Stockinger B
Proc Natl Acad Sci U S A. 1984 Jan;81(1):220-3. doi: 10.1073/pnas.81.1.220.
Induction of neonatal tolerance leads to a profound reduction in cytotoxic T-lymphocyte precursor frequencies against the tolerated alloantigen ("tolerogen") as evaluated by limiting-dilution analysis. The curves obtained were linear within the range tested and, thus, did not yield evidence for any dissociation of cytotoxic precursors from regulatory cell populations. However, it could be shown that cytotoxic T-lymphocyte precursor frequencies against the tolerogen increased drastically if the tolerant spleen cells were adsorbed, prior to limiting-dilution culture, on monolayers of syngeneic blasts expressing receptors for the tolerogen but not if they were adsorbed on syngeneic blasts against third-party antigens. This finding implies that cytotoxic precursor cells against the tolerogen are not clonally deleted in tolerant animals but rather are suppressed by a regulatory cell population that is present at high frequency and presumably acts in an anti-idiotypic fashion.
通过有限稀释分析评估,诱导新生期耐受会导致针对耐受同种异体抗原(“耐受原”)的细胞毒性T淋巴细胞前体频率大幅降低。在所测试的范围内获得的曲线呈线性,因此,没有产生细胞毒性前体与调节细胞群体解离的证据。然而,可以证明,如果在有限稀释培养之前,将耐受的脾细胞吸附在表达耐受原受体的同基因胚细胞单层上,那么针对耐受原的细胞毒性T淋巴细胞前体频率会急剧增加,但如果将其吸附在针对第三方抗原的同基因胚细胞上则不会。这一发现意味着,在耐受动物中,针对耐受原的细胞毒性前体细胞并非克隆性缺失,而是被高频存在的调节细胞群体所抑制,推测该调节细胞群体以抗独特型方式发挥作用。