Blackman M J, Morris A G
J Gen Virol. 1984 May;65 ( Pt 5):955-61. doi: 10.1099/0022-1317-65-5-955.
Interferon (IFN) production by spleen cells from normal mice, mice acutely infected with Semliki Forest virus (SFV) or mice immune to SFV was measured after stimulation in vitro with either infectious or inactivated SFV. All three classes of spleen cells made IFN-alpha beta in response to infectious SFV. Spleen cells taken from mice late, but not early, after infection, or from immune mice, made IFN-gamma in response to inactivated SFV. Amounts of INF-gamma and IFN-alpha beta were similar. Normal spleen cells made no IFN (of any type) in response to inactivated SFV. The cell type producing IFN-alpha beta appeared to be the macrophage, whilst both T-lymphocytes and macrophages were necessary for IFN-gamma production. During the acute infection, the ability of spleen cells to lyse both virus-infected and uninfected target cells arose earlier than the ability to produce IFN-gamma. However, cytotoxicity towards uninfected cells fell to near background levels by day 7, whilst cytotoxicity towards infected targets remained high at that time, when IFN-gamma production was at its peak. IFN-gamma production is therefore temporally associated with cytotoxicity specifically directed against virus-infected targets, and the ability to produce IFN-gamma is a late response to SFV infection.
用感染性或灭活的塞姆利基森林病毒(SFV)体外刺激后,检测正常小鼠、急性感染SFV的小鼠或对SFV免疫的小鼠脾脏细胞产生干扰素(IFN)的情况。所有三类脾脏细胞在对感染性SFV作出反应时都会产生αβ干扰素。感染后晚期(而非早期)的小鼠或免疫小鼠的脾脏细胞在对灭活的SFV作出反应时会产生γ干扰素。γ干扰素和αβ干扰素的量相似。正常脾脏细胞对灭活的SFV不产生(任何类型的)干扰素。产生αβ干扰素的细胞类型似乎是巨噬细胞,而γ干扰素的产生则需要T淋巴细胞和巨噬细胞。在急性感染期间,脾脏细胞裂解病毒感染和未感染靶细胞的能力比产生γ干扰素的能力出现得更早。然而,到第7天时,对未感染细胞的细胞毒性降至接近背景水平,而此时对感染靶细胞的细胞毒性仍然很高,γ干扰素的产生也处于峰值。因此,γ干扰素的产生在时间上与针对病毒感染靶细胞的细胞毒性相关,并且产生γ干扰素的能力是对SFV感染的晚期反应。