Naive B Cell Output in HIV-Infected and HIV-Uninfected Children.
Anti-Retroviral Agents
/ therapeutic use
B-Lymphocytes
/ chemistry
Cell Proliferation
Child
Child, Preschool
Cohort Studies
DNA
/ analysis
Female
Flow Cytometry
HIV Infections
/ drug therapy
Humans
Immunity, Cellular
Infant
Infant, Newborn
Ki-67 Antigen
/ analysis
Male
Models, Theoretical
South Africa
ART
HIV
KRECs
bone marrow
child
naive B cell output
Journal
AIDS research and human retroviruses
ISSN: 1931-8405
Titre abrégé: AIDS Res Hum Retroviruses
Pays: United States
ID NLM: 8709376
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
pubmed:
10
10
2018
medline:
30
1
2020
entrez:
10
10
2018
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30298747
doi: 10.1089/AID.2018.0170
pmc: PMC6863188
doi:
Substances chimiques
Anti-Retroviral Agents
0
Ki-67 Antigen
0
MKI67 protein, human
0
DNA
9007-49-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
33-39Subventions
Organisme : Wellcome Trust
ID : 095182/Z/10/Z
Pays : United Kingdom
Références
PLoS Med. 2013 Oct;10(10):e1001542
pubmed: 24204216
J Immunol. 2009 Oct 1;183(7):4329-36
pubmed: 19734223
N Engl J Med. 2008 Nov 20;359(21):2233-44
pubmed: 19020325
J Vis Exp. 2014 Dec 06;(94):null
pubmed: 25549107
J Immunol. 1984 Oct;133(4):1710-5
pubmed: 6206131
J Transl Med. 2013 Aug 14;11:188
pubmed: 23941115
Proc Biol Sci. 2015 Dec 22;282(1821):20143085
pubmed: 26702035
S Afr Med J. 2015 Sep 21;105(7):589-95
pubmed: 26428758
J Transl Med. 2012 May 16;10:94
pubmed: 22591651
Clin Diagn Lab Immunol. 2004 Nov;11(6):1002-7
pubmed: 15539497
Immunology. 2005 Sep;116(1):1-12
pubmed: 16108812
Lancet. 2013 Nov 9;382(9904):1555-63
pubmed: 24209829
Annu Rev Microbiol. 1996;50:825-54
pubmed: 8905100
AIDS. 2014 Jan 14;28(2):209-14
pubmed: 24072195
J Immunol. 2007 Jun 15;178(12):8212-20
pubmed: 17548660
Mol Cell Biol. 1996 Feb;16(2):609-18
pubmed: 8552089
Stem Cells. 2004;22(6):1111-20
pubmed: 15536200
J Immunol. 2013 Apr 15;190(8):3985-93
pubmed: 23475214
Blood. 2004 Mar 15;103(6):2180-6
pubmed: 14604962