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2,3,7,8-四氯二苯并对二恶英对人淋巴细胞中超抗原诱导的IgM分泌的直接抑制作用

Direct suppression of superantigen-induced IgM secretion in human lymphocytes by 2,3,7,8-TCDD.

作者信息

Wood S C, Holsapple M P

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298.

出版信息

Toxicol Appl Pharmacol. 1993 Oct;122(2):308-13. doi: 10.1006/taap.1993.1200.

Abstract

The superantigen, toxic shock syndrome toxin (TSST-1), can activate T-cells to proliferate and secrete lymphokines and can act as a nominal antigen to induce proliferation and immunoglobulin secretion in human B-cells. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an environmental toxicant that produces potent suppression of murine immunocompetence. The present studies were initiated in order to examine the direct effects of TCDD upon human lymphocytes stimulated with TSST-1. TCDD had no effect upon TSST-1-induced T-cell proliferation and produced only a nonsignificant suppression (15%) of TSST-1-induced B-cell proliferation only at the highest concentration tested (30 nM). In contrast, TSST-1-induced B-cell differentiation, as manifested by IgM secretion, was significantly suppressed by TCDD over the concentration range tested (i.e., 0.3 to 30 nM) in trials using B-cells from four separate donors. However, there was obvious variability in the sensitivity to TCDD in that we detected IC50 values of < 0.3, < 0.3, approximately 5.0, and approximately 25.0 nM in the four trials. These results suggest that human B-cell function, following stimulation by TSST-1, can be modulated by direct exposure to TCDD.

摘要

超抗原中毒性休克综合征毒素(TSST-1)可激活T细胞增殖并分泌淋巴因子,还可作为名义抗原诱导人B细胞增殖和免疫球蛋白分泌。2,3,7,8-四氯二苯并对二恶英(TCDD)是一种环境毒物,可有效抑制小鼠免疫能力。开展本研究是为了检测TCDD对受TSST-1刺激的人淋巴细胞的直接作用。TCDD对TSST-1诱导的T细胞增殖无影响,仅在最高测试浓度(30 nM)时对TSST-1诱导的B细胞增殖产生不显著的抑制作用(15%)。相比之下,在使用来自四个不同供体的B细胞进行的试验中,TSST-1诱导的B细胞分化(以IgM分泌为表现)在测试浓度范围(即0.3至30 nM)内被TCDD显著抑制。然而,对TCDD的敏感性存在明显差异,因为我们在四项试验中检测到的半数抑制浓度(IC50)值分别<0.3、<0.3、约5.0和约25.0 nM。这些结果表明,TSST-1刺激后的人B细胞功能可通过直接暴露于TCDD进行调节。

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