Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015;1(3):196-202.
doi: 10.1016/S2055-6640(20)30501-X. Epub 2015 Jun 30.

Soluble CD163 and monocyte populations in response to antiretroviral therapy and in relationship with neuropsychological testing among HIV-infected children

Affiliations

Soluble CD163 and monocyte populations in response to antiretroviral therapy and in relationship with neuropsychological testing among HIV-infected children

Jintanat Ananworanich et al. J Virus Erad. 2015.

Abstract

Background: Monocytes play a central role in HIV neuropathogenesis, but there are limited data on monocyte subsets and markers of monocyte activation in perinatally HIV-infected children.

Objective: To determine the relationship between monocyte subsets, the sCD163 monocyte activation marker, and neuropsychological performance among perinatally HIV-infected children initiating antiretroviral therapy (ART).

Methods: ART-naïve children from the PREDICT study were categorised into two groups: those on ART for ≥24 weeks (ART group, n =201) and those untreated (no ART group, n =79). This analysis used data from the baseline and week 144 including sCD163 and frequencies of activated monocytes (CD14+/CD16+/HLA-DR+), perivascular monocytes (CD14+/CD16+/CD163+ and CD14low/CD16+/CD163+), and neuropsychological testing scores: Verbal and Performance Intelligence Quotient (VIQ and PIQ), Beery Visuomotor Integration (VMI) and Children's Color Trails 2 (CT2).

Results: Baseline demographic and HIV disease parameters were similar between groups. The median age was 6 years, CD4 was 20% (620 cells/mm3), and HIV RNA was 4.8 log10. By week 144, the ART vs the no ART group had significantly higher CD4 (938 vs 552 cells/mm3) and lower HIV RNA (1.6 vs 4.38 log10 copies/mL, P <0.05). sCD163 declined in the ART vs no ART group (median changes -2533 vs -159 ng/mL, P <0.0001). Frequencies of all monocyte subsets declined in the treated but not the untreated group (P <0.05). Higher CD14+/CD16+/HLA-DR+ percentage was associated with higher VIQ, Beery VMI and CT2 scores. Higher percentages of CD14+/CD16+/CD163+ and CD14low/CD16+/CD163+ were associated with higher CT2 and VIQ, respectively.

Conclusion: ART significantly reduced sCD163 levels and frequencies of activated and perivascular monocytes. Higher frequencies of these cells correlated with better neuropsychological performance suggesting a protective role of monocyte-macrophage immune activation in perinatal HIV infection in terms of neuropsychological function.

Keywords: ART; HIV; children; immune activation; monocyte; neurocognition; neuropsychological testing; sCD163.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Soluble CD163 (sCD163) and monocyte subsets at baseline and week 144 in children who are on ART vs those not on ART. (a) sCD163 levels; (b) Frequency of CD14+/CD16+/HLA-DR+ cells; (c): Frequency of CD14+/CD16+/CD163+ cells: (d) Frequency of CD14low/CD16+/CD163+ cells NB: There were 201 children in the ART group (●) and 78 in the no ART group (♦)
Figure 2.
Figure 2.
The associations between verbal intelligence quotient (VIQ) scores and sCD163 and monocyte subsets at week 144 (a) VIQ vs sCD163 levels; (b) VIQ vs frequency of CD14+/CD16+/HLA-DR+ cells; (c) VIQ vs frequency of CD14+/CD16+/CD163+ cells; (d) VIQ vs. frequency of CD14low/CD16+/CD163+ cells. NB: There were 201 children in the ART group (●) and 78 in the no ART group (♦)

Similar articles

Cited by

References

    1. Brahmbhatt H, Boivin M, Ssempijja V et al. . Neurodevelopmental benefits of antiretroviral therapy in Ugandan children aged 0–6 years with HIV. J Acquir Immune Defic Syndr 2014; 67: 316– 322. - PMC - PubMed
    1. Puthanakit T, Ananworanich J, Vonthanak S et al. . Cognitive function and neurodevelopmental outcomes in HIV-infected Children older than 1 year of age randomized to early versus deferred antiretroviral therapy: the PREDICT neurodevelopmental study. Pediatr Infect Dis J 2013; 32: 501– 508. - PMC - PubMed
    1. Smith R and Wilkins M.. Perinatally acquired HIV infection: long-term neuropsychological consequences and challenges ahead. Child Neuropsychol 2015; 21: 234– 268. - PubMed
    1. Laughton B, Cornell M, Boivin M and Van Rie A.. Neurodevelopment in perinatally HIV-infected children: a concern for adolescence. J Int AIDS Soc 2013; 16: 18603. - PMC - PubMed
    1. Laughton B, Cornell M, Grove D et al. . Early antiretroviral therapy improves neurodevelopmental outcomes in infants. AIDS 2012; 26: 1685– 1690. - PMC - PubMed

LinkOut - more resources