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In vitro suppression of interleukin 2 production by Mycobacterium leprae antigen.

机译:麻风分枝杆菌抗原在体外抑制白介素2的产生。

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摘要

The suppressive activity of three different lots and sources of Mycobacterium leprae (M. leprae) was studied by measuring the inhibitory effect on interleukin 2 (IL-2) production in normal subjects. All three M. leprae preparations had suppressive activity on IL-2 production when peripheral blood mononuclear leucocytes (PBML) were stimulated with the mitogens PHA-P or Con A in a dose response. M. leprae also had suppressive activity on IL-2 production when PBML were stimulated with the specific antigen, PPD. The inhibitory activity of M. leprae on IL-2 was not due to the direct interaction of M. leprae and IL-2 because direct mixing of IL-2 with different concentrations of M. leprae did not alter the activity of IL-2. Incorporation of M. leprae for 0, 6 and 12 h in PHA-P and PBML cultures had no inhibitory effect on IL-2 production; however, after 14, 16 and 18 h of M. leprae incorporation, significant inhibitory effects were noted on IL-2 production. The suppressive mechanism of M. leprae was studied by incorporating M. leprae into PBML or adherent cells. The suppressive activity could be detected in both M. leprae-stimulated PBML and M. leprae-stimulated monocyte supernatant fluids. The suppressive mechanism of M. leprae was further evaluated by incorporating 1 and 2 micrograms/ml of indomethacin in PBML containing PHA-P and M. leprae. The suppressive activity of M. leprae was significantly diminished by indomethacin, suggesting that the inhibitory effect of M. leprae may result from the induction of PBML and adherent cells to produce the immunosuppressive activity of prostaglandin(s).
机译:通过测量对正常受试者白介素2(IL-2)产生的抑制作用,研究了三种不同批次和来源的麻风分枝杆菌(M. leprae)的抑制活性。当用促细胞分裂剂PHA-P或Con A刺激剂量反应时,外周血单核白细胞(PBML)时,所有三种麻风分枝杆菌制剂均具有抑制IL-2产生的活性。当用特异性抗原PPD刺激PBML时,麻风分枝杆菌还具有抑制IL-2产生的活性。麻风分枝杆菌对IL-2的抑制活性不是由于麻风分枝杆菌与IL-2的直接相互作用,因为将IL-2与不同浓度的麻风分枝杆菌直接混合不会改变IL-2的活性。在PHA-P和PBML培养物中掺入麻风分枝杆菌0、6和12小时对IL-2的产生没有抑制作用。然而,在麻风分枝杆菌掺入14、16和18小时后,注意到对IL-2产生显着的抑制作用。通过将麻风分枝杆菌掺入PBML或贴壁细胞中来研究麻风分枝杆菌的抑制机制。在麻风分枝杆菌刺激的PBML和麻风分枝杆菌刺激的单核细胞上清液中均可检测到抑制活性。通过在含有PHA-P和麻风分枝杆菌的PBML中掺入1和2微克/ ml消炎痛,进一步评估麻风分枝杆菌的抑制机制。吲哚美辛显着减弱了麻风杆菌的抑制活性,表明麻风杆菌的抑制作用可能是由于诱导PBML和粘附细胞产生前列腺素的免疫抑制活性而引起的。

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