Evidence map›Paper›PMID 39321807›Full record

ArticleImmunity2024

Multidimensional profiling of human T cells reveals high CD38 expression, marking recent thymic emigrants and age-related naive T cell remodeling.

Pavla Bohacova, Marina Terekhova, Petr Tsurinov, Riley Mullins, Kamila Husarcikova, Irina Shchukina, Alina Ulezko Antonova, Barbora Echalar, Jan Kossl, Adam Saidu and 14 more

Abstract read
In one paragraph

Article in Immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  10. Immune responses in aging adults.The Journal of clinical investigation · 2026
    Review
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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

24 authors.

Pavla BohacovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Marina TerekhovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Petr TsurinovJetBrains Research, Paphos 8021, Cyprus.
Riley MullinsDepartment of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Kamila HusarcikovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Irina ShchukinaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Alina Ulezko AntonovaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Barbora EchalarDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jan KosslDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Adam SaiduDepartment of Emergency Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Thomas FrancisCentre for Human and Applied Physiological Sciences, School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 1UL, UK.
Chelsea MannieDivision of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Laura ArthurDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Stephen D R HarridgeCentre for Human and Applied Physiological Sciences, School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 1UL, UK.
Daniel KreiselDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Philip A MuddDepartment of Emergency Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; The Andrew M. and Jane M. Bursky Center for Human Immunology & Immunotherapy Programs, Washington University School of Medicine, St. Louis, MO 63110, USA; Center for Vaccines and Immunity to Microbial Pathogens, Washington University School of Medicine, St. Louis, MO 63110, USA.
Angela M TaylorDepartment of Medicine, Cardiovascular Division, University of Virginia, Charlottesville, VA 22903, USA.
Coleen A McNamaraDepartment of Medicine, Cardiovascular Division, University of Virginia, Charlottesville, VA 22903, USA; Beirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, VA 22903, USA.
Marina CellaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sidharth V PuramDepartment of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA; Rob Ebert and Greg Stubblefield Head and Neck Tumor Center at Siteman Cancer Center, St. Louis, MO 63110, USA.
Theo van den BroekCenter for Translational Immunology, University Medical Centre Utrecht, Utrecht University, Utrecht 3584CX, the Netherlands.
Femke van WijkCenter for Translational Immunology, University Medical Centre Utrecht, Utrecht University, Utrecht 3584CX, the Netherlands.
Pirooz EghtesadyDivision of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Maxim N ArtyomovDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: martyomov@wustl.edu.

Funding

Project 4: APOB-specific CD4 and CD8 T cells exacerbate atherosclerosisP01HL136275 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Catherine C Hedrick · 2017 to 2026
$25.5M
NHLBI NIH HHS P01 HL136275
6 · The paper itself

Abstract

Thymic involution is a key factor in human immune aging, leading to reduced thymic output and a decline in recent thymic emigrant (RTE) naive T cells in circulation. Currently, the precise definition of human RTEs and their corresponding cell surface markers lacks clarity. Analysis of single-cell RNA-seq/ATAC-seq data distinguished RTEs by the expression of SOX4, IKZF2, and TOX and CD38 protein, whereby surface CD38

Indexed as

ADP-ribosyl Cyclase 1AgingCD8-Positive T-LymphocytesThymus GlandAdultAgedAged, 80 and overCD4-Positive T-LymphocytesFemaleGene Expression ProfilingHumansMaleMembrane GlycoproteinsMiddle AgedReceptors, CXCR3Single-Cell AnalysisADP-ribosyl Cyclase 1CD38 protein, humanCXCR3 protein, humanMembrane GlycoproteinsReceptors, CXCR3aginghumannaive T cellsPBMCrecent thymic emigrants

Identifiers

PMID39321807
PMCPMC13138122

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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.