Chi D S, Chen J P
Tex Rep Biol Med. 1975;33(4):493-508.
Immunoassay for fibrinogen and/or fibrin degradation products (FDP) is generally in the clot and hence assay of serum may not reveal the true concentration of FDP in blood. We have developed a hemagglutination inhibition immunoassay for FDP in human plasma. D fragment appears to possess an antigenic determinant, called D-neoantigen, not found in native fibrinogen. Rabbit antiserum produced against D fragment was absorbed with immunosorbent columns coupled with fibrinogen and normal human serum, respectively, so that it contained only those antibodies directed against the neoantigenic determinant of D fragment. In this immunoassay, sheep erythrocytes (SRBC) were stabilized with glutaraldehyde and subsequently sensitized with D fragment by means of tannic acid. Hemagglutination of absorbed anti-D-neoantigen serum against SRBC sensitized with D fragment was titered to be 1:256. The hemagglutination was inhibited by D fragment but not by fibrinogen; the sensitivity of detecting D fragment was 8 mug/ml. Human plasma from normal subjects did not inhibit. This appears to be the first report of a hemagglutination inhibition immunoassay for FDP in plasma.
纤维蛋白原和/或纤维蛋白降解产物(FDP)的免疫测定通常在凝块中进行,因此血清测定可能无法揭示血液中FDP的真实浓度。我们开发了一种用于人血浆中FDP的血凝抑制免疫测定法。D片段似乎具有一种抗原决定簇,称为D-新抗原,在天然纤维蛋白原中未发现。分别用与纤维蛋白原和正常人血清偶联的免疫吸附柱吸收针对D片段产生的兔抗血清,使其仅含有针对D片段新抗原决定簇的那些抗体。在这种免疫测定中,用戊二醛稳定绵羊红细胞(SRBC),随后通过鞣酸用D片段致敏。吸收的抗D-新抗原血清对用D片段致敏的SRBC的血凝效价测定为1:256。血凝被D片段抑制,但不被纤维蛋白原抑制;检测D片段的灵敏度为8微克/毫升。正常受试者的人血浆不产生抑制作用。这似乎是关于血浆中FDP的血凝抑制免疫测定的首次报道。