Hl. Smits et al., INTERMETHOD VARIATION IN DETECTION OF HUMAN PAPILLOMAVIRUS DNA IN CERVICAL SMEARS, Journal of clinical microbiology, 33(10), 1995, pp. 2631-2636
In order to investigate the reliability of detection of human papillom
avirus (HPV) DNA in cervical smears, we have compared the performance
of two HPV PCR systems, the CPI/IIG and MY09/11 primer-mediated PCRs a
nd the Hybrid Capture System HPV DNA detection test (hybrid capture as
say), in detecting HPV DNA in cervical smears. We also included in our
study the MY09/11B PCR plus SHARP (solution hybridization assay for P
CR products) Signal System, This SHARP Signal System was recently deve
loped to detect RaY09/ 11B-generated biotinylated PCR products, The de
tection rate of the hybrid capture assay was lower than those of the C
PI/IIG and MY09/11 PCRs and the MY09/11B PCR plus SHARP Signal System.
The detection rates of the CPI/IIG PCR and the MY09/11B PCR plus SHAR
P Signal System were similar and higher than that of the conventional
MY09/11 PCR system. The agreement beyond chance of the PCR methods was
nearly perfect (kappa value between 0.82 and 0.84). The agreement bey
ond chance of the hybrid capture assay and the PCR methods was fair to
good (kappa value between 0.64 and 0.70). The systems detected HPV DN
A in different hut overlapping sets of smears, Our results indicate th
at each of the detection methods alone underestimates the prevalence o
f HPV.