An anti-CD6 antibody for the treatment of COVID-19 patients with cytokine-release syndrome: report of three cases.
Aged, 80 and over
Anti-Inflammatory Agents
/ therapeutic use
Antibodies, Monoclonal, Humanized
/ therapeutic use
Antigens, CD
/ immunology
Antigens, Differentiation, T-Lymphocyte
/ immunology
Biomarkers
/ blood
COVID-19
/ pathology
Critical Illness
Cytokine Release Syndrome
/ drug therapy
Drug Therapy, Combination
Female
Humans
Interleukin-6
/ blood
Male
Middle Aged
SARS-CoV-2
Treatment Outcome
COVID-19 Drug Treatment
CD6 molecule
COVID-19
IL-6
SARS-CoV-2
coronavirus 2
cytokine-release syndrome
itolizumab
monoclonal antibody
Journal
Immunotherapy
ISSN: 1750-7448
Titre abrégé: Immunotherapy
Pays: England
ID NLM: 101485158
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
pubmed:
6
1
2021
medline:
2
2
2021
entrez:
5
1
2021
Statut:
ppublish
Résumé
In COVID-19, the inflammatory cytokine-release syndrome is associated with the progression of the disease. Itolizumab is a monoclonal antibody that recognizes human CD6 expressed in activated T cells. The antibody has shown to be safe and efficacious in the treatment of moderate to severe psoriasis. Its effect is associated with the reduction of pro-inflammatory cytokines release, including IFN-γ, IL-6 and TNF-α. Here, we report the outcome of three severe and critically ill COVID-19 patients treated with itolizumab as part of an expanded access protocol. Itolizumab was able to reduce IL-6 concentrations in all the patients. Two of the three patients showed respiratory and radiological improvement and were fully recovered. We hypothesize this anti-inflammatory therapy in addition to antiviral and anticoagulant therapy could reduce COVID-19 associated morbidity and mortality.
Identifiants
pubmed: 33397150
doi: 10.2217/imt-2020-0235
pmc: PMC7784786
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Antibodies, Monoclonal, Humanized
0
Antigens, CD
0
Antigens, Differentiation, T-Lymphocyte
0
Biomarkers
0
CD6 antigen
0
Interleukin-6
0
itolizumab
XQQ2RHV14N
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
289-295Subventions
Organisme : Center of Molecular Immunology
Pays : International