See R H, Chow A W
Department of Medicine, University of British Columbia, Vancouver, Canada.
Infect Immun. 1992 Nov;60(11):4957-60. doi: 10.1128/iai.60.11.4957-4960.1992.
We previously demonstrated that the induction by staphylococcal toxic shock syndrome toxin 1 (TSST-1) of tumor necrosis factor alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) secretion by human monocytes requires direct T cell-monocyte contact. In the present study, a role for the adhesion molecule lymphocyte function associated antigen 1 (LFA-1) in TSST-1-induced cytokine secretion by human monocytes among 12 normal healthy donors was investigated. Monoclonal antibodies to the alpha chain (anti-CD11a) and to the beta chain (anti-CD18) of LFA-1 significantly inhibited TSST-1-induced TNF-alpha and IL-1 beta secretion (P < 0.025; Wilcoxon signed-rank test, two tailed), while a control monoclonal antibody directed against the monocyte CD14 antigen had no effect. These results suggest that LFA-1 may play an important role in the secretion of TNF-alpha and IL-1 beta by TSST-1-stimulated human monocytes, likely by promoting cell-cell adhesion between monocytes and lymphocytes.
我们之前证明,葡萄球菌中毒性休克综合征毒素1(TSST-1)诱导人单核细胞分泌肿瘤坏死因子α(TNF-α)和白细胞介素-1β(IL-1β)需要T细胞与单核细胞直接接触。在本研究中,我们调查了12名正常健康供体中,黏附分子淋巴细胞功能相关抗原1(LFA-1)在TSST-1诱导人单核细胞分泌细胞因子中的作用。针对LFA-1α链的单克隆抗体(抗CD11a)和β链的单克隆抗体(抗CD18)显著抑制了TSST-1诱导的TNF-α和IL-1β分泌(P < 0.025;Wilcoxon符号秩检验,双侧),而针对单核细胞CD14抗原的对照单克隆抗体则没有作用。这些结果表明,LFA-1可能在TSST-1刺激的人单核细胞分泌TNF-α和IL-1β中发挥重要作用,可能是通过促进单核细胞与淋巴细胞之间的细胞间黏附来实现的。