Tocilizumab therapy in 5 solid and composite tissue transplant recipients with early ARDS due to SARS-CoV-2.


Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
11 2020
Historique:
received: 30 04 2020
revised: 21 05 2020
accepted: 21 05 2020
pubmed: 2 6 2020
medline: 29 12 2020
entrez: 2 6 2020
Statut: ppublish

Résumé

There are emerging data depicting the clinical presentation of coronavirus disease 19 (COVID-19) in solid organ transplant recipients but negligible data-driven guidance on clinical management. A biphasic course has been described in some infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), beginning with a flu-like illness followed by an intense inflammatory response characterized by elevated c-reactive protein (CRP), interleukin 6 (IL-6), and acute respiratory distress syndrome (ARDS) associated with high mortality. The exuberant and possibly dysregulated immune response has prompted interest in therapeutic agents that target the cytokines involved, particularly IL-6. Tocilizumab is an IL-6 receptor antagonist with a record of use for a variety of rheumatologic conditions and cytokine release syndrome due to chimeric antigen receptor T-cell therapy but experience in solid organ and composite tissue transplant recipients (SOT/CTTRs) with SARS-CoV-2-related ARDS has not been previously reported in detail. We present the clinical course of 5 SOT/CTTRs with SARS-CoV-2-related ARDS that received tocilizumab with favorable short-term outcomes in 4. Responses were characterized by reductions in CRP, discontinuation of vasopressors, improved oxygenation and respiratory mechanics, and variable duration of ventilator support. Four bacterial infections occurred within 2 weeks of tocilizumab administration. We discuss safety concerns and the need for randomized comparative trials to delineate tocilizumab's clinical utility in this population.

Identifiants

pubmed: 32476261
doi: 10.1111/ajt.16080
pmc: PMC7300992
pii: S1600-6135(22)21566-4
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
tocilizumab I031V2H011

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3191-3197

Informations de copyright

© 2020 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Auteurs

Jose A Morillas (JA)

Department of Infectious Diseases, Cleveland Clinic, Cleveland, Ohio.

Francisco Marco Canosa (F)

Department of Infectious Diseases, Cleveland Clinic, Cleveland, Ohio.

Pavithra Srinivas (P)

Department of Pharmacy, Cleveland Clinic, Cleveland, Ohio.

Tannaz Asadi (T)

Department of Infectious Diseases, Hillcrest Hospital, Cleveland, Ohio.

Cassandra Calabrese (C)

Department of Rheumatologic and Immunologic Disease, Cleveland Clinic, Ohio.

Prabalini Rajendram (P)

Department of Critical Care Medicine, Cleveland Clinic, Cleveland, Ohio.

Marie Budev (M)

Department of Pulmonary Medicine, Cleveland Clinic, Cleveland, Ohio.
Transplantation Center, Cleveland Clinic, Cleveland, Ohio.

Emilio D Poggio (ED)

Department of Nephrology and Hypertension, Cleveland Clinic, Cleveland, Ohio.
Transplantation Center, Cleveland Clinic, Cleveland, Ohio.

K V Narayanan Menon (KV)

Department of Hepatology, Cleveland Clinic, Cleveland, Ohio.
Transplantation Center, Cleveland Clinic, Cleveland, Ohio.

Brian Gastman (B)

Department of Plastic Surgery, Cleveland Clinic, Cleveland, Ohio.
Transplantation Center, Cleveland Clinic, Cleveland, Ohio.

Christine Koval (C)

Department of Infectious Diseases, Cleveland Clinic, Cleveland, Ohio.
Transplantation Center, Cleveland Clinic, Cleveland, Ohio.

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