环孢素A (CyA)和甲基强的松龙(MP)对免疫反应的影响。2单核细胞- T细胞相互作用导致淋巴因子产生的进一步研究。

K Bendtzen, J Petersen, B Søeberg
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摘要

免疫抑制药物环孢素A (CyA)和甲基强的松龙(MP)可抑制回忆抗原激发的单核细胞对淋巴细胞迁移抑制因子(LIF)的分泌。这两种情况下的抑制在去除药物后是可逆的,并且不能证明T抑制细胞参与其介质。cya诱导的效应在淋巴细胞激活的早期(小于60分钟)发挥作用,而MP在抗原后60分钟后仍然抑制LIF的释放。与早期的研究结果相反,这些药物不能影响巨噬细胞(M-phi’s)在肉豆蔻酸佛醇刺激下释放的T细胞活化因子(TAF)和淋巴细胞活化因子(LAF)。MP(而非CyA)显著降低结核菌素培养的M-phi产生TAF。此外,部分纯化的TAF和LAF在CyA(而不是MP)存在的情况下都能恢复LIF的产生,这种效果不会被T细胞产物T细胞生长因子所模仿。然而,这两种药物的抑制作用被外源性cGMP所消除。因此,CyA似乎阻碍了TAF/LAF与免疫T细胞之间的相互作用,而MP在Mo水平上影响抗原诱导的T细胞活化以及淋巴因子的产生和/或释放水平。两种药物的作用似乎与涉及cGMP的细胞内事件有关。
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Effects of cyclosporin A (CyA) and methylprednisolone (MP) on the immune response. II. Further studies of the monocyte - T cell interactions leading to lymphokine production.

The immunosuppressive drugs cyclosporin A (CyA) and methylprednisolone (MP) abolished the elaboration of the lymphokine leukocyte migration inhibitory factor (LIF) by mononuclear cells challenged by recall antigen. Suppression in both cases was reversible upon removal of the drugs, and participation of T suppressor cells of their mediators could not be demonstrated. The CyA-induced effect was exerted in the early stage of lymphocyte activation (less than 60 min), whereas MP still inhibited LIF release when added 60 min after the antigen. In contrast to earlier findings that the drugs failed to affect the release of T cell-activating factor (TAF) and lymphocyte-activating factor (LAF) from macrophages (M-phi's) stimulated by phorbol myristate acetate. MP (but not CyA) markedly reduced TAF production by M-phi's incubated with tuberculin. M-phireover, partially purified TAF and LAF both restored LIF production in the presence of CyA (but not MP), an effect not mimicked by the T cell product T cell growth factor. However, suppression by both drugs was abrogated by exogenous cGMP. Hence, CyA seems to obstruct the interaction between TAF/LAF and the immune T cell, whereas MP affects antigen-induced T cell activation at the Mo level as well as the level of lymphokine production and/or release. The effects of both drugs seem related to intracellular events involving cGMP.

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