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用组织相容性同种抗血清致敏的人淋巴细胞激活人补体。

Activation of human complement by human lymphoid cells sensitized with histocompatibility alloantisera.

作者信息

Ferrone S, Cooper N R, Pellegrino M A, Reisfeld R A

出版信息

Proc Natl Acad Sci U S A. 1973 Dec;70(12):3665-8. doi: 10.1073/pnas.70.12.3665.

Abstract

Cultured human lymphoid cells sensitized with human histocompatibility (HL-A) antibodies were able to activate the human complement system in vitro. Some HL-A alloantisera selectively activated the alternate complement pathway while other antisera activated only the classical pathway. A third group of alloantisera was equally able to initiate complement action by way of either pathway. The mechanism of complement activation did not correlate with the HL-A antigen present on the cells or the HL-A specificity of the alloantisera, indicating that the antigenic determinants or distribution on the cell surface play on direct role in selecting the pathway of activation. In this completely homologous system the alternate pathway was found to have the same cytolytic potential as the classical pathway. Thus, an altered or damaged membrane is not a prerequisite for the production of cytolytic damage by the alternate pathway. A complete understanding of the mechanism of interaction of membrane bound antigens and antibodies with the complement system may provide a versatile tool for the investigation of membrane antigen expression.

摘要

用人组织相容性(HL - A)抗体致敏的培养人淋巴细胞能够在体外激活人补体系统。一些HL - A同种抗血清选择性激活替代补体途径,而其他抗血清仅激活经典途径。第三组同种抗血清通过任一途径均能同样启动补体作用。补体激活机制与细胞上存在的HL - A抗原或同种抗血清的HL - A特异性无关,这表明细胞表面的抗原决定簇或分布在选择激活途径中不发挥直接作用。在这个完全同源的系统中,发现替代途径与经典途径具有相同的细胞溶解潜力。因此,膜改变或受损并非替代途径产生细胞溶解损伤的先决条件。对膜结合抗原和抗体与补体系统相互作用机制的全面理解可能为研究膜抗原表达提供一个通用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3813/427302/57279b25e0eb/pnas00139-0397-a.jpg

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