Huang D, Schwacha M G, Eisenstein T K
Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Infect Immun. 1996 Sep;64(9):3786-92. doi: 10.1128/iai.64.9.3786-3792.1996.
Previous reports from our laboratory have shown that 7 days after infection of C3HeB/FeJ mice with an attenuated strain of Salmonella typhimurium, there is profound suppression of responses to B- and T-cell mitogens and suppression of the capacity of spleen cells to mount a primary, in vitro plaque-forming-cell (PFC) response to sheep erythrocytes. Inhibition of the PFC response was shown to be mediated by nitric oxide (NO), as NG-monomethyl-L-arginine (NMMA) gave complete reversal of suppression. The experiments reported here examined the role of NO in suppression of the response to the mitogen concanavalin A (ConA). In contrast to the PFC system, it was found that addition of NMMA to ConA-stimulated immune spleen cells resulted in less than 20% reversal of suppression. However, addition to NMMA resulted in a 50% reversal of suppression in cocultures of immune and normal spleen cells at a ratio of 1:4. A complete restoration of ConA-induced responses was achieved in cocultures incubated in medium containing a reduced concentration of L-arginine plus 1.25 mM NMMA. Investigation of why NMMA alone was not 100% effective in reversing suppression showed that addition of ConA significantly augmented production of nitrite and gamma interferon (IFN-gamma) in cocultures containing immune cells. Addition of anti-IFN-gamma reduced nitrite levels in the cultures, although results with the combination of anti-IFN-gamma and NMMA were not significantly better than results with NMMA alone. These findings suggest that suppression in cultures stimulated with ConA is difficult to reverse completely with NMMA alone because of an overproduction of NO, which can be offset by either reducing the L-arginine concentration or blocking IFN-gamma. The quantitative relationship between nitrite levels and suppression in cocultures was examined. It was found that suppression did not correlate directly with the nitrite concentration but rather with the log10 of the nitrite concentration. Nitrite levels above 15 microM gave almost complete suppression, and levels between 1 and 10 microM gave a wide range of suppression. These results strongly support NO as the suppressor factor in Salmonella-induced immunosuppression of responses to ConA and, by inference, suppression of responses to mitogens induced by other microbes. The results show that involvement of NO cannot always be demonstrated by simple addition of NMMA to suppressed mitogen-stimulated spleen cell cultures.
我们实验室之前的报告显示,用减毒鼠伤寒沙门氏菌感染C3HeB/FeJ小鼠7天后,对B细胞和T细胞有丝分裂原的反应受到显著抑制,并且脾细胞对绵羊红细胞产生初级体外空斑形成细胞(PFC)反应的能力也受到抑制。PFC反应的抑制被证明是由一氧化氮(NO)介导的,因为NG-单甲基-L-精氨酸(NMMA)能完全逆转抑制作用。本文报道的实验研究了NO在抑制对有丝分裂原刀豆球蛋白A(ConA)反应中的作用。与PFC系统不同,发现向ConA刺激的免疫脾细胞中添加NMMA导致抑制作用的逆转不足20%。然而,在免疫脾细胞与正常脾细胞按1:4比例共培养时,添加NMMA导致抑制作用逆转了50%。在含有降低浓度L-精氨酸加1.25 mM NMMA的培养基中培养的共培养物中,ConA诱导的反应完全恢复。对单独使用NMMA不能100%有效逆转抑制作用的原因进行研究发现,添加ConA显著增加了含有免疫细胞的共培养物中亚硝酸盐和γ干扰素(IFN-γ)的产生。添加抗IFN-γ降低了培养物中的亚硝酸盐水平,尽管抗IFN-γ和NMMA联合使用的结果并不比单独使用NMMA的结果显著更好。这些发现表明,在用ConA刺激的培养物中,单独使用NMMA很难完全逆转抑制作用,因为NO产生过多,这可以通过降低L-精氨酸浓度或阻断IFN-γ来抵消。研究了共培养物中亚硝酸盐水平与抑制作用之间的定量关系。发现抑制作用与亚硝酸盐浓度没有直接相关性,而是与亚硝酸盐浓度的log10相关。亚硝酸盐水平高于15 microM时几乎产生完全抑制,而水平在1至10 microM之间时产生广泛的抑制作用。这些结果有力地支持了NO作为沙门氏菌诱导的对ConA反应免疫抑制中的抑制因子,并由此推断,也是其他微生物诱导的对有丝分裂原反应抑制中的抑制因子。结果表明,不能总是通过简单地向受抑制的有丝分裂原刺激的脾细胞培养物中添加NMMA来证明NO的参与。