Moriya N, Sanjoh K, Yokoyama S, Hayashi T
Department of Pediatrics, Yamagata University School of Medicine, Japan.
J Immunol. 1987 Nov 15;139(10):3281-6.
Signals required for expression of HLA-DR (DR) antigen in phytohemagglutinin (PHA)-activated human peripheral blood T cells were examined. T cells were purified by a four-step procedure, which included depletion of glass-adherent cells, 53% Percoll gradient centrifugation, nylon wool column passage, and treatment with mouse monoclonal antibodies directed to human HLA-DR antigen and Leu M1 antigen plus complement. Purified T cells responded poorly to PHA but with the combination stimuli of PHA and recombinant human interleukin 2 (rIL-2), resting T cells proliferated as well as T cells cultured with 10% monocytes and PHA. But well proliferated T cells in the absence of monocytes expressed very poor DR antigen after 7 to 8 days of culture. DR expression of T cells was restored by the addition of 10% monocytes. Allogeneic monocytes also helped proliferative responses of PHA-activated T cells but did not help the expression of DR antigen. These results suggested that signals required for T cell proliferation (PHA and rIL-2) were not sufficient for DR expression in this system and further monocytes were essentially required in a HLA-restricted manner. In the next experiment, we examined the role of membrane molecules in monocytes for transmission of signals that induce activated T cells to express DR antigen. Autologous monocytes were fixed with 1% paraformaldehyde and added to T cells in the presence of PHA and rIL-2. Fixed monocytes could help DR antigen expression of PHA-activated T cells as well as viable monocytes. But when fixed monocytes were pretreated with anti-HLA-DR monoclonal antibody, they could not help DR expression of T cells any longer. These results suggested that for the expression of DR antigen, PHA-activated T cells had to first recognize self DR antigen expressed on the surface of monocytes before proliferation occurred.
研究了在植物血凝素(PHA)激活的人外周血T细胞中表达HLA - DR(DR)抗原所需的信号。通过四步程序纯化T细胞,该程序包括去除玻璃黏附细胞、53% Percoll梯度离心、尼龙毛柱过柱以及用针对人HLA - DR抗原和Leu M1抗原的小鼠单克隆抗体加补体处理。纯化的T细胞对PHA反应不佳,但在PHA和重组人白细胞介素2(rIL - 2)的联合刺激下,静息T细胞的增殖情况与用10%单核细胞和PHA培养的T细胞相同。但在无单核细胞的情况下,增殖良好的T细胞在培养7至8天后表达的DR抗原非常少。添加10%单核细胞可恢复T细胞的DR表达。同种异体单核细胞也有助于PHA激活的T细胞的增殖反应,但无助于DR抗原的表达。这些结果表明,在该系统中T细胞增殖所需的信号(PHA和rIL - 2)不足以使DR表达,并且进一步表明单核细胞以HLA限制的方式是必不可少的。在接下来的实验中,我们研究了单核细胞膜分子在诱导活化T细胞表达DR抗原的信号传递中的作用。用1%多聚甲醛固定自体单核细胞,并在PHA和rIL - 2存在的情况下将其添加到T细胞中。固定的单核细胞与活单核细胞一样有助于PHA激活的T细胞表达DR抗原。但是,当用抗HLA - DR单克隆抗体预处理固定的单核细胞时,它们不再有助于T细胞的DR表达。这些结果表明,对于DR抗原的表达,PHA激活的T细胞在增殖发生之前必须首先识别单核细胞表面表达的自身DR抗原。