Fry A M, Jones L A, Kruisbeek A M, Matis L A
Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892.
Science. 1989 Nov 24;246(4933):1044-6. doi: 10.1126/science.2511630.
During T cell differentiation, self tolerance is established in part by the deletion of self-reactive T cells within the thymus (negative selection). The presence of T cell receptor (TCR)-alpha beta + T cells in older athymic (nu/nu) mice indicates that some T cells can also mature without thymic influence. Therefore, to determine whether the thymus is required for negative selection, TCR V beta expression was compared in athymic nu/nu mice and their congenic normal littermates. T cells expressing V beta 3 proteins are specific for minor lymphocyte stimulatory (Mlsc) determinants and are deleted intrathymically due to self tolerance in Mlsc+ mouse strains. Here it is shown that V beta 3+ T cells are deleted in Mlsc+ BALB/c nu/+ mice, but not in their BALB/c nu/nu littermates. Thus, the thymus is required for clonal deletion during T cell development.
在T细胞分化过程中,自身耐受性部分是通过胸腺内自身反应性T细胞的缺失(阴性选择)来建立的。老年无胸腺(nu/nu)小鼠中存在T细胞受体(TCR)-αβ + T细胞,这表明一些T细胞也可以在没有胸腺影响的情况下成熟。因此,为了确定阴性选择是否需要胸腺,对无胸腺nu/nu小鼠及其同基因正常同窝小鼠的TCR Vβ表达进行了比较。表达Vβ3蛋白的T细胞对次要淋巴细胞刺激(Mlsc)决定簇具有特异性,并且由于Mlsc +小鼠品系中的自身耐受性而在胸腺内被删除。此处表明,Vβ3 + T细胞在Mlsc + BALB/c nu/+小鼠中被删除,但在其BALB/c nu/nu同窝小鼠中未被删除。因此,胸腺是T细胞发育过程中克隆删除所必需的。