Naive B Cell Output in HIV-Infected and HIV-Uninfected Children

AIDS Res Hum Retroviruses. 2019 Jan;35(1):33-39. doi: 10.1089/AID.2018.0170. Epub 2018 Dec 26.

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.

Keywords: ART; HIV; KRECs; bone marrow; child; naive B cell output.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Retroviral Agents / therapeutic use*
  • B-Lymphocytes / chemistry
  • B-Lymphocytes / immunology*
  • Cell Proliferation*
  • Child
  • Child, Preschool
  • Cohort Studies
  • DNA / analysis
  • Female
  • Flow Cytometry
  • HIV Infections / drug therapy*
  • HIV Infections / immunology*
  • Humans
  • Immunity, Cellular*
  • Infant
  • Infant, Newborn
  • Ki-67 Antigen / analysis
  • Male
  • Models, Theoretical
  • South Africa

Substances

  • Anti-Retroviral Agents
  • Ki-67 Antigen
  • MKI67 protein, human
  • DNA