Understanding Autoimmune Disease

This booklet contains information about autoimmune diseases. You will not find everything there is to know about autoimmune diseases here, however. In fact, the information presented here may prompt you to think of more questions about autoimmune diseases because autoimmune diseases are complex.

We have tried to anticipate which terms will need further definition and clarification. Those terms, when they first appear in the text, are in italics. Italicized words and phrases are defined in the Glossary at the end of the booklet.

You will find more in-depth and detailed resources at your local library or through your health care provider. The Internet is a valuable source of information as well. Start by doing a search on the National Institutes of Health (NIH) Web site at http://www.nih.gov/ for information on the broad range of research conducted by NIH, including autoimmune diseases.

What Are Autoimmune Diseases?

The word "auto" is the Greek word for self. The immune system is a complicated network of cells and cell components (called molecules) that normally work to defend the body and eliminate infections caused by bacteria, viruses, and other invading microbes. If a person has an autoimmune disease, the immune system mistakenly attacks self, targeting the cells, tissues, and organs of a person's own body. A collection of immune system cells and molecules at a target site is broadly referred to as inflammation.

There are many different autoimmune diseases, and they can each affect the body in different ways. For example, the autoimmune reaction is directed against the brain in multiple sclerosis and the gut in Crohn's disease. In other autoimmune diseases such as systemic lupus erythematosus (lupus), affected tissues and organs may vary among individuals with the same disease. One person with lupus may have affected skin and joints whereas another may have affected skin, kidney, and lungs. Ultimately, damage to certain tissues by the immune system may be permanent, as with destruction of insulin-producing cells of the pancreas in Type 1 diabetes mellitus.

Who Is Affected by Autoimmune Diseases?

Many of the autoimmune diseases are rare. As a group, however, autoimmune diseases afflict millions of Americans. Most autoimmune diseases strike women more often than men; in particular, they affect women of working age and during their childbearing years.

Some autoimmune diseases occur more frequently in certain minority populations. For example, lupus is more common in African-American and Hispanic women than in Caucasian women of European ancestry. Rheumatoid arthritis and scleroderma affect a higher percentage of residents in some Native American communities than in the general U.S. population. Thus, the social, economic, and health impact from autoimmune diseases is far-reaching and extends not only to family but also to employers, co-workers, and friends.

What Are the Causes of Autoimmune Diseases?

Are they contagious? No autoimmune disease has ever been shown to be contagious or "catching." Autoimmune diseases do not spread to other people like infections. They are not related to AIDS, nor are they a type of cancer.

Are they inherited? The genes people inherit contribute to their susceptibility for developing an autoimmune disease. Certain diseases such as psoriasis can occur among several members of the same family. This suggests that a specific gene or set of genes predisposes a family member to psoriasis. In addition, individual family members with autoimmune diseases may inherit and share a set of abnormal genes, although they may develop different autoimmune diseases. For example, one first cousin may have lupus, another may have dermatomyositis, and one of their mothers may have rheumatoid arthritis.

Examples of Autoimmune Diseases: (Listed by the Main Target Organ)
Nervous System:		Gastrointestinal System:
	Multiple sclerosis		Crohn's Disease
	Myasthenia gravis		Ulcerative colitis
	Autoimmune neuropathies		Primary biliary cirrhosis
	such as Guillain-Barré		Autoimmune hepatitis
	Autoimmune uveitis
			Endocrine Glands:
	Blood:		Type 1 or immune-mediated
	Autoimmune hemolytic anemia		diabetes mellitus
	Pernicious anemia		Grave's Disease
	Autoimmune thrombocytopenia		Hashimoto's thyroiditis
			Autoimmune oophoritis and
	Blood Vessels:		orchitis
	Temporal arteritis		Autoimmune disease of the
	Anti-phospholipid syndrome		adrenal gland
	Vasculitides such as
	Wegener's granulomatosis		Multiple Organs Including the
	Behcet's disease		Musculoskeletal System:*
			Rheumatoid arthritis
	Skin:		Systemic lupus erythematosus
	Psoriasis		Scleroderma
	Dermatitis herpetiformis		Polymyositis, dermatomyositis
	Pemphigus vulgaris		Spondyloarthropathies such as
	Vitiligo		ankylosing spondylitis
			Sjogren's syndrome

*These diseases are also called connective tissue (muscle, skeleton, tendons, fascia, etc.) diseases.

The development of an autoimmune disease may be influenced by the genes a person inherits together with the way the person's immune system responds to certain triggers or environmental influences.

What other factors may influence the development of autoimmune diseases? Some autoimmune diseases are known to begin or worsen with certain triggers such as viral infections. Sunlight not only acts as a trigger for lupus but can worsen the course of the disease. It is important to be aware of the factors that can be avoided to help prevent or minimize the amount of damage from the autoimmune disease. Other less understood influences affecting the immune system and the course of autoimmune diseases include aging, chronic stress, hormones, and pregnancy.

How Does the Immune System Work?

The immune system defends the body from attack by invaders recognized as foreign. It is an extraordinarily complex system that relies on an elaborate and dynamic communications network that exists among the many different kinds of immune system cells that patrol the body. At the heart of the system is the ability to recognize and respond to substances called antigens whether they are infectious agents or part of the body (self antigens).

Cells and molecules of the immune system protect the nose from attack by a virus.

T cell (lymphocyte) with a T-cell receptor on its surface

T and B Cells

Most immune system cells are white blood cells, of which there are many types. Lymphocytes are one type of white blood cell, and two major classes of lymphocytes are T cells and B cells. T cells are critical immune system cells that help to destroy infected cells and coordinate the overall immune response. The T cell has a molecule on its surface called the T-cell receptor. This receptor interacts with molecules called MHC (major histocompatibility complex). MHC molecules are on the surfaces of most other cells of the body and help T cells recognize antigen fragments. B cells are best known for making antibodies. An antibody binds to an antigen and marks the antigen for destruction by other immune system cells. Other types of white blood cells include macrophages and neutrophils.

Macrophages and Neutrophils

Macrophages and neutrophils circulate in the blood and survey the body for foreign substances. When they find foreign antigens, such as bacteria, they engulf and destroy them. Macrophages and neutrophils destroy foreign antigens by making toxic molecules such as reactive oxygen intermediate molecules. If production of these toxic molecules continues unchecked, not only are the foreign antigens destroyed, but tissues surrounding the macrophages and neutrophils are also destroyed. For example, in individuals with the autoimmune disease called Wegener's granulomatosis, overactive

A macrophage engulfing a bacterium and releasing packets of toxic molecules (reactive oxygen intermediates) that break down and destroy the bacterium.

macrophages and neutrophils that invade blood vessels produce many toxic molecules and contribute to damage of the blood vessels. In rheumatoid arthritis, reactive oxygen intermediate molecules and other toxic molecules are made by overproductive macrophages and neutrophils invading the joints. The toxic molecules contribute to inflammation, which is observed as warmth and swelling, and participate in damage to the joint.

MHC and Co-Stimulatory Molecules

MHC molecules are found on all cell surfaces and are an active part of the body's defense team. For example, when a virus infects a cell, a MHC molecule binds to a piece of a virus (antigen) and displays the antigen on the cell's surface. Cells that have the capability of displaying antigen with MHC are called antigen-presenting cells. Each MHC molecule that displays an antigen is recognized by a matching or compatible T-cell receptor. Thus, an antigen-presenting cell is able to communicate with a T cell about what may be occurring inside the cell.

Upper left: a virus attacking a nerve cell. Lower right: a T cell with a T-cell receptor recognizing a piece of a virus (antigen) on the MHC of the infected nerve cell.

However, for the T cell to respond to a foreign antigen on the MHC, another molecule on the antigen-presenting cell must send a second signal to the T cell. A corresponding molecule on the surface of the T cells recognizes the second signal. These two secondary molecules of the antigen-presenting cell and the T cell are called co-stimulatory molecules. There are several different sets of co-stimulatory molecules that can participate in the interaction of antigen-presenting cell with a T cell.

Once the MHC and the T-cell receptor interact, and the co-stimulatory molecules interact, there are several possible paths that the T cell may take. These include T cell activation, tolerance, or T cell death. The subsequent steps depend in part on which co-stimulatory molecules interact and how well they interact. Because these interactions are so critical to the response of the immune system, researchers are intensively studying them to find new therapies that could control or stop the immune system attack on self tissues and organs.

An antigen-presenting cell (for example, a macrophage) with a foreign antigen on its MHC is recognized by a T-cell receptor. In addition, co-stimulatory molecules on the antigen-presenting cell and the T cell interact.

Cytokines and Chemokines

One way T cells can respond after the interaction of the MHC and the T-cell receptor, and the interaction of the co-stimulatory molecules, is to secrete cytokines and chemokines. Cytokines are proteins that may cause surrounding immune system cells to become activated, grow, or die. They also may influence non-immune system tissues. For example, some cytokines may contribute to the thickening of the skin that occurs in people with scleroderma.

After the antigen-presenting cell and T cell interact through the MHC, T-cell receptor and co-stimumlatory and molecules, the T cell becomes activated, sending cytokine signals to other cells.

Chemokines are small cytokine molecules that attract cells of the immune system. Overproduction of chemokines contributes to the invasion and inflammation of the target organ, which occurs in autoimmune diseases. For example, overproduction of chemokines in the joints of people with rheumatoid arthritis may result in invasion of the joint space by destructive immune system cells such as macrophages, neutrophils, and T cells.

Antibodies

B cells are another critical type of immune system cell. They participate in the removal of foreign antigens from the body by using a surface molecule to bind the antigen or by making specific antibodies that can search out and destroy specific foreign antigens. However, the B cell can only make antibodies when it receives the appropriate command signal from a T cell. Once the T cell signals the B cell with a type of cytokine that acts as a messenger molecule, the B cell is able to produce a unique antibody that targets a particular antigen.

A T cell sends messenger molecules, e.g. cytokines, to the B cell, which allows the B cell to start making antibodies.

Autoantibodies

In some autoimmune diseases, B cells mistakenly make antibodies against tissues of the body (self antigens) instead of foreign antigens. Occasionally, these autoantibodies either interfere with the normal function of the tissues or initiate destruction of the tissues. People with myasthenia gravis experience muscle weakness because autoantibodies attack a part of the nerve that stimulates muscle movement. In the skin disease pemphigus vulgaris, autoantibodies are misdirected against cells in the skin. The accumulation of antibodies in the skin activates other molecules and cells to break down, resulting in skin blisters.

Immune Complexes and the Complement System

When many antibodies are bound to antigens in the bloodstream, they form a large lattice network called an immune complex. Immune complexes are harmful when they accumulate and initiate inflammation

A large immune complex.

within small blood vessels that nourish tissues. Immune complexes, immune cells, and inflammatory molecules can block blood flow and ultimately destroy organs such as the kidney. This can occur in people with systemic lupus erythematosus.

If immune complexes accumulate in the kidney, they may promote movement of other inflammatory cells and molecules into the kidney.

A group of specialized molecules that form the complement system helps to remove immune complexes. The different types of molecules of the complement system, which are found in the bloodstream and on the surfaces of cells, make immune complexes more soluble. Complement molecules prevent formation and reduce the size of immune complexes so they do not accumulate in the wrong places (organs and tissues of the body). Rarely, some people inherit defective genes for a complement molecule from their parents. Because these individuals cannot make a normal amount or type of complement molecule, their immune systems are unable to prevent immune complexes from being deposited in different tissues and organs. These people develop a disease that is not autoimmune but resembles lupus erythematosus.

Genetic Factors

Genetic factors can affect an individual's immune system and its responses to foreign antigens in several ways. Genes determine the variety of MHC molecules that individuals carry on their cells. Genes also influence the potential array of T-cell receptors present on T cells. In fact, some MHC genes are associated with autoimmune diseases. However, genes are not the only factors involved in determining a person's susceptibility to an autoimmune disease. For example, some individuals who carry disease-associated MHC molecules on their cells will not develop an autoimmune disease.

How Are Autoimmune Diseases Diagnosed?

The diagnosis of an autoimmune disease is based on an individual's symptoms, findings from a physical examination, and results from laboratory tests. Autoimmune diseases can be difficult to diagnose, particularly early in the course of the disease. Symptoms of many autoimmune diseases—such as fatigue—are nonspecific. Laboratory test results may help but are often inadequate to confirm a diagnosis.

If an individual has skeletal symptoms such as joint pain and a positive but nonspecific lab test, she or he may be diagnosed with the confusing name of early or "undifferentiated" connective tissue disease. In this case, a physician may want the patient to return frequently for follow up. The early phase of disease may be a very frustrating time for both the patient and physician. On the other hand, symptoms may be short-lived, and inconclusive laboratory tests may amount to nothing of a serious nature.

In some cases, a specific diagnosis can be made. A diagnosis shortly after onset of a patient's symptoms will allow for early aggressive medical therapy; and for some diseases, patients will respond completely to treatments if the reason for their symptoms is discovered early in the course of their disease.

Although autoimmune diseases are chronic, the course they take is unpredictable. A doctor cannot foresee what will happen to the patient based on how the disease starts. Patients should be monitored closely by their doctors so environmental factors or triggers that may worsen the disease can be discussed and avoided and new medical therapy can be started as soon as possible. Frequent visits to a doctor are important in order for the physician to manage complex treatment regimens and watch for medication side effects.

How Are Autoimmune Diseases Treated?

Autoimmune diseases are often chronic, requiring lifelong care and monitoring, even when the person may look or feel well. Currently, few autoimmune diseases can be cured or made to "disappear" with treatment. However, many people with these diseases can live normal lives when they receive appropriate medical care.

Physicians most often help patients manage the consequences of inflammation caused by the autoimmune disease. For example, in people with Type 1 diabetes, physicians prescribe insulin to control blood sugar levels so that elevated blood sugar will not damage the kidneys, eyes, blood vessels, and nerves. However, the goal of scientific research is to prevent inflammation from causing destruction of the insulin-producing cells of the pancreas, which are necessary to control blood sugars.

On the other hand, in some diseases such as lupus or rheumatoid arthritis, medication can occasionally slow or stop the immune system's destruction of the kidneys or joints. Medications or therapies that slow or suppress the immune system response in an attempt to stop the inflammation involved in the autoimmune attack are called immunosuppressive medications. These drugs include corticosteroids (prednisone), methotrexate, cyclophosphamide, azathioprine, and cyclosporin. Unfortunately, these medications also suppress the ability of the immune system to fight infection and have other potentially serious side effects.

In some people, a limited number of immuno-suppressive medications may result in disease remission. Remission is the medical term used for "disappearance" of a disease for a significant amount of time. Even if their disease goes into remission, patients are rarely able to discontinue medications. The possibility that the disease may restart when medication is discontinued must be balanced with the long-term side effects from the immunosuppressive medication.

A current goal in caring for patients with autoimmune diseases is to find treatments that produce remissions with fewer side effects. Much research is focused on developing therapies that target various steps in the immune response. New approaches such as therapeutic antibodies against specific T cell molecules may produce fewer long-term side effects than the chemotherapies that now are routinely used.

Ultimately, medical science is striving to design therapies that prevent autoimmune diseases. To this end, a significant amount of time and resources are spent studying the immune system and pathways of inflammation.

What Are Some Examples of Autoimmune Diseases?

Rheumatoid Arthritis

In people with rheumatoid arthritis, the immune system predominantly targets the lining (synovium) that covers various joints. Inflammation of the synovium is usually symmetrical (occurring equally on both sides of the body) and causes pain, swelling, and stiffness of the joints. These features distinguish rheumatoid arthritis from osteoarthritis, which is a more common and degenerative "wear-and-tear" arthritis.

An inflamed joint—the synovium—is attacked by cells and molecules of the immune system.

Currently available therapy focuses on reducing inflammation of the joints with anti-inflammatory or immunosuppresssive medications. Sometimes, the immune system may also target the lung, blood vessels, or eye; occasionally patients may also develop symptoms of other autoimmune diseases such as Sjogren's the inflammation, itching, and scaling. For more severe cases, oral medications are used. Psoriasis is common and may affect more than 2 out of 100 Americans. Psoriasis often runs in families.

Multiple Sclerosis

Multiple sclerosis is a disease in which the immune system targets nerve tissues of the central nervous system. Most commonly, damage to the central nervous system occurs intermittently, allowing a person to lead a fairly normal life. At the other extreme, the symptoms may become constant, resulting in a progressive disease with possible blindness, paralysis, and premature death. Some medications such as beta interferon are helpful to people with the intermittent form of multiple sclerosis.

In young adults, multiple sclerosis is the most common disabling disease of the nervous system. Multiple sclerosis afflicts 1 in 700 people in this country. Researchers continue to search for triggers of the disease.

Immune-Mediated or Type 1 Diabetes Mellitus

Type 1 diabetes mellitus results from autoimmune destruction of the insulin-producing cells of the pancreas. Insulin is required by the body to keep the blood sugar (glucose) level under control. High levels of glucose are responsible for the symptoms and the complications of the disease. However, most of the insulin-producing cells are destroyed before the patient develops symptoms of diabetes. Symptoms include fatigue, frequent urination, increased thirst, and possible sudden confusion.

Type 1 diabetes mellitus is usually diagnosed before the age of 30 and may be diagnosed as early as the first month of life. Together with Type 2 diabetes (not considered an autoimmune disease), diabetes mellitus is the leading cause of kidney damage, loss of eyesight, and leg amputation. Close control of sugar levels decreases the rate at which these events occur. There is a genetic predisposition to Type 1 diabetes, which occurs in 1 out of 800 people in the United States. Among individuals who have a close relative with Type 1 diabetes, those at high risk for developing disease can be identified. Efforts are now under way to evaluate prevention strategies for these family members at risk.

Sunlight is one of the triggers of lupus and can worsen the progression of the disease.

Inflammatory Bowel Diseases

This medical term is used for both Crohn's disease and ulcerative colitis, two diseases in which the immune system attacks the gut (intestine). Patients may have diarrhea, nausea, vomiting, abdominal cramps, and pain that can be difficult to control. Illness in afflicted individuals can result from intestinal inflammation and from side effects of the drugs used for the disease. For example, daily use of high-dose corticosteroid (prednisone) therapy, which is needed to control severe symptoms of Crohn's disease, can predispose patients to infections, bone thinning (osteoporosis), and fractures. For patients with ulcerative colitis, surgical removal of the lower intestine (colon) will eliminate the disease and their increased risk for colon cancer. More than 1 in 500 Americans has some type of inflammatory bowel disease.

Systemic Lupus Erythematosus

Patients with systemic lupus erythematosus most commonly experience profound fatigue, rashes, and joint pains. In severe cases, the immune system may attack and damage several organs such as the kidney, brain, or lung. For many individuals, symptoms and damage from the disease can be controlled with available anti-inflammatory medications. However, if a patient is not closely monitored, the side effects from the medications can be quite serious. Lupus occurs in 1 out of 2,000 Americans and in as many as 1 in 250 young, African-American women.

Psoriasis

Psoriasis is an immune system disorder that affects the skin, and occasionally the eyes, nails, and joints. Psoriasis may affect very small areas of skin or cover the entire body with a buildup of red scales called plaques. The plaques are of different sizes, shapes, and severity and may be painful as well as unattractive. Bacterial infections and pressure or trauma to the skin can aggravate psoriasis. Most treatments focus on topical skin care to relieve the inflammation, itching, and scaling. For more severe cases, oral medications are used. Psoriasis is common and may affect more than 2 out of 100 Americans. Psoriasis often runs in families.

Scleroderma

This autoimmune disease results in thickening of the skin and blood vessels. Almost every patient with scleroderma has Raynaud's, which is a spasm of the blood vessels of the fingers and toes. Symptoms of Raynaud's include increased sensitivity of the fingers and toes to the cold, changes in skin color, pain, and occasionally ulcers of the fingertips or toes. In people with scleroderma, thickening of skin and blood vessels can result in loss of movement and shortness of breath or, more rarely, in kidney, heart, or lung failure. The estimated number of people with any type of scleroderma varies from study to study but may range from 1 to 4 affected individuals for every 10,000 Americans (or as many as 1 out of 2500 individuals).

Autoimmune Thyroid Diseases

Hashimoto's thyroiditis and Grave's disease result from immune system destruction or stimulation of thyroid tissue. Symptoms of low (hypo-) or overactive (hyper-) thyroid function are nonspecific and can develop slowly or suddenly; these include fatigue, nervousness, cold or heat intolerance, weakness, changes in hair texture or amount, and weight gain or loss. The diagnosis of thyroid disease is readily made with appropriate laboratory tests.

The thyroid gland affect many parts of the body.

The symptoms of hypothyroidism are controlled with replacement thyroid hormone pills; however, complications from over- or under-replacement of the hormone can occur. Treatment of hyperthyroidism requires long-term anti-thyroid drug therapy or destruction of the thyroid gland with radioactive iodine or surgery. Both of these treatment approaches carry certain risks and long-term side effects. Autoimmune thyroid diseases afflict as many as 4 out of 100 women and are frequently found in families where there are other autoimmune diseases.

What Research Is Under Way on Autoimmune Diseases?

The National Institute of Allergy and Infectious Diseases (NIAID) supports research studies on the function of the immune system in various diseases. A basic understanding of the human immune system is central to the understanding of the development of an autoimmune disease (disease pathogenesis). Scientists searching for ways to prevent and treat autoimmune disease are studying disease pathogenesis and investigating new ways to modify the immune system.

Specifically, investigators supported by NIAID are focusing on: 1) studies of the immune system during the progression of an autoimmune disease; 2) analysis of the influence of genetics on autoimmune disease expression and progression; 3) the role of infectious agents in autoimmune diseases; 4) studies of animal models of autoimmune diseases; and 5) the effects of therapeutic intervention on the immune system in an autoimmune disease.

In addition, studies of a specific autoimmune disease such as multiple sclerosis can provide new and additional insights into the pathogenesis of autoimmune diseases affecting other organ systems. Therefore, NIAID also supports studies on specific autoimmune diseases in cooperation with other Institutes of the National Institutes of Health that focus on organ-specific autoimmune diseases.

Resources

National Institutes of Health (NIH) Resources

The following NIH components support medical research and/or provide information on varying aspects of autoimmune diseases.

National Institute of Allergy and Infectious Diseases
Office of Communications
Bldg. 31/Rm. 7A50
31 Center Drive, MSC 2520
Bethesda, MD 20892-2520
(301) 496-5717
http://www.niaid.nih.gov/publications/
and
http://www.niaid.nih.gov/recruit/recruit.htm (for clinical trials information)

National Institute of Arthritis and Musculoskeletal and Skin Diseases
Information Clearinghouse/NIH
1 AMS Circle
Bethesda, MD 20892-3675
Fast Facts: (301) 881-2731 (to receive information by fax)
Clearinghouse: (301) 495-4484
http://www.nih.gov/niams/healthinfo/

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information Clearinghouse
1 Information Way
Bethesda, MD 20892-3560
Diabetes, Digestive, and Kidney Diseases Information:
(301) 654-3810

NIDDK Information Office (Thyroid Diseases)
Bldg. 31/Rm. 9A04
31 Center Drive
Bethesda, MD 20892-3560
(301) 496-3583
http://www.niddk.nih.gov/

National Institute of Neurological Disorders and Stroke
Office of Scientific and Health Reports
P.O. Box 5801
Bethesda, MD 20824
(301) 496-5751
http://www.ninds.nih.gov/hlthinhp.htm

NIH Clinical Center
Patient Recruitment and Referral Center—for specific NIH clinical trials information
4 West Drive, MSC 2655
Quarters 15 D-2
Bethesda, MD 20892-2655
(301) 411-1222
http://clinicalstudies.info.nih.gov/referring_patient.html

Office of Rare Diseases, NIH
Bldg. 31/Rm. 1B03
31 Center Drive
Bethesda, MD 20892
(301) 402-4336
http://cancernet.nci.nih.gov/ord/p_home.htm

Other Resources Sponsored by the Department of Health and Human Services

National Health Information Center
(800) 336-4797 or (301) 565-4167
Health Finder: http://www.healthfinder.gov/

Combined Health Information Database
http://chid.nih.gov/

Private Sector Organizations

The following list is astarting point for additional information on autoimmune diseases. Many of the organizations have extensive educational resources, local chapters, and support groups. The Internet Web site of many organizations can refer you to other disease-oriented groups (for example, the Arthritis Foundation has alink to the Lupus Foundation).

American Autoimmune Related Diseases Association
15475 Gratiot Avenue
Detroit, MI 48205
(800) 598-4668 or (313) 371-8600
http://www.aarda.org/

American Diabetes Association
1660 Duke Street
Alexandria, VA 22314
(800) 232-3472 or (703) 549-1500
http://www.diabetes.org/

American Liver Foundation
1425 Pompton Avenue
Cedar Grove, NJ 07009
(800) 233-0179 and (973) 256-2550
http://sadieo.ucsf.edu/alf/alffinal/homepagealf.html

American Thyroid Association Montefiore Medical Center
111 East 210th Street
Bronx, NY 10467
Fax: (718) 882-6085
http://www.thyroid.org/

Arthritis Foundation
1650 Bluegrass Lakes Pkwy.
Alpharetta, GA 30009
(800) 283-7800 or (800) 207-8633
http://www.arthritis.org/

Crohn's and Colitis Foundation of America
National Headquarters
386 Park Avenue South, 17th Floor
New York, NY 10016-8804
(800) 932-2423
(800) 343-3637 (Warehouse)
http://www.ccfa.org/

Juvenile Diabetes Foundation International
120 Wall Street
New York, NY 10005-4001
(800) JDF-CURE or (800) 533-2873
http://www.jdfcure.com/

Lupus Foundation of America
1300 Piccard Drive, Suite 200
Rockville, MD 20850-4303
(800) 558-0121 and (301) 670-9292
http://www.lupus.org/lupus

Myasthenia Gravis Foundation of America
222 S. Riverside Plaza, Suite 1540
Chicago, IL 60606
(800) 541-5454 or (312) 258-0522
http://www.med.unc.edu/mgfa/

Myositis Association of America
1420 Huron Court
Harrisonburg, VA 22801
(540) 433-7686
http://www.myositis.org/

National Alopecia Areata Foundation
710 CStreet, Suite 11
San Rafael, CA 94901-3853
or
P.O. Box 150760
San Rafael, CA 94915-0760
(415) 456-4644
Fax: (415) 456-4274
http://weber.u.washington.edu/~dvictor/natl.html

National Multiple Sclerosis Society
733 Third Avenue, 6th Floor
New York, NY 10017-3288
(800) 344-4867 or (212) 986-3240
Fax: (212) 986-7981
http://www.nmss.org/
e-mail: [email protected]

National Organization for Rare Disorders
P.O. Box 8923
New Fairfield, CT 06812-1783
(800) 999-6673
http://www.nord-rdb.com/~orphan

National Psoriasis Foundation
6600 SW 92nd Avenue, Suite 300
Portland, OR 97223
(800) 723-9166 or (503) 244-7404
http://www.psoriasis.org/

National Sjogren's Syndrome Association
5815 N. Black Canyon Highway, Suite 103
Phoenix, AZ 85015-2200
(602) 433-9844
http://www.sjogrens.org/

National Vitiligo Foundation
P.O. Box 6337
Tyler, TX 75703
(903) 531-0074
Fax: (903) 531-9767
http://www.nvfi.org/

Sjogren's Syndrome Foundation
333 N. Broadway
Jericho, NY 11753
1-800-4-SJOGRENS or (516) 933-6365
http://www.sjogrens.com/

Spondylitis Association of America
P.O. Box 5872
Sherman Oaks, CA 91413
(800) 777-8189 or (888) 777-1594
http://www.spondylitis.org/

The S.L.E. Foundation
149 Madison Avenue, Suite 205
New York, NY 10016
(800) 745-8787
http://www.lupus.org/lupus

United Scleroderma Foundation
89 Newbury Street, Suite 201
Danvers, MA 01923
800) 722-HOPE
Fax: (978) 750-9902
http://www.scleroderma.org/

Wegener's Foundation
3705 South George Mason Drive, Suite 1813
Falls Church, VA 22041
(703) 931-5852

Wegener's Granulomatosis Support Group
P.O. Box 28660
Kansas City, MO 64188-8668
(800) 277-9474
Fax: (816) 436-8211
http://www.wgsg.org/

Glossary

antibody: a molecule (also called an immunoglobulin) produced by a B cell in response to an antigen. The binding of antibody to antigen leads to the antigen's destruction.

antigen: a substance or molecule that is recognized by the immune system. The molecule can be from a foreign material such as a bacterium or virus, or the molecule can be from the same organism (one's own body) and called a self antigen.

antigen-presenting cell: a cell that displays an antigen with an MHC molecule on the cell surface.

autoantibody: antibodies that are made against the body's own organs and tissues rather than foreignparts of bacteria or viruses.

autoimmune disease: condition in which the immune system mistakenly attacks the body's own organs and tissues.

B cell: a type of lymphocyte, which is an immune system cell. Among its many roles, the B cell produces antibodies that bind antigens.

cells: the building blocks that make up tissues, organs, and bloodstream of the body. Immune system cells normally move throughout the bloodstream and reside temporarily in the lymph nodes, spleen, and thymus.

chemokine: a substance manufactured by cells and tissues, that stimulates movement and activation of immune system cells to the area where the chemokine is produced.

clinical trial: a prospective, scientific evaluation in human volunteers of a treatment regimen, device, or procedure used for the prevention, diagnosis, or treatment of a disease.

complement system: this series of molecules works together to perform many immune system functions. For example, the complement system helps to dissolve and remove immune complexes and to kill foreign cells.

co-stimulatory molecules: pairs of molecules on the surfaces of two cells that work together with the MHC and T-cell receptors of those cells. The co-stimulatory molecules help to stimulate or decrease the immune response produced by the two cells.

cytokines: chemical substances that have varied effects on many cells of the body. For example, some cytokines can cause growth and activation of immune system cells.

gene: a unit of genetic material that is inherited from a parent. A gene carries the directions that a cell uses to perform a specific function.

immune complex: a cluster of interlocking antigens and antibodies forming a large network of molecules.

inflammation: a collection of immune system cells and molecules that invade tissues and organs as part of an immune system response.

lymphocyte: a type of white blood cell of the immune system. T cells and B cells are lymphocytes that look similar under the microscope but have different functions.

macrophage: a type of white blood cell that functions as a patrol cell and engulfs and kills foreign infectious invaders.

MHC (major histocompatibility complex) molecules: molecules that are found on cell surfaces and display antigen; the antigen-MHC molecules may then interact with a T-cell receptor.

molecule: a small physical unit made up of chemical substances such as proteins, sugars or fats. Molecules are the building blocks of a cell.

neutrophil: a type of immune system cell that combats infectious agents, in particular bacteria. Neutrophils contain granules filled with potent chemicals that can destroy bacteria or other nearby cells when the chemicals are released.

reactive oxygen intermediate molecules: toxic molecules that are released by immune cells and help to destroy invading microbes. These molecules can sometimes destroy healthy body tissues nearby.

T-cell: a type of lymphocyte. T cells have T-cell receptors and, sometimes, co-stimulatory molecules on their cell surfaces. The T cell helps to orchestrate the immune system and can issue "orders" for other cells to make cytokines and chemokines.

T-cell receptor: a molecule found on the surface of T cells. The T-cell receptor can recognize and interact with a corresponding MHC molecule that is displaying an antigen.

tolerance: a state in which the T cell can no longer respond to antigen.

Last Updated December 18, 1998 (kap)

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