Evidence map›Paper›PMID 33827115›Full record

ArticleBlood2021

CD27 is required for protective lytic EBV antigen-specific CD8+ T-cell expansion.

Yun Deng, Bithi Chatterjee, Kyra Zens, Hana Zdimerova, Anne Müller, Patrick Schuhmachers, Laure-Anne Ligeon, Antonino Bongiovanni, Riccarda Capaul, Andrea Zbinden and 4 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. A tonsil organoid model reveals Epstein-Barr virus-infected germinal center B cell states during primary infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

14 authors at 4 institutions in 4 countries.

Yun DengViral Immunobiology, Institute of Experimental Immunology, and.ORCID 0000-0002-8204-9021
Bithi ChatterjeeViral Immunobiology, Institute of Experimental Immunology, and.
Kyra ZensViral Immunobiology, Institute of Experimental Immunology, and.ORCID 0000-0001-7979-076X
Hana ZdimerovaViral Immunobiology, Institute of Experimental Immunology, and.
Anne MüllerViral Immunobiology, Institute of Experimental Immunology, and.ORCID 0000-0002-7470-5279
Patrick SchuhmachersViral Immunobiology, Institute of Experimental Immunology, and.ORCID 0000-0003-2052-738X
Laure-Anne LigeonViral Immunobiology, Institute of Experimental Immunology, and.
Antonino BongiovanniCellular Microbiology of Infectious Pathogens Group, Center for Infection and Immunity of Lille, and.ORCID 0000-0001-9876-2940
Riccarda CapaulInstitute of Medical Virology, University of Zurich, Zurich, Switzerland.
Andrea ZbindenInstitute of Medical Virology, University of Zurich, Zurich, Switzerland.
Angelika HollerInstitute of Immunity and Transplantation, Royal Free Campus, University College London, London, United Kingdom; and.
Hans StaussInstitute of Immunity and Transplantation, Royal Free Campus, University College London, London, United Kingdom; and.
Wolfgang HammerschmidtResearch Unit Gene Vectors, Helmholtz Zentrum München, German Research Center for Environmental Health and German Center for Infection Research, Munich, Germany.ORCID 0000-0002-4659-0427
Christian MünzViral Immunobiology, Institute of Experimental Immunology, and.ORCID 0000-0001-6419-1940
University of Zurich · CHThe Royal Free Hospital · GBHelmholtz Zentrum München · DEInstitut Pasteur de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary immunodeficiencies in the costimulatory molecule CD27 and its ligand, CD70, predispose for pathologies of uncontrolled Epstein-Barr virus (EBV) infection in nearly all affected patients. We demonstrate that both depletion of CD27+ cells and antibody blocking of CD27 interaction with CD70 cause uncontrolled EBV infection in mice with reconstituted human immune system components. While overall CD8+ T-cell expansion and composition are unaltered after antibody blocking of CD27, only some EBV-specific CD8+ T-cell responses, exemplified by early lytic EBV antigen BMLF1-specific CD8+ T cells, are inhibited in their proliferation and killing of EBV-transformed B cells. This suggests that CD27 is not required for all CD8+ T-cell expansions and cytotoxicity but is required for a subset of CD8+ T-cell responses that protect us from EBV pathology.

Indexed as

Immunity, CellularAnimalsB-LymphocytesCD8-Positive T-LymphocytesCell Transformation, ViralEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansMiceMice, Inbred NODMice, TransgenicPhosphoproteinsTrans-ActivatorsTumor Necrosis Factor Receptor Superfamily, Member 7PhosphoproteinsSM protein, Human herpesvirus 4Trans-ActivatorsTumor Necrosis Factor Receptor Superfamily, Member 7CD27CD39DLBCLEpstein-Barr virushumanized miceIMMUNOBIOLOGY/B-cell neoplasmsIMMUNOBIOLOGY/Cytotoxic T cellsIMMUNOBIOLOGY/Host-pathogen interactionsIMMUNOBIOLOGY/T-cell costimulationIMMUNOBIOLOGY/T-Cell Mediated Immunity

Identifiers

PMID33827115
PMCPMC8351885
OpenAlexW3145743621

What OpenQuestion holds

Textmetadata
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.