Transfer factor in the age of molecular biology: a review.

J M Dwyer
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引用次数: 8

Abstract

Current data suggests that the transferring of immunologically specific information by transfer factor molecules requires interaction with a cell that has been genetically programmed to be antigen reactive but at the time of interaction is unprimed. Contact with transfer factor molecules would allow a naive recipient, on a first encounter with antigen, to make a secondary rather than a primary immunological response. Transfer factor molecules for each and every antigenic determinant are thus necessary. Transfer factors made from animals or humans are capable of transferring antigen specificity across a species barrier. Even primitive species have cells from which one can make transfer factors. The molecules are, therefore, well conserved and it is reasonable to suggest that they are important for normal immunological functioning. Proposed mechanisms of action must explain the fact that transfer factors obtained from the cells of high responder animals are capable of transferring delayed hypersensitivity to low responder animals while the reverse is not true. Transfer factor molecules are likely to interact with the variable regions of the alpha and/or beta chain of T cell receptors to change their avidity and affinity for antigen in a way that otherwise would only occur after an encounter with antigen.

分子生物学时代的传递因子研究进展。
目前的数据表明,通过传递因子分子传递免疫特异性信息需要与基因编程为抗原反应性的细胞相互作用,但在相互作用时未启动。与传递因子分子接触可以使初次接触抗原的幼稚受体产生二次而不是一次免疫反应。因此,每个抗原决定因素的转移因子分子是必要的。由动物或人制成的转移因子能够跨越物种屏障转移抗原特异性。即使是原始物种也有可以制造转移因子的细胞。因此,这些分子是很保守的,有理由认为它们对正常的免疫功能很重要。所提出的作用机制必须解释这样一个事实,即从高反应动物的细胞中获得的转移因子能够将延迟超敏反应转移到低反应动物,而反之则不成立。传递因子分子可能与T细胞受体α和/或β链的可变区域相互作用,以改变其对抗原的亲和力和亲和力,否则只有在与抗原相遇后才会发生这种情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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