Romero-Steiner Sandra, Caba Joseph, Rajam Gowrisankar, Langley Travis, Floyd Andrea, Johnson Scott E, Sampson Jacquelyne S, Carlone George M, Ades Edwin
Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333, USA.
Vaccine. 2006 Apr 12;24(16):3224-31. doi: 10.1016/j.vaccine.2006.01.042. Epub 2006 Feb 2.
Pneumococcal surface adhesin A (PsaA) is a pneumococcal vaccine candidate. In this study, we detect functional antibodies to PsaA by using carboxylate-modified fluospheres coated with either recombinant non-lipidated PsaA (rPsaA) or synthetic peptides with relevant epitopes of PsaA. Peptides P1-P3 were derived from phage display sequences; peptides P4-P7 were homologous to rPsaA. P1- and P4-coated fluospheres had similar adherence to Detroit 562 nasopharyngeal cells when compared to rPsaA-coated fluospheres. Homologous and heterologous competitive inhibitions with peptides in solution determined the specificity of the adherence. There was no significant difference (P=0.25) between the inhibition of adherence of rPsaA- and P4-coated fluospheres. This study indicates that P1 and P4 contain a functional epitope(s) for the adherence of PsaA to nasopharyngeal cells making them suitable targets for the measurement of functional antibodies to PsaA.
肺炎球菌表面黏附素A(PsaA)是一种肺炎球菌疫苗候选物。在本研究中,我们通过使用包被有重组非脂化PsaA(rPsaA)或具有PsaA相关表位的合成肽的羧酸盐修饰荧光球来检测针对PsaA的功能性抗体。肽P1 - P3源自噬菌体展示序列;肽P4 - P7与rPsaA同源。与包被rPsaA的荧光球相比,包被P1和P4的荧光球对底特律562鼻咽细胞的黏附性相似。溶液中肽的同源和异源竞争性抑制作用确定了黏附的特异性。rPsaA包被和P4包被的荧光球黏附抑制之间无显著差异(P = 0.25)。本研究表明,P1和P4含有PsaA黏附至鼻咽细胞的功能性表位,使其成为测量针对PsaA的功能性抗体的合适靶点。