Evidence map›Paper›PMID 32565132›Full record

ReviewCytotherapy2020

Emerging trends in COVID-19 treatment: learning from inflammatory conditions associated with cellular therapies.

Maria Cancio, Rachele Ciccocioppo, Patricia R M Rocco, Bruce L Levine, Vincenzo Bronte, Catherine M Bollard, Daniel Weiss, Jaap Jan Boelens, Patrick J Hanley

Open access · hybridAbstract readReview
In one paragraph

Review in Cytotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  11. COVID-19 and metabolic comorbidities: An update on emerging evidences for optimal therapies.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2021
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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

9 authors at 7 institutions in 3 countries.

Maria CancioMemorial Sloan Kettering Cancer Center, New York, New York, USA. Electronic address: Canciom@mskcc.org.
Rachele CiccocioppoDepartment of Medicine, A.O.U.I Policlinico G.B Rossi and University of Verona, Verona, Italy.
Patricia R M RoccoLaboratory of Pulmonary Investigation, Carlos Chagas Filho Institute of Biophysics, Federal university of Rio de Janeiro, Rio de Janeiro, Brazil.
Bruce L LevineCenter for Cellular Immunotherapies and Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Vincenzo BronteDepartment of Medicine, A.O.U.I Policlinico G.B Rossi and University of Verona, Verona, Italy.
Catherine M BollardCenter for Cancer and Immunology Research, Center for Cancer and Blood Disorders, Children's National Hospital and the George Washington University Cancer Center, George Washington University, Washington, DC, USA.
Daniel WeissUniversity of Vermont Medical Center, Burlington, Vermont, USA.
Jaap Jan BoelensMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Patrick J HanleyCenter for Cancer and Immunology Research, Center for Cancer and Blood Disorders, Children's National Hospital and the George Washington University Cancer Center, George Washington University, Washington, DC, USA.
Memorial Sloan Kettering Cancer Center · USUniversity of Verona · ITCenter for Cancer and Blood Disorders · USGeorge Washington University · USUniversidade Federal do Rio de Janeiro · BRUniversity of Pennsylvania · USUniversity of Vermont Medical Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Coronavirus disease 2019 (SARS-CoV2) is an active global health threat for which treatments are desperately being sought. Even though most people infected experience mild to moderate respiratory symptoms and recover with supportive care, certain vulnerable hosts develop severe clinical deterioration. While several drugs are currently being investigated in clinical trials, there are currently no approved treatments or vaccines for COVID-19 and hence there is an unmet need to explore additional therapeutic options. At least three inflammatory disorders or syndromes associated with immune dysfunction have been described in the context of cellular therapy. Specifically, Cytokine Release Syndrome (CRS), Immune Reconstitution Inflammatory Syndrome (IRIS), and Secondary Hemophagocytic Lymphohistiocytosis (sHLH) all have clinical and laboratory characteristics in common with COVID19 and associated therapies that could be worth testing in the context of clinical trials. Here we discuss these diseases, their management, and potential applications of these treatment in the context of COVID-19. We also discuss current cellular therapies that are being evaluated for the treatment of COVID-19 and/or its associated symptoms.

Indexed as

Adrenal Cortex HormonesCoronavirus InfectionsCOVID-19COVID-19 Drug TreatmentCytokine Release SyndromeHumansImmune Reconstitution Inflammatory SyndromeImmunization, PassiveInterleukin-1Interleukin-6Interleukin-6 InhibitorsKiller Cells, NaturalLymphohistiocytosis, HemophagocyticPandemicsPlasmapheresisPneumonia, ViralAdrenal Cortex HormonesIL6 protein, humanInterleukin-1Interleukin-6Interleukin-6 InhibitorsSTAT Transcription Factorscellular therapyCOVID-19CRScytokine releaseHLHhyperimmune responseimmunotherapyIRISSARS-CoV-2

Identifiers

PMID32565132
PMCPMC7252029
OpenAlexW3023176883

What OpenQuestion holds

Textmetadata
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.