Evidence map›Paper›PMID 33304584›Full record

ArticleClinical & translational immunology2020

Treatment of COVID-19 patients with the anti-CD6 antibody itolizumab.

Armando Caballero, Lázaro M Filgueira, Julio Betancourt, Naivy Sánchez, Carlos Hidalgo, Alberto Ramírez, Alejandro Martinez, Rolando E Despaigne, Alberto Escalona, Henrry Diaz and 18 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. CD6-mediated inhibition of T cell activation via modulation of Ras.Cell communication and signaling : CCS · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Disease-drug and drug-drug interaction in COVID-19: Risk and assessment.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2021
    Review
  12. 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

28 authors at 5 institutions in 2 countries.

Armando CaballeroIntensive Care Unit Arnaldo Milián Castro University Hospital Santa Clara Cuba.
Lázaro M FilgueiraIntensive Care Unit Manuel "Piti" Fajardo Rivero Hospital Santa Clara Cuba.
Julio BetancourtIntensive Care Unit Manuel "Piti" Fajardo Rivero Hospital Santa Clara Cuba.
Naivy SánchezIntensive Care Unit Manuel "Piti" Fajardo Rivero Hospital Santa Clara Cuba.
Carlos HidalgoIntensive Care Unit Manuel "Piti" Fajardo Rivero Hospital Santa Clara Cuba.
Alberto RamírezIntensive Care Unit Salvador Allende Hospital Havana Cuba.
Alejandro MartinezIntensive Care Unit Salvador Allende Hospital Havana Cuba.
Rolando E DespaigneIntensive Care Unit Joaquín Castillo Hospital Havana Cuba.
Alberto EscalonaIntensive Care Unit Faustino Pérez Hospital Matanzas Cuba.
Henrry DiazIntensive Care Unit Frank País Hospital Havana Cuba.
Elio MeriñoIntensive Care Unit Frank País Hospital Havana Cuba.
Lilia M OrtegaIntensive Care Unit Pedro Kouri Institute Havana Cuba.
Ulises CastilloEmergency Department Ministry of Cuban Health Havana Cuba.
Mayra RamosClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Danay SaavedraClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Yanelda GarcíaClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Geydi LorenzoClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Meylán CepedaClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Maylén ArencibiaClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Leticia CabreraClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Milagros DomecqClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Daymys EstévezClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Carmen ValenzuelaClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Patricia LorenzoClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Lizet SánchezClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Zaima MazorraClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.
Kalet LeónResearch Direction Center of Molecular Immunology (CIM) Havana Cuba.
Tania CrombetClinical Research Direction Center of Molecular Immunology (CIM) Havana Cuba.ORCID https://orcid.org/0000-0002-2550-7292
Center of Molecular Immunology (Cuba) · CUHospital Infantil Manuel de Jesús Rivera · NIHospital Oncológico Docente "Conrado Benítez García" · CUInstituto de Medicina Tropical “Pedro Kourí” · CUUniversity of Matanzas · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCOVID-19 can lead to a hyperinflammatory state. CD6 is a glycoprotein expressed on mature T lymphocytes which is a crucial regulator of the T-cell activation. Itolizumab is a humanised antibody targeting CD6. Nonclinical and clinical data in autoimmune diseases indicate that it lowers multiple cytokines primarily involving the Th1/Th17 pathway. The primary objective of this study was to assess the impact of itolizumab in arresting the lung function deterioration of COVID-19 patients. Secondary objectives included safety, duration of ventilation, 14-day mortality and evaluation of interleukin 6 concentration.

methodsPatients with confirmed SARS-CoV-2 received itolizumab in combination with other therapies included in the national protocol for COVID-19.

resultsSeventy critical, severe or moderate patients were treated with itolizumab in 10 Cuban hospitals. Median age was 68, and 94% had comorbidities. After 72 h, most patients improved the PO

conclusionsThe opportune administration of itolizumab might interrupt the hyperinflammatory cascade and prevent COVID-19 morbidity and mortality.

Indexed as

CD6COVID‐19cytokine release syndromeitolizumabmonoclonal antibodySARS‐CoV2

Identifiers

PMID33304584
PMCPMC7688906
OpenAlexW3108663934

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.