A major goal expressed by NIAID and other agencies charged with development of the U.S. biodefense research strategy is a broad spectrum activity that mitigates catastrophic biothreats across a wide spectrum of agents. Such therapeutic activities have been difficult to identify and require new understanding and paradigms of the immune system or the pathogens. The novel discovery that reduced expression of CD45, a protein associated with immune cells, profoundly modulates the immune response capability in a manner that protects the host against a variety of lethal pathogens provides opportunities for novel therapeutic interventions that target the host immune system to achieve the goal of a broad spectrum activity. The approach is based on findings using a series of mice genetically modified to express reduced levels of CD45. Reduced CD45 expression was shown to provide survival protection from three Category A (B. anthracis, Ebola virus and Marburg virus) and one Category C (influenza) biodefense pathogens. Since these four pathogens represent highly diverse infectious organisms and pathologies, it is likely that the reduction of CD45 will also provide therapeutic benefit against additional pathogens. Thus, the significance of the proposed studies is not only the potential for pathogen protection from a biodefense standpoint but also for pandemic disease control. The reduction of CD45 expression to enhance immune protection against biodefense pathogens represents a new and unexpected property of CD45 and a novel approach for immunotherapy. Since permanent, genetically-reduced CD45 expression, as occurs when only one functional gene copy is present, produces no detectable adverse effects in mouse or human, a therapeutic that induces transient reduction of CD45 function is very likely to have an excellent safety profile, particularly if only CD45 is targeted. One approach to such selective targeting is to utilze CD45-specific genetic sequences. CD45-specific siRNA will be delivered using a unique lipid-polymer hybrid nanoparticle platform to achieve selective CD45 reduction. This feasibility study will test and advance this technology, initially using cultured cells followed by evaluation of CD45 reduction and modulation of immune function in mice.
Public Health Relevance Statement: Public Health Relevance: Reduction of CD45 expression protects against lethal infections from diverse bacterial and viral pathogens providing opportunities for a broad spectrum therapeutic. The ultimate goal of this project is to inhibit CD45 production with small interfering RNA (siRNA) to a level that provides survival benefit to a variety of biothreats. Advanced nanoparticle technology will be used to deliver the siRNA to the appropriate cells.
Project Terms: Adverse effects; Bacillus anthracis; base; Biocompatible; biodefense; biothreat; Cancer Center; Categories; Cell Culture System; Cell Line; Cells; Charge; Communicable Diseases; Cultured Cells; design; Development; Disease model; disorder control; Dose; Drug Delivery Systems; Ebola virus; Encapsulated; Engineering; Evaluation; Feasibility Studies; Frankfurt-Marburg Syndrome Virus; Future; Genes; Genetic; Goals; Hematopoietic; Human; Hybrids; Immune; immune function; Immune response; Immune system; Immune Targeting; immunoregulation; Immunotherapy; In Vitro; in vivo; Infection; Infectious Agent; Infectious Disease Immunology; Influenza; influenzavirus; Leukocytes; Lipids; medical schools; Microbe; Modeling; Molecular Biology; Mus; nanoengineering; nanomedicine; nanoparticle; Nanotechnology; National Institute of Allergy and Infectious Disease; novel; novel strategies; novel therapeutic intervention; pandemic disease; Particle Size; pathogen; Pathology; Polymers; Production; Property; Protein Tyrosine Phosphatase; Proteins; PTPRC gene; public health relevance; Research; Safety; Series; Signal Transduction; Small Interfering RNA; Strategic Planning; Structure; Surface; Technology; Testing; Therapeutic; Viral; Work
