Gaps and opportunities in sepsis translational research.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 36470831.
- Also identified by DOI 10.1016/j.ebiom.2022.104387 and PMC identifier 9783171.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Infection initiates sepsis, but the clinical disease arises through the innate immune response of the host. A rapidly evolving understanding of the biology of that response has not been paralleled by the development of successful new treatment. The COVID-19 pandemic has begun to change this revealing the promise of distinct therapeutic approaches and the feasibility of new approaches to evaluate them. We review the history of mediator-targeted therapy for sepsis and explore the conceptual, biological, technological, and organizational challenges that must be addressed to enable the development of effective treatments for a leading cause of global morbidity and mortality.
Medical subject headings
- COVID-19
- Sepsis