Itoh Y, Ogasawara K, Gotohda T, Takami K, Naruse H, Onoe K
Section of Pathology, Institute of Immunological Science, Hokkaido University, Sapporo, Japan.
Int Immunol. 1992 Jul;4(7):779-87. doi: 10.1093/intimm/4.7.779.
When C57BL/10(B10) mice were immunized with a pigeon cytochrome c related peptide, 50V (AEGFSYTVANKNKGIT), two helper T cell populations with different specificity were activated. A major T cell population reacted with a 50V analog, 50V54A (AEGFSYTVANKAKGIT), more potently than with the immunogen, 50V, in a heteroclitic fashion, whereas the other minor T cell population responded only to 50V. By contrast, when bm12 mice were immunized with 50V, the minor T cell population responding only to 50V could hardly be demonstrated. The apparent deletion of the minor T cell population in bm12 mice seems to be attributable to negative selection under the influence of I-Abm12 molecules, since the minor T cell population was undetectable in both I-Ab and I-Abm12 restricted T cells from (B10 x bm12)F1 mice. Thus, three mutant points on the I-A molecule in bm12 mice appear to be involved in the seemingly negative selection of the certain T cell repertoire. The present finding demonstrates that a T cell repertoire generated under the influence of a MHC product (Ab) on one parental strain is eliminated by a different MHC product (Abm12) on the other parental strain of F1 cross. The mechanism underlying the apparent negative selection is discussed.
当用鸽细胞色素c相关肽50V(AEGFSYTVANKNKGIT)免疫C57BL/10(B10)小鼠时,激活了两个具有不同特异性的辅助性T细胞群体。一个主要的T细胞群体以异质性方式与50V类似物50V54A(AEGFSYTVANKAKGIT)反应,比与免疫原50V反应更强,而另一个次要的T细胞群体仅对50V有反应。相比之下,当用50V免疫bm12小鼠时,几乎无法证明仅对50V有反应的次要T细胞群体。bm12小鼠中次要T细胞群体的明显缺失似乎归因于I-Abm12分子影响下的阴性选择,因为在(B10×bm12)F1小鼠的I-Ab和I-Abm12限制性T细胞中均未检测到次要T细胞群体。因此,bm12小鼠I-A分子上的三个突变点似乎参与了特定T细胞库的看似阴性选择。本研究结果表明,在一个亲本品系的MHC产物(Ab)影响下产生的T细胞库被F1杂交另一个亲本品系的不同MHC产物(Abm12)消除。讨论了明显阴性选择的潜在机制。