HLA-B58
HLA-B (alpha)-β2MG with bound peptide | ||
major histocompatibility complex (human), class I, B58 | ||
Alleles | *5801, *5802 | |
Structure (See HLA-B) | ||
Shared data | ||
Locus | chr.6 6p21.31 |
HLA-B58 (B58) is an HLA-B serotype. B58 is a split antigen from the B17 broad antigen, the sister serotype B57.[1] The serotype identifies the more common HLA-B*58 gene products.[2] (For terminology help see: HLA-serotype tutorial) B*5801 is associated with allopurinol induced inflammatory necrotic skin disease.
Serotype
B*58 | B58 | B17 | Sample |
allele | % | % | size (N) |
*5801 | 79 | 4 | 2096 |
*5802 | 72 | 3 | 837 |
Allele distribution
freq | ||
ref. | Population | (%) |
[4] | Cameroon Pygmy Baka | 15.0 |
[4] | India Khandesh Pawra | 15.0 |
[4] | Cameroon Sawa | 11.5 |
[4] | Taiwan Hakka | 10.9 |
[4] | Kenya Nandi | 10.0 |
[4] | India West Bhils | 9.0 |
[4] | China South Han | 8.9 |
[4] | China Inner Mongolia | 8.8 |
[4] | India North Delhi | 8.8 |
[4] | Thailand Northeast | 8.4 |
[4] | Guinea Bissau | 7.8 |
[4] | Thailand | 7.7 |
[4] | India Mumbai Marathas | 7.4 |
[4] | India Andhra Pradesh Golla | 7.2 |
[4] | Kenya Luo | 7.0 |
[4] | Senegal Niokholo Mandenka | 6.9 |
[4] | India New Delhi | 6.8 |
[4] | Oman | 6.8 |
[4] | Russia Tuva (2) | 6.7 |
[4] | South Korea (3) | 6.5 |
[4] | Italy Sardinia (3) | 6.4 |
[4] | Burkina Faso Fulani | 6.1 |
[4] | Taiwan Siraya | 5.9 |
[4] | India North Hindus | 5.8 |
[4] | Burkina Faso Mossi | 5.7 |
[4] | Cameroon Yaounde | 5.4 |
[4] | Cameroon Bamileke | 5.2 |
[4] | Singapore Riau Malay | 5.0 |
[4] | Saudi Arabia Guraiat and Hail | 4.6 |
[4] | France Corsica | 4.5 |
[4] | Sudanese | 4.5 |
[4] | Zimbabwe Harare Shona | 4.4 |
[4] | Burkina Faso Rimaibe | 4.3 |
[4] | Iran Baloch | 4.0 |
[4] | South African Natal Zulu | 4.0 |
[4] | Tunisia | 4.0 |
[4] | Uganda Kampala | 4.0 |
[4] | Cameroon Beti | 3.7 |
[4] | Tunisia Ghannouch | 3.7 |
[4] | Taiwan Pazeh | 3.6 |
[4] | Tunisia Tunis | 3.4 |
[4] | Italy North (1) | 3.3 |
[4] | Israel Ashkenazi and Non Ashkenazi Jews | 3.2 |
[4] | India West Coast Parsis | 3.0 |
[4] | China North Han | 2.9 |
[4] | Ivory Coast Akan Adiopodoume | 2.3 |
[4] | Mali Bandiagara | 2.2 |
[4] | Mexico Zaptotec Oaxaca | 2.2 |
[4] | South Africa Natal Tamil | 2.0 |
[4] | China Yunnan Nu | 1.9 |
[4] | Bulgaria | 1.8 |
[4] | China Tibet Autonomous Region Tibetans | 1.6 |
[4] | France South East | 1.6 |
[4] | Israel Arab Druse | 1.5 |
[4] | Czech Republic | 1.4 |
[4] | Georgia Tibilisi Georgians | 1.4 |
[4] | Jordan Amman | 1.4 |
[4] | Morocco Nador Metalsa (berber) | 1.4 |
[4] | Croatia | 1.3 |
[4] | Romanian | 1.3 |
[4] | Spain Eastern Andalusia | 1.2 |
[4] | Australian Aborigine Cape York Peninsula | 1.0 |
B*5802 | ||
[4] | Cameroon Bamileke | 14.3 |
[4] | Kenya Luo | 12.5 |
[4] | Cameroon Yaounde | 10.9 |
[4] | Cameroon Pygmy Baka | 10.0 |
[4] | Cameroon Beti | 9.8 |
[4] | Kenya Nandi | 8.5 |
[4] | South African Natal Zulu | 8.5 |
[4] | Cameroon Sawa | 7.7 |
[4] | Zimbabwe Harare Shona | 6.4 |
[4] | Cape Verde Northwestern Islands | 5.6 |
[4] | Uganda Kampala | 4.4 |
[4] | Central Africa Republic Mbenzele Pygmy | 4.0 |
[4] | Zambia Lusaka | 2.3 |
[4] | Iran Baloch | 1.0 |
[4] | Tunisia | 1.0 |
Disease
HLA-B*5801 is involved in allopurinol sensitive drug induced Stevens–Johnson syndrome.[5][6] Allopurinol is a frequent cause of severe cutaneous adverse reactions, including drug-hypersensitivity syndrome, Stevens–Johnson syndrome, and toxic epidermal necrolysis (SJS/TEN).[7] The association with allopurinol sensitivity in JSJ/TEN was extremely strong in Asia, and somewhat less associated in Europeans.[8]
References
- ↑ Ways JP, Coppin HL, Parham P (1985). "The complete primary structure of HLA-Bw58". J. Biol. Chem. 260 (22): 11924–33. PMID 2995352.
- ↑ Marsh SG, Albert ED, Bodmer WF, et al. (2005). "Nomenclature for factors of the HLA system, 2004". Tissue Antigens. 65 (4): 301–69. doi:10.1111/j.1399-0039.2005.00379.x. PMID 15787720.
- ↑ derived from IMGT/HLA
- 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database: http://www.allelefrequencies.net". Tissue Antigens. 61 (5): 403–7. doi:10.1034/j.1399-0039.2003.00062.x. PMID 12753660. External link in
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(help) - ↑ Chung WH, Hung SI, Chen YT (August 2007). "Human leukocyte antigens and drug hypersensitivity". Curr Opin Allergy Clin Immunol. 7 (4): 317–23. doi:10.1097/ACI.0b013e3282370c5f. PMID 17620823.
- ↑ Tassaneeyakul W, Jantararoungtong T, Chen P, Lin PY, Tiamkao S, Khunarkornsiri U, Chucherd P, Konyoung P, Vannaprasaht S, Choonhakarn C, Pisuttimarn P, Sangviroon A, Tassaneeyakul W (2009). "Strong association between HLA-B*5801 and allopurinol-induced Stevens–Johnson syndrome and toxic epidermal necrolysis in a Thai population". Pharmacogenet Genomics. 19 (9): 704–9. doi:10.1097/FPC.0b013e328330a3b8. PMID 19696695.
- ↑ Hung SI, Chung WH, Liou LB, et al. (March 2005). "HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol". Proc. Natl. Acad. Sci. U.S.A. 102 (11): 4134–9. doi:10.1073/pnas.0409500102. PMC 554812. PMID 15743917.
- ↑ Lonjou C, Borot N, Sekula P, et al. (February 2008). "A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs". Pharmacogenet. Genomics. 18 (2): 99–107. doi:10.1097/FPC.0b013e3282f3ef9c. PMID 18192896.
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