The Hypersensitivity, Autoimmune, and Immune-mediated [HAI] Diseases Study Section reviews applications that address basic and clinically-related immunological mechanisms of autoimmunity and immune-mediated diseases. Both human and animal models as well as in vitro systems, molecular, cellular, genomic and proteomic approaches are used to address immune-mediated disease questions.
The List of Reviewers lists all present, whether permanent or temporary, to provide the full scope of expertise present on that date. Lists are posted 30 days before the meeting and are tentative, pending any last minute changes.
The membership panel is a list of chartered members only.
- Immunological processes related to autoimmune diseases such as systemic lupus erythematosus, Sjögren’s syndrome, multiple sclerosis, type I diabetes, autoimmune arthritis, and idiopathic inflammatory myopathies.
- Environmental and genetic factors involved in immune pathway triggers and autoimmunity.
- Maintenance and breakage of central tolerance, peripheral tolerance and immune homeostasis.
- Strategies for reestablishing a normal immune balance for treatment of autoimmune diseases.
Shared Interests and Overlaps
Applications that focus on inflammatory diseases, hypersensitivity, allergic diseases, and asthma that currently fit the HAI Study Section are being moved to the Hypersensitivity, Allergies and Mucosal Immunology (HAMI) recurring Special Emphasis Panel.
There are shared interests with Innate Immunity and Inflammation Study Section (III) in innate immune mechanisms and inflammation. Applications focusing on basic and/or effector functions of innate immune cells in in vitro and in vivo models of inflammation and innate immunity may be reviewed by III. Applications examining innate immune mechanisms involved in autoimmune disease development or progression may be reviewed by HAI.
There are shared interests with Transplantation, Tolerance and Tumor Immunology Study Section (TTT). Applications focusing on central and peripheral tolerance in tumor and transplant models may be reviewed by TTT. Applications examining mechanism leading to effector:regulatory immune cell imbalance, central and peripheral tolerance breakage and autoimmune disease may be reviewed by HAI.
There are shared interests with Cellular and Molecular Immunology A (CMIA)/Cellular and Molecular Immunology Study Section B (CMIB) in basic immune mechanisms. Applications examining the development, differentiation, activation, cellular, biochemical, structural and biophysical mechanisms of innate/adaptive immune cells and systems may be reviewed by CMIA/CMIB. Applications examining molecular and cellular mechanisms, such as transcriptional and translational control events that alter immune cell function leading to tolerance breakage and autoimmune disease onset or progression may be reviewed by HAI.
There are shared interests with Arthritis, Connective Tissue and Skin Study Section (ACTS) in inflammation of the joints, connective tissues and skin. Applications examining the biology of the joint, connective tissue and skin may be reviewed by ACTS. Applications examining the immunological aspects of rheumatic diseases may be reviewed by HAI.
There are shared interests in neuroimmunology with the Clinical Neuroimmunology and Brain Tumors Study Section (CNBT), with Neuroendocrinology, Neuroimmunology, Rhythms and Sleep Study Section(NNRS) and with Cellular and Molecular Biology of Glia Study Section (CMBG) study sections. Applications examining neural tissue and processes associated with neural diseases may be reviewed by CNBT, NNRS or CMBG. Applications focusing on the immunomodulatory mechanisms and immunopathology of inflammatory neural diseases such as multiple sclerosis may be reviewed by HAI.
There are shared interests with Cellular Aspects of Diabetes and Obesity (CADO). Applications examining differentiation, development, growth, function and immune regulation of adipocytes, pancreatic islets or beta cell replacement due to diabetes may be reviewed by CADO. Applications examining immunological mechanisms related to type 1 diabetes onset and progression may be reviewed in HAI.