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Phenotypic characterization of NK cells in 5-year-old children exposed to maternal HIV and antiretroviral therapy in early-life.
- Source :
-
BMC immunology [BMC Immunol] 2024 Dec 19; Vol. 25 (1), pp. 82. Date of Electronic Publication: 2024 Dec 19. - Publication Year :
- 2024
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Abstract
- Background: HIV-exposed uninfected (HEU) children are at increased risk of morbidity during the first years of life. Although the immune responses of HEU infants in early-life are relatively well described, studies of natural killer (NK) cells in older HEU children are lacking. NK cell subsets were analysed in HEU children and compared to those in HIV unexposed uninfected (HUU) children aged ~ five years.<br />Methods: Multi-parametric flow cytometry was used to characterize peripheral blood-derived NK cell CD56, CD16, CD57, NKG2A and KIR3DL1/KIR2DL2/L3 expression, including intracellular perforin and granzyme B. NK cell subsets were compared between HEU children exposed to prenatal antiretroviral therapy (ART) from conception [long-term (HEULT)]; those exposed to ART during pregnancy [medium-term (HEUMT)] with continued exposure throughout the breastfeeding period and HUU peers. Furthermore, clinical data of the children, including sick clinic visits and hospitalizations documented in morbidity diaries from birth to 5 years were compared between HEU and HUU groups. Frequencies of CD56 <superscript>bright</superscript> and CD56 <superscript>dim</superscript> NK cell were correlated with these clinical parameters.<br />Results: 139 children were enrolled however, 133 comprising 43 HEULT, 38 HEUMT and 52 HUU were included in the main analyses. Total NK cell, CD56 <superscript>bright</superscript> nor CD56 <superscript>dim</superscript> NK cell proportions differed between HEU and HUU children. However, HEULT children had lower frequencies of CD56 <superscript>dim</superscript> NK cells compared to HEUMT children, (p = 0.002) which maintained significance after controlling for preterm birth, p = 0.012. No differences were observed between HEULT and HUU. The expressions of NKG2A, KIR3DL1/KIR2DL2/L3 and CD57 on CD56 <superscript>bright</superscript> and CD56 <superscript>dim</superscript> NK cells were similar between the three groups. Furthermore, the frequencies of granzyme B and perforin double positive NK cells were similar between the HUU with HEULT and HEUMT children. CD56 <superscript>dim</superscript> NK cell counts had a significant moderate negative correlation with recurrent respiratory infections (rho=-0.38; p = 0.010) in HUU children and negatively correlated with total sick clinic visits in HEUMT (rho=-0.40, p = 0.064).<br />Conclusion: The proportions of total NK cell, CD56 <superscript>bright</superscript> and CD56 <superscript>dim</superscript> NK cells, NK cells inhibitory and differentiation surface marker expression and cytolytic granule-positive cells were similar between HEU and HUU children. These data suggest that early-life HIV/ART exposure may not result in major changes in NK cell subsets at 5 years of age.<br />Competing Interests: Declarations. Ethics approval: This study was approved by the Joint Research Ethics Committee for the University of Zimbabwe College of Health Sciences and Parirenyatwa Group Hospitals (JREC/81/20) and the Medical Research Council of Zimbabwe (MRCZ/A/2662). Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Female
Pregnancy
Child, Preschool
Male
Granzymes metabolism
Perforin metabolism
Prenatal Exposure Delayed Effects immunology
Immunophenotyping
Infant
Infant, Newborn
Anti-Retroviral Agents therapeutic use
CD56 Antigen metabolism
Receptors, KIR3DL1 metabolism
Pregnancy Complications, Infectious drug therapy
Pregnancy Complications, Infectious immunology
HIV-1 immunology
Killer Cells, Natural immunology
HIV Infections drug therapy
HIV Infections immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1471-2172
- Volume :
- 25
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- BMC immunology
- Publication Type :
- Academic Journal
- Accession number :
- 39702040
- Full Text :
- https://doi.org/10.1186/s12865-024-00674-4