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DOI 10.1159/000442512

Медицинская библиотека · Acta cytologica · 2015

Multiple Human Papilloma Virus Infections and Their Impact on the Development of High-Risk Cervical Lesions.

Salazar Katrina L, Zhou Haijun Steve, Xu Jiaqiong, Peterson Leif E, Schwartz Mary R, Mody Dina R, Ge Yimin

Сравнительное исследованиеСтатьяПеревод в очереди

Аннотация

OBJECTIVE

Individuals are often infected with multiple genotypes of human papillomavirus (HPV) simultaneously, but the role these infections play in the development of cervical disease is not well established. This study aimed to determine the association of multiple HPV infections with high-risk cervical lesions (hrCLs).

STUDY

DESIGN

HPV genotyping was performed on 798 SurePath specimens collected between December 1, 2009, and April 30, 2011. The cases were classified as hrCL (n = 90) or non-hrCL (n = 708) based on cytology diagnoses. The association between hrCL and HPV infection patterns was analyzed.

RESULTS

Multiple HPV infections were frequently encountered (38.2%) in the cohort. Increased frequency of hrCLs was associated with a single high-risk HPV (hrHPV) infection. An additive or synergistic effect was not observed for hrCL in multiple HPV infections. The hrCL rates appeared to decrease in various patterns of multiple HPV infections, but the reduction was not statistically significant.

CONCLUSIONS

Multiple HPV infections are common with no additive or synergistic effect on the development of hrCL. Conversely, reduced hrCL rates were observed in various patterns of multiple HPV infections compared to their single-genotype infection counterparts, suggestive of possible intergenotypic competition or more effective immune response triggered by multiple infections. Further studies in larger cohorts are needed.

Для цитирования: Salazar Katrina L, Zhou Haijun Steve, Xu Jiaqiong, Peterson Leif E, Schwartz Mary R, Mody Dina R, Ge Yimin. Multiple Human Papilloma Virus Infections and Their Impact on the Development of High-Risk Cervical Lesions.. Acta cytologica. 2015. DOI: 10.1159/000442512.

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