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 Complement Total CH50 Test measures overall activity of the complement system, a key part of the immune response that helps fight infections and regulate inflammation. Abnormal results may indicate autoimmune diseases such as lupus, complement deficiencies, or immune complex disorders. Doctors use this blood test to evaluate immune function, investigate recurrent infections, and monitor treatment in patients with suspected immune or autoimmune conditions.

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Also Known As: Total Complement Test, Total Complement Activity Test

The Complete Blood Count with Differential and Platelets Test is a comprehensive blood test that checks red blood cells, white blood cells, hemoglobin, hematocrit, and platelets. The differential analyzes types of white blood cells to detect infections, anemia, clotting abnormalities, immune conditions, and certain cancers. This essential test is often ordered for routine health exams, diagnosis, and monitoring treatment progress.

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Also Known As: CBC Test, CBC with Differential and Platelets Test, CBC w/Diff and Platelets Test, Full Blood Count Test, Complete Blood Count Test

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The Comprehensive Metabolic Panel (CMP) Test measures 21 markers to assess metabolic health, liver and kidney function, and electrolyte balance. It includes glucose, calcium, sodium, potassium, chloride, CO2, albumin, globulin, A/G ratio, total protein, bilirubin, ALP, AST, ALT, BUN, creatinine, BUN/creatinine ratio, and eGFR. The CMP helps detect diabetes, liver or kidney disease, and supports routine screening and chronic condition monitoring.

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Also Known As: CMP Test, Chemistry Panel Test, Chem Test, Chem 21 Test, Chem 14 Test 

The Comprehensive Sjögren’s Syndrome Diagnostic Panel evaluates key autoimmune markers including ANA with reflex to titer, SS-A and SS-B antibodies, rheumatoid factor, thyroid peroxidase antibody, and mitochondrial antibody with reflex. This blood test helps diagnose Sjögren’s syndrome, an autoimmune disease affecting tear and saliva glands, while also detecting related autoimmune or connective tissue disorders to guide treatment and patient care.

Also Known As: Sjögren's Syndrome Diagnostic Panel Comprehensive

The Coxsackie B Virus Antibodies test is a diagnostic blood test used to detect antibodies produced by the immune system in response to a Coxsackie B virus infection. Coxsackie B viruses belong to the enterovirus family and are associated with a range of illnesses, from mild flu-like symptoms to more severe conditions such as viral myocarditis and meningitis. This test measures the presence of specific antibodies against Coxsackie B viruses, helping to confirm recent or past infections and assess the immune response to the virus. The test is particularly useful in identifying cases where Coxsackie B virus may be the underlying cause of unexplained cardiac, neurological, or systemic symptoms.
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The Creatine 24 Hour Urine Test measures creatine excretion to evaluate muscle metabolism, kidney function, and possible metabolic disorders. Abnormal levels may indicate muscular dystrophy, kidney impairment, or issues with creatine utilization. By tracking creatine over a full day, this test provides valuable insight into energy metabolism, aiding the assessment of neuromuscular health, renal function, and inherited metabolic conditions.

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Urine Collection

The Creatine Kinase Isoenzymes Panel evaluates CK-MM, CK-MB, and CK-BB fractions to differentiate the source of elevated creatine kinase. It aids in diagnosing heart attack, skeletal muscle injury, or central nervous system damage. By analyzing isoenzyme distribution, the test supports clinical evaluation of myocardial infarction, myopathies, neurotrauma, and systemic conditions.

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The Creatine Kinase (CK) Isoenzymes with Total CK Panel measures overall CK levels and breaks them into isoenzymes (CK-MM, CK-MB, CK-BB) to identify muscle, heart, or brain injury. Elevated CK-MB may suggest a heart attack, while CK-MM points to skeletal muscle damage, and CK-BB indicates brain injury. Doctors order this test for chest pain, muscle weakness, or trauma. Results provide critical insight for diagnosing and monitoring tissue damage.

Also Known As: CPK Isoenzymes Test

The Creatine Kinase (CK) Total Test measures CK enzyme levels in blood to detect muscle injury, inflammation, or stress. Elevated CK may indicate muscle disorders, heart attack, strenuous exercise, or conditions such as rhabdomyolysis, while low levels are less common. Doctors use this test to evaluate unexplained muscle pain, weakness, or chest pain and to monitor recovery. It provides insight into muscle, cardiac, and overall metabolic health.

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Also Known As: CK Total Test, Creatine Phosphokinase, CPK Test

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The Direct Antiglobulin Test (DAT), also known as the Direct Coombs test, is a laboratory test used to detect antibodies or complement proteins attached to the surface of red blood cells (RBCs). The presence of these antibodies or complement components suggests an immune-mediated process leading to red blood cell destruction, also known as hemolysis. This test is essential in diagnosing immune-related hemolytic anemia, transfusion reactions, hemolytic disease of the newborn (HDN), and autoimmune disorders affecting red blood cells.
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The Direct Antiglobulin Test with Reflex to Anti C3 and Anti IgG evaluates immune-mediated red blood cell destruction by detecting antibodies or complement proteins. Abnormal findings may suggest autoimmune hemolytic anemia, drug-induced hemolysis, or transfusion reaction. Reflex testing helps distinguish complement activation from IgG involvement, offering insight into immune regulation and hematologic health.

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Also Known As: Direct Coombs Test, Coombs Direct Test, DAT Test

The DNA (ds) Antibody Test detects double-stranded DNA antibodies, often linked to systemic lupus erythematosus (SLE) and other autoimmune diseases. High levels may indicate lupus activity, kidney involvement, or autoimmune flare-ups. Doctors order this test for patients with joint pain, fatigue, rash, or suspected connective tissue disease. Results provide critical insight for diagnosing lupus, monitoring disease progression, and guiding treatment decisions.

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The Early Sjögren’s Syndrome Profile tests for antibodies to carbonic anhydrase VI (CA VI), salivary protein 1 (SP-1), and parotid specific protein (PSP) across IgG, IgA, and IgM isotypes. These novel biomarkers may appear before classic SS-A/SS-B antibodies, helping identify Sjögren’s syndrome earlier. This profile supports assessment of early autoimmune damage to salivary and lacrimal glands.

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ENA (Extractable Nuclear Antigen) panel including Jo-1, RNP, Scl-70, SS-A, SS-B, and Sm antibodies. Designed to support evaluation of systemic lupus, Sjögren’s syndrome, systemic sclerosis, mixed connective tissue disease, and inflammatory myopathies through targeted autoimmune antibody testing.

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Panel Contains Test: Extractable Nuclear Antigen Panel

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The HLA DRB1 DQB1 Low Resolution Test determines genetic variations within the HLA class II region, specifically DRB1 and DQB1 alleles. These markers play an important role in immune system regulation and are associated with autoimmune conditions such as type 1 diabetes, celiac disease, and rheumatoid arthritis. This test provides insight into genetic predisposition, transplant matching, and immune-related disease risk.

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Also Known As: HLA Class II DNA Typing Test, HLA DR DQ Test

The HLA-B27 Antigen Test detects the presence of the HLA-B27 protein on white blood cells, which is linked to autoimmune conditions. A positive result may indicate higher risk for ankylosing spondylitis, reactive arthritis, or other spondyloarthropathies. Doctors order this test to investigate chronic back pain, joint inflammation, or autoimmune family history. Results provide critical insight into genetic predisposition, immune system activity, and inflammatory disease risk.

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Most Popular

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 IgA Subclasses Panel evaluates IgA1 and IgA2 subclasses, which are critical for mucosal defense and immune balance. Deficiencies may increase susceptibility to sinus, lung, or digestive infections and may also be linked to autoimmune disease. This test supports assessment of antibody function, systemic health, and conditions tied to mucosal immunity and immune dysregulation.

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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.