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创伤患者自然杀伤细胞活性受抑制的机制。

Mechanism of suppression of natural killer cell activity in trauma patients.

作者信息

Joshi P, Hauser C J, Jones Q, Kennedy R, Thomae K R, Zhou X

机构信息

Department of Surgery, University of Mississippi Medical Center, Jackson 39216, USA.

出版信息

Res Commun Mol Pathol Pharmacol. 1998 Sep;101(3):241-8.

PMID:9874282
Abstract

Trauma patients develop a severe immunosuppression that includes suppression of natural killer (NK) cell activity although numbers of NK cells are not reduced. The mechanism of suppression of NK cell activity after major trauma is not known. The aim of the present study was to investigate the in vitro effect of plasma samples from trauma patients (TP) on the cytotoxic activity of normal NK cells. Buffycoat mononuclear cells (5x10(5)/well) were preincubated with either TP or plasma samples from age and sex matched healthy controls (CP) for 0, 16 or 40 h. These effector cells were then cultured with 51Cr labeled K-562 cells (2x10(4)/well) for 4 h at 37 degrees C and % lysis was calculated. No significant differences in % lysis between CP and TP were found with 0 or 16 h preincubation, however 40 h preincubation with TP severely suppressed NK cell function (p=0.003) as compared to preincubation with CP for the same period. Addition of neutralizing anti-IL-4, anti-TGF-beta1, or anti-IL-10 antibodies did not reverse the NK cell suppression. There was a partial reversal of NK cell suppression by catalase but not by SOD or L-NMMA. Removal of monocytes from buffycoat mononuclear cells also significantly reversed the NK cell suppression. These data suggest that suppression of NK cell activity in trauma patients may be an accessory cell dependent phenomenon and may partially depend on production of reactive oxygen metabolites (ROM).

摘要

创伤患者会出现严重的免疫抑制,包括自然杀伤(NK)细胞活性受到抑制,尽管NK细胞数量并未减少。重大创伤后NK细胞活性受抑制的机制尚不清楚。本研究的目的是调查创伤患者(TP)血浆样本对正常NK细胞细胞毒性活性的体外影响。将血沉棕黄层单核细胞(5×10⁵/孔)与TP或年龄和性别匹配的健康对照(CP)的血浆样本预孵育0、16或40小时。然后将这些效应细胞与51Cr标记的K-562细胞(2×10⁴/孔)在37℃下培养4小时,并计算裂解百分比。预孵育0或16小时时,CP和TP之间的裂解百分比没有显著差异,然而,与同期CP预孵育相比,TP预孵育40小时严重抑制了NK细胞功能(p = 0.003)。添加中和抗IL-4、抗TGF-β1或抗IL-10抗体并不能逆转NK细胞的抑制。过氧化氢酶可部分逆转NK细胞的抑制,但超氧化物歧化酶或L-NMMA则不能。从血沉棕黄层单核细胞中去除单核细胞也能显著逆转NK细胞的抑制。这些数据表明,创伤患者NK细胞活性的抑制可能是一种依赖辅助细胞的现象,并且可能部分取决于活性氧代谢产物(ROM)的产生。

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