Optimized enzyme-linked immunosorbent assay for detecting cytomegalovirus infections during clinical trials of recombinant vaccines

• Published in: Journal of clinical virology Vol. 96; pp. 99 - 104
• Main Authors: Pagnon, Anke, Piras, Fabienne, Gimenez-Fourage, Sophie, Dubayle, Joseline, Arnaud-Barbe, Nadège, Hessler, Catherine, Caillet, Catherine
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.11.2017
• Subjects: Antibodies, Viral - blood; Antigens, Viral - immunology; Clinical Trials as Topic; Cytomegalovirus; Cytomegalovirus Infections - diagnosis; Cytomegalovirus Infections - prevention & control; Cytomegalovirus Vaccines - administration & dosage; Diagnostic Tests, Routine - methods; ELISA; Enzyme-Linked Immunosorbent Assay - methods; Glycoprotein B; Humans; Immunoglobulin G - blood; Sensitivity and Specificity; Vaccine; Vaccines, Synthetic - administration & dosage; HSV2 gD; Cytomegalovirus; Glycoprotein B; OD; Vaccine; gB; CMV; Ig; ELISA
• ISSN: 1386-6532; 1873-5967; 1873-5967
• DOI: 10.1016/j.jcv.2017.10.004

•Clinical trials of CMV gB vaccines require an ELISA to detect CMV-specific antibodies.•Current ELISAs require time consuming pre-absorption and verification steps.•We developed an IgG ELISA using UL32/pp150 [862–1048] as a capture antigen.•The assay eliminates the need for gB pre-absorption and verification.•The assay is specific, sensitive, reproducible, and accurate over a wide range. In clinical trials of cytomegalovirus (CMV) glycoprotein B (gB) vaccines, CMV infection is detected by first depleting serum of anti-gB antibodies and then measuring anti-CMV antibodies with a commercially available enzyme-linked immunosorbent assay (ELISA) kit, with confirmation of positive findings by immunoblot. Identification of CMV immunoantigens for the development of an ELISA that detects specifically CMV infection in clinical samples from individuals immunized with gB vaccines. Sensitivity and specificity of ELISAs using antigenic regions of CMV proteins UL83/pp65, UL99/pp28, UL44/pp52, UL80a/pp38, UL57, and UL32/pp150 were measured. An IgG ELISA using a UL32/pp150 [862–1048] capture peptide was the most specific (93.7%) and sensitive (96.4%) for detecting CMV-specific antibodies in sera. The ELISA successfully detected CMV-specific antibodies in 22 of 22 sera of subjects who had been vaccinated with a gB vaccine but who had later been infected with CMV. The ELISA was linear over a wide range of CMV concentrations (57–16,814 ELISA units/mL) and was reproducible as indicated by a 5% intra-day and 7% inter-day coefficients of variation. The signal was specifically competed by UL32/pp150 [862–1048] peptide but not by CMV-gB or herpes simplex virus 2 glycoprotein D. Lipid and hemoglobin matrix did not interfere with the assay. The UL32/pp150 [862–1048] IgG ELISA can be used for the sensitive and specific detection of CMV infection in gB-vaccinated individuals.