HLA-B27

The HLA-B27 test is primarily ordered to help strengthen or confirm a suspected diagnosis of ankylosing spondylitis (AS), Reiter’s syndrome (reactive arthritis), or sometimes anterior uveitis. The HLA-B27 test is not a definitive test that can be used to diagnose or rule out a disorder. It is used as one piece of evidence in a constellation of signs, symptoms, and lab tests to support or rule out the diagnosis of certain autoimmune disorders, such as AS and Reiter's syndrome. Both AS and Reiter’s syndrome are chronic progressive conditions that occur more frequently in men than women, and the first symptoms usually occur when a patient is in his early 30's. Ankylosing spondylitis is characterized by pain, inflammation, and a gradual stiffening of the spine, neck and chest. Reiter’s syndrome is a group of symptoms that includes inflammation of the joints, urethra, eyes, and skin lesions. Often, the initial symptoms of these autoimmune disorders are subtle and may take several years before characteristic degenerative changes to bones and joints are visible on X-rays. Anterior uveitis is associated with recurring inflammation of the structures of one or both eyes.

The HLA-B27 test may be ordered as part of a group of tests used to diagnose and evaluate conditions causing arthritis-like chronic joint pain, stiffness, and inflammation. This group of tests may include an RF (rheumatoid factor) with either an ESR (erythrocyte sedimentation rate) or a CRP (C-Reactive protein). HLA-B27 is sometimes ordered to help evaluate someone with recurrent uveitis that is not caused by a recognizable disease process.

An HLA-B27 test may be ordered when a patient has acute or chronic pain and inflammation in his spine, neck, chest, eyes, and/or joints, and the doctor suspects an autoimmune disorder that is associated with the presence of HLA-B27. Doctors frequently must rely on their clinical findings and the HLA-B27 test result when diagnosing ankylosing spondylitis, and other HLA-B27 related disorders, because the characteristic changes to the bones may not be detectible for several years. Under these circumstances, HLA-B27 is not diagnostic but adds additional information, increasing or decreasing the likelihood that the patient has ankylosing spondylitis. An HLA-B27 may also be ordered when a patient has recurrent uveitis.

HLA-B27 will be present or absent. If it is present, then the HLA-B27 antigen exists on the surface of the body’s white blood cells and other nucleated (containing a nucleus) cells. If a patient has HLA-B27 and has symptoms such as chronic pain, inflammation, and/ or degenerative changes to his bones (as seen on X-ray), then it supports a diagnosis of AS, Reiter’s syndrome, or another autoimmune disorder that is associated with the presence of HLA-B27. This is especially true if the patient is young, male, and if he experienced his first symptoms before the age of 40.

 

If HLA-B27 is not present, then the association is not there. This does not, however, mean that the person does not have the suspected condition, as a certain percentage of patients with each disorder will be HLA-B27 negative.

A positive HLA-B27 in a person who does not have symptoms or a family history of HLA-B27 associated disease is not clinically significant. It does not help predict the likelihood of developing an autoimmune disease. If a patient does have an associated disorder, the presence of HLA-B27 cannot be used to tell which disease is present, how quickly it will progress, its severity, prognosis, or the degree of organ involvement.

Whether or not HLA antigens will be present is genetically determined. Their production is controlled by genes that are passed from parents to children. If one of your family members has a HLA-B27 related disease that affects the joints of the spine (AS or other related condition) and you have the HLA-B27 antigen, then you have a higher risk of developing a similar disease.

With new genetic testing methods, it is now possible to separate HLA-B27 into subtypes. So far, about fifteen different subtypes have been identified. The most common in the U.S. are HLA B27*05 and HLA B27*02. How the presence of these specific subtypes affects the likelihood of developing an autoimmune disease is not yet known.