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瘤型麻风患者单核细胞衍生的可溶性抑制因子

Monocyte-derived soluble suppressor factor(s) in patients with lepromatous leprosy.

作者信息

Sathish M, Bhutani L K, Sharma A K, Nath I

出版信息

Infect Immun. 1983 Dec;42(3):890-9. doi: 10.1128/iai.42.3.890-899.1983.

Abstract

Peripheral blood monocytes from polar lepromatous leprosy (LL) patients were unable to support Mycobacterium leprae-induced in vitro lymphoproliferation of HLA-D-matched T cells from tuberculoid leprosy subjects, whereas those from responder individuals were able to do so. Monocyte-rich adherent cells from untreated LL patients released de novo soluble factors which inhibited antigen-induced lymphoproliferation to a greater extent and mitogenic responses to a lesser extent. Suppressive activity varied in different LL patients. However, the degree of suppression was similar in soluble factors obtained de novo and after treatment of adherent cells with heat-killed and freshly extracted, cryopreserved M. leprae. Treated patients showed less inhibition with de novo released soluble factors (27 +/- 7.7%) as compared to parallel soluble factors obtained after antigen treatment (44 +/- 4.8%) or with de novo soluble factors from untreated LL patients (62 +/- 14.2%). Similar supernatants from tuberculoid individuals showed no or insignificant effects on antigen-induced lymphoproliferation. The suppressive activity of LL soluble factors was produced for up to 72 h, was heat stable at 56 degrees C for 30 min, was indomethacin resistant, and resided in the greater than 25,000 molecular weight fraction.

摘要

来自极地瘤型麻风(LL)患者的外周血单核细胞无法支持麻风杆菌诱导的来自结核样型麻风患者的 HLA - D 匹配 T 细胞的体外淋巴细胞增殖,而来自有反应个体的外周血单核细胞则能够支持。未经治疗的 LL 患者富含单核细胞的贴壁细胞会从头释放可溶性因子,这些因子在更大程度上抑制抗原诱导的淋巴细胞增殖,在较小程度上抑制有丝分裂反应。不同 LL 患者的抑制活性有所不同。然而,从头获得的可溶性因子以及用热杀死的和新鲜提取、冷冻保存的麻风杆菌处理贴壁细胞后获得的可溶性因子的抑制程度相似。与抗原处理后获得的平行可溶性因子(44±4.8%)或未经治疗的 LL 患者的从头可溶性因子(62±14.2%)相比,接受治疗的患者从头释放的可溶性因子的抑制作用较小(27±7.7%)。来自结核样型个体的类似上清液对抗原诱导的淋巴细胞增殖没有或只有微不足道的影响。LL 可溶性因子的抑制活性可持续产生长达 72 小时,在 56℃下 30 分钟热稳定,对消炎痛有抗性,且存在于分子量大于 25,000 的组分中。

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