Evidence map›Paper›PMID 34409752›Full record

ArticleImmunity, inflammation and disease2021

Impaired T helper cell responses in human immunodeficiency virus-exposed uninfected newborns.

Yesenia Brito-Pérez, Rodrigo T Camacho-Pacheco, Noemi Plazola-Camacho, Diana Soriano-Becerril, Irma A Coronado-Zarco, Gabriela Arreola-Ramírez, Gabriela González-Pérez, Alma Herrera-Salazar, Julio Flores-González, Mextli Y Bermejo-Haro and 7 more

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 14 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

17 authors at 2 institutions in 1 country.

Yesenia Brito-PérezInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Rodrigo T Camacho-PachecoInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Noemi Plazola-CamachoInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Diana Soriano-BecerrilInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Irma A Coronado-ZarcoNeonatology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Gabriela Arreola-RamírezNeonatology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Gabriela González-PérezDepartment of Physiology and Cellular Development, National Institute of Perinatology (INPer), Mexico City, Mexico.
Alma Herrera-SalazarInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Julio Flores-GonzálezInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.ORCID 0000-0003-4707-718X
Mextli Y Bermejo-HaroInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Brenda G Casorla-CervantesInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Ismael A Soto-LópezInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Jessica Hernández-PinedaInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.
Claudia Sandoval-MontesDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México.
Sandra Rodríguez-MartínezDepartamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México, México.
Ricardo Figueroa-DamianInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.ORCID 0000-0002-7749-2985
Ismael Mancilla-HerreraInfectology and Immunology Department, National Institute of Perinatology (INPer), Mexico City, Mexico.ORCID 0000-0001-8195-8082
Instituto Nacional de Perinatología · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHIV-exposed uninfected (HEU) newborns suffer from higher risks of opportunistic infections during the first months of life compared to HIV-unexposed uninfected (HUU) newborns. Alterations in thymic mass, amounts of T helper (Th) cells, T-cell receptor diversity, and activation markers have been found in HEU newborns, suggesting alterations in T cell ontogeny and differentiation. However, little is known about the ability of these cells to produce specialized Th responses from CD4

methodTo characterize the Th cell profile, we evaluated the frequency of Th

resultsLower percentages of differentiated Th

conclusionHEU neonates are born with reduced proportions of differentiated Th

Indexed as

HIV InfectionsT-Lymphocytes, Helper-InducerHIVHumansInfant, NewbornInterferon-gammaInterferon-gammaHIV-exposed uninfected newbornsTh1/Th2/Th17/Treg/CD4+CD25++ T cells and Th1 differentiationTh cells

Identifiers

PMID34409752
PMCPMC8589403
OpenAlexW3195294673

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.