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对不同同种异体抗原的自然杀伤(NK)活性的特异性抑制。

Specific inhibition of natural killer (NK) activity against different alloantigens.

作者信息

Fossum S, Ager A, Rolstad B

机构信息

Anatomical Institute, Oslo University, Norway.

出版信息

Immunogenetics. 1987;26(6):329-38. doi: 10.1007/BF00343700.

Abstract

Allogeneic lymphocyte cytotoxicity (ALC), i.e., rapid rejection of i.v. injected allogeneic lymphocytes in unprimed hosts, is an example of NK activity. Apparently anomalous rejection patterns, such as acceptance of F1 hybrid cells by parental hosts and rejection of parental cells by F1 hybrid hosts in many strain combinations, would fit the hypothesis that the effector cells in ALC recognize the absence of certain self-molecules (passwords) rather than the presence of nonself determinants. However, cold target inhibition studies showed that ALC displays allospecificity: when a mixture of radiolabeled AO and DA cells were injected i.v. into euthymic or athymic PVG rats, adding a surplus of cold DA cells reduced killing only of labeled DA cells and vice versa. Furthermore, semiallogeneic cold target cells were ineffective in inhibiting elimination of fully allogeneic cells, which supports the argument against a modification of the hypothesis that self-determinants inhibit a postbinding stage of lysis. Finally, (DA x AO)F1 cells injected into (DA x PVG)F1 hosts were rapidly rejected, despite the fact that donor and host shared expressed DA determinants. In sum, our results show that a hypothesis based on inhibition of killing by self-determinants can only be sustained with extensive modifications, and favor the alternative mechanism that the effector cells positively recognize the presence of allospecific determinants on the target cell surface.

摘要

同种异体淋巴细胞毒性(ALC),即在未致敏宿主中对静脉注射的同种异体淋巴细胞的快速排斥反应,是自然杀伤细胞活性的一个例子。明显异常的排斥模式,例如在许多品系组合中亲代宿主对F1杂交细胞的接受以及F1杂交宿主对亲代细胞的排斥,符合这样一种假设,即ALC中的效应细胞识别某些自身分子(密码)的缺失而非非自身决定簇的存在。然而,冷靶抑制研究表明ALC具有同种特异性:当将放射性标记的AO细胞和DA细胞的混合物静脉注射到有胸腺或无胸腺的PVG大鼠中时,加入过量的冷DA细胞仅减少对标记的DA细胞的杀伤,反之亦然。此外,半同种异体冷靶细胞在抑制完全同种异体细胞的清除方面无效,这支持了反对修改自身决定簇抑制裂解后结合阶段这一假设的观点。最后,尽管供体和宿主共享表达的DA决定簇,但注射到(DA×PVG)F1宿主中的(DA×AO)F1细胞仍被快速排斥。总之,我们的结果表明,基于自身决定簇抑制杀伤的假设只有经过大量修改才能成立,并且支持另一种机制,即效应细胞积极识别靶细胞表面同种特异性决定簇的存在。

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