R01AA031710
Project Grant
Overview
Grant Description
INTESTINAL PROTEASES IN ALCOHOL-ASSOCIATED LIVER DISEASE - PROJECT SUMMARY ALCOHOL-ASSOCIATED HEALTH PROBLEMS ARE A MAJOR MEDICAL BURDEN IN INDUSTRIALIZED COUNTRIES. PATIENTS WITH ALCOHOL-ASSOCIATED LIVER DISEASE (ALD) SHOW INTESTINAL DYSBIOSIS AND GUT BARRIER DYSFUNCTION. INCREASED INTESTINAL PERMEABILITY ALLOWS MICROBE-ASSOCIATED MOLECULAR PATTERNS (MAMPS) SUCH AS LIPOPOLYSACCHARIDES (LPS) TO TRANSLOCATE TO THE LIVER AND CAUSE PROGRESSION OF ALD. THE MOLECULAR MECHANISMS HOW ALCOHOL MEDIATES DISRUPTION OF TIGHT JUNCTIONS ARE INCOMPLETELY UNDERSTOOD. USING MULTIPLEXED QUANTITATIVE PROTEOMICS AS AN UNBIASED APPROACH, OUR PRELIMINARY RESULTS DEMONSTRATE THAT FECAL SAMPLES FROM PATIENTS WITH ALCOHOL-ASSOCIATED HEPATITIS (AH) CONTAIN AN INCREASED ABUNDANCE OF HOST-DERIVED PROTEASES AS COMPARED WITH HEALTHY CONTROLS AND PATIENTS WITH ALCOHOL USE DISORDER (AUD). FECAL CATHEPSIN B (CTSB) LEVELS WERE ASSOCIATED WITH INCREASED MORTALITY IN PATIENTS WITH AH. OUR LABORATORIES FURTHER DEMONSTRATE THAT CTSB IS PREDOMINANTLY EXPRESSED IN MACROPHAGES IN THE INTESTINE AND ITS SECRETION IS UPREGULATED AFTER CHRONIC ETHANOL FEEDING IN MICE. FECAL SUPERNATANT FROM PATIENTS WITH AH INDUCES BARRIER DISRUPTION IN A CACO2 CELL MONOLAYER, WHICH IS BLOCKED WITH THE SPECIFIC CTSB INHIBITOR CA-074. THIS IS SUPPORTED BY DATA DEMONSTRATING THAT ORAL ADMINISTRATION OF THE GUT-RESTRICTED CTSB INHIBITOR CA-074 STABILIZES THE GUT BARRIER AND REDUCES ETHANOL-INDUCED LIVER DISEASE IN MICE. THE TESTABLE CENTRAL HYPOTHESIS OF THIS PROPOSED COLLABORATIVE AND MULTIDISCIPLINARY RESEARCH APPLICATION IMPLICATES THAT THE ETHANOL-MEDIATED INDUCTION OF CTSB IN INTESTINAL MACROPHAGES CONTRIBUTES TO GUT BARRIER DYSFUNCTION BY DIRECTLY DEGRADING INTESTINAL TIGHT JUNCTION PROTEINS AND PROMOTING ALD. THROUGH THE PROPOSED STUDIES WE WILL CHARACTERIZE HOST GUT PROTEASES AND THE IMMUNE RESPONSE IN A HUMAN COHORT AND A MOUSE MODEL OF ETHANOL-INDUCED LIVER DISEASE. TOWARDS THIS GOAL, WE WILL CHARACTERIZE HUMAN PROTEASES IN FECAL SAMPLES AND INTESTINAL BIOPSIES OF PATIENTS WITH ALD. WE PREDICT THAT INCREASED FECAL CTSB CORRELATES WITH CLINICAL SEVERITY AND OUTCOME IN PATIENTS WITH ALD (AIM 1). WE WILL MECHANISTICALLY DETERMINE THE ROLE OF CTSB IN CONTRIBUTING TO INTESTINAL TIGHT JUNCTION DISRUPTION. WE WILL CHARACTERIZE THE SOURCE, REGULATION AND SUBSTRATES OF CTSB USING MOUSE INTESTINAL MACROPHAGES AND HUMAN INTESTINAL ORGANOIDS. WE WILL USE MICE WITH A MYELOID SPECIFIC DELETION OF CTSB AND SUBJECT THEM TO CHRONIC-PLUS BINGE ETHANOL FEEDING (AIM 2). WE WILL USE A PHARMACOLOGICAL INTERVENTION WITH AN INTESTINE RESTRICTED AND SPECIFIC CTSB INHIBITOR IN A MOUSE MODEL OF ETHANOL FEEDING (AIM 3). WE BELIEVE THESE STUDIES WILL PROVIDE IMPORTANT INSIGHTS INTO ALCOHOL-MEDIATED CHANGES OF INTESTINAL PROTEASES THAT RESULT IN GUT BARRIER DYSFUNCTION AND PROMOTE ALD. EVENTUALLY THIS APPROACH WILL LEAD TO NEW THERAPEUTIC TARGETS FOR PATIENTS WITH ALD.
Funding Goals
TO DEVELOP A SOUND FUNDAMENTAL KNOWLEDGE BASE WHICH CAN BE APPLIED TO THE DEVELOPMENT OF IMPROVED METHODS OF TREATMENT AND MORE EFFECTIVE STRATEGIES FOR PREVENTING ALCOHOLISM AND ALCOHOL-RELATED PROBLEMS. THE NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM (NIAAA) SUPPORTS RESEARCH IN A BROAD RANGE OF DISCIPLINES AND SUBJECT AREAS RELATED TO BIOMEDICAL AND GENETIC FACTORS, PSYCHOLOGICAL AND ENVIRONMENTAL FACTORS, ALCOHOL-RELATED PROBLEMS AND MEDICAL DISORDERS, HEALTH SERVICES RESEARCH, AND PREVENTION AND TREATMENT RESEARCH. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION AND TECHNOLOGY TRANSFER THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
California
United States
Geographic Scope
State-Wide
Related Opportunity
San Diego University Of California was awarded
Intestinal Proteases in Alcohol-Associated Liver Disease
Project Grant R01AA031710
worth $3,182,397
from National Institute on Alcohol Abuse and Alcoholism in September 2025 with work to be completed primarily in California United States.
The grant
has a duration of 4 years and
was awarded through assistance program 93.273 Alcohol Research Programs.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
9/20/25
Start Date
8/31/29
End Date
Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
Activity Timeline
Additional Detail
Award ID FAIN
R01AA031710
SAI Number
R01AA031710-80819600
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75N500 NIH National Institute on Alcohol Abuse and Alcoholism
Funding Office
75N500 NIH National Institute on Alcohol Abuse and Alcoholism
Awardee UEI
UYTTZT6G9DT1
Awardee CAGE
50854
Performance District
CA-90
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Modified: 9/24/25