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“非特异性”主要组织相容性复合体非限制性杀伤细胞及其受体。

'Nonspecific' MHC-unrestricted killer cells and their receptors.

作者信息

Hersey P, Bolhuis R

机构信息

Immunology and Oncology Unit, David Maddison Clinical Sciences Building, Royal Newcastle Hospital, NSW, 2300 Australia.

Department of Immunology, Rotterdam Radio-Therapeutic Institute and The Dr Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.

出版信息

Immunol Today. 1987;8(7-8):233-9. doi: 10.1016/0167-5699(87)90173-3.

Abstract

The receptors involved in apparently nonspecific, MHC- unrestricted effector cell-target cell interaction and lysis continue to raise controversy. They bind to distinct ligands on their target cells and activate diverse cellular functions such as gene expression, lymphokine production, proliferation and/or cytolytic activity by the effector cells. Several distinct receptors may mediate MHC-unrestricted cytotoxicity. Here, Peter Hersey and Reinder Bolhuis review evidence that the four main receptors involved in triggering this form of lytic activity are the CD2 molecule (the sheep red cell receptor), CD3-associated αβ chain T-cell receptor (TCR), the γδ chain TCR-CD3 complex and the CD16 molecule (the IgG0Fc receptor). The apparent non-specificity specificity of killing is a reflection of the widespread expression of natural ligands for these receptors on target cells.

摘要

参与明显非特异性、不受主要组织相容性复合体(MHC)限制的效应细胞与靶细胞相互作用及裂解过程的受体,一直存在争议。它们与靶细胞上不同的配体结合,并激活多种细胞功能,如效应细胞的基因表达、淋巴因子产生、增殖和/或细胞溶解活性。几种不同的受体可能介导不受MHC限制的细胞毒性。在此,彼得·赫西和赖德·博尔胡伊斯综述了相关证据,表明参与引发这种裂解活性形式的四种主要受体是CD2分子(绵羊红细胞受体)、与CD3相关的αβ链T细胞受体(TCR)、γδ链TCR - CD3复合体以及CD16分子(IgG0Fc受体)。杀伤作用表面上的非特异性实际上反映了这些受体的天然配体在靶细胞上广泛表达的情况。

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