Evavold Lab
Synthetic immunity and cell death regulation
Lab Overview
The Evavold lab studies fundamental cellular decision making towards different cell fates using cell death programs as a model system. We have a particular interest in the intersection of microbiology and metabolism with impact on host cell survival or death.
Regulated cell death can serve different functions within the innate immune system. For example, immunologically silent cell death can remove unnecessary, damaged, or pre-malignant cells during development and homeostasis. Alternatively, during the early containment of a pathogen, inflammatory cell death can alert the immune system to a foreign invader. However, inflammatory cell death can become pathogenic during systemic infection or contribute to sterile autoimmunity and chronic inflammation. Conversely, acquired resistance to cell death programs can promote cancer progression or resistance to chemotherapies. Dysfunction of cell death regulation may underlie much of the pathology related to human diseases. Thus, we aim to uncover novel regulation in these processes using precision screening that combines genomic or chemical perturbations with synthetic biology models of discrete signaling nodes.
Charles Evavold, PhD
Principal Investigator
Affiliation
- Core Member and Early Independence Fellow, Ragon Institute of Mass General, MIT, and Harvard
- Instructor, Harvard University
About
Dr. Charlie Evavold received his PhD in Immunology from Harvard University. He received his BS in Physics and Astronomy with a double major in Chemistry from Emory University. Charlie is one of the inaugural Ragon Early Independence Fellows on the basic science track.
Related Research Foci
- Artificial Intelligence and Machine Learning
- Cancer Immunology
- Fundamental Immunology
- Infectious Disease Pathogenesis
Related Areas of Study
- Aging
- Cancer
- Infectious Disease
Looking for Collaboration?
Contact UsSelected Publications
Gasdermin D pore-forming activity is redox-sensitive
Cell Reports 2023, 42(1):112008
Putting the p (hosphor) in pyroptosis
Cell Host & Microbe 2022, Volume 30, Issue 12, p1650-1652
Glycine inhibits NINJ1 membrane clustering to suppress plasma membrane rupture in cell death
Elife 2022, 11:e78609
Biting the hand that feeds: Metabolic determinants of cell fate during infection
Frontiers in Immunology 2022, 13:923024
Diverse Control Mechanisms of the Interleukin-1 Cytokine Family
Frontiers in Cell and Developmental Biology 2022, 10:910983
Control of gasdermin D oligomerization and pyroptosis by the Ragulator-Rag-mTORC1 pathway
Cell 2021, Volume 184, Issue 17, Pages 4495-4511.e19
HDAC6 mediates an aggresome-like mechanism for NLRP3 and pyrin inflammasome activation
Science 2020, Vol 369, Issue 6510
Inflammasomes: threat-assessment organelles of the innate immune system
Immunity 2019, Volume 51, Issue 4, p609–624