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人类T细胞对在小鼠肥大细胞瘤P815的DNA转染细胞上表达的克隆HLA I类基因产物的识别。

Human T cell recognition of cloned HLA class I gene products expressed on DNA transfectants of mouse mastocytoma P815.

作者信息

Maryanski J L, Moretta A, Jordan B, De Plaen E, Van Pel A, Boon T, Cerottini J C

出版信息

Eur J Immunol. 1985 Nov;15(11):1111-7. doi: 10.1002/eji.1830151109.

DOI:10.1002/eji.1830151109
PMID:2933264
Abstract

Cloned genes for human major histocompatibility complex (MHC) class I antigens were introduced by DNA-mediated gene transfer into a high-efficiency transfection recipient (HTR) cell line previously derived from mouse mastocytoma P815. Cell surface expression of HLA-A3, AW24 and CW3 gene products on P815 transfectants was demonstrated by radioimmune assay and by flow cytometry. The human MHC class I gene products were apparently expressed on P815 transfectants in a form recognized by human cytolytic T lymphocytes (CTL). Human CTL generated in unidirectional mixed lymphocyte culture against AW24+ donor lymphocytes clearly lysed P815-HLA-AW24+ transfectant target cells, but not untransfected P815(HTR) controls. Moreover, P815-HLA transfectants could stimulate in vitro a significant alloreactive human CTL response. Lysis of P815-HLA transfectant target cells by human CTL was inhibited by a monoclonal antibody directed against human MHC class I gene products. These mouse cell transfectants may be useful for the study of human T cell responses.

摘要

通过DNA介导的基因转移,将人类主要组织相容性复合体(MHC)I类抗原的克隆基因导入先前从小鼠肥大细胞瘤P815衍生而来的高效转染受体(HTR)细胞系。通过放射免疫测定和流式细胞术证明了P815转染细胞上HLA - A3、AW24和CW3基因产物的细胞表面表达。人类MHC I类基因产物显然以人类细胞毒性T淋巴细胞(CTL)可识别的形式在P815转染细胞上表达。在单向混合淋巴细胞培养中针对AW24 +供体淋巴细胞产生的人类CTL能够明显裂解P815 - HLA - AW24 +转染靶细胞,但不能裂解未转染的P815(HTR)对照细胞。此外,P815 - HLA转染细胞能够在体外刺激显著的同种异体反应性人类CTL反应。针对人类MHC I类基因产物的单克隆抗体可抑制人类CTL对P815 - HLA转染靶细胞的裂解。这些小鼠细胞转染体可能对研究人类T细胞反应有用。

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Eur J Immunol. 1985 Nov;15(11):1111-7. doi: 10.1002/eji.1830151109.
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引用本文的文献

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Synthetic peptides as antigens and competitors in recognition by H-2-restricted cytolytic T cells specific for HLA.合成肽作为被H-2限制的、针对HLA的溶细胞性T细胞识别中的抗原和竞争者。
J Exp Med. 1988 Apr 1;167(4):1391-405. doi: 10.1084/jem.167.4.1391.
3
Recognition of oligonucleotide-encoded T cell epitopes introduced into a gene unrelated to the original antigen.对引入与原始抗原无关基因中的寡核苷酸编码T细胞表位的识别。
J Exp Med. 1989 Jan 1;169(1):297-302. doi: 10.1084/jem.169.1.297.
4
Site-directed mutagenesis of an HLA-A3 gene identifies amino acid 152 as crucial for major-histocompatibility-complex-restricted and alloreactive cytotoxic-T-lymphocyte recognition.HLA - A3基因的定点诱变确定第152位氨基酸对于主要组织相容性复合体限制的和同种异体反应性细胞毒性T淋巴细胞识别至关重要。
Proc Natl Acad Sci U S A. 1987 Jul;84(14):5014-8. doi: 10.1073/pnas.84.14.5014.
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DNA sequence of HLA-A11: remarkable homology with HLA-A3 allows identification of residues involved in epitopes recognized by antibodies and T cells.HLA - A11的DNA序列:与HLA - A3具有显著同源性,有助于鉴定与抗体和T细胞识别的表位相关的残基。
Immunogenetics. 1987;25(4):241-50. doi: 10.1007/BF00404694.
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