J. Reina et al., CORRELATION BETWEEN HUMAN CYTOMEGALOVIRUS QUANTITATIVE P72 ANTIGENEMIA AND VIREMIA, Clinical and diagnostic virology, 7(1), 1996, pp. 63-67
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.