An HLA-binding-motif-aided peptide epitope library: A novel library design for the screening of HLA-DR4-restricted antigenic peptides recognized by CD4+T cells

Takeshi Tana, Nobuhiro Kamikawaji, Christopher J. Savoie, Tohru Sudo, Yurika Kinoshita, Takehiko Sasazuki

研究成果: ジャーナルへの寄稿記事

8 引用 (Scopus)

抜粋

Susceptibility to a series of autoimmune diseases is strongly associated with particular HLA class II alleles. Identification of T cell clones and antigenic epitopes bound by HLA class II molecules involved in autoimmune diseases is critical to understanding the etiology of these HLA class II- associated diseases. However, establishment of T cell clones in autoimmune diseases is difficult because the antigenic peptides are unknown. Peptide library methods which include all possible peptide sequences offer a potentially powerful tool for the detection of cross-reactive antigenic peptides recognized by T cells. Here, we reduced the number of peptides per mixture by utilizing the known binding motifs of peptides for the HLA- DRB1*0405 molecule and evaluated the effectiveness of this library design. Each library mixture evoked a strong proliferative response in the unprimed peripheral blood lymphocytes (PBL) from HLA-DRB1*0405-positive donors but little or no response in the PBL from HLA-DRB1*0405-negative donors. The library also detected antigenic peptides that activated three antigen- specific T cell lines restricted by HLA-DRB1*0405, with different specificities. The motif-based approach thus presents a powerful method for monitoring T cells in large, heterogeneous T cell populations and is useful for the identification of the mimic peptide epitopes of T cell lines and clones.

元の言語英語
ページ(範囲)14-21
ページ数8
ジャーナルJournal of Human Genetics
43
発行部数1
DOI
出版物ステータス出版済み - 6 13 1998

    フィンガープリント

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

これを引用