HLA-DR18
HLA-DR18 (DR18) is a HLA-DR serotype that recognizes the DRB1*0302 and *0303 gene products. Compared to DR17 which is found at high frequency in Western Europe, DR18 is found more in SE Europe and Central Asia.
major histocompatibility complex, class II, DR18 | |
Haplotypes groups | DRA*01:DRB1*0302 DRA*01:DRB5*0303 |
Structure (See HLA-DR) | |
Identifiers | alpha *0101 |
Symbol(s) | HLA-DRA |
EBI-HLA | DRA*0101 |
Identifiers | beta 1 *0302 *0303 |
Symbol(s) | HLA-DRB1 |
EBI-HLA | DRB5*0302 |
EBI-HLA | DRB1*0303 |
Shared data | |
Locus | chr.6 6p21.31 |
Serology
DRB1* | DR18 | DR3 | DR17 | Sample |
allele | % | % | % | size (N) |
0302 | 66 | 24 | 3 | 317 |
0303 | 60 | 40 | 5 | |
DR18 recognizes the DRB1*0302 and *0303, the thoroughness of recognition is fair, but better than DR3.
Disease associations
DR18 seropositivity is associated with rheumatoid polyarthritis[2]
DRB1*0302 is positively associated with juvenile diabetes,[3] nuclear helicase Mi-2 autoantibodies in inflammatory inclusion body myositis.[4]
Genetic Linkage
DR18 Haplotypes | |||
Serotypes | DRA | DRB1 | DRB3 |
---|---|---|---|
DR18(3)-DR52 | *0101 | *0302 | *0101 |
DQA1 | DQB1 | DRB1 | |
D18(3)-DQ2(2.5) | *0501 | *0201 | *0302 |
HLA-A | HLA -B | DRB1 | |
A33-B58-DR18(3) | *3301 | *5801 | *0302 |
HLA-DR18 is genetically linked to DR52 and HLA-DQ2 serotypes. These serotypes are the result of gene products from the HLA-DRB3* and HLA DQA1*0501 and HLA DQB1*0201 alleles.
References
- derived from IMGT/HLA
- Dieye A, Diallo S, Diatta M, Thiam A, Ndiaye R, Bao O, Sarthou J (1997). "[Identification of HLA-DR alleles for susceptibility to rheumatoid polyarthritis in Senegal]". Dakar Med. 42 (2): 111–3. PMID 9827131.
- Shawkatova I, Michalkova D, Barak L, Fazekasova H, Kuba D, Buc M (2006). "HLA class II allele frequencies in type 1A diabetes mellitus Slovak patients". Bratislavské Lekárske Listy. 107 (3): 76–9. PMID 16796128.
- Sivakumar K, Semino-Mora C, Dalakas MC (1997). "An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families". Brain. 120 ( Pt 4) (4): 653–661. doi:10.1093/brain/120.4.653. PMID 9153127.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.