Evidence map›Paper›PMID 34980186›Full record

ArticleImmunity & ageing : I & A2022

The effect of age on CD4+ T-cell recovery in HIV-suppressed adult participants: a sub-study from AIDS Clinical Trial Group (ACTG) A5321 and the Bone Loss and Immune Reconstitution (BLIR) study.

Jingxian Chen, Kehmia Titanji, Anandi N Sheth, Rajesh Gandhi, Deborah McMahon, Ighovwerha Ofotokun, M Neale Weitzmann, Kristina De Paris, Julie B Dumond

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Jingxian ChenEshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. cjx7128@gmail.com.
Kehmia TitanjiDivision of Endocrinology & Metabolism & Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Anandi N ShethDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Rajesh GandhiDepartment of Infectious Disease, Massachusetts General Hospital and Ragon Institute, Boston, MA, USA.
Deborah McMahonDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Ighovwerha OfotokunDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
M Neale WeitzmannDivision of Endocrinology & Metabolism & Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Kristina De ParisDepartment of Microbiology & Immunology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Julie B DumondEshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. jdumond@unc.edu.ORCID http://orcid.org/0000-0002-3500-5819
Emory University · USUniversity of North Carolina at Chapel Hill · USRagon Institute of MGH, MIT and Harvard · USUniversity of Pittsburgh · US

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Neuro HPA Project 1U54AG062334 · NIA · EMORY UNIVERSITY · PI Ighovwerha Ofotokun · 2018 to 2026
$12.2M
Effect of HIV Infection and HAART on Bone HomeostasisR01AR059364 · NIAMS · EMORY UNIVERSITY · PI OFOTOKUN, IGHOVWERHA, WEITZMANN, MERVYN NEALE · 2009 to 2013
$3.2M
IL-4, a key regulator of bone turnover in HIV and ARTR01AR070091 · NIAMS · EMORY UNIVERSITY · PI OFOTOKUN, IGHOVWERHA, WEITZMANN, MERVYN NEALE · 2016 to 2020
$3.2M
Bone Loss and Immune Reconstitution in HIV/AIDSR01AG040013 · NIA · EMORY UNIVERSITY · PI OFOTOKUN, IGHOVWERHA, WEITZMANN, MERVYN NEALE · 2011 to 2015
$2.8M
Characterization and modulation of mucosal immunity for HIV prevention in womenK23AI114407 · NIAID · EMORY UNIVERSITY · PI SHETH, ANANDI NAYAN · 2014 to 2018
$898k
Reversing HIV-induced B cell dysfunction with bisphosphonatesK01HL131333 · NHLBI · EMORY UNIVERSITY · PI TITANJI, KEHMIA NUBONYIN · 2016 to 2020
$591k
Immune Regulation of Bone HomeostasisI01BX000105 · VA · VETERANS HEALTH ADMINISTRATION · PI WEITZMANN, MERVYN NEALE · 2009 to 2022
–
Biomedical Laboratory Research and Development, VA Office of Research and Development 5I01BX000105BLRD VA I01 BX000105National Institute of Allergy and Infectious Diseases K23AI11440NHLBI NIH HHS K01 HL131333NHLBI NIH HHS K01HL131333NIAID NIH HHS K23 AI114407NIAID NIH HHS P30 AI050410NIAMS NIH HHS R01 AR059364NIAMS NIH HHS R01AR059364, R01AR070091 and R01AR06815NIAMS NIH HHS R01 AR070091NIA NIH HHS R01 AG040013NIA NIH HHS R01AG040013, U54AG062334NIA NIH HHS U54 AG062334
6 · The paper itself

Abstract

Older age could be a risk factor for suboptimal CD4+ T-cell recovery in HIV-infected patients despite successful viral suppression. However, evaluation of this effect could be confounded by age-related immune processes such as decreased thymus output, increased immune activation and exhaustion. Here, we established a semi-mechanistic population model simultaneously describing naïve and memory CD4+ T-cell trajectories in 122 participants. Covariate analysis accounting for immune activation showed that older age was significantly associated with faster apparent elimination rate of the naïve T-cells. In addition, female sex predicted slower apparent elimination rate of memory T-cells. Simulations showed that the median maximal CD4+ T-cell count on ART treatment was 593 cells/μL (IQR 442-794) in patients aged 50 years or above and 738 cells/μL (IQR 548-1002) in patients aged 18-35 years. The differences in the percentage of subjects achieving sufficient immune reconstitution (CD4+ T-cell count> 500 cells/μL) between the two age groups were 15, 21 and 26% at year 1, 4 years and steady state, respectively, suggesting that advanced age may have a greater impact on long-term CD4+ T-cell recovery.

Indexed as

AgingHIVImmune recoveryNonlinear mixed effects modelingPharmacodynamic modeling

Identifiers

PMID34980186
PMCPMC8722153
OpenAlexW4206241463

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.