Thomson A W, Moon D K, Geczy C L, Nelson D S
Immunology. 1983 Feb;48(2):291-9.
Cyclosporin A (Cs A) exerted a dose-related inhibitory effect on antigen (ovalbumin, OVA) and phytohaemagglutinin (PHA)-induced transformation of guinea-pig lymph node cells (LNC). Whereas 0.05 micrograms/ml was sufficient to depress these responses markedly, it required 100-fold this concentration of Cs A to inhibit the production of lymphocyte activating factor (LAF) by lipopolysaccharide (LPS) stimulated peritoneal macrophages. Addition of Cs A together with insoluble concanavalin A (iCon A) to LNC cultures resulted in suppressed lymphokine production, as assessed by measurement of migration inhibition factor (MIF), the generation of macrophage procoagulant activity (MPCA) and the release of lymphocyte-derived-macrophage chemotactic factor (LDCF). Cs A also inhibited MIF and procoagulant production by sensitized peritoneal exudate cells in response to antigen, at the same concentrations which blocked lymphocyte transformation. In contrast, Cs A had no direct effect on the migration of peritoneal cells from capillary tubes, or on the responses of macrophages to preformed MIF, the lymphokine inducing MPCA or LDCF. Overnight incubation of macrophages with Cs A did, however, result in mild inhibition of their basal level of procoagulant activity.
环孢菌素A(CsA)对抗原(卵清蛋白,OVA)和植物血凝素(PHA)诱导的豚鼠淋巴结细胞(LNC)转化具有剂量相关的抑制作用。虽然0.05微克/毫升就足以显著抑制这些反应,但抑制脂多糖(LPS)刺激的腹腔巨噬细胞产生淋巴细胞激活因子(LAF)则需要CsA浓度的100倍。将CsA与不溶性伴刀豆球蛋白A(iConA)一起添加到LNC培养物中会导致淋巴因子产生受到抑制,这通过测量迁移抑制因子(MIF)、巨噬细胞促凝活性(MPCA)的产生以及淋巴细胞衍生的巨噬细胞趋化因子(LDCF)的释放来评估。CsA在阻断淋巴细胞转化的相同浓度下,也抑制致敏腹腔渗出细胞对抗原产生的MIF和促凝剂。相反,CsA对腹腔细胞从毛细管中的迁移没有直接影响,对巨噬细胞对预先形成的MIF、诱导MPCA或LDCF的淋巴因子的反应也没有直接影响。然而,巨噬细胞与CsA过夜孵育确实会导致其促凝活性的基础水平受到轻度抑制。