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A promiscuous T cell hybridoma restricted to various I-A molecules
Authors:Masahito Katoh,Yasushi Itoh,Kazumasa Ogasawara,Kiichi Kajino,Hiroki Nishihori,Akio Takahashi,Naoto Matsuki,Kazuya Iwabuchi,Takato O. Yoshida,Robert A. Good,Kazunori Ono  
Affiliation:Masahito Katoh,Yasushi Itoh,Kazumasa Ogasawara,Kiichi Kajino,Hiroki Nishihori,Akio Takahashi,Naoto Matsuki,Kazuya Iwabuchi,Takato O. Yoshida,Robert A. Good,Kazunori Onoé
Abstract:
In a previous study, we identified T cell receptor and major histocompatibility complex (MHC) contact sites on the pigeon cytochrome c p43-58 peptide. Positions 46 and 54 of p43-58 were shown to be the MHC-binding sites. Specific amino acids were identified on the MHC-binding sites which bound to the relevant I-A molecule. In the present study, using NOD (I-Ag7) mice, we established a T cell hybridoma, NOE33-1-2, specific for a p43-58 analog 46R50E54A with arginine (R) and alanine (A) at positions 46 and 54, respectively. Interestingly, NOE 33-1-2 recognized 46R50E54A in the presence of not only I-Ag7, but also I-Ad, s, u and v. In contrast to previous reports that promiscuous T cells were able to recognize peptide antigens with various HLA-DR or I-E molecules consist of monomorphic α and polymorphic β chains, the promiscuous T cell clone NOE33-1-2 recognized peptides with various I-A molecules lacking the monomorphic chain.
Keywords:Major histocompatibility complex class II  T cell hybridoma  Promiscuous recognition
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