Older age at infection and nulliparity are associated with long-term non-progression in female sex workers infected with non-subtype B HIV-1

Author:

Mochache Vernon1ORCID,Richardson Barbra A1,Masese Linnet N1,Graham Susan M1,Mandaliya Kishorchandra1,Kinuthia John23,Jaoko Walter3,Overbaugh Julie4,McClelland R Scott5

Affiliation:

1. University of Maryland, Center for International Health, Education and Biosecurity, Nairobi, Kenya

2. Kenyatta National Hospital, Department of Research, Nairobi, Kenya

3. University of Nairobi, Faculty of Medicine, Nairobi, Kenya

4. Fred Hutchison Cancer Research Center, Seattle, Washington, USA

5. University of Washington, Department of Epidemiology, Seattle, Washington, USA

Abstract

Studies have reported on HIV-infected, antiretroviral therapy (ART)-naïve individuals who show minimal disease progression despite prolonged infection. The characteristics of these long-term non-progressors (LTNPs) are not well-characterized in populations predominantly infected with non-subtype B HIV-1. Female sex workers in Mombasa, Kenya who acquired HIV-1 were studied to ascertain immunologic disease progression. Long-term non-progression was defined as an ART-naïve duration of infection ≥7 years and a majority of CD4+ cell counts ≥600 cells/µl with a non-declining CD4+ trend. Correlates of long-term non-progression were determined using multivariable logistic regression. Between February 1993 and March 2014, 332 women acquired HIV-1. Of these, 77 (23%) had ≥7 years of follow-up and 13 (17%) were categorized as LTNPs. Factors associated with long-term non-progression included age >30 years at infection (aOR = 9.41, 95% CI: 1.48–59.86, P = 0.005) and nulliparity (aOR = 20.19, 95% CI: 1.36–299.90, P = 0.03). Each log10 copies/ml increase in viral load (VL) set point was associated with a lower likelihood of being a LTNP (aOR = 0.31, 95% CI: 0.12–0.79, P = 0.01). These findings suggest that age and parity may influence the likelihood of long-term non-progression through mechanisms that are not mediated by the effects of these variables on VL. Future studies should seek to determine whether the associations presented are reproducible.

Funder

National Institute of Allergy and Infectious Diseases

University of Washington Centre for AIDS Research

National Institute of Child Health and Human Development

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Public Health, Environmental and Occupational Health,Dermatology

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