Inhibition of HIV infectivity by lactoperoxidase-produced hypothiocyanite.

Journal de biologie buccale Pub Date : 1990-12-01
M Pourtois, C Binet, N Van Tieghem, P Courtois, A Vandenabbeele, L Thiry
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引用次数: 0

Abstract

HIV aliquots, from a supernatant of ARV-4 cell line, were mixed with an equal volume of a OSCN.generating glucose-glucose oxidase + thiocyanate-lacteroperoxidase solution, and then pre-incubated at 37 degrees C for periods of 30 secs to one hour. These mixtures were then inoculated into cultures of phytohaemagglutinin-stimulated lymphocytes. Viral growth was monitored with an ELISA quantitating the specific p24 protein either in the culture cells or in the supernatant. In control experiments, the virus produced both intra- and extra-cellular p24. In the controls, concentration of p24 per 10(6) lymphocytes grew rapidly. By contrast, HIV that was pretreated with the OSCN generating system for 30 sec., produced very little p24, and no detectable amount of this protein could be found after 2 min. pre-treatment.

乳酸过氧化物酶产生的下硫氰酸酯对HIV感染的抑制作用。
从ARV-4细胞系的上清液中提取HIV等量液,与等体积的OSCN混合。生成葡萄糖-葡萄糖氧化酶+硫氰酸盐-乳酸过氧化物酶溶液,然后在37℃下预孵育30秒至1小时。然后将这些混合物接种到植物血凝素刺激淋巴细胞中。用ELISA定量测定培养细胞或上清液中特定的p24蛋白来监测病毒生长。在对照实验中,病毒同时产生细胞内和细胞外的p24。在对照组中,p24 / 10(6)淋巴细胞的浓度迅速上升。相比之下,用OSCN生成系统预处理30秒的HIV产生很少的p24,预处理2分钟后无法检测到该蛋白的含量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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