Sample results
Common Variable Immunodeficiency (CVID) is a primary immune disorder characterized by significantly reduced levels of immunoglobulins (antibodies) in the blood. It is caused by genetic defects that impair B cells from producing adequate amounts of IgG, IgA, and sometimes IgM antibodies. The IgG, IgA, Indirect Immunofluorescence test is the most important test for diagnosis because it measures multiple immunoglobulin levels simultaneously to confirm antibody deficiency.
Common Variable Immunodeficiency is caused by genetic mutations that affect B cells, preventing them from maturing properly and producing adequate antibodies. While the exact genetic defects vary between individuals, these mutations impair the immune system's ability to make immunoglobulins like IgG, IgA, and IgM. Without sufficient antibodies, your body cannot effectively fight off bacteria, viruses, and other pathogens, leading to recurrent infections throughout life.
The IgG, IgA, Indirect Immunofluorescence test is the most important test for Common Variable Immunodeficiency because it measures multiple critical antibody levels in a single comprehensive panel. This test detects significantly reduced levels of IgG and IgA immunoglobulins, which are the hallmark findings needed to confirm CVID diagnosis. The IgA test can also be used as a supplementary measure to specifically assess Immunoglobulin A deficiency, which contributes to increased susceptibility to respiratory and gastrointestinal infections. Together, these tests provide the essential antibody measurements that distinguish CVID from other causes of recurrent infections.
You should get tested if you experience frequent bacterial infections like pneumonia, bronchitis, or sinus infections that keep coming back despite treatment. Testing is also important if you have chronic diarrhea, ear infections that won't resolve, or unusual infections that healthy people rarely get. Adults who suddenly develop recurrent infections in their 20s or 30s, or children with persistent infections affecting the lungs, ears, or sinuses should consider immunoglobulin testing to identify potential antibody deficiencies early.
What this means
Your test came back negative, meaning no anti-epithelial cell surface antibodies were detected in your blood. This is the expected and healthy result, suggesting no active autoimmune blistering disease affecting the connections between skin cells.
Recommended actions
Continue monitoring any skin symptoms and report new blistering to your doctor
Maintain good skin care practices and protect skin from excessive friction
If you develop unexplained blisters or sores, consider retesting
Follow up with your dermatologist if symptoms persist despite negative results
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Sample results
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