Tenner-Racz K, Racz P, Thomé C, Meyer C G, Anderson P J, Schlossman S F, Letvin N L
Department of Hematology, Allgemeines Krankenhaus St. Georg. Hamburg, Germany.
Am J Pathol. 1993 Jun;142(6):1750-8.
A novel monoclonal antibody (mAB) TIA-1, which recognizes a 15-kd granule-associated protein of cytotoxic T lymphocytes and natural killer cells, has been applied to sections of lymph nodes with human immunodeficiency virus (HIV)-induced lymphadenopathy (follicular hyperplasia and lymphocyte depletion). The protein recognized by this mAB induces apoptosis in permeabilized lymphocytes in vitro. While this mAB reacted with approximately 46% of paracortical CD8+ cells in control nodes, it reacted with 75% of such cells in HIV-induced follicular hyperplasia. Germinal centers of the control nodes contained few TIA-1 + cells; in follicular hyperplasia caused by HIV-1, almost all germinal center CD8+ cells were TIA-1 +. Both in the control nodes and in HIV-induced follicular hyperplasia the majority of TIA-1 + cells coexpressed CD45R0. A marked loss of CD8+TIA-1+ cells was seen in lymphocyte-depleted nodes of patients with AIDS. The loss of these cytotoxic T lymphocytes may have a significant impact on the progression of the disease.
一种新型单克隆抗体(mAB)TIA-1,可识别细胞毒性T淋巴细胞和自然杀伤细胞中一种15kd的颗粒相关蛋白,已应用于患有人类免疫缺陷病毒(HIV)引起的淋巴结病(滤泡增生和淋巴细胞耗竭)的淋巴结切片。该单克隆抗体识别的蛋白在体外可诱导通透化淋巴细胞发生凋亡。在对照淋巴结中,此单克隆抗体与约46%的副皮质CD8+细胞发生反应,而在HIV引起的滤泡增生中,它与75%的此类细胞发生反应。对照淋巴结的生发中心含很少的TIA-1+细胞;在由HIV-1引起的滤泡增生中,几乎所有生发中心CD8+细胞都是TIA-1+。在对照淋巴结和HIV引起的滤泡增生中,大多数TIA-1+细胞都共表达CD45R0。在艾滋病患者的淋巴细胞耗竭淋巴结中可见CD8+TIA-1+细胞显著减少。这些细胞毒性T淋巴细胞的减少可能对疾病进展有重大影响。