4.6 Review

Targeting Persistent Human Papillomavirus Infection

Journal

VIRUSES-BASEL
Volume 9, Issue 8, Pages -

Publisher

MDPI AG
DOI: 10.3390/v9080229

Keywords

HPV; persistent infection; cervical cancer; therapeutics; vaccines; episome maintenance; E2 protein

Categories

Funding

  1. National Institutes of Health (NIH) [R01CA187718]
  2. NCI Cancer Center Support Grant [NCI P30 CA016520]

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While the majority of Human papillomavirus (HPV) infections are transient and cleared within a couple of years following exposure, 10-20% of infections persist latently, leading to disease progression and, ultimately, various forms of invasive cancer. Despite the clinical efficiency of recently developed multivalent prophylactic HPV vaccines, these preventive measures are not effective against pre-existing infection. Additionally, considering that the burden associated with HPV is greatest in regions with limited access to preventative vaccination, the development of effective therapies targeting persistent infection remains imperative. This review discusses not only the mechanisms underlying persistent HPV infection, but also the promise of immunomodulatory therapeutic vaccines and small-molecular inhibitors, which aim to augment the host immune response against the viral infection as well as obstruct critical viral-host interactions.

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