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细菌超抗原作为抗肿瘤剂:葡萄球菌肠毒素A诱导人淋巴细胞产生肿瘤细胞毒性

Bacterial superantigens as anti-tumour agents: induction of tumour cytotoxicity in human lymphocytes by staphylococcal enterotoxin A.

作者信息

Lando P A, Hedlund G, Dohlsten M, Kalland T

机构信息

Kabi Pharmacia Therapeutics AB, Lund, Sweden.

出版信息

Cancer Immunol Immunother. 1991;33(4):231-7. doi: 10.1007/BF01744942.

Abstract

Activation of lymphocytes by interleukin-2 (IL-2) induces lymphokine-activated killer (LAK) cells that show promising effects on tumour growth in clinical trials. We examined the effect of the superantigen staphylococcal enterotoxin A (SEA) on anti-tumour activity of freshly prepared human lymphocytes. Picomolar amounts of SEA rapidly induced cytotoxic activity against K562 and Raji cells as well as some natural-killer(NK)-resistant tumour cell lines. Cytotoxic activity was not dependent on target cell expression of either major histocompatibility complex (MHC) class I or II antigens as shown using mutated cell lines. Cell-sorting experiments showed that the activity was expressed by NK (CD5-CD56+) as well as T (CD5+) cells, although the former contained the majority of cytotoxic activity. NK cells could not be directly activated by SEA. In contrast, SEA activated purified T cells to the same extent as in bulk cultures. It is suggested that SEA activation of NK cells is secondary to that brought about by lymphokines produced by T cells. Activation of LAK cells with SEA was comparable in magnitude as well as target cell spectrum to that of IL-2. In addition to the LAK-like cytotoxic activity induced by SEA, a superimposed cytotoxicity towards target cells expressing MHC class II antigens coated with SEA was observed. This staphylococcal-enterotoxin-dependent cell-mediated cytotoxicity (SDCC) was exclusively mediated by T cells. It is well established that MHC class II antigens function as receptors for staphylococcal enterotoxins on mammalian cells and that the complex between MHC class II antigen and--SEA apparently functions as a target structure for activated T cells with target cell lysis as a consequence. Activation of T lymphocytes with IL-2 also resulted in the capability to mediate SDCC. Staphylococcal enterotoxins represent a novel way of inducing anti-tumour activity in human lymphocytes, which could be of value in therapeutic applications.

摘要

白细胞介素-2(IL-2)激活淋巴细胞可诱导产生淋巴因子激活的杀伤(LAK)细胞,在临床试验中,这些细胞对肿瘤生长显示出有前景的效果。我们研究了超抗原葡萄球菌肠毒素A(SEA)对新鲜制备的人淋巴细胞抗肿瘤活性的影响。皮摩尔量的SEA可迅速诱导对K562和Raji细胞以及一些天然杀伤(NK)抗性肿瘤细胞系的细胞毒活性。使用突变细胞系表明,细胞毒活性不依赖于主要组织相容性复合体(MHC)I类或II类抗原的靶细胞表达。细胞分选实验表明,活性由NK(CD5-CD56+)细胞以及T(CD5+)细胞表达,尽管前者含有大部分细胞毒活性。SEA不能直接激活NK细胞。相反,SEA激活纯化的T细胞的程度与在大量培养物中相同。提示SEA对NK细胞的激活继发于T细胞产生的淋巴因子所引起的激活。SEA激活LAK细胞在强度以及靶细胞谱方面与IL-2相当。除了SEA诱导的LAK样细胞毒活性外,还观察到对表达包被有SEA的MHC II类抗原的靶细胞有叠加的细胞毒性。这种葡萄球菌肠毒素依赖性细胞介导的细胞毒性(SDCC)完全由T细胞介导。众所周知,MHC II类抗原在哺乳动物细胞上作为葡萄球菌肠毒素的受体起作用,并且MHC II类抗原与SEA之间的复合物显然作为活化T细胞的靶结构,结果导致靶细胞裂解。用IL-2激活T淋巴细胞也导致介导SDCC的能力。葡萄球菌肠毒素代表了一种在人淋巴细胞中诱导抗肿瘤活性的新方法,这在治疗应用中可能具有价值。

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