B cells in pSS add to our understanding of the distinct memory B cell subsets in pSS. Reduction of peripheral memory CD27(+) B cells, most strikingly of the CD27(+)IgM(+) subset, may indicate a lack of appropriate censoring mechanisms and incomplete differentiation processes within the ectopic lymphoid tissues in pSS. This ectopically formed lymphoid tissue might protect autoreactive memory B cells from deletion by physiological check-points and, thereby, may contribute to the perpetuation of the disease as well as to an enhanced lymphoma risk. Thus, B cells may be potential targets of direct or indirect treatment in pSS.
记忆 B 细胞的异常似乎与原发性干燥综合征 (pSS)及其恶性并发症 B 细胞淋巴瘤的发病机制密切相关。最近对 pSS 中 B 细胞的研究增加了我们对 pSS 中不同记忆 B 细胞亚群的理解。外周记忆 CD27(+)B 细胞减少,尤其是 CD27(+)IgM(+)亚群减少,可能表明 pSS 异位淋巴组织中缺乏适当的清除机制和不完全的分化过程。这种异位形成的淋巴组织可能使自身反应性记忆 B 细胞免受生理检查点的删除,从而有助于疾病的持续存在和淋巴瘤风险的增加。因此,B 细胞可能是 pSS 直接或间接治疗的潜在靶点。