Chen J S, Lorenz R G, Goldberg J, Allen P M
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
J Immunol. 1991 Dec 1;147(11):3672-8.
An immunodominant epitope of bovine RNase restricted by I-Ek molecules was identified using a T cell hybridoma recognizing RNase. This epitope was localized to the peptide RNase(90-105). Single conservative amino acid substitutions were made at each of the positions 94 through 105. It was found that only at one position, Asn-103, were conservative substitutions not allowed. This residue was shown to be the critical residue in determining T cell specificity. The ability of RNase(90-105) and the well-defined T cell epitope, HEL(46-61) to stimulate mouse strains expressing different independent H-2 haplotypes was examined using a T cell proliferation assay. The response to HEL(46-61) was completely restricted to mice expressing an I-Ak molecule. In striking contrast, 6 of 10 different mouse strains, H-2b,f,k,q,s,u, mounted vigorous T cell responses to RNase(90-105). The response was restricted to both I-A and I-E molecules, including I-Ab, I-Af, I-Ek, I-Aq, and I-As. H-2d mice were nonresponders to RNase(90-105), which was shown to be due to the failure of RNase(90-105) to bind to I-Ad molecules. A variant RNase(90-105) peptide was generated, containing an I-Ad binding motif, that could bind to I-Ad molecules. Despite its ability to bind, this variant peptide was not able to stimulate a response in H-2d mice. This result demonstrates that the ability of a peptide to bind to an Ia molecule is necessary but not always sufficient for a response to occur. Thus, in contrast to the highly restricted HEL(46-61) determinant, the RNase(90-105) determinant is permissive in its binding to Ia molecules. These results show that in the universe of T cell inducing epitopes contains both highly restricted and broadly restricted epitopes are found.
利用识别核糖核酸酶的T细胞杂交瘤鉴定了受I-Ek分子限制的牛核糖核酸酶的一个免疫显性表位。该表位定位于肽段核糖核酸酶(90 - 105)。在94至105位的每个位置进行了单个保守氨基酸替换。结果发现,只有在一个位置,即天冬酰胺-103,不允许进行保守替换。该残基被证明是决定T细胞特异性的关键残基。使用T细胞增殖试验检测了核糖核酸酶(90 - 105)和明确的T细胞表位HEL(46 - 61)刺激表达不同独立H-2单倍型的小鼠品系的能力。对HEL(46 - 61)的反应完全局限于表达I-Ak分子的小鼠。与之形成鲜明对比的是,10种不同小鼠品系中的6种,即H-2b、f、k、q、s、u,对核糖核酸酶(90 - 105)产生了强烈的T细胞反应。该反应局限于I-A和I-E分子,包括I-Ab、I-Af、I-Ek、I-Aq和I-As。H-2d小鼠对核糖核酸酶(90 - 105)无反应,这被证明是由于核糖核酸酶(90 - 105)未能与I-Ad分子结合。产生了一种变体核糖核酸酶(90 - 105)肽,其含有I-Ad结合基序,能够与I-Ad分子结合。尽管其具有结合能力,但这种变体肽不能刺激H-2d小鼠产生反应。这一结果表明,肽与Ia分子结合的能力是反应发生的必要条件,但并不总是充分条件。因此,与高度受限的HEL(46 - 61)决定簇不同,核糖核酸酶(90 - 105)决定簇在与Ia分子结合方面具有宽容性。这些结果表明,在T细胞诱导表位的范畴中,既存在高度受限的表位,也存在广泛受限的表位。