Evidence map›Paper›PMID 10642595›Full record

ArticleThe Journal of clinical investigation2000

Stable mixed chimerism and tolerance using a nonmyeloablative preparative regimen in a large-animal model.

C A Huang, Y Fuchimoto, R Scheier-Dolberg, M C Murphy, D M Neville, D H Sachs

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 208 citations in OpenAlex.

  1. Trial
  2. Review
  3. Animal models for transplant immunology: bridging bench to bedside.Clinical transplantation and research · 2024
    Review
  4. Review
  5. Review
  6. CD3e-immunotoxin spares CD62LFrontiers in immunology · 2022
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Donor Lymphocyte Infusion-Mediated Graft-versus-Host Responses in a Preclinical Swine Model of Haploidentical Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2016
    Article
  17. Role of Bone Marrow Maturity, Insulin-Like Growth Factor 1 Receptor, and Forkhead Box Protein N1 in Thymic Involution and Rejuvenation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  18. Article
  19. Review
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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

6 authors at 4 institutions in 1 country.

C A HuangTransplantation Biology Research Center, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts 02129, USA.
Y Fuchimoto
R Scheier-Dolberg
M C Murphy
D M Neville
D H Sachs
Harvard University · USHarvard University Press · USMassachusetts General Hospital · USNational Institutes of Health · US

Funding

MIXED HEMATOPOIETIC CELL CHIMERISM IN A MODELR01HL063430 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SACHS, DAVID H · 1999 to 2002
$1.2M
Tolerance In Organ Transplantation &Autoimmune DiseaseZ01MH002747 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI NEVILLE, DAVID M. · 1996 to 2007
$1.1M
BONE MARROW CULTURE AND ENGRAFTMENT IN A SWINE MODELR01HL046532 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SACHS, DAVID H · 1991 to 1999
–
NHLBI NIH HHS 1RO1 HL-63430NHLBI NIH HHS 5RO1 HL-46532
6 · The paper itself

Abstract

Bone marrow transplantation (BMT) has considerable potential for the treatment of malignancies, hemoglobinopathies, and autoimmune diseases, as well as the induction of transplantation allograft tolerance. Toxicities associated with standard preparative regimens for bone marrow transplantation, however, make this approach unacceptable for all but the most severe of these clinical situations. Here, we demonstrate that stable mixed hematopoietic cell chimerism and donor-specific tolerance can be established in miniature swine, using a relatively mild, non-myeloablative preparative regimen. We conditioned recipient swine with whole-body and thymic irradiation, and we depleted their T-cells by CD3 immunotoxin-treatment. Infusion of either bone marrow cells or cytokine-mobilized peripheral blood stem cells from leukocyte antigen-matched animals resulted in stable mixed chimerism, as detected by flow cytometry in the peripheral blood, thymus, and bone marrow, without any clinical evidence of graft-versus-host disease (GvHD). Long-term acceptance of donor skin and consistent rejection of third-party skin indicated that the recipients had developed donor-specific tolerance.

Indexed as

Hematopoietic Stem Cell TransplantationAnimalsBone Marrow TransplantationCD3 ComplexCell LineageChimeraDrug Administration ScheduleFlow CytometryGraft SurvivalImmune ToleranceImmunotoxinsLeukocyte CountLymphocyte DepletionPlatelet CountSkin TransplantationSwineCD3 ComplexImmunotoxins

Identifiers

PMID10642595
PMCPMC377429
OpenAlexW2088962680

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.