Evidence map›Paper›PMID 31472079›Full record

ReviewTransplant international : official journal of the European Society for Organ Transplantation2020

Tolerogenic dendritic cells in organ transplantation.

Jordi Ochando, Farideh Ordikhani, Stefan Jordan, Peter Boros, Angus W Thomson

Open access · bronzeAbstract readReview
In one paragraph

Review in Transplant international : official journal of the European Society for Organ Transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
3.6field-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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
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  13. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
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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

5 authors at 3 institutions in 2 countries.

Jordi OchandoDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Farideh OrdikhaniDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Stefan JordanDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Peter BorosDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Angus W ThomsonDepartment of Surgery and Department of Immunology, Starzl Transplantation Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0001-6731-8871
Icahn School of Medicine at Mount Sinai · USInstituto de Salud Carlos III · ESUniversity of Pittsburgh · US

Funding

TRAINING PROGRAM IN CANCER THERAPYT32CA078207 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI James J Manfredi · 1999 to 2026
$11.6M
Transplant Pathology and Tissue Imaging Core (Core B)U19AI131453 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEMETRIS, ANTHONY J · 2017 to 2022
$8.4M
Regulatory Dendritic Cell Therapy in Live Donor Renal Transplant RecipientsU01AI136779 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2018 to 2022
$4.3M
Regulation of Liver DC Function and Transplant ToleranceR01AI118777 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2017 to 2021
$2.3M
Myeloid Specific Targeted Nanoimunotherapy for Organ Transplant AcceptanceR01AI139623 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI OCHANDO, JORDI · 2018 to 2022
$2.3M
NCI NIH HHS T32 CA078207NIAID NIH HHS R01 AI118777NIAID NIH HHS R01 AI139623NIAID NIH HHS U01 AI136779NIAID NIH HHS U19 AI131453NIH HHS R01 AI 118777NIH HHS R01 AI 139623NIH HHS U01 AI 136779NIH HHS U19 AI 131453
6 · The paper itself

Abstract

Dendritic cells (DCs) are specialized cells of the innate immune system that are characterized by their ability to take up, process and present antigens (Ag) to effector T cells. They are derived from DC precursors produced in the bone marrow. Different DC subsets have been described according to lineage-specific transcription factors required for their development and function. Functionally, DCs are responsible for inducing Ag-specific immune responses that mediate organ transplant rejection. Consequently, to prevent anti-donor immune responses, therapeutic strategies have been directed toward the inhibition of DC activation. In addition however, an extensive body of preclinical research, using transplant models in rodents and nonhuman primates, has established a central role of DCs in the negative regulation of alloimmune responses. As a result, DCs have been employed as cell-based immunotherapy in early phase I/II clinical trials in organ transplantation. Together with in vivo targeting through use of myeloid cell-specific nanobiologics, DC manipulation represents a promising approach for the induction of transplantation tolerance. In this review, we summarize fundamental characteristics of DCs and their roles in promotion of central and peripheral tolerance. We also discuss their clinical application to promote improved long-term outcomes in organ transplantation.

Indexed as

Immune ToleranceOrgan TransplantationTransplantation ToleranceAnimalsDendritic CellsT-Lymphocytesdendritic cellsimmune toleranceorgan transplantation

Identifiers

PMID31472079
PMCPMC6983332
OpenAlexW2970957056

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.