{"title":"Correlation between human cytomegalovirus quantitative p72 antigenemia and viremia","authors":"Jordi Reina, Isabel Blanco, Maria Munar","doi":"10.1016/S0928-0197(96)00249-8","DOIUrl":null,"url":null,"abstract":"<div><p><strong>Objective:</strong> We present a prospective study of the correlation between the human cytomegalovirus (HCMV) quantitative antigenemia with monoclonal antibody to p72 protein (immediate-early antigen) and the number of infected cell foci detected in the shell-vial culture. A comparative study was made of the value of quantitative antigenemia (pp65 and p72) in 14 patients.</p><p><strong>Results:</strong> The average value of the pp65 antigenemia was 195 pp65-positive PMNLs per 10<sup>5</sup> PMNLs (range 10–1000) and that of the p72, 21 p72-positive PMNLs per 10<sup>5</sup> PMNLs (range 0–120) (<em>P</em> < 0.001). The p72 antigenemia value represented 10.7% of the pp65 value (range 4.4–70%). A statistical correlation was observed between the total number of infected cell foci detected in the shell-vial culture and the total number of p72-positive PMNLs (<em>P</em> < 0.001), but not with the number of pp65-positive PMNLs (<em>P</em> = 0.4). A study of the number of infected cell foci detected in the shell-vial per 100 000 PMNLs inoculated showed a statistical correlation with the value of the p72 antigenemia (<em>P</em> < 0.001).</p><p><strong>Conclusions:</strong> According to results, there seems to be a general population of PMNLs carrying viral particles which are detected by means of the pp65 monoclonal antibody, and a subpopulation carrying active and replicative viral particles which is detected with the p72 antibody. This last subpopulation would be responsible for the formation of infected cell foci in the shell-vial culture. However due to the technical difficulties presented by the routine performance of p72 antigenemia, we recommend the routine application of the quantitative shell-vial culture and the use of the number of infected cell foci × 100 000 PMNLs inoculated as a parameter of replicative viral load for the diagnosis of infection and disease caused by HCMV.</p></div>","PeriodicalId":79479,"journal":{"name":"Clinical and diagnostic virology","volume":"7 1","pages":"Pages 63-67"},"PeriodicalIF":0.0000,"publicationDate":"1996-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0928-0197(96)00249-8","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and diagnostic virology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928019796002498","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Objective: We present a prospective study of the correlation between the human cytomegalovirus (HCMV) quantitative antigenemia with monoclonal antibody to p72 protein (immediate-early antigen) and the number of infected cell foci detected in the shell-vial culture. A comparative study was made of the value of quantitative antigenemia (pp65 and p72) in 14 patients.
Results: The average value of the pp65 antigenemia was 195 pp65-positive PMNLs per 105 PMNLs (range 10–1000) and that of the p72, 21 p72-positive PMNLs per 105 PMNLs (range 0–120) (P < 0.001). The p72 antigenemia value represented 10.7% of the pp65 value (range 4.4–70%). A statistical correlation was observed between the total number of infected cell foci detected in the shell-vial culture and the total number of p72-positive PMNLs (P < 0.001), but not with the number of pp65-positive PMNLs (P = 0.4). A study of the number of infected cell foci detected in the shell-vial per 100 000 PMNLs inoculated showed a statistical correlation with the value of the p72 antigenemia (P < 0.001).
Conclusions: According to results, there seems to be a general population of PMNLs carrying viral particles which are detected by means of the pp65 monoclonal antibody, and a subpopulation carrying active and replicative viral particles which is detected with the p72 antibody. This last subpopulation would be responsible for the formation of infected cell foci in the shell-vial culture. However due to the technical difficulties presented by the routine performance of p72 antigenemia, we recommend the routine application of the quantitative shell-vial culture and the use of the number of infected cell foci × 100 000 PMNLs inoculated as a parameter of replicative viral load for the diagnosis of infection and disease caused by HCMV.