Horgan C, Brown K, Pincus S H
Laboratory of Microbial Structure and Function, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840.
J Immunol. 1992 Jul 1;149(1):127-35.
Activation of C by immune complexes (IC) in tissues and the inflammatory consequences are major determinants in the pathogenesis of many autoimmune disorders. To assess the factors involved in C activation by such IC, we examined the binding of C components by chimeric IgG1 antibodies bound to immobilized Ag. We previously reported that alterations in the H chain V regions can affect the binding of first component of C (C1q) and a major breakdown product of the third C component (C3b) when otherwise identical antibodies were bound to immobilized (Tyr, Glu)-Ala-Lys. To evaluate C activation of these antibodies in well defined IC, we utilized a 9-amino acid peptide conjugated to BSA as Ag. The peptide:BSA conjugate was bound similarly by the two IgG1 antibodies which differed mainly in the CDR3 regions, but also in 9 other amino acids in the H chain V region. When soluble IC were prepared with the two antibodies, they activated C similarly. However, C activation by solid phase Ag:antibody complexes differed; we found that antibody 10B bound more C1q and C3b than antibody B11 did, unless the Ag was present at high density on the plates. These data suggest that the variable region differences affect C activation by these antibody when they are bound to immobilized Ag. Furthermore, these results underscore the differences in C activation by the same antibody depending upon whether the IC are free in solution or immobilized.
免疫复合物(IC)在组织中激活补体(C)及其引发的炎症后果是许多自身免疫性疾病发病机制的主要决定因素。为了评估此类IC激活C的相关因素,我们检测了与固定化抗原结合的嵌合IgG1抗体与补体成分的结合情况。我们之前报道过,当其他方面相同的抗体与固定化的(酪氨酸、谷氨酸)-丙氨酸-赖氨酸结合时,重链V区的改变会影响补体第一成分(C1q)和第三补体成分的主要裂解产物(C3b)的结合。为了评估这些抗体在明确界定的IC中的补体激活情况,我们使用了一种与牛血清白蛋白(BSA)偶联的9个氨基酸的肽作为抗原。该肽:BSA偶联物与两种主要在互补决定区3(CDR3)区域不同、重链V区还有9个其他氨基酸不同的IgG1抗体的结合情况相似。当用这两种抗体制备可溶性IC时,它们激活补体的情况相似。然而,固相抗原:抗体复合物激活补体的情况有所不同;我们发现,除非平板上的抗原高密度存在,否则抗体10B比抗体B11结合更多的C1q和C3b。这些数据表明,可变区差异会影响这些抗体与固定化抗原结合时的补体激活。此外,这些结果强调了同一抗体激活补体的差异,这取决于IC是游离于溶液中还是固定化的。