Molina J M
Service des Maladies Infectieuses et Tropicales, Hôpital Saint-Louis, Paris.
Pathol Biol (Paris). 1993 Oct;41(8 Pt 2):777-80.
The cytokine network, which is involved in the regulation of normal immune responses, may play a role in the pathogenesis of human immunodeficiency virus (HIV) infection, by altering the replication of HIV in target cells. In vitro data, suggest that certain cytokines like "tumor necrosis factor" alpha (TNF alpha) "granulocyte-macrophage colony-stimulating factor" (GM-CSF) and interleukin-6 (IL-6) could up-regulate HIV expression in T-cells and macrophages. Other cytokines like alpha interferon, are potent inhibitors of HIV replication. Surprisingly, the macrophage and the T-lymphocyte, the main source of cytokines in the body, do not produce any of these cytokines following HIV infection. B-lymphocytes however, spontaneously release TNF alpha and IL-6, that might enhance HIV replication in nearby monocytes and T-lymphocytes. This situation may occur in lymph nodes, a major reservoir of HIV.
参与正常免疫反应调节的细胞因子网络,可能通过改变人类免疫缺陷病毒(HIV)在靶细胞中的复制,在HIV感染的发病机制中发挥作用。体外数据表明,某些细胞因子,如肿瘤坏死因子α(TNFα)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-6(IL-6),可上调T细胞和巨噬细胞中的HIV表达。其他细胞因子,如α干扰素,是HIV复制的有效抑制剂。令人惊讶的是,体内细胞因子的主要来源——巨噬细胞和T淋巴细胞,在HIV感染后不会产生这些细胞因子中的任何一种。然而,B淋巴细胞会自发释放TNFα和IL-6,这可能会增强附近单核细胞和T淋巴细胞中的HIV复制。这种情况可能发生在HIV的主要储存库——淋巴结中。