Evidence map›Paper›PMID 34526991›Full record

ReviewFrontiers in immunology2021

Cellular Therapies in Solid Organ Allotransplantation: Promise and Pitfalls.

Brian I Shaw, Jeffrey R Ord, Chloe Nobuhara, Xunrong Luo

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Brian I ShawDepartment of Surgery, Duke University, Durham, NC, United States.
Jeffrey R OrdSchool of Medicine, Duke University, Durham, NC, United States.
Chloe NobuharaSchool of Medicine, Duke University, Durham, NC, United States.
Xunrong LuoDepartment of Medicine, Division of Nephrology, Duke University, Durham, NC, United States.

Funding

Stimulating Access to Research in Residency (StARR) - NIAIDR38AI140297 · NIAID · DUKE UNIVERSITY · PI Rachel G Greenberg, David H. Harpole · 2018 to 2026
$2.4M
NIAID NIH HHS R38 AI140297
6 · The paper itself

Abstract

Donor specific transfusions have been the basis of tolerance inducing protocols since Peter Medawar showed that it was experimentally feasible in the 1950s. Though trials of cellular therapies have become increasingly common in solid organ transplantation, they have not become standard practice. Additionally, whereas some protocols have focused on cellular therapies as a method for donor antigen delivery-thought to promote tolerance in and of itself in the correct immunologic context-other approaches have alternatively focused on the intrinsic immunosuppressive properties of the certain cell types with less emphasis on their origin, including mesenchymal stem cells, regulatory T cells, and regulatory dendritic cells. Regardless of intent, all cellular therapies must contend with the potential that introducing donor antigen in a new context will lead to sensitization. In this review, we focus on the variety of cellular therapies that have been applied in human trials and non-human primate models, describe their efficacy, highlight data regarding their potential for sensitization, and discuss opportunities for cellular therapies within our current understanding of the immune landscape.

Indexed as

Cell- and Tissue-Based TherapyOrgan TransplantationAnimalsCombined Modality TherapyGraft RejectionGraft SurvivalHematopoietic Stem Cell TransplantationHumansImmune ToleranceImmunosuppression TherapyMesenchymal Stem CellsMesenchymal Stem Cell TransplantationTissue DonorsT-Lymphocyte SubsetsTransplantation, Homologousallosensitizationallotransplantationdonor specific antibodiesdonor specific transfusion (DST)mesenchymal stem cellsensitizationtolerance

Identifiers

PMID34526991
PMCPMC8435835

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.