Evidence map›Paper›PMID 30298747›Full record

ArticleAIDS research and human retroviruses2019

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

Helen Payne, Gabriel Chain, Stuart Adams, Patricia Hunter, Natasha Luckhurst, Kimberly Gilmour, Joanna Lewis, Abdel Babiker, Mark Cotton, Avy Violari and 3 more

Open access · hybridAbstract read
In one paragraph

Article in AIDS research and human retroviruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 55% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Helen Payne1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Gabriel Chain1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Stuart Adams1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Patricia Hunter1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Natasha Luckhurst1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Kimberly Gilmour1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Joanna Lewis1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Abdel Babiker1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Mark Cotton5 Children's Infectious Diseases Clinical Research Unit, Department of Paediatrics and Child Health, Stellenbosch University, Cape Town, South Africa.
Avy Violari6 Perinatal HIV Research Unit, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Diana Gibb1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Robin Callard1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Nigel Klein1 UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Great Ormond Street Hospital · GBUniversity College London · GBPerinatal HIV Research Unit · ZAStellenbosch University · ZA

Funding

Wellcome Trust 095182/Z/10/Z
6 · The paper itself

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.

Indexed as

Cell ProliferationImmunity, CellularAnti-Retroviral AgentsB-LymphocytesChildChild, PreschoolCohort StudiesDNAFemaleFlow CytometryHIV InfectionsHumansInfantInfant, NewbornKi-67 AntigenMaleAnti-Retroviral AgentsDNAKi-67 AntigenMKI67 protein, humanARTbone marrowchildHIVKRECsnaive B cell output

Identifiers

PMID30298747
PMCPMC6863188
OpenAlexW2897360194

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.