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将非肽抗原,尤其是药物,呈递给特异性T细胞。

Presentation of non-peptide antigens, in particular drugs, to specific T cells.

作者信息

von Greyerz S, Zanni M, Schnyder B, Pichler W J

机构信息

Institute of Immunology and Allergology, Inselspital, Bern, Switzerland.

出版信息

Clin Exp Allergy. 1998 Sep;28 Suppl 4:7-11.

PMID:9761023
Abstract

Drugs are non-peptide antigens that can be recognized by specific T cells. It has been thought for many years that small molecular compounds can only be stimulating for T cells after covalent binding to MHC-embedded peptides. As most drug-specific T cell clones can react to glutaraldehyde fixed antigen presenting cells (APC), recognition of drugs by specific T cells does not require prior uptake and processing of haptenated proteins by APC. In fact, activated T cell clones can recognize drugs associated with the MHC-peptide complex in a non-covalent way. Such a binding is reminiscent of superantigen stimulations of T cells.

摘要

药物是非肽类抗原,可被特异性T细胞识别。多年来人们一直认为,小分子化合物只有在与嵌入MHC的肽共价结合后才能刺激T细胞。由于大多数药物特异性T细胞克隆能与戊二醛固定的抗原呈递细胞(APC)发生反应,特异性T细胞对药物的识别并不需要APC预先摄取和处理半抗原化蛋白。事实上,活化的T细胞克隆能够以非共价方式识别与MHC-肽复合物相关的药物。这种结合使人联想到T细胞的超抗原刺激。

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