The Mark Egly Foundation employs a fundamentally different research strategy from most organizations. While traditional research focuses primarily on finding cures for existing diseases, we're pioneering a complementary approach:
We seek to expand the utilization possibilities of Alpha-1 Antitrypsin to improve patient outcomes across multiple disease categories—with an emphasis on prevention rather than only remediation.
Our mission is to collaborate with the medical and research community, inviting scientists and clinicians to take Mark's groundbreaking discoveries and expand upon them, exploring new therapeutic applications that can transform healthcare.
Research Goal: Fund studies exploring Alpha-1 Antitrypsin's therapeutic potential beyond traditional AATD treatment.
Focus Areas: identified in Mark Egly's 2020 patent filing
Why It Matters: These applications can help millions of people who don't have AATD but could benefit from AAT's protective properties.
Research Goal: Develop strategies to prevent disease manifestation through proactive AAT supplementation.
Key Questions We're Exploring:
Target Populations:
Innovation: Moving from reactive treatment to proactive prevention—stopping disease before it starts.
Research Goal: Fund development of Alpha-1 Antitrypsin sources beyond human blood and plasma donation.
Critical Need: Current AAT augmentation therapy relies entirely on pooled human plasma—a limited, expensive, and potentially scarce resource. Expanding production capabilities is essential for broader therapeutic access.
Promising Approaches:
Impact: Alternative production could dramatically reduce costs, increase availability, and enable treatment for millions currently without access.
Research Goal: Establish more precise medical definitions and diagnostic criteria for AATD as a systemic condition.
Current Problem: AATD is narrowly defined based on severe genetic deficiency and lung/liver manifestations, excluding:
Research Needs:
Goal: Create diagnostic standards that capture the true scope of AAT-related disease, ensuring no patient falls through the cracks.
Research Goal: Map all tissues and systems affected by uncontrolled neutrophil elastase when AAT is deficient.
Mark's Insight: If insufficient Alpha-1 Antitrypsin fails to protect lung tissue, it logically fails to protect other tissues throughout the body.
Target Areas for Investigation:
Bone Marrow and Blood Formation
Vascular System
Connective Tissues
Neurological Tissues
Reproductive Health
Renal System
Comprehensive Mapping: We seek to identify every tissue vulnerable to neutrophil elastase attack, creating a complete picture of AAT's protective role throughout the body.
Research Goal: Demonstrate how adequate AAT levels can prevent development of secondary diseases and complications.
Hypothesis: Many "comorbidities" in various diseases may actually be manifestations of inadequate AAT protection against inflammatory tissue damage.
Research Questions:
Potential Impact: Preventing comorbidities could dramatically improve quality of life and reduce healthcare costs across numerous patient populations.
We support research that:
No idea is too novel for us to consider. We especially welcome:
We support:
Basic Research
Translational Research
Clinical Research
All research should consider:
We expect:
We encourage:
The Mark Egly Foundation is particularly interested in research exploring Alpha-1 Antitrypsin in conditions never before associated with AAT deficiency.
Examples of Frontier Research:
Our Philosophy: Any condition with an inflammatory or neutrophil elastase-mediated component is worth investigating.
If you have a research proposal aligned with our priorities:
We're open to:
Through strategic funding and collaboration, the Mark Egly Foundation aims to:
Transform Medical Practice
Advance Scientific Understanding
Improve Global Health
Build a Research Community
What makes our research strategy unique:
The Mark Egly Foundation invites researchers, clinicians, industry partners, and institutions to join us in expanding the horizons of Alpha-1 Antitrypsin research.
Together, we can:
The research opportunities are limitless. The potential impact is extraordinary.
For research inquiries, grant applications, or collaborative opportunities, please contact the Mark Egly Foundation through our website.
Let's change medicine together.