Sexually transmitted infection by herpes simplex virus type-2 (HSV-2) is a major health problem. HSV-2 genital infections can also significantly enhance susceptibility to human immunodeficiency virus. There is no vaccine or protective therapy available to control the transmission of the virus, which is on the rise. In lieu of an effective vaccine, we recently demonstrated the feasibility of a novel microbivac approach as an effective mucosal immunity boosting virucidal platform. Under this strategy, uniquely designed zinc oxide tetrapod nanoparticles (ZOTEN) provide instant microbicidal benefits to the vaginal surface via high-affinity trapping of invading HSV-2 virions. The trapping renders the virions unable to enter cells of the vaginal epithelium. As an additional advantage of this approach, innate and adaptive immune mechanisms are triggered when the virions captured on ZOTEN are presented to and processed by professional phagocytes including mucosal antigen presenting cells (APCs). We also demonstrated that ZOTEN provides adjuvant-like benefits that are very similar to those seen with alum. This proposal will test our hypothesis that inhibition of HSV-2 attachment receptor, heparan sulfate, from cells on the surface of the genital epithelium will enhance the microbivac efficacy of ZOTEN. We propose that inhibition of virus binding to cells will generate stronger infection blockade and a more robust adaptive immune response against the trapped virus. Our hypothesis is supported by brand new data that binding of anti-HSV peptide, G2, to heparan sulfate proteoglycans stops infection and in addition, triggers internalization of heparan sulfate from the surface of cells. Using a mouse model of female genital infection our central hypothesis will be tested by two specific Aims.
Aim 1 will test the first part of our hypothesis that inhibition of heparan sulfate by G2 will protect the cells on the vaginal surface from the deleterious effects of HSV-2 while enhancing the virucidal benefits of ZOTEN.
Aim 2 will test the hypothesis that in the presence of G2, the ZOTEN/HSV-2 complexes drive stronger adaptive immune responses. We also propose that dual action by the microbivac will generate strong immunotherapeutic effects, which will be confirmed by a second round of HSV-2 infection. Analyses of key cytokines/chemokines will be made to determine the status of mucosal innate immunity under various treatment conditions. Overall, our exploratory and proof-of-concept studies will establish a role for heparan sulfate inhibition in generating higher microbivac efficacy, and guide future designs for more effective prevention of genital herpes transmission and associated disease manifestations.

Public Health Relevance

Herpes simplex virus type-2 (HSV-2) is the major causative agent for sexually transmitted diseases and a co- factor for the acquisition of human immunodeficiency virus. Our study focuses on understanding molecular mechanisms that can improve innate and adaptive immune responses generated against HSV-2 particles bound to zinc oxide nanoparticles. Stronger immune responses can better guard against the deleterious effects of genital HSV-2 infection. Our proof-of-concept studies will pave the way for future translational studies to help prevent genital herpes transmission.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21AI133557-02
Application #
9625077
Study Section
Immunity and Host Defense (IHD)
Program Officer
Natarajan, Ramya
Project Start
2018-01-12
Project End
2019-12-31
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612