Multi-drug resistant (MDR) bacterial infections represent a significant threat to public health. It is estimated that the impact of antibiotic resistance will continue to grow resulting in a global economic burden of $100 trillion and causing 10 million deaths annually. Many of the therapeutics currently under development represent traditional antibiotic approaches or next generation antibiotics that will likely suffer a limited market lifespan due to the rapid emergence of resistance. To effectively address antibiotic resistance and have therapeutic options that are effective, approaches that utilize new mechanisms of action must be explored. Arrevus is developing a novel approach to addressing MDR bacterial infections using Designer Proline-rich antimicrobial peptide Chaperone protein inhibitors (DPCs), derived from insects and selectively modified, acting as inhibitors to one of the critical bacterial proteins responsible for bacterial protein folding, DnaK. Preliminary studies have demonstrated the potential of DPCs as antibiotic potentiating agents against MDR gram-positive and gram-negative bacterial pathogens. Our efforts have shown that DPCs: 1) enhance antibiotic activity; 2) reduce bacterial burden in systemic infection models; 3) have favorable preliminary safety profiles; and 4) provide an enhancement to antimicrobial agents through a novel mechanism of action. While early efforts to develop DPCs has been successful, the pace of the programs and expansion into additional indications has been hindered due to the lack of reliable in vitro screening assays that correlate with in vivo efficacy. DPCs that have displayed potency using minimum inhibitory assays have failed in subsequent in vivo efficacy studies. The objective of the proposed Phase I program is to develop and validate an in vitro assay for DPC activity.
In Aim 1, a scratch test assay using human alveolar and keratinocyte cells will be characterized for several endpoints, including scratch closure, cytokine production, and apoptosis in the presence of well-characterized DPCs and antibiotics to develop an assay that is predictive of in vivo DPC activity.
In Aim 2, the assay developed in Aim 1 will then be used to inform a medical chemistry program that is designed to identify DPCs with activity against methicillin-resistant Staphylococcus aureus. Two lead DPCs identified using the using the assay will then be evaluated for in vivo efficacy using a standard thigh infection model. Successful completion of the proposed program will provide proof-of-concept for the use of the developed in vitro assay for detecting DPC activity that is predictive of in vivo activity and will support a Phase II program that will expand the assay to use with gram- negative pathogens and evaluate lead DPCs in indication-specific models.

Public Health Relevance

Antibiotic-resistant infections are associated with an increased morbidity and mortality compared to antibiotic- sensitive infections and represent a significant threat to public health. Arrevus is developing a new class of anti- infectives, modified antimicrobial peptides, derived from insects that act via a novel mode of action to enhance the ability of antibiotics in treating antibiotic-resistant infections. Arrevus proposes to develop an in vitro assay that will predict in vivo efficacy of the modified antimicrobial peptides in order to expedite development programs for multi-drug resistant infections.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Business Technology Transfer (STTR) Grants - Phase I (R41)
Project #
1R41AI142829-01
Application #
9674732
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Xu, Zuoyu
Project Start
2018-12-01
Project End
2019-11-30
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Arrevus, Inc.
Department
Type
DUNS #
080059821
City
Research Triangle Park
State
NC
Country
United States
Zip Code
27709