Dwyer J M
Division of Clinical Immunobiology of the Prince Henry and Prince of Wales Hospitals of the University of New South Wales, Sydney, Australia.
Biotherapy. 1996;9(1-3):7-11. doi: 10.1007/BF02628650.
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.
目前的数据表明,转移因子分子传递免疫特异性信息需要与一种细胞相互作用,这种细胞在基因上被编程为对抗原具有反应性,但在相互作用时未被致敏。与转移因子分子接触会使初次接触抗原的未致敏受体做出二次而非初次免疫反应。因此,针对每个抗原决定簇都需要转移因子分子。从动物或人类制备的转移因子能够跨越物种屏障传递抗原特异性。即使是原始物种也有能制备转移因子的细胞。因此,这些分子具有高度保守性,有理由认为它们对正常免疫功能很重要。提出的作用机制必须解释这样一个事实,即从高反应性动物细胞获得的转移因子能够将迟发型超敏反应转移给低反应性动物,而反之则不成立。转移因子分子可能与T细胞受体α链和/或β链的可变区相互作用,以改变它们对抗原的亲合力和亲和力,而这种改变方式通常只有在接触抗原后才会发生。