Hyjek E M, Bartkowiak J, Drozdz R, Wasik T J, Jasinski M, Kaneko Y, Lischner H W, Kozbor D
Department of Microbiology and Immunology, Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA 19107, USA.
J Immunol. 1997 Jan 1;158(1):464-74.
Progression of HIV-induced immunodeficiency is associated with both B cell activation and an increased proportion of Vdelta1+ T cells in PBL. To examine whether the peripheral expansion of Vdelta1+ cells is driven by activated B cells, we isolated CD19+ PBL from HIV+ individuals at different stages of infection and used them to stimulate Vdelta1+ T cell clones. The Vdelta1+ T cell clones were isolated from HIV+ individuals and selected on the basis of cytotoxic activity and IFN-gamma expression in response to lymphoblastoid cell lines (LCLs) established from patients with AIDS (AIDS-related LCLs) but not LCLs of HIV- donors. Peripheral blood B cells from HIV+ patients induced IFN-gamma expression in these Vdelta1+ clones, and their stimulatory ability was associated with up-regulated expression of the CD38 activation Ag and with a 6- to 10-fold increased spontaneous Ig production. Stimulation of CD19+ PBL from HIV+ individuals with cross-linked anti-CD40 mAb or rgpl20 further augmented induction of IFN-gamma expression in the Vdelta1+ cells. The isolated Vdelta1+ T cell clones expressed the Jdelta1 gene segment, but differed in Vgamma gene segment usage and in the junctional region of TCR-delta chains, indicating Vdelta gene-determined recognition. These results provide evidence that the peripheral expansion of Vdelta1+ cells in HIV infection is associated with phenotypic and functional alterations of B cells, due to chronic activation during progression to AIDS.
HIV 诱导的免疫缺陷进展与 B 细胞活化以及外周血淋巴细胞(PBL)中 Vδ1 + T 细胞比例增加有关。为了研究 Vδ1 + 细胞的外周扩增是否由活化的 B 细胞驱动,我们从处于不同感染阶段的 HIV 阳性个体中分离出 CD19 + PBL,并使用它们刺激 Vδ1 + T 细胞克隆。Vδ1 + T 细胞克隆从 HIV 阳性个体中分离出来,并根据对从艾滋病患者建立的淋巴母细胞系(AIDS 相关 LCL)而非 HIV 阴性供体的 LCL 的细胞毒性活性和 IFN-γ 表达进行选择。HIV 阳性患者的外周血 B 细胞在这些 Vδ1 + 克隆中诱导 IFN-γ 表达,其刺激能力与 CD38 活化抗原的上调表达以及自发 Ig 产生增加 6 至 10 倍有关。用交联的抗 CD40 mAb 或 rgpl20 刺激 HIV 阳性个体的 CD19 + PBL 进一步增强了 Vδ1 + 细胞中 IFN-γ 表达的诱导。分离的 Vδ1 + T 细胞克隆表达 Jδ1 基因片段,但在 Vγ 基因片段使用和 TCR-δ 链的连接区有所不同,表明 Vδ 基因决定识别。这些结果提供了证据,表明在 HIV 感染中 Vδ1 + 细胞的外周扩增与 B 细胞的表型和功能改变有关,这是由于在进展为艾滋病期间的慢性活化所致。