Evidence map›Paper›PMID 36727571›Full record

ArticleJournal of the Pediatric Infectious Diseases Society2023

Transient Viral Rebound in Children with Perinatally Acquired HIV-1 Induces a Unique Soluble Immunometabolic Signature Associated with Decreased CD4/CD8 Ratio.

Laura Tarancon-Diez, Joaquim Peraire, Santiago Jiménez de Ory, Maria Guirro, Luis Escosa, Luis Manuel Prieto Tato, María Penín Antón, Ana Isabel Piqueras, Álvaro Vázquez Pérez, César Gavilán and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Pediatric Infectious Diseases Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

16 authors at 11 institutions in 1 country.

Laura Tarancon-DiezMolecular Immunology Laboratory, Hospital General Universitario Gregorio Marañón, Health Research Institute Gregorio Marañón (IiSGM), Madrid, Spain.
Joaquim PeraireUniversitat Rovira i Virgili, Tarragona, Spain.
Santiago Jiménez de OryCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Maria GuirroCentre for Omic Sciences, Eurecat, Centre Tecnològic de Catalunya (Joint Unit Eurecat-Universitat Rovira i Virgili), Unique Scientific and Technical Infrastructure (ICTS), 43204 Reus, Spain.
Luis EscosaCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Luis Manuel Prieto TatoServicio de Pediatría, Hospital Universitario 12 de Octubre e Instituto de Investigación I+12, 28041, Madrid, Spain.
María Penín AntónServicio de pediatría, Hospital Universitario Príncipe de Asturias, Alcalá de Henares, Spain.
Ana Isabel PiquerasPediatric Infectious Diseases Unit, Hospital Universitario y Politécnico La Fe, Hospital La Fe, Valencia, Spain.
Álvaro Vázquez PérezDepartment of Pediatrics, Virgen de las Nieves Children's Hospital, Granada, Spain.
César GavilánServicio de Pediatría, Hospital San Juan de Alicante, Sant Joan d'Alacant, Spain.
Matilde Bustillo-AlonsoServicio de Pediatría. Enfermedades Infecciosas, Hospital Universitario Miguel Servet, Zaragoza, Spain.
María Luisa NavarroCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Consuelo ViladésUniversitat Rovira i Virgili, Tarragona, Spain.
Francesc VidalUniversitat Rovira i Virgili, Tarragona, Spain.
Anna RullUniversitat Rovira i Virgili, Tarragona, Spain.
María Ángeles Muñoz-FernándezMolecular Immunology Laboratory, Hospital General Universitario Gregorio Marañón, Health Research Institute Gregorio Marañón (IiSGM), Madrid, Spain.
Centro de Investigación Biomédica en Red · ESInstituto de Salud Carlos III · ESCentre for Omic Sciences · ESHospital General Universitario Gregorio Marañón · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario 12 De Octubre · ESHospital Universitario Miguel Servet · ESHospital Universitario Príncipe de Asturias · ESHospital Universitario Virgen de las Nieves · ESHospital Universitari Sant Joan D'Alacant · ESUniversidad Rovira i Virgili · ES

Funding

Bioingeniería, Biomateriales y Nanomedicina CB22/01/00041Centro de Investigación Biomédica en Red de Enfermedades Infecciosas CB21/13/00020Fondo de Investigacion Sanitaria PI19/01337Programa de Intensificación de Investigadores INT20/00031Spanish National AIDS Network RIS-EPICLIN-06/2017
6 · The paper itself

Abstract

backgroundTo determine by multi-omic analysis changes in metabolites, lipids, and proteins as a consequence of transient viral rebound (tVR) in children with perinatally acquired HIV-1 (PHIV).

methodsPlasma samples from children with PHIV and with tVR (first episode of transient RNA-HIV viral load >20 copies/ml followed by suppression) on the time-point immediately before (pre-tVR) and after (post-tVR) the tVR were assessed. Multi-omic analyses were performed using nLC-Orbitrap, GC-qTOF-MS, and LC-qTOF-MS.

resultsComparing pre- and post-tVR time-points, HIV-1 children with tVR (n = 5) showed a trend to a decrease in ratio CD4/CD8 (p = 0.08) but no significant differences were observed in plasma metabolites, lipids, or proteins. Post-tVR condition was compared with a reference group of children with PHIV with persistent viral control (n = 9), paired by sex, age, and time under antiretroviral treatment. A total of 10 proteins, 8 metabolites, and 2 lipids showed significant differences (p < 0.05): serotransferrin, clusterin, kininogen-1, succinic acid, threonine, 2-hydroxyisovaleric acid, methionine, 2-hydroxyglutaric, triacylglyceride 50:0 (TG50:0), and diacylglyceride 34:1 (DG34:1) were upregulated while alpha-2-macroglobulin, apolipoprotein A-II, carboxylic ester hydrolase, apolipoprotein D, coagulation factor IX, peptidase inhibitor 16, SAA2-SAA4 readthrough, oleic acid, palmitoleic acid, and D-sucrose downregulated on post-tVR time-point compared to the reference group. Ratio CD4/CD8 correlated with apolipoprotein A-II, DG34:1, and methionine (p = 0.004; ρ = 0.71, p = 0.016; ρ = -0.63; and p = 0.032; ρ = -0.57, respectively). Nadir CD4+ correlated inversely with kininogen-1 (p = 0.022; ρ = -0.60) and positively with D-sucrose (p = 0.001; ρ = 0.77).

conclusionstVR followed by suppression implies changes in soluble proteins, lipids, and metabolites that correlate with immunological parameters, mainly ratio CD4/CD8, that decreased after tVR. These distinct soluble biomarkers could be considered potential biomarkers of immune progression.

Indexed as

HIV-1HIV InfectionsHIV SeropositivityApolipoprotein A-IIBiomarkersCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildHumansMethionineViral LoadApolipoprotein A-IIBiomarkersMethionineomicsratio CD4/CD8vertically HIV-1 childrenviral rebounds

Identifiers

PMID36727571
PMCPMC10112677
OpenAlexW4318897418

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.