Related Experiment Video
Updated: May 23, 2026

08:07
Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
The link between HLA-B27 and SpA--new ideas on an old problem
1Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, UK.
Rheumatology (Oxford, England)
|April 20, 2012
Summary
The human leukocyte antigen B27 (HLA-B27) is strongly linked to ankylosing spondylitis (AS). Recent advances in GWAS, B27 biology, and biologic therapies offer new insights into AS pathogenesis.
Area of Science:
- Immunogenetics
- Rheumatology
- Genomics
Background:
- The association between HLA-B27 and ankylosing spondylitis (AS) was identified in 1972.
- Despite decades of research, the precise pathogenic role of HLA-B27 in AS remains elusive.
- Recent genome-wide association studies (GWAS) have reconfirmed this strong genetic link.
Purpose of the Study:
- To review recent advancements in understanding HLA-B27 and AS.
- To propose new theories on AS pathogenesis.
- To discuss current models of AS pathogenesis.
Main Methods:
- Review of recent literature on GWAS.
- Analysis of studies on HLA-B27 biology.
- Examination of findings from biologic therapies for AS.
Main Results:
- GWAS have provided sophisticated fine-mapping confirmation of the HLA-B27 association.
- Advances in understanding B27 biology offer potential mechanisms for disease.
- Biologic therapies provide insights into inflammatory pathways in AS.
Conclusions:
- Recent developments offer a new perspective on the HLA-B27 and AS relationship.
- Coherent theories of AS pathogenesis can now be proposed.
- Further investigation into B27 biology and therapeutic responses is warranted.
More Related Videos
Related Concept Videos
Genome-wide Association Studies-GWAS
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
Single Nucleotide Polymorphisms-SNPs
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...

