A novel mouse with B cells but lacking serum antibody reveals an antibody-independent role for B cells in murine lupus.

A novel mouse with B cells but lacking serum antibody reveals an antibody-independent role for B cells in murine lupus.
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DOI:
10.1084/jem.189.10.1639
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发表时间:
1999-05-17
期刊:
The Journal of experimental medicine
影响因子:
--
通讯作者:
Shlomchik MJ
Shlomchik MJ
中科院分区:
其他
文献类型:
--
作者:
Chan OT;Hannum LG;Haberman AM;Madaio MP;Shlomchik MJ

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B细胞在系统性自身免疫中的精确作用尚未完全了解。尽管B细胞对于疾病的表达是必需的(Chan, O., 和M.J. Shlomchik. 1998.《免疫学杂志》160:51 - 59,以及Shlomchik, M.J., M.P. Madaio, D. Ni, M. Trounstine和D. Huszar. 1994.《实验医学杂志》180:1295 - 1306),但尚不清楚自身抗体产生、抗原呈递和/或其他B细胞功能对于完整的病理表型是否是必需的。为了解决这个问题,使用了两种实验方法。首先,使用表达编码表面免疫球蛋白(Ig)的突变转基因但不允许分泌循环Ig的MRL/MpJ - Faslpr(MRL/lpr)小鼠分析循环抗体和B细胞的个体贡献。这些小鼠发生了肾炎,其特征是肾脏内有细胞浸润,这表明B细胞本身在不产生可溶性自身抗体的情况下也发挥致病作用。结果表明,不依赖于血清自身抗体,表达表面Ig的功能性B细胞对于疾病表达是必不可少的,要么作为抗原特异性自身反应性T细胞的抗原呈递细胞,要么直接促进局部炎症。
The precise role of B cells in systemic autoimmunity is incompletely understood. Although B cells are necessary for expression of disease (Chan, O., and M.J. Shlomchik. 1998. J. Immunol. 160:51–59, and Shlomchik, M.J., M.P. Madaio, D. Ni, M. Trounstine, and D. Huszar. 1994. J. Exp. Med. 180:1295–1306), it is unclear whether autoantibody production, antigen presentation, and/or other B cell functions are required for the complete pathologic phenotype. To address this issue, two experimental approaches were used. In the first, the individual contributions of circulating antibodies and B cells were analyzed using MRL/MpJ-Faslpr (MRL/lpr) mice that expressed a mutant transgene encoding surface immunoglobulin (Ig), but which did not permit the secretion of circulating Ig. These mice developed nephritis, characterized by cellular infiltration within the kidney, indicating that B cells themselves, without soluble autoantibody production, exert a pathogenic role. The results indicate that, independent of serum autoantibody, functional B cells expressing surface Ig are essential for disease expression, either by serving as antigen-presenting cells for antigen-specific, autoreactive T cells, or by contributing directly to local inflammation.