Evidence map›Paper›PMID 26543876›Full record

ReviewJournal of immunology research2015

Tolerogenic Dendritic Cells on Transplantation: Immunotherapy Based on Second Signal Blockage.

Priscila de Matos Silva, Julia Bier, Lisiery Negrini Paiatto, Cassia Galdino Albuquerque, Caique Lopes Souza, Luis Gustavo Romani Fernandes, Wirla Maria da Silva Cunha Tamashiro, Patricia Ucelli Simioni

Abstract readReview
In one paragraph

Review in Journal of immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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.

Priscila de Matos SilvaDepartment of Biomedical Science, Faculty of Americana (FAM), 13477-360 Americana, SP, Brazil ; Medical School, University of Campinas (UNICAMP), 13083-887 Campinas, SP, Brazil.
Julia BierDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Lisiery Negrini PaiattoDepartment of Biomedical Science, Faculty of Americana (FAM), 13477-360 Americana, SP, Brazil ; Department of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Cassia Galdino AlbuquerqueDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Caique Lopes SouzaDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Luis Gustavo Romani FernandesDepartment of Biomedical Science, Faculty of Americana (FAM), 13477-360 Americana, SP, Brazil ; Medical School, University of Campinas (UNICAMP), 13083-887 Campinas, SP, Brazil.
Wirla Maria da Silva Cunha TamashiroDepartment of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Patricia Ucelli SimioniDepartment of Biomedical Science, Faculty of Americana (FAM), 13477-360 Americana, SP, Brazil ; Department of Genetics, Evolution and Bioagents, Institute of Biology, University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil ; Department of Biochemistry and Microbiology, Institute of Biosciences, Universidade Estadual Paulista (UNESP), 13506-900 Rio Claro, SP, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs), the most important professional antigen-presenting cells (APC), play crucial role in both immunity and tolerance. It is well known that DCs are able to mount immune responses against foreign antigens and simultaneously tolerate self-antigens. Since DCs can be modulated depending on the surrounding microenvironment, they can act as a bridge between innate and adaptive immunity. However, the mechanisms that support this dual role are not entirely clear. Recent studies have shown that DCs can be manipulated ex vivo in order to trigger their tolerogenic profile, what can be a tool to be used in clinical trials aiming the treatment of various diseases and the prevention of transplant rejection. In this sense, the blockage of costimulatory molecules on DC, in the attempt of inhibiting the second signal in the immunological synapse, can be considered as one of the main strategies under development. This review brings an update on current therapies using tolerogenic dendritic cells modulated with costimulatory blockers with the aim of reducing transplant rejection. However, although there are current clinical trials using tolerogenic DC to treat allograft rejection, the actual challenge is to modulate these cells in order to maintain a permanent tolerogenic profile.

Indexed as

Immune ToleranceTransplantation ImmunologyAdaptive ImmunityAnimalsCell CommunicationDendritic CellsGraft RejectionHumansImmunity, InnateImmunotherapySignal TransductionT-Lymphocyte SubsetsTransplantation, Homologous

Identifiers

PMID26543876
PMCPMC4620289

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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.