HLA-DPB1 ALLELE MISMATCHES BETWEEN UNRELATED HLA-A,B,C,DR (GENERIC) DQA1-IDENTICAL UNRELATED INDIVIDUALS WITH UNREACTIVE MLC

被引:13
作者
SALAZAR, M [1 ]
YUNIS, I [1 ]
ALOSCO, SM [1 ]
CHOPEK, M [1 ]
YUNIS, EJ [1 ]
机构
[1] AMER RED CROSS,DEDHAM,MA
来源
TISSUE ANTIGENS | 1992年 / 39卷 / 04期
关键词
HLA-DPB1; MHC; MLC; PCR-RFLP;
D O I
10.1111/j.1399-0039.1992.tb01936.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have used a PCR-RFLP method with one generic amplification of HLA-DPB1 second exon and 6 endonucleases to differentiate the 19 HLA-DPB1 alleles and 171 heterozygous combinations. The set of primers used in our studies produced fragment sizes different from those published before (1). The HLA-DPB1 alleles in Caucasians showed a higher frequency of DPB1*0401 and DPB1*0402, when compared to a small group of Colombians who showed a higher frequency of DPB1*0402 and DPB1*0201. We found three HLA-DPB1 alleles associated with two HLA haplotypes that result from non-random association of alleles: DPB1*0401 with HLA-A26. B38, DR4, DQA1*0301 and DPB1*0101 and DPB1*0401 with HLA-A1. B8, DR3, DQA1*0501. We also report that 70% of combinations between HLA (generic A,B,C,DR) and DQA1-identical MLC-unreactive cell mixtures showed HLA-DPB1 mismatches. suggesting that HLA-DPB1 differences are not important in MLC reactivity.
引用
收藏
页码:203 / 208
页数:6
相关论文
共 18 条
[1]   GENE POLYMORPHISM OF HLA-DPB1 AND DPA1 LOCI IN CAUCASOID POPULATION - FREQUENCIES AND DPB1-DPA1 ASSOCIATIONS [J].
ALDACCAK, R ;
FU, QW ;
THEOPHILLE, D ;
LETHIELLEUX, P ;
COLOMBANI, J ;
LOISEAU, P .
HUMAN IMMUNOLOGY, 1991, 31 (04) :277-285
[2]   EVALUATION OF HLA-CLASS-II IDENTITY BETWEEN UNRELATED INDIVIDUALS BY SEROLOGICAL TYPING, DNA-RFLP METHOD, AND MIXED LYMPHOCYTE-REACTION [J].
ALDACCAK, R ;
LOISEAU, P ;
MIRAMONT, P ;
RABIAN, C ;
RAFFOUX, C ;
COLOMBANI, J .
HUMAN IMMUNOLOGY, 1990, 29 (03) :189-201
[3]   A SPECIFIC HLA-DP-BETA ALLELE IS ASSOCIATED WITH PAUCIARTICULAR JUVENILE RHEUMATOID-ARTHRITIS BUT NOT ADULT RHEUMATOID-ARTHRITIS [J].
BEGOVICH, AB ;
BUGAWAN, TL ;
NEPOM, BS ;
KLITZ, W ;
NEPOM, GT ;
ERLICH, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (23) :9489-9493
[4]   A COMBINATION OF A PARTICULAR HLA-DP-BETA ALLELE AND AN HLA-DQ HETERODIMER CONFERS SUSCEPTIBILITY TO CELIAC-DISEASE [J].
BUGAWAN, TL ;
ANGELINI, G ;
LARRICK, J ;
AURICCHIO, S ;
FERRARA, GB ;
ERLICH, HA .
NATURE, 1989, 339 (6224) :470-473
[5]   HLA-DP TYPING BY AMPLIFIED FRAGMENT LENGTH POLYMORPHISMS (AFLPS) [J].
DEKKER, JW ;
EASTEAL, S .
IMMUNOGENETICS, 1990, 32 (01) :56-59
[6]   HUMAN MIXED-LYMPHOCYTE CULTURE REACTION - GENETICS, SPECIFICITY, AND BIOLOGICAL IMPLICATIONS [J].
DUPONT, B ;
HANSEN, JA ;
YUNIS, EJ .
ADVANCES IN IMMUNOLOGY, 1976, 23 :107-202
[7]   DNA TYPING FOR CLASS-II HLA ANTIGENS WITH ALLELE-SPECIFIC OR GROUP-SPECIFIC AMPLIFICATION .3. TYPING FOR 24 ALLELES OF HLA-DP [J].
FERNANDEZVINA, M ;
MORAES, ME ;
STASTNY, P .
HUMAN IMMUNOLOGY, 1991, 30 (01) :60-68
[8]   CELIAC-DISEASE IS ASSOCIATED WITH AN EXTENDED HLA-DR3 HAPLOTYPE WHICH INCLUDES HLA-DPW1 [J].
HALL, MA ;
LANCHBURY, JSS ;
BOLSOVER, WJ ;
WELSH, KI ;
CICLITIRA, PJ .
HUMAN IMMUNOLOGY, 1990, 27 (03) :220-228
[9]   A SIMPLE AND RAPID METHOD FOR HLA-DP GENOTYPING BY DIGESTION OF PCR-AMPLIFIED DNA WITH ALLELE-SPECIFIC RESTRICTION ENDONUCLEASES [J].
MAEDA, M ;
URYU, N ;
MURAYAMA, N ;
ISHII, H ;
OTA, M ;
TSUJI, K ;
INOKO, H .
HUMAN IMMUNOLOGY, 1990, 27 (02) :111-121
[10]   LINKAGE DISEQUILIBRIUM OF HLA-SB1 WITH THE HLA-A1, HLA-B8, HLA-DR3, HLA-SCO1 AND OF HLA-SB4 WITH THE HLA-A26, HLA-BW38, HLA-DW10, HLA-DR4, HLA-SC21 EXTENDED HAPLOTYPES [J].
MATSUI, Y ;
ALOSCO, SM ;
AWDEH, Z ;
DUQUESNOY, RJ ;
PAGE, PL ;
HARTZMAN, RJ ;
ALPER, CA ;
YUNIS, EJ .
IMMUNOGENETICS, 1984, 20 (06) :623-631