Alloreactive feature of HLA-DP-specific cytotoxic T-cell clone.

Abstract:

:The alloreactive feature of CD4+ cytotoxic T-cell clone that could specifically lyse the cells bearing DPB1*0202 sequence was described. The clone was generated from a mixed culture of peripheral blood lymphocytes derived from siblings who were HLA-A, B, C, DR, and DQ identical by serological typing and whose DNA sequence of the second exon of DPB1 was one-allele mismatched by oligonucleotide typing (responder, PDB1*0201/0402; stimulator, DPB1*0202/0402). Specific cytotoxic activity of the clone was strictly limited against the cells bearing DPB1*0202 and was not able to lyse the other tested cells bearing DPB1*0201, 0301, 0401, 0501, 0601, 0901, 1301, and 1601. The cytotoxic activity of the clone was blocked by treatment of target cells with anti-DP monoclonal antibodies (B7/21). On the other hand, treatment of target cells with blocking agents of endogenous or exogenous antigen transport pathway (brefeldin A (BFA), endogenous; chloroquine, exogenous) had no effect on the cytotoxic activity of the clone. These results strongly favor the view that the DP epitopes recognized by the clone are conformational epitopes conferred by specific amino acids in hypervariable regions of the HLA-DP second DPB1 exon and the contribution of peptides in the HLA grooves to the conformational epitope motif is less likely.

journal_name

Cell Immunol

journal_title

Cellular immunology

authors

Nishimura M,Mitsunaga S,Akaza T,Mitomi Y,Tadokoro K,Juji T

doi

10.1006/cimm.1994.1024

subject

Has Abstract

pub_date

1994-01-01 00:00:00

pages

262-70

issue

1

eissn

0008-8749

issn

1090-2163

pii

S0008-8749(84)71024-0

journal_volume

153

pub_type

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