Polin R A, Douglas S D, Kasper D L, Baker C J
J Clin Microbiol. 1982 Jun;15(6):991-3. doi: 10.1128/jcm.15.6.991-993.1982.
Neonates at risk for fulminant type III, group B streptococcal (III GBS) infection are those who lack antibody to the capsular polysaccharide. A newly developed enzyme-linked immunosorbent assay (ELISA) was compared with a standard radioactive antigen-binding assay (RABA) for quantitation of III GBS antibody in human sera. Although there was a significant correlation between the ELISA and RABA (r = 0.81; P less than 0.001) in general, the ELISA detected antibody both to core and native antigens of III GBS, whereas the RABA detected antibody to native polysaccharide exclusively. The results of the two assays were discordant when sera which had only high native or core antibody (not both) were assessed. Although the ELISA was reproducible and required less than 1 microliter of serum, interpretation of data obtained by the assay should be viewed with caution since only antibody to native III GBS has been correlated with human immunity.
有暴发性B族链球菌III型(III GBS)感染风险的新生儿是那些缺乏针对荚膜多糖抗体的婴儿。一种新开发的酶联免疫吸附测定(ELISA)与标准放射性抗原结合测定(RABA)进行了比较,以定量人血清中的III GBS抗体。虽然ELISA和RABA总体上有显著相关性(r = 0.81;P小于0.001),但ELISA检测到针对III GBS核心抗原和天然抗原的抗体,而RABA仅检测到针对天然多糖的抗体。当评估仅具有高天然抗体或核心抗体(而非两者都有)的血清时,两种测定结果不一致。虽然ELISA可重复且所需血清量少于1微升,但由于只有针对天然III GBS的抗体与人类免疫力相关,因此对该测定获得的数据解释应谨慎看待。