| Literature DB >> 34396415 |
Kh Shamsur Rahman1, Bernhard Kaltenboeck1.
Abstract
Detection of anti-Chlamydia trachomatis (Ctr) antibodies is compromised by cross-reactivity and poor sensitivity of classic Ctr-antigens. We discovered 48 strongly reactive peptide antigens of Ctr-specific B-cell epitopes from 21 immunodominant proteins. In this study, we review the utility of peptide assays for diagnosis of Ctr infections. By combining many of these Ctr-specific B-cell epitopes from several proteins in separate or mixed multipeptide assays, they achieved vastly superior assay sensitivity and specificity over standard enzyme-linked immunosorbent assays. Such multipeptide assays eliminate cross-reactivities (false positives) and correct for stochastic gaps in antibody responses (false negatives). More importantly, we developed and validated a novel microarray platform in which hundreds of peptides from many proteins are spotted in a single reaction well. This offers the possibility of high-throughput screening of many candidate peptides for routine serological fingerprinting of Ctr infections. Discovery of optimal sets of antibody responses that associate with clinical pelvic inflammatory disease (PID) may identify diagnostically useful PID biomarker antigens.Entities:
Keywords: B-cell epitope; cross-reactivity in immunoassay; pelvic inflammatory disease (PID)
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Year: 2021 PMID: 34396415 DOI: 10.1093/infdis/jiab016
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226