Lh. Smith et al., TITRATION OF HPV-11 INFECTIVITY AND ANTIBODY NEUTRALIZATION CAN BE MEASURED IN-VITRO, Journal of investigative dermatology, 105(3), 1995, pp. 438-444
Human papillomavirus type 11 (HPV-11), produced from the athymic mouse
xenograft system, was shown to infect cultured neonatal human foreski
n keratinocytes and the HaCaT keratinocyte cell line in vitro. Infecti
on was documented by the appearance of HPV-ll-specific spliced mRNA, d
etected by reverse transcriptase-polymerase chain re action, Purified
HPV-11 virions at concentrations of approximately 10(7) particles/ml c
ould successfully evoke infection in this system, Infection was comple
tely abrogated by preincubation of the HPV-11 inoculum with mouse anti
-HPV-11 monoclonal antibodies, experimentally immunized animal sera, o
r sera of human patients with HPV infection. Concurrent detection of c
ellular mRNA for the beta-actin gene, also by reverse transcriptase-po
lymerase chain reaction, provided an internal control confirming RNA r
ecovery and successful reverse transcriptase-polymerase chain reaction
. Using this approach, it was possible to determine semiquantitative t
iters for test solutions of HPV-11-neutralizing antibodies, The in vit
ro system for HPV-11 infectivity and neutralization map be useful in t
he study of the immune response to HPV-11 infection or immunization in
patients.