Determination of granulocyte-specific antigens on neutrophil Fcγ receptor IIIb by PCR-preferential homoduplex formation assay, and gene frequencies in the Japanese population

被引:22
作者
Fujiwara, K
Watanabe, Y
Mitsunaga, S
Oka, T
Yamana, A
Akaza, T
Tadokoro, K
Tokunaga, K
Shibata, Y
Juji, T
机构
[1] Japanese Red Cross, Cent Blood Ctr, Shibuya Ku, Tokyo 150, Japan
[2] Wakunaga Pharmaceut Co Ltd, Inst Biotechnol Res, Hiroshima, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Human Genet, Tokyo, Japan
[4] Univ Tokyo, Fac Med, Dept Transfus Med & Immunohematol, Tokyo 113, Japan
关键词
D O I
10.1046/j.1423-0410.1999.7740218.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Granulocyte-specific antigens play an important role in provoking immune neutropenia and transfusion reactions. We developed a new DNA-typing method, PCR-preferential homoduplex formation assay (PHFA), to determine granulocyte-specific antigens on the neutrophil Fc gamma receptor lllb (FcyRlllb, CD16b), namely the NA1, NA2, and SH antigens and their gene frequencies in the Japanese population. materials and Methods: Four hundred unrelated healthy Japanese blood donors were typed using PCR-PHFA. To confirm the accuracy of the results of Fc gamma RlllB genotyping using PCR-PHFA, PCR-sequence-specific primer(SSP) typing and PCR-restriction fragment length polymorphism (RFLP) typing were carried out in another 20 samples for comparison. Results: The results of PCR-PHFA typing agreed well with other methods. The frequencies of the Fc gamma RlllB alleles were 62.2, 37.8, 0 and 0% for NA1, NA2, SH, and 'NA-null', respectively. Conclusion: The PCR-PHFA method can be semi-automated easily with computer-based assignment and is suitable for typing both small and large numbers of samples. In the Japanese population, the frequency of NA1 is about double that in Caucasians (32.5%), and the SH allele is rare. Copyright (C) 1999 S. Karger AG. Basel.
引用
收藏
页码:218 / 222
页数:5
相关论文
共 24 条
[1]   NA GENE-FREQUENCIES IN THE GERMAN POPULATION, DETERMINED BY POLYMERASE CHAIN-REACTION WITH SEQUENCE-SPECIFIC PRIMERS [J].
BUX, J ;
STEIN, EL ;
SANTOSO, S ;
MUELLERECKHARDT, C .
TRANSFUSION, 1995, 35 (01) :54-57
[2]   Characterization of a new alloantigen (SH) on the human neutrophil Fc gamma receptor IIIb [J].
Bux, J ;
Stein, EL ;
Bierling, P ;
Fromont, P ;
Clay, M ;
Stroncek, D ;
Santoso, S .
BLOOD, 1997, 89 (03) :1027-1034
[3]   AN ABNORMALITY OF THE GENE THAT ENCODES NEUTROPHIL FC-RECEPTOR-III IN A PATIENT WITH SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
CLARK, MR ;
LIU, L ;
CLARKSON, SB ;
ORY, PA ;
GOLDSTEIN, IM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :341-346
[4]   NEUTROPHIL FC-GAMMA-RIIIB DEFICIENCY, NATURE, AND CLINICAL CONSEQUENCES - A STUDY OF 21 INDIVIDUALS FROM 14 FAMILIES [J].
DEHAAS, M ;
KLEIJER, M ;
VANZWIETEN, R ;
ROOS, D ;
VONDEMBORNE, AEGK .
BLOOD, 1995, 86 (06) :2403-2413
[5]   The NA "null" phenotype of a young man is caused by an FcγRIIIB gene deficiency while the products of the neighboring FcγRIIA and FcγRIIIA genes are present [J].
Flesch, BK ;
Achtert, G ;
Bauer, F ;
Neppert, J .
ANNALS OF HEMATOLOGY, 1998, 76 (05) :215-220
[6]   FREQUENCY OF THE POLYMORPHONUCLEAR NEUTROPHIL FC-GAMMA RECEPTOR-III DEFICIENCY IN THE FRENCH POPULATION AND ITS INVOLVEMENT IN THE DEVELOPMENT OF NEONATAL ALLOIMMUNE NEUTROPENIA [J].
FROMONT, P ;
BETTAIEB, A ;
SKOURI, H ;
FLOCH, C ;
POULET, E ;
DUEDARI, N ;
BIERLING, P .
BLOOD, 1992, 79 (08) :2131-2134
[7]   DNA-BASED TYPING OF HUMAN PLATELET ANTIGEN SYSTEMS BY POLYMERASE CHAIN REACTION-SINGLE-STRAND CONFORMATION POLYMORPHISM METHOD [J].
FUJIWARA, K ;
TOKUNAGA, K ;
ISA, K ;
MIYAMOTO, M ;
WANG, L ;
AKAZA, T ;
TADOKORO, K ;
SHIBATA, Y ;
JUJI, T .
VOX SANGUINIS, 1995, 69 (04) :347-351
[8]   Large-scale DNA typing for human platelet alloantigens by PCR-PHFA (preferential homoduplex formation assay) [J].
Fujiwara, K ;
Isa, K ;
Oka, T ;
Maekawajiri, S ;
Yamane, A ;
Akaza, T ;
Tadokoro, K ;
Juji, T ;
Shibata, Y ;
Tokunaga, K .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 95 (01) :198-203
[9]   Determination of neutrophil antigen gene frequencies in five ethnic groups by polymerase chain reaction with sequence-specific primers [J].
Hessner, MJ ;
Curtis, BR ;
Endean, DJ ;
Aster, RH .
TRANSFUSION, 1996, 36 (10) :895-899
[10]  
HUIZINGA TWJ, 1990, BLOOD, V76, P1927