Authors
Mohammad Hossein Nicknam, Mahdi Mahmoudi, Ali Akbar Amirzargar, Ahmad Reza Jamshidi, Nima Rezaei, Behrouz Nikbin
Publication date
2009/3/30
Journal
European cytokine network
Volume
20
Issue
1
Pages
17-20
Description
Background
HLA-B27 is an MHC class I molecule that is strongly associated with ankylosing spondylitis (AS). TNF-α, as an important cytokine in inflammatory joint disease, might have a role in the process of AS. This study was performed to determine HLA-B27 subtypes among Iranian patients with AS, and to investigate TNF-α gene polymorphisms in the patient groups.
Methods
Ninety seven AS patients (74 HLAB27-positive and 23 HLA-B27-negative) and 137 healthy normal subjects (2 HLA-B27-positive) were enrolled in this study. HLA-B27 positive patients were screened using the polymerase chain reaction, with sequence specific primers (PCR-SSP), for B* 27 subtyping. All patients and the controls were also investigated for determination of TNF-α polymorphisms using the same method.
Results
Just two subtypes were detected in our patients, namely B* 2705 (63.4%) and B* 2702 (36.6%). The study of TNF-α polymorphisms at position-238 showed that the A allele and AA genotype were significantly over-represented in all patient groups in comparison with the control group (p< 0.001). At position-308, while the A allele and AA genotype were significantly overrepresented in the whole patient group (p= 0.01), there was no significant difference between the AS groups and the control group.
Conclusion
It could be suggested that a polymorphism within the TNF-α gene at-238 play an important role in AS, although this polymorphism was not related to HLA-B27 subtypes.
Total citations
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