High Prevalence of High-Risk Human Papillomavirus Genotypes Other Than HPV-16 and HPV-18 in Congolese Women Living With HIV: Implication for Cervical Cancer Prevention in a Resource Limited Setting

Authors

  • Maryse N Akolbout Manguilla Marien Ngouabi University Faculty of health Sciences, Brazzaville, Congo Author
  • Christ Arcel Massamba Ndala Outpatient Treatment Center; Brazzaville, Congo Author
  • Rocide Moukouba Outpatient Treatment Center; Brazzaville, Congo Author
  • Rocide Moukouba Outpatient Treatment Center; Brazzaville, Congo Author
  • Laure Ghoma Linguissi National Institute for Health Sciences Research; Brazzaville, Congo Author
  • Valchy Miegakanda National Public Health Laboratory; Brazzaville, Congo Author
  • Norcely Makela Outpatient Treatment Center; Brazzaville, Congo Author
  • Ralph-Sydney Mboumba Bouassa Central African Regional Doctoral School (EDR) in Tropical Infectious Diseases Franceville, Gabon Author
  • Edith-Sophie Kombo Bayonne Marien Ngouabi University Faculty of health Sciences, Brazzaville, Congo Author
  • Jean Félix Peko National Institute for Health Sciences Research; Brazzaville, Congo Author

DOI:

https://doi.org/10.47363/JVRR/2023(4)158

Keywords:

High-Risk Human Papillomavirus Genotypes, HPV16, HPV-18, Cervical Cancer, CD4 T Cells Count, HIV RNA Load, Women Living With HIV

Abstract

Background: Despite the undeniable benefits provided by antiretroviral therapy (ART) in drastically reducing AIDS-related mortality, women living with HIV (WLWH) are disproportionately affected by high-risk Human Papillomavirus (HR-HPV) infection and cervical cancer. We herein assessed the distribution of HR-HPV genotypes according to HIV immunovirological prognostic parameters and their implications for the prevention of cervical cancer.

Methods: Among 276 screened WLWH on ART attending the HIV outpatient treatment clinic in Brazzaville, in the Republic of Congo, 122 tested positive for HR-HPV (mean age: 43.92 ± 9.98 years) were included in a cross-sectional study. Sociodemographic and clinical information were collected and CD4+ T cells count and HIV RNA load were determined. HR-HPV genotypes distribution was determined from cervicovaginal samples using the ABBOTT Real Time High Risk HPV kit (Abbott, Chicago, USA).

Results: A total of 122 (44.4%) WLWH were tested positive for any-HR-HPV, including 73.8% of HR-HPV genotypes other than HPV-16/HPV-18, while HPV-16 (14.7%) and HPV-18 (11.5%) were less frequently detected. Overall, nor CD4+ T cells count, HIV-1 RNA load or the duration of HIV diagnosis did have a significant impact in the distribution of HR-HPV genotypes in WLWH positive for cervical HR-HPV infection. However, around half of all HPV-16 infections occurred in women with the highest CD4+ T cells count (≥500 CD4+ T cells/μL). On the other hand, women with lower CD4+ T cells count (200 to 349 cells/μL) were more likely to carry HPV-18 DNA and HR-HPV genotypes other than HPV-16.

Conclusion: WLWH in Brazzaville in the Republic of Congo are largely infected by HR-HPV genotypes other than HPV-16 and HPV-18, suggesting a possible reduced predictive efficacy of HPV vaccine in this population. A secondary prevention with a regular screening for cervical pre-cancerous lesions should be prioritized in WLWH living in Brazzaville, in the Republic of Congo. 

Author Biographies

  • Maryse N Akolbout Manguilla, Marien Ngouabi University Faculty of health Sciences, Brazzaville, Congo

    Maryse N Akolbout Manguilla, Marien Ngouabi University Faculty of health Sciences; Brazzaville, Congo

  • Christ Arcel Massamba Ndala, Outpatient Treatment Center; Brazzaville, Congo

    Outpatient Treatment Center; Brazzaville, Congo

  • Rocide Moukouba, Outpatient Treatment Center; Brazzaville, Congo

    Outpatient Treatment Center; Brazzaville, Congo

  • Rocide Moukouba, Outpatient Treatment Center; Brazzaville, Congo


    Outpatient Treatment Center; Brazzaville, Congo

  • Laure Ghoma Linguissi, National Institute for Health Sciences Research; Brazzaville, Congo

    National Institute for Health Sciences Research; Brazzaville, Congo

  • Valchy Miegakanda, National Public Health Laboratory; Brazzaville, Congo

    National Public Health Laboratory; Brazzaville, Congo

  • Norcely Makela, Outpatient Treatment Center; Brazzaville, Congo

    Outpatient Treatment Center; Brazzaville, Congo

  • Ralph-Sydney Mboumba Bouassa, Central African Regional Doctoral School (EDR) in Tropical Infectious Diseases Franceville, Gabon

    Central African Regional Doctoral School (EDR) in Tropical Infectious Diseases Franceville, Gabon

  • Edith-Sophie Kombo Bayonne, Marien Ngouabi University Faculty of health Sciences, Brazzaville, Congo

    Marien Ngouabi University Faculty of health Sciences, Brazzaville, Congo

  • Jean Félix Peko, National Institute for Health Sciences Research; Brazzaville, Congo

    National Institute for Health Sciences Research; Brazzaville, Congo 

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Published

2023-12-20