Evidence map›Paper›PMID 33248366›Full record

ArticleCellular immunology2021

Age-related changes in PD-1 expression coincide with increased cytotoxic potential in Vδ2 T cells during infancy.

Haoting Hsu, Sarah Boudova, Godfrey Mvula, Titus H Divala, David Rach, Randy G Mungwira, Francesca Boldrin, Giulia Degiacomi, Riccardo Manganelli, Miriam K Laufer and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 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
0.4field-weighted citation impact, top 40% 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, 12 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

11 authors at 3 institutions in 4 countries.

Haoting HsuInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, United States.
Sarah BoudovaCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, United States.
Godfrey MvulaBlantyre Malaria Project, University of Malawi College of Medicine, Blantyre, Malawi.
Titus H DivalaBlantyre Malaria Project, University of Malawi College of Medicine, Blantyre, Malawi.
David RachMolecular Microbiology and Immunology Graduate Program, University of Maryland School of Medicine, Baltimore, MD, United States.
Randy G MungwiraBlantyre Malaria Project, University of Malawi College of Medicine, Blantyre, Malawi.
Francesca BoldrinDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Giulia DegiacomiDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Riccardo ManganelliDepartment of Molecular Medicine, University of Padova, Padova, Italy.
Miriam K LauferCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, United States.
Cristiana CairoInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, United States. Electronic address: ccairo@ihv.umaryland.edu.
University of Maryland, Baltimore · USUniversity of Malawi · MWUniversity of Padua · IT

Funding

Antigen exposure in utero: impacts on newborn immunity and infectious diseasesR01AI104702 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CAIRO, CRISTIANA · 2013 to 2016
$1.5M
NIAID NIH HHS R01 AI104702
6 · The paper itself

Abstract

Human Vγ9Vδ2 T cells respond to several diverse pathogens by sensing microbial cholesterol intermediates. Unlike CD4 T cells, they are poised for rapid Th1-like responses even before birth, which allows them to play a key role in the first line of defense against pathogens in early life. However, their regulation and functional maturation during infancy (in particular the acquisition of cytotoxic potential) remain understudied. We thus characterized their responses to cholesterol intermediates and Bacille Calmette-Guérin in a cohort of African neonates and 12-month-old infants. Infant Vδ2 lymphocytes exhibited intermediate or adult-like expression of markers associated with differentiation or function, intermediate proliferative responses, and adult-like cytotoxic potential. The enhancement of Vδ2 cell cytotoxic potential coincided with decreasing PD-1 and increasing NKG2A expression. Our results are consistent with the hypothesis that switching from a PD-1

Indexed as

AdultAge FactorsCell DifferentiationCells, CulturedCordocentesisFemaleFetal BloodGene ExpressionHumansInfantInfant, NewbornInterferon-gammaLymphocyte ActivationMalawiMaleNK Cell Lectin-Like Receptor Subfamily CInterferon-gammaKLRC1 protein, humanNK Cell Lectin-Like Receptor Subfamily CPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, Antigen, T-Cell, gamma-deltaBCGCord bloodCytotoxic potentialGammadelta T cellsInfantPD-1

Identifiers

PMID33248366
PMCPMC7811364
OpenAlexW3104238262

What OpenQuestion holds

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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.