Wrenshall Lucile E, Smith Deandra R, Stevens Elliot T, Miller John D
Division of Transplantation, University of Nebraska Medical Center, 983285 Nebraska Medical Center, Omaha, NE 68198-3285, USA.
J Autoimmun. 2007 Sep-Nov;29(2-3):125-33. doi: 10.1016/j.jaut.2007.06.001. Epub 2007 Aug 9.
The production of auto-antibodies is one of the predominant characteristics of autoimmune disorders. Because IL-2 deficient mice develop autoimmunity, we asked how IL-2 deficiency might impair endogenous mechanisms of B cell tolerance. To this end, we mated BALB/c anti-dsDNA H chain knock-in mice, in which B cells producing anti-dsDNA antibodies are properly regulated, with IL-2 deficient mice and assessed the phenotype of their offspring. IL-2 deficient mice expressing the anti-dsDNA H chain knock-in allele developed anti-dsDNA antibodies of both IgM and IgG isotypes. Production of these antibodies occurred through the disruption of several mechanisms of endogenous tolerance, including deletion, maturational arrest, and follicular exclusion. In summary, our results suggest that IL-2 plays an important role in regulating B cell tolerance.
自身抗体的产生是自身免疫性疾病的主要特征之一。由于白细胞介素-2(IL-2)缺陷小鼠会发生自身免疫,我们探究了IL-2缺陷可能如何损害B细胞耐受性的内源性机制。为此,我们将BALB/c抗双链DNA重链敲入小鼠(其中产生抗双链DNA抗体的B细胞受到适当调控)与IL-2缺陷小鼠进行交配,并评估其后代的表型。表达抗双链DNA重链敲入等位基因的IL-2缺陷小鼠产生了IgM和IgG两种亚型的抗双链DNA抗体。这些抗体的产生是通过破坏内源性耐受性的几种机制实现的,包括细胞缺失、成熟停滞和滤泡排斥。总之,我们的结果表明IL-2在调节B细胞耐受性中起重要作用。