CD4+ T cell-mediated immunity against prion proteins

被引:10
作者
Stoltze, L
Rezaei, H
Jung, G
Grosclaude, J
Debey, P
Schild, H
Rammensee, HG
机构
[1] Univ Tubingen, Dept Immunol, Inst Cell Biol, D-72076 Tubingen, Germany
[2] Museum Natl Hist Nat, Unite 806, EA2703, INRA, F-75005 Paris, France
[3] INRA, Unite Virol & Immunol Mol, F-78352 Jouy En Josas, France
[4] Univ Tubingen, Inst Organ Chem, D-72076 Tubingen, Germany
关键词
T lymphocyte; prion protein; MHC class II;
D O I
10.1007/s000180300054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prion protein (PrPC) is essential for susceptibility to transmissible spongiform encephalopathies. A specific conformer of this protein (PrPSC) is, according to the 'protein only' hypothesis, the principal or only component of the infectious agent, designated prion. Transmission' of prions between species is often inefficient, resulting in low attack rates and/or prolonged incubation times and is ascribed to a 'species barrier' caused by differences in the amino acid sequence of PrP between recipient and donor. In this report, we demonstrate that these differences in amino acid sequence result in presentation of distinct peptides on major histocompatibility complex class II molecules. These peptides result in activation of specific CD4(+) T cells which leads to the induction of an effective immune response against foreign PrP as demonstrated by antibody production. Therefore, CD4(+) T cells represent a crucial component of the immune system to distinguish between foreign and self PrP.
引用
收藏
页码:629 / 638
页数:10
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