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Suppression of immunoglobulin synthesis and secretion by peripheral blood lymphocytes from normal donors.

机译:正常供体外周血淋巴细胞抑制免疫球蛋白合成和分泌。

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摘要

Concanavalin A (Con A)-treated peripheral blood lymphocytes from healthy volunteer donors have been shown to suppress proliferative responses associated with thymus-derived lymphocytes (T-cells). The present investigations demonstrate that peripheral blood lymphocytes incubated with Con A for 48 hr can abrogate pokeweed mitogen-stimulated differentiation of bone-marrow-derived (B) lymphocytes to immunoglobulin-synthesizing and -secreting plasma cells. This effect was manifested when washed Con A-treated peripheral blood lymphocytes were added to pokeweed mitogen-stimulated cocultures containing fresh autologous or allogeneic mononuclear cells, and it did not appear to involve cytotoxicity. Parallel control cultures consisting of mononuclear leukocytes incubated for 48 hr in the absence of Con A also had immunoglobulin suppressor activity in mixing experiments. This effect, however, was most pronounced when preincubated cells were added to fresh autologous pokeweed mitogen-stimulated peripheral blood lymphocytes. Cell mixtures containing peripheral blood lymphocytes demonstrated a spectrum of immunoregulatory effects ranging from suppression to enhancement of pokeweed mitogen-stimulated immunoglobulin synthesis and secretion. Several functional subclasses of suppressor cells that reflect varying levels of specific activity have thus been demonstrated in human beings. Moreover, a degree of genetic identity appears to be required for the expression of "weak" immunoregulatory influences.
机译:来自健康志愿者供体的伴刀豆球蛋白A(Con A)处理的外周血淋巴细胞已显示可抑制与胸腺来源的淋巴细胞(T细胞)相关的增殖反应。本研究表明,用Con A孵育48小时的外周血淋巴细胞可以消除商陆有丝分裂原刺激的骨髓衍生(B)淋巴细胞向免疫球蛋白合成和分泌浆细胞的分化。当将经Con A处理的经洗涤的外周血淋巴细胞加入到含有新鲜自体或同种异体单核细胞的商陆有丝分裂原刺激的共培养物中时,这种效果得以体现,并且似乎没有细胞毒性。在混合实验中,由无Con A孵育48小时的单核白细胞组成的平行对照培养物也具有免疫球蛋白抑制活性。但是,当将预培养的细胞添加到新鲜的自体商陆有丝分裂原刺激的外周血淋巴细胞中时,这种作用最为明显。含有外周血淋巴细胞的细胞混合物显示出一系列的免疫调节作用,从抑制到增强商陆有丝分裂原刺激的免疫球蛋白的合成和分泌。因此已经在人类中证明了反映特定活性水平变化的抑制细胞的几种功能亚类。而且,似乎需要一定程度的遗传同一性来表达“弱”的免疫调节影响。

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