AUTOIMMUNITY: AN UNMET CLINICAL CHALLENGE Lauren Johnson with Dr. Pamela Langer.

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Presentation transcript:

AUTOIMMUNITY: AN UNMET CLINICAL CHALLENGE Lauren Johnson with Dr. Pamela Langer

Overview  What is autoimmunity?  Septic Arthritis  Narcolepsy  Ankylosing Spondylitis  Treatment  New Direction of Research

What is autoimmunity?  Affects 5-8% of individuals in Western countries  Over 80 autoimmune conditions  Rheumatoid Arthritis, Diabetes Mellitus, Multiple Sclerosis  One of the least understood conditions in medicine  Among the leading causes of death in young and middle aged women in the U.S.  Results from immune cells recognizing “self” as foreign.  Cause is unknown, but thought to occur one of two ways.

Molecular Mimicry  Naive immune system Sensitized immune system

Error in T Cell Selection  T cells must undergo “positive” and “negative” selection  Occurs before they are released into the body  Test cells against a piece of “self”  Strong reaction = deletion / cell death Not perfect

Activation Pathways

Septic Arthritis  Caused by microbial infection  Septic = whole body infection ; presence of pathogens in the bloodstream  Arthritis = joint inflammation  Easier to diagnose, usually only 1-2 joints involved  Strong immune reaction, many cells activated  Influx of cells to joint = inflammation  Leads to cartilage damage  Risk of septic shock because of high inflammation (blood leaks out of capillaries, get decreased blood supply to organs)

Risks in Septic Arthritis  Higher risk if individual has pre-existing joint disease  Taking drugs that suppress immune system  Also risk of molecular mimicry  May lead to more permanent arthritic complications  Borrelia burgdorferi is similar to our own cells  Transmitted by ticks

Narcolepsy  Chronic neurological disorder  1/2000 people  Results from inability to regulate sleep-wake cycles  Irresistible bouts of sleep throughout the day, length varies  Only recently shown to be autoimmune  2009

Reaction Against Protein in Narcolepsy  Lack of hypocretin = hormone that promotes wakefulness  Narcolepsy patients lack cells that produce hypocretin  Destroyed in autoimmune reaction  Certain variation of immune response gene is present

Ankylosing Spondylitis  Affects 1.3% of adults 25 years and older = 2.4 million people  Angkylos = bent  Spondylos = spine  Belongs to subset of autoimmunity called the spondyloarthropathies  Joint diseases of the spine associated with presence of a specific variant of an immune response gene

Damage in Ankylosing Spondylitis  Immune system cells attack spine  May be molecular mimicry component  Klebsiella pneumoniae  Causes tissue damage  Ossification = new bone formation

Risk of spinal fracture in Ankylosing Spondylitis Bamboo spine Normal spine

Current Treatment for Autoimmune Disease  Manage symptoms  Methotrexate, Prednisone, Plaquenil, Arava Therapeutic targets Inhibit T cell activity Induce T cell death Eliminate certain subsets of T cells Inhibit cytokine activity (anti-inflammatory) * Modulate gene expression

Humira  Used for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, Crohn’s disease  Slows joints damage, provides pain relief  Bind to cytokine from macrophage, relieves inflammation and pain  Tumor Necrosis Factor- α (TNF- α )

Humira Action

Future Directions  Attempting to treat the source  Identify autoimmune T cells (Gocke et al., 2009) Study structure; synthetic molecules could bind and inactivate  Track the development of the disease in hopes of preventing it (Zangini et al., 2009)  Gene Therapy  Introduce anti-inflammatory genes into cells  Introduce TNF- α receptor genes into cells Need long term expression or repeated administration

Conclusions  Many factors affect immune system  Stress, environment, genetics, diet, sleep  Factors push cells one way or another.  Sometimes results in autoimmunity.  Need to be able to recognize autoimmunity in patients.  Research  The more we understand regulation and factors, the more treatment options will be available.

Thank you!  Dr. Pamela Langer

References  Al-Ahaideb, Abdulaziz. "Septic arthritis in patients with rheumatoid arthritis." Journal of Orthopaedic Surgery and Research (2008). Journal of Orthopaedic Surgery and Research. 29 July Web. 5 Jan  Andrej, Tarkowski. "Infectious arthritis." Best Practice & Research Clinical Rheumatology 20.6 (2006): ScienceDirect. 24 Dec Web. 5 Jan  Berchtold, P., and M. Seitz. "Immunosuppression: Tightrope walk between iatrogenic side effects and therapy." Schweiz Med Wochenschrift (1996): Pubmed.gov. 21 Sept Web. 5 Jan  Brusch, John L. "Septic Arthritis." Emedicine. WebMD, 5 Jan Web. 9 Jan  Davidson, Anne, and Diamond Betty. "Autoimmune Diseases." New England Journal of Medicine (2001): New England Journal of Medicine. 2 Aug Web. 5 Jan  Fauci, Braunwald, Kasper, Hauser, Longo, Jameson, and Loscalzo. Harrison's Principles of Internal Medicine. 17th ed. Vol. II. The McGraw-Hill Companies, Inc., Print.  Favero, M., L. Punzi, V. Carraro, L. Riato, and F. Schiavon. "[Septic arthritis: a 12 years retrospective study in a rheumatological university clinic]." Reumatismo 60.4 (2008): Pubmed.gov. Oct. & nov Web. 5 Jan  Johnston, A., JE Gudjonsson, H. Sigmundsdottir, BR Ludviksson, and H. Valdimarsson. "The anti-inflammatory action of methotrexate is not mediated by lymphocyte apoptosis, but by the suppression of activation and adhesion molecules." Clinical Immunology (2005): Pubmed.gov. Feb Web. 5 Jan  Kindt, Thomas J., Barbara A. Osborne, and Richard A. Goldsby. Kuby Immunology. 6th ed. New York: W. H. Freeman, Print.