Evidence map›Paper›PMID 24056628›Full record

ArticleTransplantation2014

Effects of preexisting autoimmunity on heart graft prolongation after donor-specific transfusion and anti-CD154.

Safa Kalache, Parth Lakhani, Peter S Heeger

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Memory CD4American journal of translational research · 2017
    Article
  5. Article
  6. Article
  7. Review
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

3 authors at 2 institutions in 1 country.

Safa Kalache1 Division of Nephrology, Department of Medicine, The Immunology Institute, The Recanati-Miller Transplant Institute, Icahn School of Medicine at Mount Sinai, New York, NY. 2 Address correspondence to: Peter S. Heeger, M.D., Division of Nephrology, Department of Medicine, The Immunology Institute, The Recanati-Miller Transplant Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1243, New York, NY 10029.
Parth Lakhani
Peter S Heeger
Icahn School of Medicine at Mount Sinai · USMount Sinai Hospital · US

Funding

Translational Immunology Training ProgramT32AI078892 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Karen Leigh Edelblum, SERGIO A. LIRA · 2008 to 2026
$4.5M
GRAFT REJECTION AND DIRECT VERSUS INDIRECT RECOGNITIONR01AI043578 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HEEGER, PETER SCOTT · 1998 to 2013
$3.8M
NIAID NIH HHS R01 AI043578NIAID NIH HHS R01 AI43578NIAID NIH HHS T32 AI078892
6 · The paper itself

Abstract

backgroundAlloreactive memory T cells prevent costimulatory blockade-induced heart graft survival in mice, but whether and how preexisting autoreactive T cells affect solid-organ transplants under these conditions is unknown.

methodsWe tested the impact of preexisting cardiac myosin (CM)-specific immunity on murine heart transplant recipients treated with donor-specific transfusion (DST) plus anti-CD154 monoclonal antibody MR1.

resultsPreimmunization with CM but not control ovalbumin abrogated the graft prolonging effects of DST/MR1, whether administered 2 weeks or more than 6 weeks before transplantation. Adoptive transfer of spleen cells from CM-immunized mice into naïve recipients had similar effects. CM-specific immunity did not cross-react with donor antigens and preimmunization with CM had no impact on the survival or histology of DST/MR1-treated syngeneic heart grafts, the latter indicating that persistent autoimmunity is insufficient to cause rejection in the context of costimulatory blockade. We observed that the CM preimmunized mice produced higher frequencies of donor-reactive T cells with higher ratios of CD8/CD4Foxp3 cells, suggesting that the autoreactive memory T cells provide help for activation of alloreactive T cells despite the costimulatory blockade.

conclusionsThese mechanistic insights linking autoimmunity and alloimmunity in a model of murine heart transplantation have clinical relevance to the known association between autoimmunity and an elevated risk of acute and chronic heart transplant injury in humans.

Indexed as

Adoptive TransferHeart TransplantationAnimalsAntibodies, MonoclonalAutoantigensAutoimmunityCardiac MyosinsCD40 LigandCells, CulturedGraft RejectionGraft SurvivalImmunizationImmunologic MemoryImmunosuppressive AgentsMiceMice, Inbred BALB CAntibodies, MonoclonalAutoantigensCardiac MyosinsCD40 LigandImmunosuppressive Agents

Identifiers

PMID24056628
PMCPMC3877173
OpenAlexW2045478303

What OpenQuestion holds

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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.