Evidence map›Paper›PMID 11994414›Full record

ArticleThe Journal of clinical investigation2002

Enhanced allostimulatory activity of host antigen-presenting cells in old mice intensifies acute graft-versus-host disease.

Rainer Ordemann, Raymond Hutchinson, Jeffrey Friedman, Steven J Burakoff, Pavan Reddy, Ulrich Duffner, Thomas M Braun, Chen Liu, Takanori Teshima, James L M Ferrara

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Aging and the immune response to organ transplantation.The Journal of clinical investigation · 2017
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. IL-12hi rapamycin-conditioned dendritic cells mediate IFN-γ-dependent apoptosis of alloreactive CD4+ T cells in vitro and reduce lethal graft-versus-host disease.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2014
    Article
  14. Immunosenescence and organ transplantation.Transplantation reviews (Orlando, Fla.) · 2013
    Review
  15. Review
  16. Article
  17. Article
  18. Advances in predicting acute GVHD.British journal of haematology · 2013
    Review
  19. Article
  20. Reduced graft-versus-host disease in C3-deficient mice is associated with decreased donor Th1/Th17 differentiation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2012
    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

10 authors at 5 institutions in 1 country.

Rainer OrdemannBlood and Marrow Transplant Program, Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan Cancer Center, Ann Arbor, Michigan 48109-0942, USA.
Raymond Hutchinson
Jeffrey Friedman
Steven J Burakoff
Pavan Reddy
Ulrich Duffner
Thomas M Braun
Chen Liu
Takanori Teshima
James L M Ferrara
University of Michigan–Ann Arbor · USDana-Farber Cancer Institute · USCancer Research And Biostatistics · USPalmetto Hematology Oncology · USUniversity of Florida · US

Funding

TUMOR VACCINES AND BONE MARROW TRANSPLANTATIONP01CA039542 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JAMES L. M. FERRARA · 1985 to 2026
$47.9M
Effect of recipient age /graft vs host disease post BMTR03AG019943 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUTCHINSON, RAYMOND J · 2001 to 2001
$73k
NCI NIH HHS CA-39542NCI NIH HHS P01 CA039542NIA NIH HHS R03 AG-19943-01
6 · The paper itself

Abstract

Older bone marrow transplantation (BMT) recipients are at heightened risk for acute graft-versus-host disease (GVHD) after allogeneic BMT, but the causes of this association are poorly understood. Using well-characterized murine BMT models we have explored the mechanisms of increased GVHD in older mice. GVHD mortality, morbidity, and pathologic and biochemical indices were all worse in old recipients. Donor T cell responses were significantly increased in old recipients both in vivo and in vitro when stimulated by antigen-presenting cells (APCs) from old mice, which also secreted more TNF-alpha and IL-12 after LPS stimulation. In a B6 --> B6D2F1 model, CD4(+) donor T cells but not CD8(+) T cells mediated more severe GVHD in old mice. We confirmed the role of aged APCs in GVHD using B6D2F1 BM chimeras created with either old or young BM. Four months after chimera creation, allogeneic BMT from B6 donors caused significantly worse GVHD in old BM chimeras. APCs from these mice also stimulated greater responses from allogeneic cells in vitro. These data demonstrate a hitherto unsuspected mechanism of amplified donor T cell responses by aged allogeneic host APCs that increases acute GVHD in aged recipients in this BMT model.

Indexed as

Bone Marrow TransplantationAgingAnimalsAntigen-Presenting CellsCells, CulturedDisease Models, AnimalFemaleGraft vs Host DiseaseHumansIntestine, SmallKiller Cells, NaturalLipopolysaccharidesLymphocyte ActivationMiceMice, Inbred C57BLSurvival RateLipopolysaccharidesTumor Necrosis Factor-alpha

Identifiers

PMID11994414
PMCPMC150964
OpenAlexW2019049311

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.