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乙胺嘧啶和磺胺多辛对人淋巴细胞增殖的影响。

Effect of pyrimethamine and sulphadoxine on human lymphocyte proliferation.

作者信息

Bygbjerg I C, Odum N, Theander T G

出版信息

Trans R Soc Trop Med Hyg. 1986;80(2):295-300. doi: 10.1016/0035-9203(86)90040-4.

Abstract

The in vitro effect of pyrimethamine (PYR) on human blood mononuclear cells stimulated with phytohaemagglutinin (PHA), pokeweed mitogen (PWM) and purified protein derivative of tuberculin (PPD) was studied by 14C-thymidine incorporation, by cell counting and by total DNA estimation. PYR in concentrations 10 times higher than serum values obtained in clinical practice inhibited lymphocyte proliferation irreversibly. PYR in concentrations corresponding to clinical practice quickly and irreversibly suppressed the proliferation of PWM-stimulated cells, and more slowly the proliferation of PPD-stimulated cells. The suppression of PHA-stimulated cells was reversed after one week. The increased 14C-thymidine incorporation observed in stimulated cells exposed to PYR in vitro in the early phase of proliferation did not reflect immunopotentiation but rather blocked endogenous thymidine synthesis. Sulphadoxine (SDX), added in vitro, had no effect on the lymphocytes, while SDX plus PYR had the same effect as PYR alone. Oral intake of SDX plus PYR (Fansidar) also blocked the thymidine synthesis of mitogen-stimulated lymphocytes. The possible consequences of the findings for the use of PYR in malaria prophylaxis and therapy are discussed.

摘要

通过¹⁴C-胸腺嘧啶核苷掺入法、细胞计数法和总DNA测定法,研究了乙胺嘧啶(PYR)对用植物血凝素(PHA)、商陆有丝分裂原(PWM)和结核菌素纯蛋白衍生物(PPD)刺激的人血单核细胞的体外作用。浓度比临床实践中获得的血清值高10倍的PYR不可逆地抑制淋巴细胞增殖。对应于临床实践浓度的PYR迅速且不可逆地抑制PWM刺激细胞的增殖,对PPD刺激细胞增殖的抑制作用则较慢。PHA刺激细胞的抑制作用在一周后逆转。在增殖早期体外暴露于PYR的刺激细胞中观察到的¹⁴C-胸腺嘧啶核苷掺入增加并不反映免疫增强,而是阻断了内源性胸腺嘧啶核苷的合成。体外添加磺胺多辛(SDX)对淋巴细胞无影响,而SDX加PYR的作用与单独使用PYR相同。口服SDX加PYR(Fansidar)也阻断了有丝分裂原刺激淋巴细胞的胸腺嘧啶核苷合成。讨论了这些发现对PYR在疟疾预防和治疗中应用的可能影响。

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