| Literature DB >> 30298747 |
Helen Payne1,2, Gabriel Chain1, Stuart Adams1, Patricia Hunter1, Natasha Luckhurst1,3, Kimberly Gilmour1, Joanna Lewis1,4, Abdel Babiker1, Mark Cotton5, Avy Violari6, Diana Gibb1, Robin Callard1, Nigel Klein1.
Abstract
In this study, we aimed to quantify KREC (kappa-deleting recombination excision circle) levels and naive B cell output in healthy HIV-uninfected children, compared with HIV-infected South African children, before and after starting ART (antiretroviral therapy). Samples were acquired from a Child Wellness Clinic (n = 288 HIV-uninfected South African children, 2 weeks-12 years) and the Children with HIV Early Antiretroviral Therapy (CHER) trial (n = 153 HIV-infected South African children, 7 weeks-8 years). Naive B cell output was estimated using a mathematical model combining KREC levels to reflect B cell emigration into the circulation, flow cytometry measures of naive unswitched B cells to quantify total body naive B cells, and their rates of proliferation using the intracellular marker Ki67. Naive B cell output increases from birth to 1 year, followed by a decline and plateau into late childhood. HIV-infected children on or off ART had higher naive B cell outputs than their uninfected counterparts (p = .01 and p = .04). This is the first study to present reference ranges for measurements of KRECs and naive B cell output in healthy and HIV-infected children. Comparison between HIV-uninfected healthy children and HIV-infected children suggests that HIV may increase naive B cell output. Further work is required to fully understand the mechanisms involved and clinical value of measuring naive B cell output in children.Entities:
Keywords: ART; HIV; KRECs; bone marrow; child; naive B cell output
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Year: 2018 PMID: 30298747 PMCID: PMC6863188 DOI: 10.1089/AID.2018.0170
Source DB: PubMed Journal: AIDS Res Hum Retroviruses ISSN: 0889-2229 Impact factor: 2.205