Review
Copyright ©The Author(s) 2016.
World J Gastroenterol. Sep 7, 2016; 22(33): 7415-7430
Published online Sep 7, 2016. doi: 10.3748/wjg.v22.i33.7415
Table 1 Human papillomavirus classification
HPV groupGenotypes
High-risk types
Carcinogenic16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59
Probably carcinogenic68
Possibly carcinogenic26, 53, 66, 67, 67, 70, 73, 82
Low-risk types6, 11, 40, 42, 43, 44, 54, 61, 72, 81, 89
Table 2 Comparison of human papillomavirus detection methods
MethodsSpecimensAdvantagesDisadvantages
Southern blotting assayFresh/frozen samplesHigh specificity, ability to differentiate between episomal and integrated DNANot easily applied to FFPE samples
ISHFFPE, fresh samplesHigh specificity, ability to differentiate between episomal and integrated DNALow sensitivity, technically difficult
HPV PCRFresh/frozen samples brushing washing any body fluidHigh sensitivity, cost effectiveLow specificity, provides no quantitative measure of viral load, no confirmation of transcriptionally active virus
Real-time PCRFresh/frozen samples, FFPE brushing washing any body fluidHigh sensitivity and specificity, ability to differentiate between episomal and integrated DNALabour-intensive
Reverse Transcriptase PCRFresh/frozen samples, FFPEHigh sensitivityTime consuming, technically difficult
p16 immunostainingFresh/frozen samples FFPE brushing washingHigh sensitivity, easy and accessible to most laboratories, marker of transcriptionally active virusLow specificity
Signal amplification methodsFresh/frozen samples FFPE brushing washingEasy to performFalse positive products, no typing