Govender M, Marimuthu T, Bubb M O, Conradie J D
S Afr Med J. 1985 Aug 31;68(5):295-8.
An enzyme-linked immunosorbent assay (ELISA) was developed for the detection and quantitation of antibodies (anti-HBs) to the surface antigen of the hepatitis B virus (HBsAg). The ELISA uses HBsAg as the solid phase, and, after conjugation to horseradish peroxidase, also as the conjugate. Conditions for this assay were optimized and a rapid (1.5 hours) ELISA has evolved which works very satisfactorily for the large-scale screening of donated blood. We have used this ELISA to examine donated blood in Natal and concluded that we cannot initiate a programme of anti-HBs supplementation of parenteral blood products without hyperimmunization and plasmapheresis of selected, voluntary donors.
开发了一种酶联免疫吸附测定(ELISA),用于检测和定量针对乙型肝炎病毒(HBsAg)表面抗原的抗体(抗-HBs)。该ELISA以HBsAg作为固相,与辣根过氧化物酶结合后,也用作结合物。对该测定的条件进行了优化,一种快速(1.5小时)的ELISA已研发出来,它对大规模筛查献血非常有效。我们已使用这种ELISA检测纳塔尔地区的献血,并得出结论,如果没有对选定的自愿献血者进行超免疫和血浆置换,我们无法启动对非肠道血液制品补充抗-HBs的计划。