Evidence map›Paper›PMID 24918616›Full record

ArticleTransplantation2014

Simultaneous transplantation of hematopoietic stem cells and a vascularized composite allograft leads to tolerance.

David W Mathes, Jeff Chang, Billanna Hwang, Scott S Graves, Barry E Storer, Tiffany Butts-Miwongtum, George E Sale, Rainer Storb

Abstract read
In one paragraph

Article in Transplantation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  19. From marrow to matrix: novel gene and cell therapies for epidermolysis bullosa.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
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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

8 authors at 2 institutions in 1 country.

David W Mathes1 Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA. 2 Department of Surgery, University of Washington, Seattle, WA. 3 Plastic Surgery Service, VA Puget Sound Health Care System, Seattle, WA. 4 Department of Medicine, University of Washington, Seattle, WA. 5 School of Public Health, University of Washington, Seattle, WA. 6 Department of Pathology, University of Washington, Seattle, WA. 7 Address correspondence to: David W. Mathes, M.D., Clinical Research Division, Fred Hutchinson Cancer Research Center, PO Box 19024; D1-100 1100 Fairview Ave, N, Seattle, WA 98109.
Jeff Chang
Billanna Hwang
Scott S Graves
Barry E Storer
Tiffany Butts-Miwongtum
George E Sale
Rainer Storb
University of Washington · USFred Hutch Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Project 3: Stem Cell Allografts for Lymphoid MalignanciesP01CA078902 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SANDMAIER, BRENDA MARIE · 1999 to 2025
$46.1M
NCI NIH HHS P01 CA078902NCI NIH HHS P01CA078902NCI NIH HHS P30 CA015704NCI NIH HHS P30CA015704
6 · The paper itself

Abstract

backgroundWe have previously demonstrated that tolerance to a vascularized composite allograft (VCA) can be achieved after the establishment of mixed chimerism. We test the hypothesis that tolerance to a VCA in our dog leukocyte antigen-matched canine model is not dependent on the previous establishment of mixed chimerism and can be induced coincident with hematopoietic cell transplantation (HCT).

methodsEight dog leukocyte antigen-matched, minor antigen mismatched dogs received 200 cGy of radiation and a VCA transplant. Four dogs received donor bone marrow at the time of VCA transplantation (group 1), whereas a second group of four dogs did not (group 2). All recipients received a limited course of postgrafting immunosuppression. All dogs that received HCT and VCA were given donor, third-party, and autologous skin grafts.

resultsAll group 1 recipients were tolerant to their VCA (>62 weeks). Three of the four dogs in group 2 rejected their VCA transplants after the cessation of immunosuppression. Biopsies obtained from the muscle and skin of VCA from group 1 showed few infiltrating cells compared with extensive infiltrates in biopsies of VCA from group 2. Compared with autologous skin and muscle, elevated levels of CD3+ FoxP3+ T-regulatory cells were found in the skin and muscle obtained from the VCA of HCT recipients. All group 1 animals were tolerant to their donor skin graft and promptly rejected the third-party skin grafts.

conclusionThese data demonstrated that donor-specific tolerance to all components of the VCA can be established through simultaneous nonmyeloablative allogeneic HCT and VCA transplantation protocol.

Indexed as

Graft SurvivalHematopoietic Stem Cell TransplantationSkin TransplantationTransplantation ToleranceVascularized Composite AllotransplantationAnimalsBiomarkersCD3 ComplexComposite Tissue AllograftsCytokinesDogsForkhead Transcription FactorsGraft RejectionHistocompatibilityHistocompatibility AntigensImmunosuppressive AgentsBiomarkersCD3 ComplexCytokinesForkhead Transcription FactorsHistocompatibility AntigensImmunosuppressive AgentsMyeloablative Agonists

Identifiers

PMID24918616
PMCPMC4128556
OpenAlexW2325893453

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.