Lachgar A, Bizzini B
Laboratoire de Physiologie Cellulaire, Université Pierre et Marie Curie, Paris, France.
Cell Mol Biol (Noisy-le-grand). 1995 May;41(3):431-7.
In the present investigation we have shown that PBLs taken from HIV-positive patients suppressed T-cell proliferation when cultured for at least 12 days. When infected In vitro with HIV-1, these cells become suppressive after 6 days. PBLs collected from seronegative individuals turned out to be non-suppressive even after prolonged culturing. However, when infected in vitro with HIV they were found to be cytostatic also after 6 days. This anti-immune activity, related to HIV infection, is mediated, at least in part, by alpha IFN, since about 50% of this HIV associated activity could be quenched by alpha IFN antibodies. We also showed that this T-cell cytostasis is associated with CD8+ cells. In view of a possible use of suppressive cells for T-cell vaccination, we verified that such cellular functions were abolished by aldehyde treatment.
在本研究中,我们已表明,从HIV阳性患者获取的外周血淋巴细胞(PBLs)在培养至少12天时会抑制T细胞增殖。当在体外感染HIV-1时,这些细胞在6天后会变得具有抑制性。从血清阴性个体收集的PBLs即使经过长时间培养也无抑制性。然而,当在体外感染HIV时,发现它们在6天后也具有细胞生长抑制作用。这种与HIV感染相关的抗免疫活性至少部分由α干扰素介导,因为这种与HIV相关的活性约50%可被α干扰素抗体消除。我们还表明,这种T细胞生长抑制与CD8 +细胞有关。鉴于抑制性细胞可能用于T细胞疫苗接种,我们证实醛处理可消除此类细胞功能。