Solinger A M, Ultee M E, Margoliash E, Schwartz R H
J Exp Med. 1979 Oct 1;150(4):830-48. doi: 10.1084/jem.150.4.830.
The T-lymphocyte proliferative response to pigeon cytochrome c was studied in the mouse. H-2a and H-2k strains were responders to this antigen whereas H-2b, H-2d, H-2f, H-2ja, H-2p, H-2q, H-2r, H-2s, and H-2u strains were low or nonresponders. Genetic mapping demonstrated that two major histocompatibility complex (MHC)-linked Ir genes control the response, one in I-A, the other in I-E/I-C. The major antigenic determinant recognized in this response was localized by cross-stimulations with species variants and cyanogen bromide cleavage fragments of cytochrome c. It was found to be a topographic surface determinant composed of an isoleucine for valine substitution at residue 3, a glutamine for lysine substitution at residue 100 and a lysine for glutamic acid substitution at residue 104. Tobacco hornworm moth cytochrome c, which contains a glutamine at residue 100 but a terminal lysine at residue 103 (one amino acid closer to the glutamine), stimulated pigeon cytochrome c immune T cells better than the immunogen. This result demonstrates for the first time a functional T-cell heteroclitic proliferative response in a system under Ir gene control. Immunization with the cyanogen bromide cleavage fragments revealed that only pigeon cytochrome c fragment 81-104 was immunogenic. This fragment primed for a T-cell proliferative response whose specificity was nearly identical to that of the T-cell response primed for by the whole molecule, suggesting that the glutamine at 100 and the lysine at 104 form the immunodominant portion of the antigenic site. Furthermore, mixing experiments using the two cross-reacting antigens, hippopotamus cytochrome c and Pekin duck or chicken cytochrome c fragment (81-104), each of which contains only one of the two immunodominant substitutions, demonstrated that the T lymphocytes responding to the major antigenic determinant comprise a single family of clones that recognize both amino acids as part of the same determinant. Thus, two complementing MHC-linked Ir genes can control the immune response to a single antigenic determinant.
在小鼠中研究了对鸽细胞色素c的T淋巴细胞增殖反应。H-2a和H-2k品系对该抗原呈反应性,而H-2b、H-2d、H-2f、H-2ja、H-2p、H-2q、H-2r、H-2s和H-2u品系反应较弱或无反应。基因定位表明,两个主要组织相容性复合体(MHC)连锁的Ir基因控制该反应,一个在I-A区,另一个在I-E/I-C区。通过与细胞色素c的物种变体和溴化氰裂解片段进行交叉刺激,确定了该反应中识别的主要抗原决定簇。发现它是一种构象表面决定簇,由第3位异亮氨酸取代缬氨酸、第100位谷氨酰胺取代赖氨酸和第104位赖氨酸取代谷氨酸组成。烟草天蛾细胞色素c在第100位含有谷氨酰胺,但在第103位含有末端赖氨酸(比谷氨酰胺近一个氨基酸),其刺激鸽细胞色素c免疫T细胞的能力优于免疫原。这一结果首次在Ir基因控制的系统中证明了功能性T细胞交叉反应性增殖反应。用溴化氰裂解片段免疫表明,只有鸽细胞色素c片段81-104具有免疫原性。该片段引发的T细胞增殖反应的特异性与全分子引发的T细胞反应的特异性几乎相同,这表明第100位的谷氨酰胺和第104位的赖氨酸构成了抗原位点的免疫显性部分。此外,使用两种交叉反应抗原(河马细胞色素c和北京鸭或鸡细胞色素c片段(81-104))进行的混合实验表明,对主要抗原决定簇作出反应的T淋巴细胞由一个克隆家族组成,该家族将这两种氨基酸识别为同一决定簇的一部分。因此,两个互补的MHC连锁Ir基因可以控制对单一抗原决定簇的免疫反应。