Evidence map›Paper›PMID 22058417›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

Cutting edge: Tissue-retentive lung memory CD4 T cells mediate optimal protection to respiratory virus infection.

John R Teijaro, Damian Turner, Quynh Pham, E John Wherry, Leo Lefrançois, Donna L Farber

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 456 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
456citing papers in PubMed, 1 pooled it
10.4field-weighted citation impact, top 1% 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

456 citing papers in PubMed, 1 synthesis or guideline pooled it, 634 citations in OpenAlex.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
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  12. PD-1 Inhibits CD4+ TRM-Mediated cDC1 Mobilization via Suppressing JAML in Human NSCLC.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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396 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 1 country.

John R TeijaroDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Damian Turner
Quynh Pham
E John Wherry
Leo Lefrançois
Donna L Farber
Columbia University Irving Medical Center · USUConn Health · USUniversity of Maryland, Baltimore · USUniversity of Pennsylvania · US

Funding

The Impact of Bacterial Co-Infectin on Respiratory Virus-Specific T cell ResponseU19AI083022 · NIAID · WISTAR INSTITUTE · PI SHEN, HAO · 2009 to 2013
$10.7M
CD8 T CELL ACTIVATION AND MIGRATION IN VIVOR01AI041576 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KHANNA, KAMAL MOHAN · 1997 to 2016
$5.3M
T Cell Response to Listeria Monocytogenes InfectionR01AI076457 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI SHERIDAN, BRIAN S · 2009 to 2019
$3.8M
NIAID NIH HHS AI083022NIAID NIH HHS AI41576NIAID NIH HHS AI76457NIAID NIH HHS R01 AI041576NIAID NIH HHS R01 AI076457NIAID NIH HHS U19 AI083022
6 · The paper itself

Abstract

We identify in this article a new class of lung tissue-resident memory CD4 T cells that exhibit tissue tropism and retention independent of Ag or inflammation. Tissue-resident memory CD4 T cells in the lung did not circulate or emigrate from the lung in parabiosis experiments, were protected from in vivo Ab labeling, and expressed elevated levels of CD69 and CD11a compared with those of circulating memory populations. Importantly, influenza-specific lung-resident memory CD4 T cells served as in situ protectors to respiratory viral challenge, mediating enhanced viral clearance and survival to lethal influenza infection. By contrast, memory CD4 T cells isolated from spleen recirculated among multiple tissues without retention and failed to mediate protection to influenza infection, despite their ability to expand and migrate to the lung. Our results reveal tissue compartmentalization as a major determining factor for immune-mediated protection in a key mucosal site, important for targeting local protective responses in vaccines and immunotherapies.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell SeparationChemotaxis, LeukocyteFlow CytometryImmunity, MucosalImmunologic MemoryLungMiceMice, TransgenicOrthomyxoviridaeOrthomyxoviridae InfectionsRespiratory MucosaT-Lymphocyte Subsets

Identifiers

PMID22058417
PMCPMC3221837
OpenAlexW2155051381

What OpenQuestion holds

Textmetadata
LicenceTDM
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.