Gilles J G, Saint-Remy J M
Allergy and Clinical Immunology Unit, Université Catholique de Louvain, Brussels, Belgium.
J Clin Invest. 1994 Oct;94(4):1496-505. doi: 10.1172/JCI117489.
Anti-Factor VIII (FVIII) antibodies were prepared by a combination of salt precipitation, gel filtration chromatography, and specific adsorption over insolubilized FVIII from the serum of 10 healthy subjects with normal levels of FVIII. Antibody specificity was confirmed by the capacity to recognize soluble and insolubilized FVIII and to neutralize FVIII cofactor activity in FX activation. Epitope mapping was carried out using a competition ELISA in which affinity-purified human antibodies inhibited the binding of labeled monoclonal antibodies. In most cases, a single region of the A3 domain of the FVIII light chain was recognized by the antibodies, while the reactivity toward heavy chain epitopes differed from one antibody preparation to the other. Sera or IgG fractions of the serum before immunoadsorption over insolubilized FVIII did not bind to FVIII. The IgG fraction that was not retained on the FVIII immunosorbent contained IgG that bound to the variable part of anti-FVIII mouse monoclonal antibodies and inhibited the binding of labeled FVIII; in addition, the IgG fraction inhibited the binding of affinity-purified human antibodies to FVIII, thereby strongly suggesting the presence of anti-idiotypic antibodies. These findings indicate that the presence of anti-FVIII antibodies is a more universal phenomenon than previously thought and that anti-idiotypic antibodies capable of inhibiting the binding of anti-FVIII antibodies to FVIII are produced spontaneously.
通过盐析、凝胶过滤色谱法以及对来自10名FVIII水平正常的健康受试者血清中不溶性FVIII的特异性吸附相结合的方法制备抗因子VIII(FVIII)抗体。通过识别可溶性和不溶性FVIII以及中和FX激活中FVIII辅因子活性的能力来确认抗体特异性。使用竞争ELISA进行表位作图,其中亲和纯化的人抗体抑制标记单克隆抗体的结合。在大多数情况下,抗体识别FVIII轻链A3结构域的单个区域,而对重链表位的反应性因抗体制剂而异。在不溶性FVIII上进行免疫吸附之前,血清或血清的IgG组分不与FVIII结合。未保留在FVIII免疫吸附剂上的IgG组分含有与抗FVIII小鼠单克隆抗体可变部分结合并抑制标记FVIII结合的IgG;此外,该IgG组分抑制亲和纯化的人抗体与FVIII的结合,从而强烈提示抗独特型抗体的存在。这些发现表明,抗FVIII抗体的存在是一种比以前认为的更普遍的现象,并且能够抑制抗FVIII抗体与FVIII结合的抗独特型抗体是自发产生的。