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小鼠白血病病毒的低分子量产物可抑制小鼠体内巨噬细胞的聚集。

Macrophage accumulation in mice is inhibited by low molecular weight products from murine leukemia viruses.

作者信息

Cianciolo G J, Matthews T J, Bolognesi D P, Snyderman R

出版信息

J Immunol. 1980 Jun;124(6):2900-5.

PMID:6246170
Abstract

Low m.w. extracts from three known oncogenic viruses, Friend, Moloney, and Rauscher, inhibited the accumulation of macrophages at sites of delayed inflammatory reactions in mice. The potential biologic significance of these proteins is suggested by their potency: as little as 1.2 ng of viral protein inhibited (p less than 0.02) macrophage accumulation when injected at a site distant to the inflammatory reaction. A virus envelope protein fraction of 15,000 daltons (p15E) was likewise found to inhibit macrophage accumulation and may in part represent the active factor of the virus extracts. Certain oncogenic viruses may thus exert their immunosuppressive activity by release of potent inhibitors of systemic macrophage function.

摘要

从三种已知致癌病毒(Friend病毒、莫洛尼病毒和劳舍尔病毒)中提取的低分子量提取物,可抑制小鼠迟发性炎症反应部位巨噬细胞的聚集。这些蛋白质的效力表明了它们潜在的生物学意义:在远离炎症反应的部位注射时,低至1.2纳克的病毒蛋白就能抑制(p<0.02)巨噬细胞的聚集。同样发现,一种分子量为15000道尔顿的病毒包膜蛋白组分(p15E)可抑制巨噬细胞的聚集,它可能部分代表了病毒提取物中的活性因子。某些致癌病毒可能通过释放强效的全身巨噬细胞功能抑制剂来发挥其免疫抑制活性。

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