Loss of correlation between HIV viral load and CD4+ T-cell counts in HIV/HTLV-1 co-infection in treatment naïve Mozambican patients

Author:

Bhatt N B1,Gudo E S1,Semá C1,Bila D1,Di Mattei P2,Augusto O1,Garsia R34,Jani I V1

Affiliation:

1. Department of Immunology, Instituto Nacional de Saúde, Maputo, Mozambique

2. HIV Outpatient Clinic, Alto Maé Health Centre, Médecins Sans Frontières-Switzerland (MSF-CH), Maputo, Mozambique

3. Department of Medicine, University of Sydney, New South Wales, Australia

4. Department of Clinical Immunology, Royal Prince Alfred Hospital, Camperdown, NSW, Australia

Abstract

Seven hundred and four HIV-1/2-positive, antiretroviral therapy (ART) naïve patients were screened for HTLV-1 infection. Antibodies to HTLV-1 were found in 32/704 (4.5%) of the patients. Each co-infected individual was matched with two HIV mono-infected patients according to World Health Organization clinical stage, age ±5 years and gender. Key clinical and laboratory characteristics were compared between the two groups. Mono-infected and co-infected patients displayed similar clinical characteristics. However, co-infected patients had higher absolute CD4+ T-cell counts ( P = 0.001), higher percentage CD4+ T-cell counts ( P < 0.001) and higher CD4/CD8 ratios ( P < 0.001). Although HIV plasma RNA viral loads were inversely correlated with CD4+ T-cell-counts in mono-infected patients ( P < 0.0001), a correlation was not found in co-infected individuals ( P = 0.11). Patients with untreated HIV and HTLV-1 co-infection show a dissociation between immunological and HIV virological markers. Current recommendations for initiating ART and chemoprophylaxis against opportunistic infections in resource-poor settings rely on more readily available CD4+ T-cell counts without viral load parameters. These guidelines are not appropriate for co-infected individuals in whom high CD4+ T-cell counts persist despite high HIV viral load states. Thus, for co-infected patients, even in resource-poor settings, HIV viral loads are likely to contribute information crucial for the appropriate timing of ART introduction.

Publisher

SAGE Publications

Subject

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

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