Jintaridth Pornrutsami, Srisomsap Chantragan, Vichittumaros Kanjana, Kalpravidh Ruchaneekorn W, Winichagoon Pranee, Fucharoen Suthat, Svasti M R Jisnuson, Kasinrerk Watchara
Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok, Thailand.
Int J Hematol. 2006 Jun;83(5):408-414. doi: 10.1532/IJH97.A20515. Epub 2018 Jan 16.
Immunoglobulin Y (IgY) technology was used to generate anti-hemoglobin Bart's (Hb Bart's) IgY antibodies (Abs) for development into an enzyme-linked immunosorbent assay (ELISA) test for thalassemia diagnosis. Hb Bart's purified from the hemolysate of a patient with Hb Bart's hydrops fetalis (homozygous α-thalassemia) was used to immunize a chicken via the pectoralis muscle. After water dilution and sodium sulfate precipitation, 40 to 70 mg of IgY could be extracted from an egg. IgY, first detected in sera 2 weeks after immunization, reached the highest titer at week 4, and the titer remained stable for at least 2 weeks before declining. The pattern of Ab response in the yolk was the same as in the serum but was somewhat delayed. The IgY Abs produced reacted with γ globin, Hb Bart's, Hb F, normal cord hemolysate (Hbs F plus A), and Hb Bart's hydrops fetalis (Hbs Bart's plus Portland) and to a lesser degree with β globin, Hb A, Hb A, and adult hemolysate (Hbs A plus A), but the Abs did not react with α globin. Immunoaffinity purification with Hb A coupled to Sepharose was used to isolate an unbound IgY that reacted with Hb F, Hb Bart's, and γ globin, and this IgY was used to develop an ELISA test for thalassemia diagnosis. The results of direct ELISA analyses of 336 hemolysate samples from individuals with various known thalassemia genotypes and phenotypes and from healthy individuals confirmed the specificity of the polyclonal Abs for Hbs containing Hb F and Hb Bart's. This specificity, which was due to the Abs' strong reactivity in cases of pathologic thalassemic diseases and weak reactivity in cases of nonpathologic thalassemic diseases, depended on the levels of Hb Bart's and Hb F.
采用免疫球蛋白Y(IgY)技术制备抗血红蛋白Bart's(Hb Bart's)IgY抗体,用于开发地中海贫血诊断的酶联免疫吸附测定(ELISA)检测方法。从一名患有Hb Bart's胎儿水肿综合征(纯合子α地中海贫血)患者的溶血产物中纯化得到的Hb Bart's,通过胸肌注射免疫鸡。经水稀释和硫酸钠沉淀后,一枚鸡蛋可提取出40至70毫克的IgY。免疫后2周在血清中首次检测到IgY,第4周达到最高滴度,滴度在下降前至少稳定2周。蛋黄中的抗体反应模式与血清相同,但有所延迟。所产生的IgY抗体与γ珠蛋白、Hb Bart's、Hb F、正常脐血溶血产物(Hb F加Hb A)以及Hb Bart's胎儿水肿综合征(Hb Bart's加Hb Portland)发生反应,与β珠蛋白、Hb A、Hb A2和成人溶血产物(Hb A加Hb A2)的反应较弱,但不与α珠蛋白反应。使用与琼脂糖偶联的Hb A进行免疫亲和纯化,以分离出与Hb F、Hb Bart's和γ珠蛋白反应的未结合IgY,并将该IgY用于开发地中海贫血诊断的ELISA检测方法。对来自具有各种已知地中海贫血基因型和表型的个体以及健康个体的336份溶血产物样本进行直接ELISA分析的结果,证实了多克隆抗体对含有Hb F和Hb Bart's的血红蛋白的特异性。这种特异性归因于抗体在病理性地中海贫血疾病中的强反应性和在非病理性地中海贫血疾病中的弱反应性,取决于Hb Bart's和Hb F的水平。