Evidence map›Paper›PMID 33391276›Full record

ReviewFrontiers in immunology2020

Current Preventions and Treatments of aGVHD: From Pharmacological Prophylaxis to Innovative Therapies.

Sina Naserian, Mathieu Leclerc, Sara Shamdani, Georges Uzan

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

4 authors.

Sina NaserianINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
Mathieu LeclercService d'Hématologie Clinique et de Thérapie Cellulaire, Hôpital Henri Mondor, Créteil, France.
Sara ShamdaniINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.
Georges UzanINSERM UMR-S-MD 1197, Hôpital Paul Brousse, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Graft versus host disease (GVHD) is one of the main causes of mortality and the reason for up to 50% of morbidity after hematopoietic stem cell transplantations (HSCT) which is the treatment of choice for many blood malignancies. Thanks to years of research and exploration, we have acquired a profound understanding of the pathophysiology and immunopathology of these disorders. This led to the proposition and development of many therapeutic approaches during the last decades, some of them with very promising results. In this review, we have focused on the recent GVHD treatments from classical chemical and pharmacological prophylaxis to more innovative treatments including gene therapy and cell therapy, most commonly based on the application of a variety of immunomodulatory cells. Furthermore, we have discussed the advantages and potentials of cell-free therapy as a newly emerging approach to treat GVHD. Among them, we have particularly focused on the implication of the TNFα-TNFR2 axis as a new immune checkpoint signaling pathway controlling different aspects of many immunoregulatory cells.

Indexed as

Cell- and Tissue-Based TherapyGenetic TherapyImmunotherapyAnimalsDiffusion of InnovationGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunosuppressive AgentsRisk FactorsTreatment OutcomeImmunosuppressive Agentscell therapygraft versus host diseasehematopoietic stem cell transplantationimmunoregulationT cellsTNFα-TNFR2 signaling pathwaytolerance induction

Identifiers

PMID33391276
PMCPMC7773902

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.