Abstract:
Cervical cancer is one of the most prevalent types of cancer in women. Every
year approximately 0.5 m women are diagnosed with the disease worldwide.
Cervical cancer development is linked to the persistent infection by high-risk
mucosal human papiliomaviruses (HPVs) types. To elucidate the role of Toll-
like Receptors (TLRs) in the persistence and clearance of HPV, the association
between Toll-like Receptors (TLRs) expression and HPVs (HPV type 16, 18,
51 or 6) infection among young women who either had persistent or cleared
HPV infection were investigated. Messenger expression of TLR1, TLR2, TLR3,
TLR4, TLR6, TLR7, TLR8, and TLR9 was measured by quantitative RT-PCR
using endocervical specimens collected before and following viral acquisition
in a cohort well-characterized for HPV DNA infections. HPV16 infections that
persisted were significantly associated (p<0.05) with downregulation of Toll-
like receptor (TLRs) TLR2, TLR3, TLR7, TLR8 and TLR9 upon viral
acquisition. In contrast, HPV type 18, which are known to persist less
competently in the host than HPV16 showed down-regulation of only Toll-
Like Receptors (TLRs) 1 (p<0.005). No significant associations were found
with clearance versus persistence of HPV 6 or HPV 51. This study unravels a
novel mechanism used by HPV16 to suppress the host immune response by
deregulating the TLRs transcripts, providing evidence that abolishing innate
responses may be a crucial step involved in the carcinogenic events mediated
by human papillomaviruses. Understanding the mechanism involved In
reversing this down-regulation could lay the foundation for new therapies.