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参与小鼠细胞毒性T淋巴细胞与靶细胞附着的细胞表面受体——一项用T细胞抗原异种抗血清进行的研究。

Cell surface receptors involved in the attachment of murine cytotoxic T lymphocytes to target cells - a study with xenoantisera to T-cell antigens.

作者信息

Rabinowitz R, Levy J, Schlesinger M

出版信息

Thymus. 1983 Apr;5(3-4):127-39.

PMID:6603681
Abstract

In previous studies it was demonstrated that rabbit anti-mouse thymus sera (RAT) but not rabbit anti-brain serum (RABR), block the activity of cytotoxic T lymphocytes (CTL). The aim of the present study was to determine to what extent inhibition of the lytic activity of CTL reflects inhibition of the attachment of CTL to target cells. Following heat inactivation RAT and RABR were absorbed with mouse liver and kidney and tested for their capacity to inhibit the attachment of sensitized peritoneal exudate T lymphocytes (PEL) to various target cells. The exposure of sensitized PEL to RABR markedly reduced their capacity to form conjugates with either allogeneic or syngeneic target cells. In contrast, RAT inhibited only the formation of conjugates of sensitized PEL with the respective target cells against which they were immunized. Treatment with RAT had no effect on the formation of conjugates with irrelevant target cells. Additive experiments in which PEL were exposed to a mixture of both RAT and RABR indicated that the two antisera blocked different types of attachment. The inhibitory activity of RAT on conjugate formation could be removed by absorption with B-lymphoma cells but not with myeloma cells. Analysis of the correlation between the inhibitory effect of RAT on cell-mediated lysis (CML) and on conjugate formation revealed that the serum was about twice as effective in its capacity to inhibit CML as to inhibit the attachment of PEL to target cells. The results indicate that while RABR inhibits non-specific attachment of CTL which does not lead to cell lysis. RAT exerts its effect by interfering with immunologically specific functional receptors on CTL.

摘要

在先前的研究中已证明,兔抗小鼠胸腺血清(RAT)可阻断细胞毒性T淋巴细胞(CTL)的活性,而兔抗脑血清(RABR)则不能。本研究的目的是确定CTL裂解活性的抑制在多大程度上反映了CTL与靶细胞结合的抑制。热灭活后的RAT和RABR用小鼠肝脏和肾脏进行吸收,并测试它们抑制致敏腹膜渗出液T淋巴细胞(PEL)与各种靶细胞结合的能力。将致敏的PEL暴露于RABR后,其与同种异体或同基因靶细胞形成结合物的能力明显降低。相反,RAT仅抑制致敏的PEL与它们所免疫的相应靶细胞形成结合物。用RAT处理对与无关靶细胞形成结合物没有影响。将PEL暴露于RAT和RABR混合物的相加实验表明,这两种抗血清阻断不同类型的结合。RAT对结合物形成的抑制活性可通过用B淋巴瘤细胞吸收而去除,但不能用骨髓瘤细胞吸收。分析RAT对细胞介导的裂解(CML)和结合物形成的抑制作用之间的相关性发现,该血清抑制CML的能力约为抑制PEL与靶细胞结合能力的两倍。结果表明,RABR抑制不导致细胞裂解的CTL的非特异性结合。RAT通过干扰CTL上的免疫特异性功能受体发挥其作用。

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