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一种四价胍腙(CNI-1493)对单核细胞中细胞因子产生的靶向抑制作用,而对T淋巴细胞无此作用。

Targeted suppression of cytokine production in monocytes but not in T lymphocytes by a tetravalent guanylhydrazone (CNI-1493).

作者信息

Björk L, Tracey K J, Ulrich P, Bianchi M, Cohen P S, Akerlund K, Fehniger T E, Andersson U, Andersson J

机构信息

Department of Immunology, WennerGren Institute, Stockholm University, Sweden.

出版信息

J Infect Dis. 1997 Nov;176(5):1303-12. doi: 10.1086/514126.

Abstract

Image analysis was used to study the cytokine-inhibitory effect of the nitric oxide inhibitor tetravalent guanylhydrazone (CNI-1493) in individual immunocytochemically stained human peripheral blood mononuclear cells (PBMC). CNI-1493 inhibited lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-alpha, interleukin (IL)-1alpha, IL-1beta, IL-6, and IL-8 production whether or not LPS stimulation was enhanced by interferon (IFN)-gamma priming. Addition of TNF-alpha to CNI-1493-exposed LPS-stimulated cells partially restored the incidence of IL-1alpha-, IL-1beta-, and IL-8-producing cells. TNF-alpha production induced by costimulation by ligation of CD3 and CD28 was inhibited by CNI-1493 in monocytes but not in T lymphocytes. The prevalence of IL-2-, IFN-gamma-, and TNF-beta-producing T cells was not reduced by CNI-1493. Phorbol ester and ionomycin activation also resulted in a CNI-1493 -induced inhibition of TNF-alpha in monocytes but resistant production of TNF-alpha, IL-2, and IFN-gamma by T cells. Thus, CNI-1493 preferentially inhibited synthesis of proinflammatory cytokines in monocytes.

摘要

采用图像分析技术,研究一氧化氮抑制剂四价胍腙(CNI-1493)对单个免疫细胞化学染色的人外周血单核细胞(PBMC)的细胞因子抑制作用。无论干扰素(IFN)-γ预处理是否增强脂多糖(LPS)刺激,CNI-1493均能抑制LPS诱导的肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1α、IL-1β、IL-6和IL-8的产生。将TNF-α添加到经CNI-1493处理的LPS刺激细胞中,可部分恢复产生IL-1α、IL-1β和IL-8的细胞发生率。在单核细胞中,CNI-1493可抑制由CD3和CD28连接共刺激诱导的TNF-α产生,但对T淋巴细胞无此作用。CNI-1493不会降低产生IL-2、IFN-γ和TNF-β的T细胞的比例。佛波酯和离子霉素激活也会导致CNI-1493诱导单核细胞中TNF-α的产生受到抑制,但T细胞对TNF-α、IL-2和IFN-γ的产生具有抗性。因此,CNI-1493优先抑制单核细胞中促炎细胞因子的合成。

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