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白细胞介素-12增强抗原特异性淋巴细胞增殖与人类免疫缺陷病毒感染阶段相关。

Interleukin-12 enhancement of antigen-specific lymphocyte proliferation correlates with stage of human immunodeficiency virus infection.

作者信息

Nagy-Agren S E, Cooney E L

机构信息

Infectious Diseases Section, VAMC, Salem, VA 24153, USA. nagy-agren.

出版信息

J Infect Dis. 1999 Feb;179(2):493-6. doi: 10.1086/314596.

DOI:10.1086/314596
PMID:9878037
Abstract

The effect of interleukin (IL)-12 on T lymphocyte function was assessed in 47 human immunodeficiency virus (HIV)-infected persons of different disease stages and 16 seronegative controls. Lymphoproliferative responses (LPR) were measured to various HIV and non-HIV antigens and mitogens using peripheral blood mononuclear cells cultured with or without IL-12. Without exogenous IL-12, 96% of HIV-seropositive persons responded to mitogens, 77% to >=1 non-HIV antigen, and 11% to >=1 HIV antigen. Supplementation with IL-12 augmented LPR of HIV-seropositive persons to non-HIV antigens; however, the effect was greatest for those with higher CD4 cells (40% vs. 9% for those with >200 vs. <=200 CD4 cells/mm3). Addition of IL-12 also enhanced LPR to HIV antigens in 30% of subjects. This effect was most pronounced for those with>500 CD4 cells/mm3 (56% [P<. 05]). These findings suggest that impaired T lymphocyte recognition of foreign antigen, including HIV, can be reconstituted in part for selected HIV-seropositive persons.

摘要

在47名处于不同疾病阶段的人类免疫缺陷病毒(HIV)感染者和16名血清阴性对照者中评估了白细胞介素(IL)-12对T淋巴细胞功能的影响。使用外周血单个核细胞,在有或无IL-12的情况下培养,测量对各种HIV和非HIV抗原及有丝分裂原的淋巴细胞增殖反应(LPR)。在没有外源性IL-12的情况下,96%的HIV血清阳性者对有丝分裂原产生反应,77%对≥1种非HIV抗原产生反应,11%对≥1种HIV抗原产生反应。补充IL-12可增强HIV血清阳性者对非HIV抗原的LPR;然而,对于CD4细胞较高的人这种作用最大(CD4细胞>200/mm3的人为40%,而≤200/mm3的人为9%)。添加IL-12还使30%的受试者对HIV抗原的LPR增强。这种作用在CD4细胞>500/mm3的人中最为明显(56%[P<0.05])。这些发现表明,包括HIV在内的外来抗原的T淋巴细胞识别受损,对于部分选定的HIV血清阳性者可部分重建。

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