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胸腺素5组分对培养的人T淋巴细胞增殖的抑制作用。

Suppressive effect of thymosin fraction 5 on proliferation of cultured human T lymphocytes.

作者信息

Wolf R E, Maca R D

出版信息

Immunopharmacology. 1986 Dec;12(3):233-40. doi: 10.1016/0162-3109(86)90007-x.

DOI:10.1016/0162-3109(86)90007-x
PMID:3493229
Abstract

The effects of thymosin fraction 5 (F5), an extract of bovine thymus containing multiple polypeptides, on the proliferation of cultured T cells (CTC), a continuously proliferating subpopulation of peripheral blood T lymphocytes, stimulated by either phytohemagglutinin (PHA) or delectinated interleukin 2 (IL-2) were studied. Addition of F5 to cultures significantly and consistently inhibited CTC responsiveness to PHA, with the degree of inhibition being greater using a suboptimal concentration of mitogen. F5 did not significantly or consistently inhibit CTC proliferation induced by IL-2. These studies suggest that the suppressive effect of F5 may be primarily mediated by decreased IL-2 production instead of effects on IL-2 activity or efficiency in stimulating CTC proliferation. Since prostaglandins inhibit the proliferation of CTC in response to PHA or IL-2 (R.D. Maca (1983) Immunopharmacology 6:267), studies were undertaken to determine if the observed inhibition was mediated by effects of F5 on prostaglandin E2 (PGE2). The inhibitory effect of F5 on PHA responsiveness of CTC was not affected by the addition of indomethacin indicating that suppression by F5 is not mediated by stimulating the production or release of cyclooxygenase-derived prostaglandins, such as PGE2. Furthermore, PGE2 could not be detected in supernatants of F5-treated CTC stimulated by PHA. When PGE2 was added to F5-treated CTC cultures, the PHA response was inhibited indicating that the suppressive effects of F5 and PGE2 were additive and that F5 did not modulate the sensitivity of CTC to PGE2.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

胸腺素组分5(F5)是一种从牛胸腺提取的含有多种多肽的物质,本研究观察了其对经植物血凝素(PHA)或去纤连蛋白白细胞介素2(IL - 2)刺激的培养T细胞(CTC,外周血T淋巴细胞中持续增殖的亚群)增殖的影响。向培养物中添加F5可显著且持续地抑制CTC对PHA的反应性,使用亚最佳浓度的丝裂原时抑制程度更大。F5对IL - 2诱导的CTC增殖无显著或持续的抑制作用。这些研究提示,F5的抑制作用可能主要通过减少IL - 2的产生介导,而非通过影响IL - 2活性或刺激CTC增殖的效率。由于前列腺素可抑制CTC对PHA或IL - 2的增殖反应(R.D. Maca(1983年)《免疫药理学》6:267),因此开展研究以确定观察到的抑制作用是否由F5对前列腺素E2(PGE2)的影响介导。添加吲哚美辛并不影响F5对CTC对PHA反应性的抑制作用,这表明F5的抑制作用不是通过刺激环氧化酶衍生的前列腺素如PGE2的产生或释放介导的。此外,在经PHA刺激的F5处理的CTC上清液中未检测到PGE2。当向F5处理的CTC培养物中添加PGE2时,PHA反应受到抑制,这表明F5和PGE2的抑制作用具有相加性,且F5并未调节CTC对PGE2的敏感性。(摘要截短于250词)

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