Pang T, Blanden R V
Aust J Exp Biol Med Sci. 1976 Dec;54(6):559-71. doi: 10.1038/icb.1976.57.
The role of adherent cells in an in vitro secondary response to ectromelia virus infection was investigated. Spleen cells from ectromelia-primed mice ("responder" cells) depleted of adherent cells by either carbonyl iron treatment, adherence to plastic or passage through cotton wool columns had a markedly decreased capacity to produce a secondary response, as indicated by decreased T cell-mediated cytotoxicity against virus-infected target cells, when cultured with virus-infected "stimulator" cells. The secondary response was restored by the addition of peritoneal cells from either normal or ectromelia-immune mice. Small numbers of peritoneal cells completely reconstituted the response within a certain dose range but larger numbers produced a marked inhibition of the response. Spleen cells were less effective in restoring the response. The peritoneal cells were not merely acting as additional, infected "stimulator" or antigen-presenting cells, since they could be added as late as 3 days after culture. Reconstituting activity was not affected by pretreatment with anti-theta serum and complement and cell separation studies showed that the activity was associated mainly with Ig-negative cells and that the active cell probably bears Ia antigens on its surface. These results indicate that the adherent cells involved are probably macrophages and that they act non-specifically to produce optimum conditions for the specific response of T cells.
研究了贴壁细胞在体外对埃可病毒感染的二次应答中的作用。用羰基铁处理、贴壁于塑料或通过棉纤维柱去除贴壁细胞的来自经埃可病毒致敏小鼠的脾细胞(“应答”细胞),在与病毒感染的“刺激”细胞共培养时,产生二次应答的能力显著降低,这表现为针对病毒感染靶细胞的T细胞介导的细胞毒性降低。加入来自正常或经埃可病毒免疫小鼠的腹腔细胞可恢复二次应答。少量腹腔细胞在一定剂量范围内可完全重建应答,但大量腹腔细胞会显著抑制应答。脾细胞在恢复应答方面效果较差。腹腔细胞不仅仅作为额外的、被感染的“刺激”或抗原呈递细胞起作用,因为它们可以在培养后3天添加。重建活性不受抗θ血清和补体预处理的影响,细胞分离研究表明该活性主要与Ig阴性细胞相关,并且活性细胞表面可能带有Ia抗原。这些结果表明所涉及的贴壁细胞可能是巨噬细胞,并且它们非特异性地起作用以产生T细胞特异性应答的最佳条件。