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人类次要组织相容性肽的分离

Isolation of human minor histocompatibility peptides.

作者信息

Sekimata M, Griem P, Egawa K, Rammensee H G, Takiguchi M

机构信息

Department of Immunology, University of Tokyo, Japan.

出版信息

Int Immunol. 1992 Feb;4(2):301-4. doi: 10.1093/intimm/4.2.301.

Abstract

Incompatibility of human minor histocompatibility (hmH) antigens induces rejection of grafts in organ transplantation and graft versus host disease in bone marrow transplantation if donor and recipient are matched for human leukocyte antigen (HLA) genes. These antigens are recognized only by T cells. We describe here the isolation of hmH peptides recognized by a hmH antigen specific, HLA-B35 restricted CTL clone which was derived from a patient who rejected the kidneys from two HLA-identical sisters. Naturally occurring hmH peptides were isolated from a donor derived B cell line and an HLA-B35 transfected human B cell line by acid elution. Analysis of various HLA class I transfectant cells demonstrated that MHC class I molecules themselves determine the peptides which are naturally processed and presented to T cells.

摘要

如果供体和受体的人类白细胞抗原(HLA)基因相匹配,人类次要组织相容性(hmH)抗原的不相容性会在器官移植中引发移植物排斥反应,并在骨髓移植中引发移植物抗宿主病。这些抗原仅被T细胞识别。我们在此描述了由一名排斥来自两名HLA相同姐妹的肾脏的患者衍生出的hmH抗原特异性、HLA - B35限制性CTL克隆所识别的hmH肽的分离。通过酸洗脱从供体来源的B细胞系和HLA - B35转染的人B细胞系中分离出天然存在的hmH肽。对各种HLA I类转染细胞的分析表明,MHC I类分子自身决定了天然加工并呈递给T细胞的肽段。

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