首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Expression of passively transferred immunity against an established tumor depends on generation of cytolytic T cells in recipient. Inhibition by suppressor T cells
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Expression of passively transferred immunity against an established tumor depends on generation of cytolytic T cells in recipient. Inhibition by suppressor T cells

机译:针对已建立的肿瘤的被动转移免疫的表达取决于受体中溶细胞性T细胞的产生。抑制性T细胞的抑制

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摘要

The results of this study with the P815 mastocytoma confirm the results of previous studies that showed that the passive transfer of tumor- sensitized T cells from immunized donors can cause the regression of tumors growing in T cell-deficient (TXB) recipients, but not in normal recipients. The key additional finding was that the expression of adoptive immunity against tumors growing in TXB recipients is immediately preceded by a substantial production of cytolytic T cells in the recipients' draining lymph node. On the other hand, failure of adoptive immunity to be expressed against tumors growing in normal recipients was associated with a cytolytic T cell response of much lower magnitude, and a similar low magnitude response was generated in TXB recipients infused with normal spleen cells and in tumor-bearing control mice. Because the passively transferred sensitized T cells possessed no cytolytic activity of their own, the results indicate that the 6-8-d delay before adoptive immunity is expressed represents the time needed for passively transferred helper or memory T cells to give rise to a cytolytic T cell response of sufficient magnitude to destroy the recipient's tumor. In support of this interpretation was the additional finding that inhibition of the expression of adoptive immunity by the passive transfer of suppressor T cells from tumor- bearing donors was associated with a substantially reduced cytolytic T cell response in the recipient's draining lymph node. The results serve to illustrate that interpretation of the results of adoptive immunization experiments requires a knowledge of the events that take place in the adoptively immunized recipient. They support the interpretation that suppressor T cells function in this model to "down- regulate" the production of cytolytic effector T cells.
机译:这项关于P815肥大细胞瘤的研究结果证实了先前的研究结果,该研究表明免疫接种的供体的肿瘤敏感性T细胞的被动转移可导致T细胞缺陷(TXB)受体中的肿瘤生长消退,但不能普通收件人。关键的附加发现是,针对TXB受体中生长的肿瘤的过继性免疫表达在受体的引流淋巴结中大量产生细胞溶解性T细胞之前。另一方面,针对正常接受者生长的肿瘤表达的过继免疫失败与溶细胞性T细胞反应的幅度低得多有关,注入正常脾细胞的TXB接受者和肿瘤中也产生相似的低幅度反应轴承的对照小鼠。由于被动转移的致敏T细胞自身不具有细胞溶解活性,因此结果表明,过继免疫表达之前的6-8天延迟代表了被动转移的辅助T或记忆T细胞产生细胞溶解性T所需的时间。足以破坏受体肿瘤的细胞反应。支持该解释的另一项发现是,抑制性T细胞从荷瘤供体的被动转移对过继免疫表达的抑制与受体的引流淋巴结中溶血性T细胞反应显着降低有关。结果用于说明对过继免疫实验结果的解释需要了解过继免疫接种者发生的事件。他们支持这样的解释,即抑制性T细胞在该模型中起“下调”溶细胞性效应T细胞产生的作用。

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