See R H, Krystal G, Chow A W
Department of Medicine, University of British Columbia, Vancouver, Canada.
Can J Microbiol. 1992 Sep;38(9):937-44. doi: 10.1139/m92-151.
Staphylococcal toxic shock syndrome toxin-1 (TSST-1) as well as staphylococcal enterotoxin A (SEA) and B (SEB) have recently been shown to bind directly to the class II major histocompatibility antigen, HLA-DR. Whereas others have characterized TSST-1 and SEA binding to HLA-DR on transfected L cells or B lymphoma cell lines, we sought evidence for direct binding of TSST-1 and SEA to HLA-DR on purified human monocytes. A single class of high-affinity receptors was found for both TSST-1 (dissociation constant (Kd) 40 nM, 3.4 x 10(4) receptors per cell) and SEA (Kd 12 nM, 3.2 x 10(4) receptors per cell) on normal human monocytes. Affinity cross-linking of 125I-labeled toxins to monocytes revealed the presence of two membrane protein subunits with molecular masses consistent with the alpha and beta chains of human HLA-DR (35 and 28 kDa, respectively). The anti-HLA-DR monoclonal antibody L243, but not L203 or 2.06, inhibited radiolabeled toxin binding to human monocytes and neutralized the mitogenic response of human T lymphocytes to both toxins. However, L243 was consistently more effective in blocking radiolabeled TSST-1 than SEA binding to human monocytes from the same donors, suggesting that TSST-1 and SEA may be binding to overlapping epitopes rather than to the same epitope on HLA-DR. Because TSST-1 and SEB bind to distinct epitopes on HLA-DR and because SEA cross competes with both TSST-1 and SEB on the HLA-DR receptor, we postulate that SEA occupies a binding site within HLA-DR that overlaps both TSST-1 and SEB.(ABSTRACT TRUNCATED AT 250 WORDS)
葡萄球菌中毒性休克综合征毒素-1(TSST-1)以及葡萄球菌肠毒素A(SEA)和B(SEB)最近已被证明可直接结合II类主要组织相容性抗原HLA-DR。虽然其他人已对TSST-1和SEA与转染的L细胞或B淋巴瘤细胞系上的HLA-DR结合进行了表征,但我们寻求TSST-1和SEA与纯化的人单核细胞上的HLA-DR直接结合的证据。在正常人单核细胞上发现了针对TSST-1(解离常数(Kd)40 nM,每细胞3.4×10⁴个受体)和SEA(Kd 12 nM,每细胞3.2×10⁴个受体)的单一类高亲和力受体。¹²⁵I标记毒素与单核细胞的亲和交联显示存在两个膜蛋白亚基,其分子量与人HLA-DR的α链和β链一致(分别为35 kDa和28 kDa)。抗HLA-DR单克隆抗体L243而非L203或2.06抑制放射性标记毒素与人单核细胞的结合,并中和人T淋巴细胞对两种毒素的促有丝分裂反应。然而,L243在阻断放射性标记的TSST-1与来自相同供体的人单核细胞的结合方面始终比SEA更有效,这表明TSST-1和SEA可能结合到HLA-DR上的重叠表位而非相同表位。由于TSST-1和SEB结合到HLA-DR上不同的表位,并且由于SEA在HLA-DR受体上与TSST-1和SEB都存在交叉竞争,我们推测SEA占据了HLA-DR内与TSST-1和SEB都重叠的结合位点。(摘要截短于250字)