Systemic Lupus Erythematosis

The Immune System

Immunology Connection to Tissue Engineering Develop methods to selectively block immune response to engineered tissue Manipulate immune system tissues to prevent autoimmune diseases Scaffold compatibility

Gender Differences in Immune Response Females resist a variety of infections better than males Females may reject transplanted organs more rapidly Females have a higher frequency of autoimmune diseases

What is Lupus? An autoimmune disease Your body can not adequately distinguish between foreign materials (antigens) and its own cells and tissues. The immune system directs the development of antibodies that target bodily (antigens) components. The auto-antibodies react with the bodies own antigens, forming immune complexes which can accumulate and cause increasing inflammation- related damage.

What Causes Lupus? Cause unknown, but suspect –Genetic factors –Environmental factors

What Causes Lupus? (cont’d) Genetic causes –Hereditary, but no single gene known to cause SLE –Some people more genetically prone to Lupus –5% of children with parents who have it develop Lupus –10% of Lupus patients also have a close relative with the disease –Chromosomes 1 and 6 associated with Lupus in certain families

Observations to Support Genetic Factors in Lupus Clustering in families Identical twins > fraternal twins

Genetic factors in SLE -> different disease frequencies in different ethnic groups -> sibling recurrence-risk ratio ~15-20 (thus, if your sibling has SLE your risk is ~1% rather than ~0.05%) -> high clinical disease concordance among twins: 2-5% for dizygotic twins, 24-58% for monozygotic twins -> complement deficient patients (rare) very frequently develop SLE (40-75%) -> evidence for linkage to specific gene loci: Environmental factors?

What Causes Lupus? (cont’d) Environmental causes –Infections –Antibiotics –Ultra-violet light –Extreme stress –Certain drugs

Apoptosis and SLE: Causal Connection? Delayed clearance of apoptotic cells Abnormal exposure of intracellular components to immune response, supported by autoantibody findings in Lupus patients

Complement and SLE? Altered complement system: an SLE correlation? Reduced levels of C3 and C4 components commonly found, those with C1, C2, and C4 gene aberrations at apparent high risk

Symptoms of Lupus Flares are common –Periods where symptoms are intense, then die down Most common symptoms –Achy joints Occurs in 95% of Lupus patients –Fever more than 100 degrees F 90% –Arthritis 90% –Prolonged or extreme Fatigue 81%

Symptoms of Lupus (cont’d) –Skin rashes 74% –Anemia 71% Other symptoms –Kidney involvement, pain in chest, deep breathing, butterfly shaped rash on cheek and nose, sun or light sensitivity, hair loss, abnormal blood clotting, Raynaud’s phenomenon, seizures, mouth and nose ulcers.

SLE Characteristics Characterized by autoantibodies directed against nuclear and cytoplasmic cellular components. Result: AutoAb-antigen immune complex formation, which circulate and deposit in tissues, leading to chronic inflammation and continuous, extensive damage. Disease progresses in flares, followed by remissions Flares may include malaise, fever, joint pain, photosensitivity Lupus Flare (malar rash) Increased risk of clotting, stroke, heart disease, renal failure (advanced stages)

Lupus in Newborns - up to 10% risk if mother has certain antibodies Clinical Features: Reversible skin blood liver Irreversible heart problems

Diagnosis of Lupus Difficult to diagnose Lupus –Lupus symptoms mirror other diseases’ symptoms, and Lupus symptoms often come and go No single lab test to diagnose Lupus American College of Rheumatology (ACR) issued a list of 11 symptoms and tests to help diagnose Lupus patients. –A person with Lupus experiences at least four of these symptoms or prove positive to at least 4 of these tests. The symptoms do not have to occur at the same time though.

SLE: Major diagnostic laboratory findings: -> Positive lupus erythematosus cell preparation (a peculiar polymorphonuclear leukocyte which has ingested nuclear material) -> Hemolytic anemia, leukopenia, lymphopenia or thrombocytopenia -> Heavy proteinuria or cellular casts in urine sediment -> ***Anti-nuclear and/or anti-DNA antibodies*** Related systemic autoimmune diseases with overlapping findings: -> Rheumatoid arthritis (mainly restricted to joints, distinguished by presence of RFs) -> Sjogren’s symdrome (mainly restricted to salivary and lacrimal glands) -> Schleroderma (mainly restricted to skin) ANA LE cell 1948

Pathogenesis of SLE EnvironmentalTriggers HormonalFactors Genetic Factors

Natural History of SLE Disease flares/activity (reversible) Organ damage (irreversible) disease treatment

Time (years) SLE Activity SLE Damage

Environmental Triggers Sun exposure (photosensitivity) Drug-induced lupus Viral triggers

Ultraviolet Irradiation Causes Programmed Cell Death

SLE Treatment NSAIDS Antimalarials (HCQ Mepacrine) Corticosteroids (oral/iv/im/intralesional) Immunosuppressives –Azathioprine –Cyclosporin A –Methotrexate –MMF –Cyclophosphamide Biologicals- Rituximab Others- Prasterone,Thalidomide,Acetretin

Interview of a Lupus Patient What kind of medications do you take? –I take Plaquenil which is an anti-malarial drug that fights fatigue. I also take Advil when I get stiff. I used to take Prednisone, but I don’t have to anymore because my disease isn’t as severe anymore as it used to be. Is there any research being done to find a cure or better treatment for Lupus? –There are many groups doing research on the immune system which is a link to autoimmune diseases like Lupus. Also, since Lupus seems to attack mostly women, there are many groups trying to find a link between hormones and Lupus.