Atabani Sowsan F, Thio Chloe L, Divanovic Senad, Trompette Aurelien, Belkaid Yasmine, Thomas David L, Karp Christopher L
Division of Molecular Immunology, Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Eur J Immunol. 2005 Jul;35(7):2157-62. doi: 10.1002/eji.200526168.
A common single nucleotide polymorphism in CTLA4 has been linked with susceptibility and outcome in autoimmune and infectious diseases, respectively. Here, we show that this polymorphism is associated with the frequency of CD4(+)CD25(+) regulatory T cells in healthy human volunteers. We further show that, on a per cell basis, such regulatory T cells appear to be functionally indistinguishable across CTLA4 genotypes. These data implicate CTLA4 in regulatory T cell development, and provide a mechanism to account for the link between polymorphisms at this locus and the biological outcome of adaptive immune responses to self and to pathogens.
CTLA4 基因中的一种常见单核苷酸多态性分别与自身免疫性疾病和感染性疾病的易感性及预后相关。在此,我们表明这种多态性与健康人类志愿者中 CD4(+)CD25(+) 调节性 T 细胞的频率有关。我们进一步表明,基于单个细胞来看,此类调节性 T 细胞在不同 CTLA4 基因型之间似乎在功能上并无差异。这些数据表明 CTLA4 在调节性 T 细胞发育中起作用,并提供了一种机制来解释该基因座多态性与针对自身和病原体的适应性免疫反应的生物学结果之间的联系。