Humbert M, Galanaud P
INSERM U 131, Clamart.
Ann Med Interne (Paris). 1990;141(3):213-6.
Polyclonal B cell activation is the most visible biological manifestation of systemic lupus erythematosus (SLE) autoimmunity. Murine models and in vitro lymphocyte studies are the most important tools used to improve our comprehension of the disease. It was successively demonstrated that there is an intrinsic B lymphocyte hyperreactivity in human and murine lupus; that the B lymphocytes overreact to stimulating factors produced by T lymphocytes; and that these stimulating factors could be over-produced. This last feature contrasts with decreased interleukin 2 production and lymphocyte response to this cytokine. A more precise study of the interleukins involved in the control of the humoral response shows the importance of interleukins 4, 5, 6 and of gamma-interferon. Further investigations are needed to improve our understanding of B cell hyperreactivity during SLE. These studies will benefit from better molecular characterization of many interleukins and their receptors.
多克隆B细胞活化是系统性红斑狼疮(SLE)自身免疫最明显的生物学表现。小鼠模型和体外淋巴细胞研究是用于增进我们对该疾病理解的最重要工具。相继证实,人类和小鼠狼疮中存在内在的B淋巴细胞高反应性;B淋巴细胞对T淋巴细胞产生的刺激因子反应过度;并且这些刺激因子可能产生过多。这最后一个特征与白细胞介素2产生减少以及淋巴细胞对该细胞因子的反应形成对比。对参与体液反应控制的白细胞介素进行更精确的研究表明白细胞介素4、5、6和γ干扰素的重要性。需要进一步研究以增进我们对SLE期间B细胞高反应性的理解。这些研究将受益于对许多白细胞介素及其受体更好的分子特征描述。