Call for Abstract
Scientific Program
13th International Congress on Autoimmunity, will be organized around the theme “Unveiling the versatile therapies to achieve breakthrough in Immunity”
Autoimmunity 2019 is comprised of 15 tracks and 50 sessions designed to offer comprehensive sessions that address current issues in Autoimmunity 2019.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
- Track 1-1Achalasia
- Track 1-2Addison’s disease
- Track 1-3Lupus
- Track 1-4Meniere’s disease
- Track 1-5Narcolepsy
The study of the molecular and cellular components that comprise the immune system, including their function and interaction, is the central science of immunology. The immune system has been divided into a more primitive innate immune system and, in vertebrates, an acquired or adaptive immune system.
- Track 2-1Malignant disease
- Track 2-2Growing tumor
- Track 2-3 Apoptosis
- Track 2-4IgG1
- Track 3-1Auto-immune Disease
- Track 3-2Cancer
- Track 3-3Malignancy
- Track 3-4Rheumatic Disease
- Track 4-1Autoimmune cholangitis
- Track 4-2Autoimmune liver Disease
- Track 4-3Liver Transplantation
- Track 5-1IL-1 Family
- Track 5-2IL-1 Receptors
- Track 5-3Interferon (IFN)
- Track 5-4TGF beta Family
- Track 5-5Chemokine & Chemokine Receptor
Autoimmunity results from a break in self-tolerance involving humoral and/or cell-mediated immune mechanisms. One pathological consequence of a failure in central and/or peripheral tolerance is the generation of autoantibodies and subsequent formation of complement-fixing immune complexes that contribute to tissue damage. Prevailing pharmacological strategies for treating autoimmune diseases involve the use of broad-acting immunosuppressants that with long term use have associated toxicities.
- Track 6-1Drug Delivery Systems
- Track 6-2Tumor Necrosis Factor-alpha/Metabolism
- Track 6-3Membrane Proteins/Antagonists & Inhibitors
Self-tolerance loss is fundamental to autoimmunity. While understanding of immune regulation is expanding rapidly, the mechanisms causing loss of tolerance in most autoimmune diseases remain elusive. Autoimmunity is believed to develop when genetically predisposed individuals encounter environmental agents that trigger the disease.
- Track 7-1Autoimmunity Genetics
- Track 7-2Genetic Immunology
- Track 7-3Genetic Predisposition to Disease
- Track 7-4X Chromosome Inactivation
- Track 8-1Desensitization
- Track 8-2Immunologic
- Track 8-3Immunologic Factors & therapeutic use
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- Track 9-1Schizophrenia
- Track 9-2MHC
The complement system is an ancient and evolutionary conserved element of the innate immune mechanism. It comprises of more than 20 serum proteins most of which are synthesized in the liver. These proteins are synthesized as inactive precursor proteins which are activated by appropriate stimuli.
- Track 10-1Adaptive Immunity
- Track 10-2Complement Activation/Drug effects
- Track 10-3Drug Evaluation, Preclinical
- Track 10-4Complement Membrane Attack Complex
- Track 11-1Immunosuppressive Drugs
- Track 11-2Ulcerative colitis
- Track 12-1Autoimmune Diseases Prevention & Control
- Track 12-2Humans
- Track 12-3Risk Factors
- Track 13-1Hematopoietic Stem Cell Therapy for Autoimmune Diseases
- Track 13-2Development of Hematopoietic Stem Cell Lines for Transplantation
- Track 13-3Gene Therapy and Stem Cell Approaches for the Treatment of Autoimmune Diseases
- Track 14-1Multiple Sclerosis
- Track 14-2Myxedema
Several self-molecules have been identified as target antigens in autoimmune diseases. Since lack or loss of tolerance to these molecules is one of the key events promoting autoimmunity, researchers are exploring the possibility that the administration of antigens or peptides may stimulate tolerogenic mechanisms and delay or prevent the full phenotypic expression of autoimmune diseases.
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- Track 15-1Thymus
- Track 15-2Harnessing Treg cells
- Track 15-3Designing Peptides for Therapy