Population-Level Effects of Human Papillomavirus Vaccination Programs on Infections with Nonvaccine Genotypes

Mesher, David; Soldan, Kate; Lehtinen, Matti; Beddows, Simon; Brisson, Marc; Brotherton, Julia M.L.; Chow, Eric P.F.; Cummings, Teresa; Drolet, Mélanie; Fairley, Christopher K.; Garland, Suzanne M.; Kahn, Jessica A.; Kavanagh, Kimberley; Markowitz, Lauri; Pollock, Kevin G.; Söderlund-Strand, Anna; Sonnenberg, Pam; Tabrizi, Sepehr N.; Tanton, Clare; Unger, Elizabeth; Thomas, Sara L.

doi:10.3201/eid2210.160675

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Population-Level Effects of Human Papillomavirus Vaccination Programs on Infections with Nonvaccine Genotypes

Published Date:

Oct 2016

Publisher's site:

http://dx.doi.org/10.3201/eid2210.160675 New Site Icon

Source:

Emerg Infect Dis. 22(10):1732-1740.

[PDF-964.03 KB]

Details:

Personal Authors:

Mesher, David ; Soldan, Kate ; Lehtinen, Matti ; Beddows, Simon ; Brisson, Marc ; ... More ▼

Keywords:

[+]

Pubmed ID:

27648688

Pubmed Central ID:

PMC5038419

Description:

We analyzed human papillomavirus (HPV) prevalences during prevaccination and postvaccination periods to consider possible changes in nonvaccine HPV genotypes after introduction of vaccines that confer protection against 2 high-risk types, HPV16 and HPV18. Our meta-analysis included 9 studies with data for 13,886 girls and women ≤19 years of age and 23,340 women 20-24 years of age. We found evidence of cross-protection for HPV31 among the younger age group after vaccine introduction but little evidence for reductions of HPV33 and HPV45. For the group this same age group, we also found slight increases in 2 nonvaccine high-risk HPV types (HPV39 and HPV52) and in 2 possible high-risk types (HPV53 and HPV73). However, results between age groups and vaccines used were inconsistent, and the increases had possible alternative explanations; consequently, these data provided no clear evidence for type replacement. Continued monitoring of these HPV genotypes is important.

Document Type:

Journal Article

Collection(s):

Emerging Infectious Diseases

Funding:

R01 AI073713/AI/NIAID NIH HHS/United States
R01 AI104709/AI/NIAID NIH HHS/United States

Supporting Files:

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