Evidence map›Paper›PMID 19734208›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

CXCR3 directs antigen-specific effector CD4+ T cell migration to the lung during parainfluenza virus infection.

Jacob E Kohlmeier, Tres Cookenham, Shannon C Miller, Alan D Roberts, Jan P Christensen, Allan R Thomsen, David L Woodland

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

95 citing papers in PubMed, 137 citations in OpenAlex.

  1. Trial
  2. B cell-intrinsic CXCR3 drives efficient generation of ectopic pulmonary germinal center responses to influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. HIF-1αImmunity · 2026
    Article
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35 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

7 authors at 2 institutions in 2 countries.

Jacob E KohlmeierTrudeau Institute, Saranac Lake, NY 12983, USA.
Tres Cookenham
Shannon C Miller
Alan D Roberts
Jan P Christensen
Allan R Thomsen
David L Woodland
Trudeau Institute · USUniversity of Copenhagen · DK

Funding

Regulation of memory CD8+ T cell recruitment to the lungR01AI076499 · NIAID · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A · 2008 to 2012
$2.3M
Memory T cell subsets and pulmonary immunityR01AI067967 · NIAID · TRUDEAU INSTITUTE, INC. · PI WOODLAND, DAVID L. · 2006 to 2010
$2.2M
Research Training in Immunology and Infectious DiseasesT32AI049823 · NIAID · TRUDEAU INSTITUTE, INC. · PI COOPER, ANDREA M · 2001 to 2015
$2.1M
Recruitment of memory CD8+ T cells to the lung airwaysF32AI071478 · NIAID · TRUDEAU INSTITUTE, INC. · PI KOHLMEIER, JACOB E · 2007 to 2007
$51k
NIAID NIH HHS AI67967NIAID NIH HHS AI76499NIAID NIH HHS F32 AI071478NIAID NIH HHS F32 AI71478NIAID NIH HHS R01 AI067967NIAID NIH HHS R01 AI076499NIAID NIH HHS T32 AI049823NIAID NIH HHS T32 AI49823
6 · The paper itself

Abstract

Effector T cells are a crucial component of the adaptive immune response to respiratory virus infections. Although it was previously reported that the chemokine receptors CCR5 and CXCR3 affect trafficking of respiratory virus-specific CD8+ T cells, it is unclear whether these receptors govern effector CD4+ T cell migration to the lungs. To assess the role of CCR5 and CXCR3 in vivo, we directly compared the migration of Ag-specific wild-type and chemokine receptor-deficient effector T cells in mixed bone marrow chimeric mice during a parainfluenza virus infection. CXCR3-deficient effector CD4+ T cells were 5- to 10-fold less efficient at migrating to the lung compared with wild-type cells, whereas CCR5-deficient effector T cells were not impaired in their migration to the lung. In contrast to its role in trafficking, CXCR3 had no impact on effector CD4+ T cell proliferation, phenotype, or function in any of the tissues examined. These findings demonstrate that CXCR3 controls virus-specific effector CD4+ T cell migration in vivo, and suggest that blocking CXCR3-mediated recruitment may limit T cell-induced immunopathology during respiratory virus infections.

Indexed as

AnimalsCD4-Positive T-LymphocytesChemotaxis, LeukocyteClone CellsEpitopes, T-LymphocyteLungMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicReceptors, CCR5Receptors, CXCR3Respirovirus InfectionsSendai virusCxcr3 protein, mouseEpitopes, T-LymphocyteReceptors, CCR5Receptors, CXCR3

Identifiers

PMID19734208
PMCPMC2757292
OpenAlexW2153010224

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.