Levy E M, Beldekas J C, Mayer K H, Black P H
J Clin Immunol. 1986 Mar;6(2):152-60. doi: 10.1007/BF00918748.
A decline in T-cell lymphocyte number is the central characteristic of acquired immune deficiency syndrome (AIDS). The reason for the loss of these cells is not well understood. We investigated the hypothesis that defects in T-cell differentiation contributed to T-cell loss using an in vitro colony assay that measures T-cell precursor (CFU-T) frequency. The results indicate a substantial generalized decrease in CFU-T in people with AIDS (P less than 0.01), most of whom have Kaposi's sarcoma, and an occasionally severe decrease in CFU-T in people with ARC. Some of the cells from low colony formers suppressed colony formation by control cells. In addition, plasma from people with AIDS was less supportive of colony growth than control plasma. Decreased Ia expression on adherent mononuclear cells did not correlate with colony formation. A defect in T-cell repopulation can help explain the loss of T cells associated with AIDS.
T 细胞淋巴细胞数量的减少是获得性免疫缺陷综合征(艾滋病)的核心特征。这些细胞丢失的原因尚不清楚。我们使用一种测量 T 细胞前体(CFU-T)频率的体外集落测定法,研究了 T 细胞分化缺陷导致 T 细胞丢失的假说。结果表明,艾滋病患者的 CFU-T 普遍大幅下降(P 小于 0.01),其中大多数患有卡波西肉瘤,而艾滋病相关综合征(ARC)患者的 CFU-T 偶尔会严重下降。低集落形成者的一些细胞抑制了对照细胞的集落形成。此外,艾滋病患者的血浆比对照血浆对集落生长的支持作用更小。贴壁单核细胞上 Ia 表达的降低与集落形成无关。T 细胞再增殖缺陷有助于解释与艾滋病相关的 T 细胞丢失。