SBIR-STTR Award

Autoimmune diseases develop when the adaptive immune response targets self-antigens, leading to inflammation and tissue destruction. The innate immune system faces the same fundamental challenge as the adaptive immune system - distinguishing self from non-self antigens - and there is now considerable evidence that recognition of self nucleic acids through toll-like receptors (TLRs) can contribute significantly t sterile inflammation and autoimmunity, with the clearest example being the role played by TLR9 and TLR7 in the pathogenesis of systemic lupus erythematosus (SLE). One of the innate receptors for RNA, TLR8, is a potent stimulator of inflammatory cytokines such as IL6 and TNF- , and its expression by multiple cell types involved in inflammatory diseases suggests likely involvement in autoimmunity. However, the lack of useful animal models, a consequence of the very different ligand specificity of human TLR8 and its rodent orthologs, has proven to be a major limitation in the study of TLR8 function. We have developed new tools that we hope will help better understand the biology of TLR8 and that have provided important new evidence for a role of TLR8 signaling in rheumatoid arthritis. The key objective of this proposal is to develop small-molecule antagonists of human TLR8 that can be tested for efficacy, first in the novel animal models we have developed, and ultimately in patients. The principal activities will include:"Establishment of a cell-based screening strategy for huTLR8 antagonists."Screening multiple libraries of well-characterized compounds."Confirmation of the specificity of hits from these screening activities. If successful, this project will demonstrate the feasibility of developng a small-molecule inhibitor for human TLR8, and will provide the lead compounds that can be rigorously tested for potential use in the treatment of rheumatoid arthritis.

Public Health Relevance:
Many drugs targeting pro-inflammatory cytokines have proven clinically beneficial;however, the mechanisms and triggering signals underlying the production of these cytokines in various autoimmune diseases are still poorly understood. We have found that a key receptor of innate immune responses, human Toll-Like Receptor- 8, can mediate multiple forms of autoimmunity, most notably rheumatoid arthritis, when triggered in mice. We propose to screen compound libraries for small molecules that inhibit this receptor and the subsequent pro- inflammatory response as a therapy for rheumatoid arthritis.

Autoimmune diseases develop when the adaptive immune response targets self-antigens, leading to inflammation and tissue destruction. The innate immune system faces the same fundamental challenge as the adaptive immune system - distinguishing self from non-self antigens - and there is now considerable evidence that recognition of self nucleic acids through toll-like receptors (TLRs) can contribute significantly t sterile inflammation and autoimmunity, with the clearest example being the role played by TLR9 and TLR7 in the pathogenesis of systemic lupus erythematosus (SLE). One of the innate receptors for RNA, TLR8, is a potent stimulator of inflammatory cytokines such as IL6 and TNF-¿, and its expression by multiple cell types involved in inflammatory diseases suggests likely involvement in autoimmunity. However, the lack of useful animal models, a consequence of the very different ligand specificity of human TLR8 and its rodent orthologs, has proven to be a major limitation in the study of TLR8 function. We have developed new tools that we hope will help better understand the biology of TLR8 and that have provided important new evidence for a role of TLR8 signaling in rheumatoid arthritis. The key objective of this proposal is to develop small-molecule antagonists of human TLR8 that can be tested for efficacy, first in the novel animal models we have developed, and ultimately in patients. The principal activities will include: "Establishment of a cell-based screening strategy for huTLR8 antagonists. "Screening multiple libraries of well-characterized compounds. "Confirmation of the specificity of hits from these screening activities. If successful, this project will demonstrate the feasibility of developng a small-molecule inhibitor for human TLR8, and will provide the lead compounds that can be rigorously tested for potential use in the treatment of rheumatoid arthritis.

Public Health Relevance Statement:
Many drugs targeting pro-inflammatory cytokines have proven clinically beneficial; however, the mechanisms and triggering signals underlying the production of these cytokines in various autoimmune diseases are still poorly understood. We have found that a key receptor of innate immune responses, human Toll-Like Receptor- 8, can mediate multiple forms of autoimmunity, most notably rheumatoid arthritis, when triggered in mice. We propose to screen compound libraries for small molecules that inhibit this receptor and the subsequent pro- inflammatory response as a therapy for rheumatoid arthritis.

NIH Spending Category:
Arthritis; Autoimmune Disease

Project Terms:
Agonist; Animal Model; Antigens; Autoantigens; Autoimmune Diseases; Autoimmunity; B-Lymphocytes; base; Biological Assay; Biology; Blood; Blood Cells; cell type; Cells; Chronic Disease; cytokine; Dendritic Cells; Development; Disease; Drug Targeting; efficacy testing; Evaluation; Face; Genetic Polymorphism; Government; Human; Human Activities; human TLR7 protein; human TLR8 protein; IL6 gene; IL8 gene; Immune response; Immune system; Inflammation; Inflammatory; Inflammatory Response; inhibitor/antagonist; Injection of therapeutic agent; Interferon Type I; Interleukin-12; Interleukin-6; Lead; Libraries; Ligands; macrophage; Mediating; Modeling; monocyte; Mus; Myelogenous; neutrophil; novel; Nucleic Acids; Oligonucleotides; Orthologous Gene; Pathogenesis; Patients; Persons; Play; pre-clinical; Production; Program Development; Promotor (Genetics); Rattus; receptor; Reporter Genes; response; Rheumatoid Arthritis; RNA; Rodent; Role; screening; Signal Transduction; small molecule; small molecule libraries; Specificity; Sterility; Systemic Lupus Erythematosus; Testing; Text; Therapeutic Agents; Tissues; TLR7 gene; TLR8 gene; TNF gene; Toll-like receptors; tool; Transgenic Mice