Wicker L S, Benjamin C D, Miller A, Sercarz E E
Eur J Immunol. 1984 May;14(5):447-53. doi: 10.1002/eji.1830140512.
The antibody response to a defined protein antigen, hen egg white lysozyme (HEL) has been investigated using an aminopeptidase-treated HEL molecule, des-1,2,3-HEL (AP-HEL). Surprisingly, removal of these three N-terminal residues eliminates an epitope which is a dominant B cell determinant recognized in the primary antibody response to HEL. Thus, the initial antibody response focuses on a very small region of the molecule. Even more striking is the observation that removal of this epitope markedly reduces the immunogenicity of HEL. Therefore, the epitope is not only the focus of the primary antibody response, but is essential for the initiation of the response. This report demonstrates that a selective mechanism must be activated during the response to this protein antigen. Of the multitude of B cell determinants present on HEL, only a limited number are focused upon by the immune system.
使用经氨肽酶处理的溶菌酶分子des-1,2,3-HEL(AP-HEL),对特定蛋白质抗原——鸡卵清溶菌酶(HEL)的抗体反应进行了研究。令人惊讶的是,去除这三个N端残基消除了一个表位,该表位是在对HEL的初次抗体反应中被识别的主要B细胞决定簇。因此,初次抗体反应集中在分子的一个非常小的区域。更引人注目的是,去除这个表位会显著降低HEL的免疫原性。因此,该表位不仅是初次抗体反应的焦点,而且对于反应的启动至关重要。本报告表明,在对这种蛋白质抗原的反应过程中,必须激活一种选择性机制。在HEL上存在的众多B细胞决定簇中,只有有限数量的决定簇受到免疫系统的关注。