CORRELATION BETWEEN HUMAN CYTOMEGALOVIRUS QUANTITATIVE P72 ANTIGENEMIA AND VIREMIA

Citation
J. Reina et al., CORRELATION BETWEEN HUMAN CYTOMEGALOVIRUS QUANTITATIVE P72 ANTIGENEMIA AND VIREMIA, Clinical and diagnostic virology, 7(1), 1996, pp. 63-67
Citations number
13
Categorie Soggetti
Virology
ISSN journal
09280197
Volume
7
Issue
1
Year of publication
1996
Pages
63 - 67
Database
ISI
SICI code
0928-0197(1996)7:1<63:CBHCQP>2.0.ZU;2-7
Abstract
Objective: We present a prospective study of the correlation between t he human cytomegalovirus (HCMV) quantitative antigenemia with monoclon al antibody to p72 protein (immediate-early antigen) and the number of infected cell foci detected iii 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 w as 195 pp65-positive PMNLs per 10(5) PMNLs (range 10-1000) and that of the p72, 21 p72 positive PMNLs per 10(5) PMNLs (range 0-120) (P<0.001 ). The p72 antigenemia value represented 10.7% of the pp65 value (rang e 4.4-70%). A statistical correlation was observed between the total n umber 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 cel l foci detected in the shell-vial per 100 000 PMNLs inoculated showed a statistical correlation with the value of the p72 antigenemia (P<0.0 01). Conclusions: According to results, there seems to be a general po pulation 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 antibod y. This last subpopulation would be responsible for the formation of i nfected cell foci in the shell-vial culture. However due to the techni cal difficulties presented by the routine performance of p72 antigenem ia, we recommend the routine application of the quantitative shell-via l culture and the use of the number of infected cell foci x 100 000 PM NLs inoculated as a parameter of replicative viral load for the diagno sis of infection and disease caused by HCMV.