Tsujihata Y, So T, Hashimoto Y, Ueda T, Imoto T
Graduate School of Pharmaceutical Sciences, Kyushu University, Maidashi, Higashi-ku, 812-8582, Fukuoka, Japan.
Mol Immunol. 2001 Sep;38(5):375-81. doi: 10.1016/s0161-5890(01)00068-2.
We determined if a single amino acid substitution in a self protein causes autoantibody responses. Mouse lysozyme (ML) was used as a model self protein, and a mutant ML (F57L ML) was prepared by replacing 57Phe of ML to Leu, an approach which resulted in introducing into ML the immunogenic sequence of peptide 50-61 of hen egg lysozyme (HEL) restricted to I-A(k) MHC class II molecule. We found that F57L ML but not native ML primed HEL specific T cells and triggered ML specific autoantibody responses in B10.A and C3H mice (I-A(k), I-E(k)). Peptide regions, ML 14-69 and ML 98-130, were major epitopes of autoantibodies in both strains of mice. These findings indicate that a single amino acid substitution in self proteins can cause an autoantibody response when the mutated region is presented by MHC class II molecules and recognized by T cells.
我们确定了自身蛋白中的单个氨基酸替换是否会引发自身抗体反应。小鼠溶菌酶(ML)被用作模型自身蛋白,通过将ML的57位苯丙氨酸替换为亮氨酸制备了一种突变型ML(F57L ML),这种方法导致在ML中引入了受I-A(k) MHC II类分子限制的鸡卵溶菌酶(HEL)50-61肽段的免疫原性序列。我们发现,F57L ML而非天然ML在B10.A和C3H小鼠(I-A(k),I-E(k))中引发了HEL特异性T细胞,并触发了ML特异性自身抗体反应。肽段区域ML 14-69和ML 98-130是这两种小鼠品系中自身抗体的主要表位。这些发现表明,当突变区域由MHC II类分子呈递并被T细胞识别时,自身蛋白中的单个氨基酸替换可引发自身抗体反应。