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. 2008 Feb;46(2):732-9.
doi: 10.1128/JCM.01322-07. Epub 2007 Dec 12.

Cervical human papillomavirus (HPV) infection and HPV type 16 antibodies in South African women

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Cervical human papillomavirus (HPV) infection and HPV type 16 antibodies in South African women

Dianne J Marais et al. J Clin Microbiol. 2008 Feb.

Abstract

There is a high incidence of cervical cancer in South African women. No large studies to assess human papillomavirus virus (HPV) infection or HPV type 16 (HPV-16) exposure have occurred in the region, a requirement for policy making with regards to HPV screening and the introduction of vaccines. Control women (n = 1,003) enrolled in a case control study of hormonal contraceptives and cervical cancer were tested for 27 cervical HPV types by reverse line blot analysis. The seroprevalence of HPV-16 immunoglobulin G (IgG) and IgA antibodies was assessed by a virus-like particle-based enzyme-linked immunoassay of 908 and 904 control women, respectively, and of 474 women with cervical cancer. The cervical HPV prevalence was 26.1%. The HPV-16 IgG seroprevalence was 44.4% and the HPV-16 IgA seroprevalence was 28.7% in control women, and these levels were significantly higher (61.8% and 52.7%, respectively) for women with cervical cancer (odds ratio [OR], 2.1 and 2.8, respectively). The cervical HPV prevalence showed an association with cervical disease, and the HPV-16 IgG prevalence decreased while the HPV-16 IgA prevalence increased with increasing age (P < 0.05). The prevalence of oncogenic HPV types (including HPV-16) decreased with age, whereas nononcogenic HPV types showed limited association with age. Multivariate analysis revealed cervical HPV infection to be associated with herpes simplex virus type 2 infection (OR, 1.7) and increasing years of education (OR, 1.9). HPV-16 IgG antibodies were inversely associated with current smoking status (OR, 0.6), and the presence of HPV-16 IgA antibodies was inversely associated with the use of alcohol (OR, 2.1) and inversely associated with the use of oral contraceptives (OR, 0.6). High levels of exposure to HPV, and particularly HPV-16, were evident in this population. The apparent increase of serum HPV-16 IgA with increasing age requires further investigation.

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Figures

FIG. 1.
FIG. 1.
Prevalence of serum antibodies, cervical oncogenic and nononcogenic HPV types, and HPV-16 infection according to age. Also shown are the prevalence of serum HPV-16 IgG and IgA, oncogenic cervical HPV infection, nononcogenic HPV infection, and HPV-16 infection stratified according to the age of control women. The HPV-16 IgG 95% CIs for the various prevalence rates by age are the following: <30 years, 47.6 to 71.3; 30 to 39 years, 40.2 to 53.9; 40 to 49 years, 40.4 to 51.1; >50 years, 29.7 to 41.4. The HPV-16 IgA 95% CIs for the various prevalence rates by age are the following: <30 years, 7.5 to 25.5; 30 to 39 years, 16.2 to 27.5; 40 to 49 years, 28 to 38; >50 years, 27.3 to 38.9. For nononcogenic HPV types, the 95% CIs for the various prevalence rates by age are the following: <30 years, 4.8 to 19.5; 30 to 39 years, 5.5 to 13; 40 to 49 years, 4.8 to 10.1; >50 years, 5.7 to 12.5. For oncogenic HPV types, the 95% CIs for the various prevalence rates by age are the following: <30 years, 28.6 to 50.9; 30 to 39 years, 22.1 to 33.6; 40 to 49 years, 13.6 to 21.3; >50 years, 13.1 to 22. For HPV-16 DNA, the 95% CIs for the various prevalence rates by age are the following: <30 years, 1.6 to 13.2; 30 to 39 years, 2.1 to 7.6; 40 to 49 years, 1.7 to 5.5; >50 years, 1.1 to 5.1.

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References

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