Lutz H U, Stammler P, Fasler S
Laboratory for Biochemistry, Swiss Federal Institute of Technology, Zurich.
Biomed Biochim Acta. 1990;49(2-3):S224-9.
Several naturally occurring antibodies stimulate alternative complement pathway C3b deposition. One type of these antibodies, human anti-band 3 antibody, is involved in opsonizing senescent and oxidatively stressed red cells with C3b (Proc. Natl. Acad. Sci. USA 84[1987]7368). The mechanism was investigated, by which it stimulates alternative complement pathway. Anti-band 3 antibodies are preferred targets for nascent C3b which forms ester bonds with IgG and generates C3b-IgG complexes. Since C3b-IgG and free C3b can equally well nucleate alternative convertases and since C3b in C3b-IgG is protected from degradation (J. Exp. Med. 160[1984]1640), generation of C3b-IgG complexes means stimulation of alternative complement pathway. Anti-band 3 antibodies are preferred targets for the shortlived, nascent C3b since they bind to native C3 by a site distant from the antigen binding site. In vitro generation of C3b-IgG complexes confirmed a preferential formation of C3b-anti-band 3 complexes. Thus, an affinity for C3 may be all what is required to make an antibody a stimulator of the alternative complement pathway and thereby a potent opsonin.
几种天然存在的抗体可刺激补体替代途径C3b的沉积。其中一种抗体,即人抗带3抗体,参与用C3b调理衰老和氧化应激的红细胞(《美国国家科学院院刊》84[1987]7368)。对其刺激补体替代途径的机制进行了研究。抗带3抗体是新生C3b的首选靶点,新生C3b与IgG形成酯键并生成C3b-IgG复合物。由于C3b-IgG和游离C3b同样能够很好地启动替代转化酶,并且由于C3b-IgG中的C3b受到保护不被降解(《实验医学杂志》160[1984]1640),C3b-IgG复合物的生成意味着补体替代途径的激活。抗带3抗体是短命的新生C3b的首选靶点,因为它们通过远离抗原结合位点的一个位点与天然C3结合。C3b-IgG复合物的体外生成证实了C3b-抗带3复合物的优先形成。因此,对C3的亲和力可能是使一种抗体成为补体替代途径激活剂从而成为一种有效的调理素所需要的全部条件。