TY - JOUR
T1 - Determination of granulocyte-specific antigens on neutrophil Fcγ receptor IIIb by PCR-preferential homoduplex formation assay, and gene frequencies in the Japanese population
AU - Fujiwara, Koki
AU - Watanabe, Yoshihisa
AU - Mitsunaga, Shigeki
AU - Oka, Takanori
AU - Yamane, Akio
AU - Akaza, Tatsuya
AU - Tadokoro, Kenji
AU - Tokunaga, Katsushi
AU - Shibata, Yoichi
AU - Juji, Takeo
PY - 1999/12
Y1 - 1999/12
N2 - Background and 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 Fcγ receptor IIIb (FcγRIIIb, 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 FcγRIIIB 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 FcγRIIIB 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.
AB - Background and 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 Fcγ receptor IIIb (FcγRIIIb, 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 FcγRIIIB 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 FcγRIIIB 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.
UR - http://www.scopus.com/inward/record.url?scp=0033369216&partnerID=8YFLogxK
U2 - 10.1046/j.1423-0410.1999.7740218.x
DO - 10.1046/j.1423-0410.1999.7740218.x
M3 - 記事
C2 - 10717601
AN - SCOPUS:0033369216
SN - 0042-9007
VL - 77
SP - 218
EP - 222
JO - Vox Sanguinis
JF - Vox Sanguinis
IS - 4
ER -