Evidence map›Paper›PMID 34695149›Full record

ArticlePLoS pathogens2021

CD4+ T cell immunity to Salmonella is transient in the circulation.

Newton G Peres, Nancy Wang, Paul Whitney, Sven Engel, Meghanashree M Shreenivas, Ian Comerford, Dianna M Hocking, Anna B Erazo, Irmgard Förster, Andreas Kupz and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Optimal generation of hepatic tissue-resident memory CD4 T cells requires IL-1 and IL-2.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Review
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

15 authors at 5 institutions in 3 countries.

Newton G PeresDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-6681-1469
Nancy WangDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0001-7623-1858
Paul WhitneyDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Sven EngelDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Meghanashree M ShreenivasDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-7905-1091
Ian ComerfordSchool of Biological Science, Faculty of Sciences, The University of Adelaide, South Australia, Australia.ORCID 0000-0001-8753-4774
Dianna M HockingDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-3485-0586
Anna B ErazoDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.
Irmgard FörsterImmunology & Environment, Life and Medical Sciences (LIMES) Institute, University of Bonn, Bonn, Germany.ORCID 0000-0002-7644-5642
Andreas KupzCentre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.ORCID 0000-0002-9259-7873
Thomas GebhardtDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-3768-9468
Shaun R McCollSchool of Biological Science, Faculty of Sciences, The University of Adelaide, South Australia, Australia.ORCID 0000-0003-0949-4660
Stephen J McSorleyCenter for Comparative Medicine, University of California, Davis, California, United States of America.
Sammy BedouiDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0002-7443-0543
Richard A StrugnellDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, Melbourne, Australia.ORCID 0000-0003-0614-5641
The University of Melbourne · AUThe University of Adelaide · AUUniversity of Bonn · DEAustralian Institute of Tropical Health and Medicine · AUUniversity of California, Davis · US

Funding

Sustained adaptive immunity in the mucosaP01AI056172 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MCSORLEY, STEPHEN J · 2003 to 2017
$22.3M
Target antigen identification to improve Salmonella vaccinationR01AI139410 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI STEPHEN J MCSORLEY, Renee M Tsolis · 2018 to 2026
$2.9M
Salmonella-specific Th1 cell function and residenceR01AI139047 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MCSORLEY, STEPHEN J · 2019 to 2023
$1.9M
NIAID NIH HHS P01 AI056172NIAID NIH HHS R01 AI139047NIAID NIH HHS R01 AI139410
6 · The paper itself

Abstract

While Salmonella enterica is seen as an archetypal facultative intracellular bacterial pathogen where protection is mediated by CD4+ T cells, identifying circulating protective cells has proved very difficult, inhibiting steps to identify key antigen specificities. Exploiting a mouse model of vaccination, we show that the spleens of C57BL/6 mice vaccinated with live-attenuated Salmonella serovar Typhimurium (S. Typhimurium) strains carried a pool of IFN-γ+ CD4+ T cells that could adoptively transfer protection, but only transiently. Circulating Salmonella-reactive CD4+ T cells expressed the liver-homing chemokine receptor CXCR6, accumulated over time in the liver and assumed phenotypic characteristics associated with tissue-associated T cells. Liver memory CD4+ T cells showed TCR selection bias and their accumulation in the liver could be inhibited by blocking CXCL16. These data showed that the circulation of CD4+ T cells mediating immunity to Salmonella is limited to a brief window after which Salmonella-specific CD4+ T cells migrate to peripheral tissues. Our observations highlight the importance of triggering tissue-specific immunity against systemic infections.

Indexed as

AnimalsCD4-Positive T-LymphocytesFemaleImmunologic MemoryLiverMaleMiceMice, Inbred C57BLSalmonella Infections, AnimalSalmonella typhimurium

Identifiers

PMID34695149
PMCPMC8568161
OpenAlexW3209129552

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.