All Autoimmune Tests

Over 80 diseases result from autoimmune responses, and the following tests are used to confirm the diagnosis and monitor the various autoimmune disorders.

Your body's immune system naturally helps fight against harmful bacteria and other foreign substances. This natural response revolves around antibodies and specific immune cells. Autoimmune diseases occur when your body's immune system fights against normal constituents, instead of harmful bacteria and other foreign substances. It has everything to do with your immune system failing to discern between "self" vs. "non-self" constituents. This failure to discern may produce immune cells or antibodies (or auto-antibodies) that target the body's own cells, tissues, and/or organs. These attacks cause inflammation and tissue damage that result in autoimmune disorders. 

SEE BELOW THE LIST OF TESTS FOR MORE INFORMATION ABOUT Autoimmune diseases

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The Acetylcholine Receptor Binding Antibody Test detects antibodies targeting acetylcholine receptors, a hallmark of myasthenia gravis. This autoimmune disorder affects nerve-to-muscle communication, causing weakness and fatigue. The test helps confirm diagnosis, differentiate from other neuromuscular diseases, and guide treatment. Elevated antibody levels support early detection and ongoing management of myasthenia gravis.

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The Acetylcholine Receptor Blocking Antibody Test evaluates autoantibodies that block acetylcholine receptors, impairing nerve-to-muscle signaling. It is commonly ordered in the workup of suspected myasthenia gravis, where these antibodies contribute to muscle fatigue and weakness. This test, often performed with AChR binding and modulating antibody assays, provides valuable insight into autoimmune mechanisms affecting neuromuscular transmission.

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The Acetylcholine Receptor Modulating Antibody Test measures autoantibodies that cause loss or alteration of acetylcholine receptors on muscle cells, impairing nerve transmission. Elevated levels are commonly linked to myasthenia gravis, an autoimmune disorder causing muscle weakness. This test aids in identifying immune-mediated neuromuscular disease and helps evaluate disease severity.

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The Actin Smooth Muscle IgG Antibody Test detects autoantibodies against smooth muscle actin, often linked to autoimmune hepatitis and chronic liver disease. Elevated levels may indicate liver inflammation, cirrhosis, or other autoimmune conditions. Doctors use this blood test with liver panels and additional antibody tests to aid in diagnosis, monitor disease progression, and guide treatment decisions for patients with suspected autoimmune liver disorders.

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Also Known As: Actin IgG Antibody Test

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The ANA Screen IFA with Reflex to Titer and Pattern Test detects antinuclear antibodies in blood to evaluate autoimmune activity. If positive, further testing identifies antibody concentration (titer) and fluorescence pattern, helping diagnose conditions like lupus, rheumatoid arthritis, or Sjögren’s syndrome. Doctors order this test to investigate symptoms such as joint pain, fatigue, rash, or swelling and to guide treatment for autoimmune and connective tissue disorders.

Also Known As: ANA Test, Antinuclear Antibody Screen Test

The ANA IFA Panel Comprehensive screens for autoimmune disorders by detecting antinuclear antibodies and specific markers including dsDNA, Sm, Sm/RNP, Scl-70, and Sjögren’s SS-A/SS-B. Doctors order this panel for patients with joint pain, rash, fatigue, or suspected lupus, scleroderma, or Sjögren’s syndrome. Results provide critical insight into autoimmune activity, helping confirm diagnosis, monitor disease progression, and guide treatment decisions.

Also Known As: Comprehensive ANA Panel



The ANCA Screen with Reflex to ANCA Titer detects antineutrophil cytoplasmic antibodies, often linked to autoimmune vasculitis such as granulomatosis with polyangiitis and microscopic polyangiitis. If the screen is positive, a titer is performed to measure antibody levels for greater diagnostic accuracy. Doctors use this test to evaluate unexplained inflammation, kidney or lung issues, and guide treatment decisions in autoimmune and systemic vasculitis care.

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Also Known As: ANCA Test, cANCA Test, pANCA Test, Serine Protease 3 Test, Acticytoplasmic Test, 3-ANCA test, PR3-ANCA Test, MPO-ANCA test

The ANCA Vasculitides Test measures antibodies that target neutrophils, helping identify autoimmune vasculitis. It aids in diagnosing conditions including granulomatosis with polyangiitis and microscopic polyangiitis. This test provides insight into systemic inflammation, kidney disease, and respiratory involvement, supporting evaluation of autoimmune disorders linked to vascular and organ damage.

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The Apolipoprotein A1 and B Test measures Apo A1, the main protein in HDL cholesterol, and Apo B, the primary protein in LDL and VLDL cholesterol. Together, these markers and the ApoB/A1 ratio provide a clearer picture of cardiovascular risk than standard lipid panels. High ApoB or low Apo A1 may signal heart disease, stroke, or atherosclerosis. Doctors use this test to evaluate cholesterol balance, monitor therapy, and guide prevention of cardiovascular conditions.

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Also Known As: Apo A1 and B Test, Apolipoprotein Evaluation Test

The Beta-2-Glycoprotein I IgG IgA IgM Antibodies Test detects autoantibodies linked to antiphospholipid syndrome (APS), a disorder that increases risk of abnormal blood clotting. Measuring all three antibody classes provides a thorough evaluation of immune activity. Elevated results may be associated with recurrent miscarriages, venous or arterial thrombosis, and autoimmune conditions, supporting diagnosis and monitoring of clotting-related disorders.


The Beta-2-Glycoprotein I IgA Antibody Test detects IgA antibodies targeting beta-2 glycoprotein I, helping identify autoimmune conditions and clotting disorders. Positive results may indicate antiphospholipid syndrome, thrombotic risk, or pregnancy complications. This test provides insight into immune activity, vascular health, and systemic conditions linked to abnormal coagulation and inflammation.

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The Beta-2-Glycoprotein I IgG Antibody Test detects IgG antibodies targeting beta-2 glycoprotein I, helping assess autoimmune disorders and clotting risk. Positive results may indicate antiphospholipid syndrome, pregnancy complications, or thrombotic conditions. This test provides insight into vascular health, immune response, and systemic disorders related to antibody activity and coagulation balance.

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The Beta-2-Glycoprotein I IgM Antibody Test detects IgM antibodies targeting beta-2 glycoprotein I to help assess autoimmune activity and clotting disorders. Positive findings may suggest antiphospholipid syndrome, thrombotic risk, or recurrent miscarriage. This test provides insight into vascular health, immune regulation, and systemic disorders tied to antibody activity and coagulation balance.

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The Beta-2-Microglobulin (B2M) Test measures levels of B2M, a protein found on most cell surfaces and released into the blood. Elevated levels may indicate multiple myeloma, lymphoma, chronic infections, or kidney disease. Doctors order this test to evaluate cancer stage, prognosis, or kidney function. Results provide essential insight into disease progression, immune activity, and treatment monitoring for blood cancers and renal disorders.

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Also Known As: B2M Test, β2-Microglobulin Test, Thymotaxin Test

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The Vitamin B7 Test measures biotin levels in the blood to assess nutritional status and detect deficiency. Biotin is essential for energy metabolism, enzyme activity, and maintaining healthy hair, skin, and nails. Low levels may result from poor diet, genetic conditions, alcoholism, or long-term antibiotic use, leading to fatigue, hair loss, or skin rashes. Doctors use this test to diagnose deficiency, monitor supplementation, and support overall metabolic health.

Also Known As: Biotin Test

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The C-Reactive Protein (CRP) Test measures CRP levels in blood to detect inflammation in the body. Elevated CRP may indicate infections, autoimmune disorders, or chronic diseases such as arthritis, cardiovascular disease, or inflammatory bowel disease. Doctors use this test to assess acute illness, monitor treatment response, and evaluate risk for heart disease. The CRP test provides key insight into inflammation, immune health, and overall wellness.

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Also Known As: CRP Test, Inflammation Test

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The High-Sensitivity C-Reactive Protein (hs-CRP) Test measures very low levels of CRP in blood to evaluate inflammation and cardiovascular risk. Elevated hs-CRP may indicate increased risk for heart disease, heart attack, or stroke even before symptoms appear. Doctors use this test along with cholesterol and other markers to assess overall heart health, guide prevention strategies, and monitor treatment. It also helps evaluate chronic inflammation and metabolic conditions.

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Also Known As: Cardiac CRP Test, High Sensitivity C-Reactive Protein Test

The C3a DesArg Fragment Test measures levels of C3a desarginated, a stable breakdown product of complement activation. Elevated concentrations reflect immune system activation and may indicate autoimmune disease, sepsis, allergic reactions, or inflammatory conditions. This test provides insight into complement pathway activity, helping evaluate immune dysregulation, monitor disease progression, or assess systemic inflammation.


The Cardio IQ™ hs-CRP Test measures high-sensitivity C-reactive protein in the blood to assess inflammation linked to cardiovascular risk. Elevated levels may indicate a higher risk of heart disease or other inflammatory conditions.

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Also Known As: Cardiac CRP Test, High Sensitivity C-reactive Protein Test

How familiar are you with autoimmune diseases? 

Your body’s immune system naturally helps fight against harmful bacteria and other foreign substances. This natural response revolves around antibodies and specific immune cells. Autoimmune diseases occur when your body’s immune system fights against normal constituents, instead of harmful bacteria and other foreign substances. It has everything to do with your immune system failing to discern between “self” vs. “non-self” constituents.  This failure to discern may produce immune cells or antibodies (or auto-antibodies) that target the body’s own cells, tissues, and/or organs.  These attacks cause inflammation and tissue damage that result in autoimmune disorders. 

Over 80 diseases have been classified as resulting from autoimmune responses, and there is evidence to suggest that there are 40 other diseases that may have an autoimmune basis.

According to the National Institutes of Health, nearly 24 million people in the US suffer from autoimmune disease. While the majority of these diseases are, in fact, rare, the number of people suffering from them continues to rise. These diseases affect women on a larger scale than men. In the case of Lupus, women are ten times more likely to be affected.

Medical professionals are unaware of what causes most autoimmune diseases, save for the fact that genetic predisposition seems to play its part. There are some autoimmune diseases, like rheumatic fever, where a virus or bacterial infection is what leads to the confused immune response. T-cells are antibodies and immune cells that attack good cells.  The T-cells misidentify the good cells as the microbes that are infecting the body.

There are two main types of autoimmune diseases, systemic and localized. The systemic autoimmune diseases are disorders that lead to multi-organ damage. In contrast, the localized autoimmune disorders lead to direct damage to a single organ or tissue. The lines can be blurred between the two types; however, as medical professionals point out that the damage caused by localized autoimmune disorders often indirectly impacts other organs and systems in the body.

There are also instances where certain autoimmune diseases do not cause antibodies to attack a particular organ or tissue but rather a certain type of cell. One example involves anti-phospholipid antibodies and how they attack regular platelet phospholipids. This happens inside blood vessels, and the event can lead to improper blood clot formation and thrombosis.

Autoimmune diseases aren’t always easily recognizable either, especially systemic disorders. Multiple symptoms that frequently change in severity can leave doctors searching for a diagnosis for an extended period of time. Any vague and slow to develop signs and symptoms, although present, can also serve to be misleading to medical professionals. There are a variety of symptoms that stem from the various autoimmune diseases, including joint pain, fever, and fatigue. Many people also report a feeling of generally being unwell.

Which lab tests are used to detect autoimmune disorders depends on which disease a medical professional suspects to be the culprit. Blood tests are commonly used for diagnosis because doctors need to know what autoantibodies are in attack mode. Two inflammation tests, CRP (or C-reactive protein) and ESR (or erythrocyte sedimentation rate), are also commonly used in diagnosis. Sometimes a person may have more than a single autoimmune disease.  As examples, individuals who suffer from Addison disease often are type 1 diabetics, and people with sclerosing cholangitis often suffer from ulcerative colitis.

Below is a list of several of the more well-known autoimmune diseases. You can also find out additional information from the AARDA (American Autoimmune Related Diseases Association) about these diseases and more.

  • Addison Disease
  • Antiphospholipid Syndrome
  • Autoimmune Hepatitis
  • Celiac Disease
  • Graves’ Disease
  • Guillain-Barre Syndrome
  • Hashimoto Thyroiditis
  • Inflammatory Bowel Disease
  • Multiple Sclerosis
  • Myasthenia Gravis
  • Pernicious Anemia
  • Primary Biliary Cirrhosis
  • Sclerosing Cholangitis (see Autoimmune-associated Liver Diseases)
  • Reactive Arthritis
  • Rheumatoid Arthritis
  • Juvenile Rheumatoid Arthritis
  • Sarcoidosis
  • Scleroderma
  • Sjögren Syndrome
  • Lupus (Systemic Lupus Erythematosus or SLE)
  • Type 1 Diabetes
  • Vasculitis

Sarcoidosis is a medical condition caused by immune system cells clumping together to form lumps called granulomas. Granulomas can develop in any part of the body, but the most common (and serious) sites where they form are in the lungs, eyes, lymph nodes, and skin. Granulomas often disappear on their own within two to three years. Sometimes, though, granulomas clump together. When this occurs in an important organ, it can cause it to become inflamed. If the granulomas persist for long enough, they can impede the function of the organ and cause fibrosis, that is, permanent scarring. 

The precise cause of sarcoidosis is not well understood. Many risk factors are believed to contribute to the disease, including genetic predisposition, immune system overreactions when exposed to bacteria or viruses, and environmental triggers like chemicals and allergens. 

Sarcoidosis occurs in people of all ages and communities, but sufferers are most commonly over the age of 55 and of Northern European or African descent. In the United States, African American women are the demographic group most often diagnoses with sarcoidosis. The US reports more than 25,000 new cases of sarcoidosis per year. 

The severity and duration of sarcoidosis vary from patient to patient: 

  • You may have sarcoidosis without ever noticing symptoms. Mild cases may cause non-specific symptoms that are easily mistaken for other conditions. 
  • You may experience an acute case of sarcoidosis which resolves on its own within a few years. This is called “remission.” Acute sarcoidosis may or may not return in the future. 
  • You may have chronic sarcoidosis, growing worse over time. 

The National Heart Lung and Blood Institute reports that half of all sarcoidosis sufferers will go into remission within three years of being diagnosed. At 10 years after diagnosis, two-thirds of sufferers will be in remission. 

Sarcoidosis does not cause long-term health effects for most sufferers. However, about one-third of those with the disease will experience organ damage to some extent. People who suffer sarcoidosis in their lungs or hearts may experience severe consequences, including death. Sarcoidosis can, on rare occasions, cause blindness. 

Symptoms  

The symptoms you may experience with sarcoidosis vary widely in type and severity. The specific tissues and organs affected by the disease matter and symptoms can change over time. Some people with sarcoidosis experience no symptoms at all. Some symptoms are very similar to those caused by other health conditions.

Examples of these include: 

  • Fever 
  • Weight loss 
  • Fatigue 
  • Loss of appetite 
  • Night sweats 
  • Swollen and/or painful joints 
  • Swollen lymph nodes 

The symptoms may be different, depending on which organs are affected: 

The Lungs 

According to the American Lung Association, up to 90 percent of all sarcoidosis cases affect the lungs. Sarcoidosis symptoms in the lungs tend to worsen over time as scar tissue forms, and the lungs become stiff. Common symptoms include: 

  • Dry coughing 
  • Shortness of breath 
  • Wheezing or strained breathing 
  • Pain, tightness, or discomfort in the chest 

The Skin 

Skin issues occur in roughly one-quarter of all sarcoidosis cases. Signs and symptoms include: 

  • Sores appearing on the cheeks, nose, eyelids, and ears 
  • Bumpy rashes on the ankles or shins — these appear reddish and raised, and may feel tender, warm, or itchy 
  • Inflammation and raised skin around scars 
  • Skin discoloration 

The Eyes 

Symptoms that affect the eyes include: 

  • Light sensitivity 
  • Blurred vision 
  • Pain or itching 
  • Excessive tears 
  • Red or burning eyes 
  • Inflammation 

The Heart 

Symptoms that are common when the heart is affected include: 

  • Abnormal heart rhythm 
  • Chest pain 
  • Rapid heartbeat 
  • Symptoms like congestive heart failure, including shortness of breath, coughing, wheezing, and swollen legs and ankles. 

The Nervous System 

Symptoms affecting the nervous system and brain include: 

  • Headaches 
  • Seizures 
  • Loss of coordination 
  • Fatigue 
  • Tremors 

Skeleton and/or Muscles 

If sarcoidosis granulomas occur in the bones or muscles, they may cause pain and/or joint stiffness. 

Other symptoms 

May also cause the following effects: 

  • Swollen salivary glands 
  • Enlarged liver 
  • Enlarged spleen 
  • Kidney stones 
  • Kidney failure (rare) 

Testing

Testing for sarcoidosis involves determining which tissues are affected as well as accurately diagnosing the disease. Tests are also used to gauge the severity of the disease and monitor its progress. It’s also important to rule out other conditions that may cause similar granulomas. These include tuberculosis and certain fungal infections. 

Lab Tests 

  • ACE (Angiotensin Converting Enzyme) This test is useful for diagnosing Sarcoidosis and monitoring both the progress of the disease and its response to treatment. Sarcoidosis causes elevated ACE levels, but other conditions can also have this effect. Examples include diabetes, hyperthyroidism, tuberculosis, and fungal infections. 
  • Liver Panel or CMP (Comprehensive Metabolic Panel) This is a battery of tests that assess the function of the liver and or kidneys. They can tell if those organs have been damaged by the disease. 
  • CBC (Complete Blood Count) This test may be ordered to evaluate red and white blood cells. 
  • C-Reactive Protein (CRP) A key test to detect inflammation. ESR (Erythrocyte Sedimentation Rate) testing may be used as an alternative. 
  • Calcium Elevated calcium levels in the blood or urine may be a sign of sarcoidosis. This is because the granulomas produce vitamin D, which increases calcium absorption in the intestines. 
  • Vitamin D A vitamin D test is often used as a follow-up if elevated calcium levels are detected. 
  • Cerebrospinal Fluid (CSF) Analysis This test may be used to confirm or deny sarcoidosis in the brain or nervous system. 
  • AFB TestingSputum CulturesFungal Tests These are all used to rule out other conditions that may cause signs and symptoms like sarcoidosis.