Evidence map›Paper›PMID 20194716›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

CXC chemokine ligand (CXCL) 9 and CXCL10 are antagonistic costimulation molecules during the priming of alloreactive T cell effectors.

Joshua M Rosenblum, Naohiko Shimoda, Austin D Schenk, Howard Zhang, Danielle D Kish, Karen Keslar, Joshua M Farber, Robert L Fairchild

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

38 citing papers in PubMed, 87 citations in OpenAlex.

  1. Suppression of cardiac allograft vasculopathy by a macrophage efferocytosis receptor.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
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  6. Observational
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  11. Article
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  13. Gastrointestinal neuroimmune disruption in a mouse model of Gulf War illness.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  14. Cancer-cell-secreted CXCL11 promoted CD8Journal for immunotherapy of cancer · 2019
    Article
  15. Article
  16. Review
  17. Review
  18. Observational
  19. Article
  20. 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

8 authors at 3 institutions in 2 countries.

Joshua M RosenblumDepartment of Pathology, Case Western Reserve University, Cleveland, OH 44106, USA. jmr55@case.edu
Naohiko Shimoda
Austin D Schenk
Howard Zhang
Danielle D Kish
Karen Keslar
Joshua M Farber
Robert L Fairchild
Cleveland Clinic Lerner College of Medicine · USNational Institutes of Health · USSapporo University · JP

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
POSTTRANSPLANT INFLAMMATORY RESPONSER01AI040459 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI Robert L Fairchild · 1997 to 2026
$9.4M
Characterization Of Novel Chemokine Receptors In LymphocytesZIAAI000749 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FARBER, JOSHUA M · 2009 to 2011
$4.0M
Induction of T Cell Chemoattractants in Acute RejectionR01AI051620 · NIAID · CLEVELAND CLINIC LERNER COM-CWRU · PI FAIRCHILD, ROBERT L · 2003 to 2007
$1.7M
NHLBI NIH HHS F30 HL940052NIAID NIH HHS AI40459NIAID NIH HHS R01 AI040459NIAID NIH HHS R01 AI051620NIAID NIH HHS R01 AI51620NIGMS NIH HHS T32 GM007250NIGMS NIH HHS T32GM07250
6 · The paper itself

Abstract

Donor Ag-reactive CD4 and CD8 T cell production of IFN-gamma is a principal effector mechanism promoting tissue injury during allograft rejection. The CXCR3-binding chemokines CXCL9 and CXCL10 recruit donor-reactive T cells to the allograft, but their role during the priming of donor-reactive T cells to effector function is unknown. Using a murine model of MHC-mismatched cardiac transplantation, we investigated the influence of CXCL9 and CXCL10 during donor-reactive T cell priming. In allograft recipient spleens, CXCL9 and CXCL10 were expressed as early as 24 h posttransplant and increased with similar kinetics, concurrently with CXCR3 expression on T cells. CXCL9, but not CXCL10, expression required NK cell production of IFN-gamma. The absence of CXCL9 in donor allografts, recipients, or both significantly decreased the frequency of donor-reactive CD8 T cells producing IFN-gamma and increased the frequency of donor-reactive CD8 T cells producing IL-17A. In contrast, the absence of CXCL10 increased the frequency of IFN-gamma-producing CD8 T cells in a CXCL9-dependent manner. These data provide novel evidence that donor-reactive CD8 T cells use the CXCR3 chemokine axis as a costimulation pathway during priming to allografts where CXCL9 promotes the development of IFN-gamma-producing CD8 T cells, and CXCL10 antagonizes this skewing.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell SeparationChemokine CXCL10Chemokine CXCL9Flow CytometryGraft RejectionGraft SurvivalHeart TransplantationInterferon-gammaLymphocyte ActivationMiceMice, TransgenicReverse Transcriptase Polymerase Chain ReactionT-LymphocytesChemokine CXCL10Chemokine CXCL9Interferon-gamma

Identifiers

PMID20194716
PMCPMC2885704
OpenAlexW1786787856

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.