Evidence map›Paper›PMID 12952928›Full record

ArticleThe Journal of clinical investigation2003

Hematopoietic chimerism and central tolerance created by peripheral-tolerance induction without myeloablative conditioning.

Edward Seung, John P Mordes, Aldo A Rossini, Dale L Greiner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. T-cell activation and transplantation tolerance.Transplantation reviews (Orlando, Fla.) · 2012
    Review
  6. Article
  7. Article
  8. Review
  9. Treg-therapy allows mixed chimerism and transplantation tolerance without cytoreductive conditioning.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2010
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Murine mobilized peripheral blood stem cells have a lower capacity than bone marrow to induce mixed chimerism and tolerance.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2008
    Article
  15. Article
  16. Review
  17. Article
  18. Viral infection: a potent barrier to transplantation tolerance.Clinical & developmental immunology · 2008
    Review
  19. Article
  20. Elimination of insulitis and augmentation of islet beta cell regeneration via induction of chimerism in overtly diabetic NOD mice.Proceedings of the National Academy of Sciences of the United States of America · 2007
    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

4 authors at 1 institution in 1 country.

Edward SeungProgram in Immunology and Virology,University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
John P Mordes
Aldo A Rossini
Dale L Greiner
University of Massachusetts Chan Medical School · US

Funding

ROLE OF CBL AND PHOSPHATIDYLINOSITOL 3-KINASE IN CD40 SIGNALINGP01DK053006 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MORDES, JOHN PETER · 1997 to 2007
$8.9M
INTERCELLULAR SIGNALS AND INTESTINAL AGANGLIONOSISR01DK052530 · NIDDK · UNIVERSITY OF WASHINGTON · PI KAPUR, RAJ P. · 1997 to 2000
$241k
SINGLE CYCLE SIV PARTICLES--A NOVEL VACCINE STRATEGYR21AI042669 · NIAID · AARON DIAMOND AIDS RESEARCH CENTER · PI ZHANG, LINQI · 1997 to 1998
–
NIAID NIH HHS AI-42669NIDDK NIH HHS DK-52530NIDDK NIH HHS DK-53006NIDDK NIH HHS P01 DK053006
6 · The paper itself

Abstract

Allogeneic hematopoietic chimerism leading to central tolerance has significant therapeutic potential. Realization of that potential has been impeded by the need for myeloablative conditioning of the host and development of graft-versus-host disease (GVHD). To surmount these impediments, we have adapted a costimulation blockade-based protocol developed for solid organ transplantation for use in stem cell transplantation. The protocol combines donor-specific transfusion (DST) with anti-CD154 mAb. When applied to stem cell transplantation, administration of DST, anti-CD154 mAb, and allogeneic bone marrow leads to hematopoietic chimerism and central tolerance with no myeloablation and no GVHD. Tolerance in this system results from deletion of both peripheral host alloreactive CD8+ T cells and nascent intrathymic alloreactive CD8+ T cells. In the absence of large numbers of host alloreactive CD8+ T cells, the transfusion that precedes transplantation need not be of donor origin, suggesting that both allospecific and non-allospecific mechanisms regulate engraftment. Agents that interfere with peripheral transplantation tolerance impair establishment of chimerism. We conclude that robust allogeneic hematopoietic chimerism and central tolerance can be established in the absence of host myeloablative conditioning using a peripheral transplantation tolerance protocol.

Indexed as

Transplantation ConditioningAnimalsBlood TransfusionBone Marrow TransplantationCD40 LigandFemaleGraft vs Host DiseaseHematopoiesisLymphocyte DepletionMaleMiceMice, Inbred BALB CMice, Inbred C57BLMice, Inbred CBAReceptors, Interleukin-2Transplantation ChimeraCD40 LigandReceptors, Interleukin-2

Identifiers

PMID12952928
PMCPMC182209
OpenAlexW2146569288

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.