Knowledge (XXG)

HLA-DP

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decided because of the complex genetic characteristics of DPB1 alleles compared to alleles of other HLA loci. The majority of the HLA-DPB1 alleles cannot be simply grouped together by their nucleotide sequences. This name assignment has been the most confusing system within the HLA nomenclature. In the 2010 HLA nomenclature update, all DPB1 alleles, except DPB1*0202 and *0402, discovered after DPB1*9901 were reassigned with new numbers. For example, DPB1*0102 becomes DPB1*100:01 and DPB1*0203 becomes DPB1*101:01.
171:. Each DP subunit (α-subunit, β-subunit) is composed of a α-helical N-terminal domain, an IgG-like β-sheet, a membrane spanning domain, and a cytoplasmic domain. The α-helical domain forms the sides of the peptide binding groove. The β-sheet regions form the base of the binding groove and the bulk of the molecule as well as the inter-subunit (non-covalent) binding region. 192:(APC)(macrophages, dendritic cells, and B-lymphocytes). Normally, these APC 'present' class II receptor/antigens to a great many T-cells, each with unique T-cell receptor (TCR) variants. A few TCR variants that recognize these DQ/antigen complexes are on CD4 positive T-cells. These T-cells, called T-helper (T 187:
of humans, however this antigen is an artifact of the era of organ transplantation. HLA DP functions as a cell surface receptor for foreign or self antigens. The immune system surveys antigens for foreign pathogens when presented by MHC receptors (like HLA-DP). The MHC Class II antigens are found on
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Before the April 2010 HLA nomenclature update, new HLA-DPB1 allele names were assigned within the existing nomenclature system. For example, the allele discovered after HLA-DPB1*9901 was assigned as DPB1*0102, the subsequent allele was named DPB1*0202, then *0302 and so on. This name assignment was
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Marsh, S. G. E., Albert, E. D., Bodmer, W. F., Bontrop, R. E., Dupont, B., Erlich, H. A., Fernández-Viña, M., Geraghty, D. E., Holdsworth, R., Hurley, C. K., Lau, M., Lee, K. W., Mach, B., Maiers, M., Mayr, W. R., Müller, C. R., Parham, P., Petersdorf, E. W., Sasazuki, T., Strominger, J. L.,
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These 'cis'-isoforms will account for at least 50% of the DP isoforms. The other, trans isoforms are typically more rare, isoforms result from random 'trans' combinations of haplotypes in individuals as a result of 'trans' paternal/maternal gene product isoforms.
802:. This tool allows you to enter an HLA allele name and will provide you with both the current and new versions of the allele name. New alleles that have never been assigned with a name prior to the April 2010 update are: 200:
consume or destroy cells by apoptotic signaling and present self-antigens. Self antigens, in the right context, form a regulatory T-cell population that protects self tissues from immune attack or autoimmunity.
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complex DP locus is more frequently substituted, either as a result of its distance from other loci, or because it was not as actively selected in the evolution of
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The α-chain and β- of DP is encoded by the HLA-DPA1 locus and HLA-DPB1 loci, respectively. This cluster is located at the proximal (centromeric) end of the
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Each combination of DPA1 allele gene product with each combination of DPB1 'gene' product can potentially recombine to produce one isoform.
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To aid in migration of data to the new nomenclature the WHO Nomenclature Committee for Factors of the HLA System has provided the
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in the human population. In a typical population there are many DP alpha and beta. Most isoforms are not common.
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complex on human chromosome 6 (see protein boxes on right for links). Less is known about HLA-DP relative to
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encoding loci and therefore is much more equilibrated with respect to other HLA loci. In the
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antigen that is composed of 2 subunits, DPα and DPβ. DPα and DPβ are encoded by two loci,
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All renamed alleles are listed in the HLA-DPB1 Nomenclature Conversion Chart below.
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DP(αβ) Isoforms given one maternal (m) and one paternal (p) chromosome 6
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Svejgaard, A., Terasaki, P. I., Tiercy, J. M., Trowsdale, J. (2010).
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ftp://ftp.ebi.ac.uk/pub/databases/imgt/mhc/hla/Nomenclature_2009.txt
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The name 'HLA-DP' originally describes a transplantation antigen of
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but the sequencing of DP types and determination of more frequent
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It is distal from 969: 8: 931:: CS1 maint: multiple names: authors list ( 863:HLA Allele and Haplotype Frequency Database 235:Understanding the Heterodimeric DP Isoforms 976: 962: 954: 155:HLA DP Receptor with bound peptide and TCR 908: 824: 804: 452: 386: 249: 874: 851:The IMGT/HLA Database - HLA Dictionary. 924: 15: 793:IMGT/HLA Nomenclature Conversion Tool 7: 560:HLA-DPB1 Allele Nomenclature Change 833:HLA-DPA1*01:03/DPB1*04:02 (DP402) 828:HLA-DPA1*01:03/DPB1*04:01 (DP401) 127:Class II (or HLA-D) region in the 14: 1176:Minor histocompatibility antigen 985:Major histocompatibility complex 901:10.1111/j.1399-0039.2010.01466.x 185:major histocompatibility complex 147:Structure, Functions, Genetics 1: 107:is a protein/peptide-antigen 52: 365:DP genes are highly variable 1237:Genes on human chromosome 6 846:Nomenclature of HLA Alleles 1258: 1206:Cluster of differentiation 404: 1196:Human blood group systems 581: 552:DPB1*11:01 - DPB1*129:01 551: 343:, isoforms and 2 trans, 328: 273: 266: 261: 113:graft-versus-host disease 51: 26: 457: 190:antigen presenting cells 123:, that are found in the 1201:Cell adhesion molecules 1171:Human leukocyte antigen 129:Human Leukocyte Antigen 1227:Protein heteropolymers 156: 45:Immune recognition and 1232:Human MHC haplogroups 198:cytotoxic lymphocytes 169:cell-surface receptor 154: 36:cell surface receptor 821:Common DP Haplotypes 47:antigen presentation 241: 856:2012-09-25 at the 798:2012-08-04 at the 239: 157: 62:Chromosomal locus 1214: 1213: 1181:Blood transfusion 837: 836: 818: 817: 789: 788: 557: 556: 443: 442: 361: 360: 102: 101: 98: 97: 1249: 978: 971: 964: 955: 948: 943: 937: 936: 930: 922: 912: 879: 825: 805: 571: 450: 446:HLA-DPB1 Alleles 384: 380:HLA-DPA1 Alleles 356: 353: 349: 346: 342: 339: 335: 332: 323: 320: 314: 311: 306: 298: 295: 289: 286: 281: 276: 269: 264: 252: 242: 183:category of the 164:HLA-DP is an αβ- 53: 16: 1257: 1256: 1252: 1251: 1250: 1248: 1247: 1246: 1217: 1216: 1215: 1210: 1159: 1031: 988: 982: 952: 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777:DPB1*124:01 769:DPB1*123:01 761:DPB1*122:01 753:DPB1*121:01 737:DPB1*119:01 729:DPB1*118:01 721:DPB1*117:01 713:DPB1*116:01 705:DPB1*115:01 697:DPB1*114:01 689:DPB1*113:01 681:DPB1*112:01 673:DPB1*111:01 665:DPB1*110:01 657:DPB1*109:01 649:DPB1*108:01 641:DPB1*107:01 633:DPB1*106:01 625:DPB1*105:01 617:DPB1*104:01 609:DPB1*103:01 601:DPB1*102:01 593:DPB1*101:01 585:DPB1*100:01 567: 563: 445: 444: 379: 378: 369: 362: 228: 223: 208: 181:MHC class II 178: 163: 104: 103: 56:Subunit name 32:Protein type 20:MHC class II 1191:Calgranulin 994:MHC class I 812:DPB1*128:01 810:DPB1*127:01 166:heterodimer 1221:Categories 869:References 742:DPB1*2302N 141:haplotypes 782:DPB1*2802 774:DPB1*2702 766:DPB1*2602 758:DPB1*2502 750:DPB1*2402 734:DPB1*2202 726:DPB1*2102 718:DPB1*2002 710:DPB1*1902 702:DPB1*1802 694:DPB1*1702 686:DPB1*1602 678:DPB1*1502 670:DPB1*1402 662:DPB1*1302 654:DPB1*1102 646:DPB1*1002 638:DPB1*0902 630:DPB1*0802 622:DPB1*0602 614:DPB1*0502 606:DPB1*0403 598:DPB1*0302 590:DPB1*0203 582:DPB1*0102 453:HLA-DPB1 387:HLA-DPA1 160:Structure 1186:Arrestin 919:20356336 854:Archived 796:Archived 315:(Trans) 299:(Trans) 229:Super B8 224:Super B8 205:Genetics 175:Function 121:HLA-DPB1 117:HLA-DPA1 109:receptor 87:HLA-DPB1 71:HLA-DPA1 42:Function 987:classes 910:2848993 547:*10:01 539:*09:01 531:*08:01 523:*07:01 515:*06:01 507:*05:01 499:*04:02 492:*04:01 484:*03:01 476:*02:02 469:*02:01 461:*01:01 439:*04:01 436:*03:03 429:*02:04 420:*01:10 375:Alleles 324:(Cis ) 290:(Cis ) 259:allele 1128:HLA-DR 1096:HLA-DQ 1079:HLA-DP 1062:HLA-DO 1045:HLA-DM 917:  907:  434:*03:02 432:*03:01 427:*02:03 425:*02:02 423:*02:01 418:*01:09 416:*01:08 414:*01:07 412:*01:06 410:*01:05 408:*01:04 406:*01:03 350:& 336:& 219:HLA-DQ 215:HLA-DR 137:HLA-DR 133:HLA-DQ 105:HLA-DP 94:21.31 78:21.31 1164:Other 1027:HLA-G 1022:HLA-F 1017:HLA-E 1012:HLA-C 1007:HLA-B 1002:HLA-A 933:link 915:PMID 544:*10 536:*09 528:*08 520:*07 512:*06 504:*05 489:*04 481:*03 466:*02 458:*01 401:*04 275:DPA1 251:DPB1 217:and 135:and 119:and 111:and 59:Gene 22:, DP 905:PMC 897:doi 398:*03 395:*02 392:*01 305:(p) 280:(m) 268:(p) 263:(m) 245:HLA 125:MHC 1223:: 1153:β5 1148:β4 1143:β3 1138:β1 1121:β3 1116:β2 1111:β1 1106:α2 1101:α1 1089:β1 1084:α1 929:}} 925:{{ 913:. 903:. 893:75 891:. 887:. 357:. 231:. 1133:α 1072:β 1067:α 1055:β 1050:α 977:e 970:t 963:v 935:) 921:. 899:: 355:β 352:α 348:β 345:α 341:β 338:α 334:β 331:α 322:β 319:α 313:β 310:α 297:β 294:α 288:β 285:α 194:h 83:β 67:α

Index

MHC class II
cell surface receptor
HLA-DPA1
Chromosome 6p
HLA-DPB1
Chromosome 6p
receptor
graft-versus-host disease
HLA-DPA1
HLA-DPB1
MHC
Human Leukocyte Antigen
HLA-DQ
HLA-DR
haplotypes

heterodimer
cell-surface receptor
MHC class II
major histocompatibility complex
antigen presenting cells
cytotoxic lymphocytes
HLA superlocus
HLA-DR
HLA-DQ
Super B8
DP genes are highly variable
IMGT/HLA Nomenclature Conversion Tool
Archived
Wayback Machine

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