Related Experiment Video
Updated: May 31, 2026

Quantification of Autoreactive Antibodies in Mice upon Experimental Autoimmune Encephalomyelitis
Published on: December 1, 2023
HLA associations with multiple sclerosis in Greece
Ioanna Kouri1, Stylianos Papakonstantinou, Vaios Bempes
1Neurosurgery Institute, Medical School, University of Ioannina, Ioannina, Greece. ioannakouri@yahoo.gr
Background:
Multiple sclerosis (MS) is a demyelinating inflammatory disease of the central nervous system originated by a complex interplay of environmental and genetic factors. The association of MS with the human leukocyte antigen (HLA) class II alleles was investigated in MS patients in northwest Greece, in the geographical region of Epirus.
Objective:
Our aim was to estimate the prevalence of the HLA-DRB1*1501, HLA-DQB1*0602 and HLA-DQA1*0102 alleles, consisting the most common susceptibility haplotype in North European and North American Caucasians.
Methods:
We studied 126 MS patients and 93 age and sex matched healthy controls. HLA typing was performed by a polymerase chain reaction (PCR) amplification with sequence-specific primers (PCR-SSP) method.
Results:
We found that HLA-DRB1*1501, HLA-DQB1*0602 and HLA-DQA1*0102 alleles were significantly more frequent among patients (34% versus 11%, p=0.00015; 69% versus 51%, p=0.01; 76% versus 55%, p=0.002, respectively). HLA-DRB1*1501, HLA-DQB1*0602, HLA-DQA1*0102 haplotype was significantly more common among patients (p=0.00067). HLA-DRB1*1501 and HLA-DQB1*0602 alleles were more frequently detected in patients with initial symptoms from the brainstem or the cerebellum (p=0.024). No significant correlation was observed among these alleles with sex, disease clinical course, or age at onset.
Conclusion:
This is the first study to investigate genetic susceptibility to MS in Greece. Our results are in line with previous reports in North European and North American patients.
Insights
This study investigated human leukocyte antigen (HLA) alleles in Greek multiple sclerosis (MS) patients, finding specific HLA variants are more common in those with MS. These findings align with research in other Caucasian populations.
Area of Science:
- Immunogenetics
- Neurology
- Human Genetics
Background:
- Multiple sclerosis (MS) is a central nervous system inflammatory disease influenced by genetic and environmental factors.
- The role of human leukocyte antigen (HLA) class II alleles in MS susceptibility is well-established in North European and North American Caucasians.
- This study examines HLA associations in a Greek MS population from Epirus.
Purpose of the Study:
- To estimate the prevalence of HLA-DRB1*1501, HLA-DQB1*0602, and HLA-DQA1*0102 alleles in Greek MS patients.
- To determine if these alleles, forming a common susceptibility haplotype, are associated with MS in this population.
- To explore correlations between these alleles and clinical characteristics of MS.
Main Methods:
- A case-control study involving 126 MS patients and 93 healthy controls from northwest Greece.
- Human leukocyte antigen (HLA) typing was performed using the polymerase chain reaction with sequence-specific primers (PCR-SSP) method.
- Statistical analysis was used to compare allele frequencies between patients and controls.
Main Results:
- HLA-DRB1*1501, HLA-DQB1*0602, and HLA-DQA1*0102 alleles were significantly more frequent in MS patients compared to controls.
- The combined HLA-DRB1*1501, HLA-DQB1*0602, HLA-DQA1*0102 haplotype was also significantly more common in patients.
- HLA-DRB1*1501 and HLA-DQB1*0602 were associated with initial symptoms affecting the brainstem or cerebellum.
Conclusions:
- This is the first study to investigate genetic susceptibility to MS in Greece.
- The findings support the association of specific HLA alleles with MS in the Greek population.
- Results are consistent with previous studies in North European and North American Caucasian populations.
Related Concept Videos
Multiple Sclerosis l: Introduction
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
Graves' Disease I: Introduction
Myasthenia Gravis ll: Pathophysiology
