Evidence map›Paper›PMID 17641205›Full record

ArticleBlood2007

CCR1/CCL5 (RANTES) receptor-ligand interactions modulate allogeneic T-cell responses and graft-versus-host disease following stem-cell transplantation.

Sung W Choi, Gerhard C Hildebrandt, Krystyna M Olkiewicz, David A Hanauer, Meghana N Chaudhary, Ines A Silva, Clare E Rogers, Daphne T Deurloo, Jacki M Fisher, Chen Liu and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

50 citing papers in PubMed, 83 citations in OpenAlex.

  1. Atorvastatin for the Prophylaxis of Acute Graft-versus-Host Disease in Patients Undergoing HLA-Matched Related Donor Allogeneic Hematopoietic Stem Cell Transplantation (allo-HCT).Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2016
    Trial
  2. Trial
  3. Trial
  4. Efficiency and safety of five different agents forFrontiers in molecular biosciences · 2026
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. The Relationship ofJournal of clinical medicine · 2023
    Article
  13. Article
  14. C-C chemokine receptor 5 and acute graft-versus-host disease.Immunity, inflammation and disease · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Chemokine CCL5 promotes robust optic nerve regeneration and mediates many of the effects of CNTF gene therapy.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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

13 authors at 2 institutions in 2 countries.

Sung W ChoiDepartment of Pediatrics, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, MI, USA.
Gerhard C Hildebrandt
Krystyna M Olkiewicz
David A Hanauer
Meghana N Chaudhary
Ines A Silva
Clare E Rogers
Daphne T Deurloo
Jacki M Fisher
Chen Liu
David Adams
Stephen W Chensue
Kenneth R Cooke
University of Michigan–Ann Arbor · USUniversity of Florida · US

Funding

Mechanisms of Leukocyte Recruitment During IPS After BMTR01HL072258 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COOKE, KENNETH R · 2003 to 2007
$1.7M
NHLBI NIH HHS 5R01 HL 072258-04NHLBI NIH HHS R01 HL072258
6 · The paper itself

Abstract

Acute graft-versus-host disease (GVHD) and leukemic relapse are serious complications of allogeneic stem-cell transplantation (SCT). Recruitment of activated T cells to host target tissues or sites of leukemic infiltration (graft-versus-leukemia [GVL]) is likely mediated by chemokine receptor-ligand interactions. We examined the contribution of donor cell CCR1 expression to the development of GVHD and GVL using a well-established murine SCT model (B6 --> B6D2F1) and CCR1-deficient mice (CCR1(-/-)). Allo-SCT with CCR1(-/-) donor cells significantly reduced systemic and target organ GVHD severity, and CCR1 expression on both T cells and accessory cells contributed to GVHD mortality. Significant GVL activity was preserved following CCR1(-/-) SCT, but the survival advantage diminished with increasing tumor burden. We then explored the effects of CCR1 expression on allo-specific T-cell responses. Although cytolytic effector function was maintained on a per-cell basis, T-cell proliferation and IFNgamma secretion were significantly reduced both in vivo and in vitro. T-cell function was partially dependent on interactions between CCR1 and CCL5. Collectively, these data demonstrate that CCR1 expression on donor cells contributes to the development of both GVHD and GVL, and suggest that CCR1/CCL5 receptor-ligand interactions modulate allo-specific T-cell responses occurring in this context.

Indexed as

AnimalsChemokine CCL5Gene Expression RegulationGraft vs Host DiseaseLymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutProtein BindingReceptors, CCR1Stem Cell TransplantationSurvival AnalysisT-LymphocytesTransplantation, HomologousCcl5 protein, mouseCcr1 protein, mouseChemokine CCL5Receptors, CCR1

Identifiers

PMID17641205
PMCPMC2200916
OpenAlexW2007402176

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.