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蛋白质结合多糖PSK对可溶性抑制因子的淋巴细胞表面结合位点的阻断作用。

Blocking of lymphocyte surface binding sites for the soluble suppressor factor by protein-bound polysaccharide, PSK.

作者信息

Toge T, Yamaguchi Y, Kegoya Y, Baba N, Yanagawa E, Hattori T

机构信息

Department of Surgery, Hiroshima University, Japan.

出版信息

Int J Immunopharmacol. 1989;11(1):9-12. doi: 10.1016/0192-0561(89)90093-3.

Abstract

The ability of protein-bound polysaccharide (PSK) to block the suppressive activity of soluble suppressor factor (SSF) was investigated. The suppressive activity of SSF derived from U-937 cells on phytohemagglutinin (PHA)-induced lymphocyte proliferative (LP) response was significantly reduced in the presence of PSK. The release of SSF was not inhibited by the treatment of U-937 cells with PSK. The suppressive activity of SSF on LP response to PHA was significantly decreased by the pretreatment of responder lymphocytes with PSK. Studies to determine lymphocyte receptor activity were performed. PSK competed with wheat germ agglutinin (WGA) which recognized the same receptor as SSF on the surface of the lymphocyte. Neither PSK nor serum competed with anti-CD4 monoclonal antibody. Thus, PSK may inhibit SSF-mediated suppression by competing for specific binding sites on the surface of responder lymphocytes.

摘要

研究了蛋白结合多糖(PSK)阻断可溶性抑制因子(SSF)抑制活性的能力。在PSK存在的情况下,源自U - 937细胞的SSF对植物血凝素(PHA)诱导的淋巴细胞增殖(LP)反应的抑制活性显著降低。用PSK处理U - 937细胞不会抑制SSF的释放。用PSK预处理应答淋巴细胞可显著降低SSF对PHA诱导的LP反应的抑制活性。进行了确定淋巴细胞受体活性的研究。PSK与小麦胚芽凝集素(WGA)竞争,WGA与淋巴细胞表面与SSF相同的受体结合。PSK和血清均不与抗CD4单克隆抗体竞争。因此,PSK可能通过竞争应答淋巴细胞表面的特异性结合位点来抑制SSF介导的抑制作用。

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