Ankylosing spondylitis (AS) is a long-lasting inflammatory disease that mainly hits the spine. It’s been debated whether it’s an autoimmune disorder in modern medicine.
Recent studies show that AS is both an autoimmune and autoinflammatory condition. It’s one of the most complex autoimmune diseases affecting millions globally.
Genetic factors, like the HLA-B27 gene, are key in AS development. Knowing if AS is an autoimmune disease is vital for diagnosis and treatment.
At Liv Hospital, we combine international expertise and the latest research to help AS patients.
Key Takeaways
- Ankylosing spondylitis is a chronic inflammatory condition affecting the spine.
- AS is classified as both an autoimmune and autoinflammatory disease.
- Genetic factors like the HLA-B27 gene are significant in AS development.
- Understanding AS as an autoimmune disease aids in diagnosis and treatment.
- Liv Hospital provides complete care for AS patients using the latest research and protocols.
Understanding Ankylosing Spondylitis

Ankylosing Spondylitis is a chronic condition that affects the spine and other joints. It causes severe pain and discomfort, mainly in the lower back and hips. We will look into the basics of AS, including its definition, prevalence, and symptoms.
What is Ankylosing Spondylitis?
Ankylosing Spondylitis (AS) is a chronic inflammatory disease. It mainly affects the spine and sacroiliac joints. The inflammation can cause severe pain and discomfort.
In some cases, this inflammation can lead to the fusion of vertebrae, known as ankylosis. The exact cause of AS is unknown. It is believed to involve genetic and environmental factors. The HLA-B27 gene is associated with AS, but having this gene does not mean one will definitely develop it.
Prevalence and Demographics
AS affects a significant portion of the global population. The prevalence rates vary across different regions. It is estimated that AS affects 0.1 to 1.4 percent of the population, depending on the presence of the HLA-B27 gene.
The condition is more common in young males, typically beginning in late adolescence or early adulthood. It can also occur in females and older individuals. The male-to-female ratio varies, but males are generally more frequently affected.
Primary Symptoms and Affected Areas
The primary symptoms of AS include:
- Chronic back pain and stiffness, mainly in the lower back and hips.
- Inflammation of the sacroiliac joints and spine.
- Reduced mobility due to pain and stiffness.
- In some cases, peripheral joint involvement, where other joints such as the hips, shoulders, and knees are affected.
Other areas that can be affected include the eyes, heart, and lungs. This can lead to complications such as uveitis, aortic regurgitation, and pulmonary fibrosis.
Is Ankylosing Spondylitis an Autoimmune Disease?

Ankylosing spondylitis (AS) is tricky to classify because it has traits of both autoimmune and autoinflammatory diseases. We’ll look into the autoimmune and autoinflammatory sides of AS. We’ll talk about the roles of certain cytokines and genetic factors.
The Autoimmune Characteristics of AS
AS has some features of autoimmune diseases, like immune cells in affected areas and the chance of autoantibodies. But, it lacks specific autoantibodies found in diseases like rheumatoid arthritis. This makes it hard to say it’s only an autoimmune disease.
The immune response in AS involves many immune cells, like T cells and dendritic cells. These cells play a big part in causing the disease.
The Autoinflammatory Components
The autoinflammatory parts of AS involve innate immune cells and pro-inflammatory cytokines. Understanding these parts helps us see how the disease starts and find ways to treat it.
Autoinflammatory mechanisms start the inflammation in AS. This happens before the adaptive immune response kicks in.
Key Inflammatory Cytokines: IL-17 and IL-23
IL-17 and IL-23 are key cytokines in AS. They cause inflammation and bone growth, leading to the disease’s main symptoms. Trying to block these cytokines is a big part of treating AS.
The work of IL-17 and IL-23 is important for enthesitis, a key feature of AS.
Genetic Factors in AS Development
Genetics play a big role in AS, with HLA-B27 being the biggest risk factor. Other genes also affect how likely someone is to get AS and how severe it will be.
Having HLA-B27 makes getting AS more likely. But, it’s not the only thing needed for the disease to start.
Conclusion: The Dual Nature of Ankylosing Spondylitis
Ankylosing spondylitis (AS) is a complex condition. It shows traits of both autoimmune diseases and autoinflammatory disorders. Understanding its dual nature is key to finding effective treatments.
Genetic and environmental factors play a big role in AS. Research has found that certain inflammatory cytokines, like IL-17 and IL-23, are important. These findings have led to new treatments that aim to control the immune response.
Managing AS requires a detailed approach. Recognizing its autoimmune and autoinflammatory aspects helps healthcare providers give better care. This not only improves treatment results but also boosts the quality of life for those with AS.
Our study highlights the need to consider AS’s dual nature in medical practice. This way, we can better meet the needs of patients with this chronic condition. It leads to more effective management of auto immune disease arthritis.
FAQ
Is ankylosing spondylitis considered an autoimmune disease?
What are the primary symptoms of ankylosing spondylitis?
How do genetic factors contribute to the development of ankylosing spondylitis?
What is the role of IL-17 and IL-23 in ankylosing spondylitis?
Can ankylosing spondylitis be associated with other autoimmune diseases?
Is ankylosing spondylitis the same as lupus?
How does ankylosing spondylitis affect the body?
What is the current understanding of the autoimmune and autoinflammatory characteristics of ankylosing spondylitis?
References
National Center for Biotechnology Information. Evidence-Based Medical Insight. Retrieved from https://pubmed.ncbi.nlm.nih.gov/24534717/