BTK inhibitors for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2): A systematic review

Michael Stack1, Keith Sacco1, Riccardo Castagnoli1

  • 1Laboratory of Clinical Immunology and Microbiology, Immunodeficiency Genetics Section, NIAID, NIH, Bethesda, MD, USA.

Abstract

Insights

Bruton tyrosine kinase (BTK) inhibitors may reduce oxygen needs and hospitalization for severe COVID-19 patients. Further research is needed to confirm these promising findings for BTK inhibition in critical care.

Area of Science:

  • Immunology
  • Pharmacology
  • Critical Care Medicine

Background:

  • Bruton tyrosine kinase (BTK) plays a key role in B cell and macrophage signaling.
  • BTK inhibition is hypothesized to mitigate lung injury in severe COVID-19.
  • Existing clinical data on BTK inhibitors for COVID-19 is inconclusive.

Purpose of the Study:

  • To evaluate the clinical outcomes of Bruton tyrosine kinase inhibitors (BTKinibs) in patients with COVID-19.
  • To synthesize evidence on the efficacy of BTK inhibitors in managing severe COVID-19 symptoms.

Main Methods:

  • Systematic search of PubMed, Embase, and Web of Science:Core databases up to December 30, 2020.
  • Inclusion of clinical studies with at least 5 COVID-19 patients treated with BTKinibs.
  • Exclusion of case reports and reviews to focus on robust clinical data.

Main Results:

  • Six studies met the inclusion criteria from 125 identified articles.
  • Common outcomes assessed included oxygen requirements and hospitalization rates/duration.
  • Three studies indicated reduced oxygen needs, and all three evaluating hospitalization found favorable outcomes with BTKinibs.

Conclusions:

  • BTK inhibitor use in COVID-19 patients was associated with decreased oxygen requirements.
  • BTK inhibition demonstrated potential for reducing hospitalization rates and duration.
  • These findings suggest a potential therapeutic role for BTK inhibitors in severe COVID-19.