Volume 35, Issue 1 pp. 54-57
Full Access

NA gene frequencies in the German population, determined by polymerase chain reaction with sequence-specific primers

Jiirgen Bux MD

Corresponding Author

Jiirgen Bux MD

Research Assistant

Institut für Klinische Immunologie und Transfusionsmedizin, Justus-Liebig-University, Langhanstrasse 7, D-35385 Giessen, Germany.Search for more papers by this author
Ernst-Ludwig Stein

Ernst-Ludwig Stein

Ernst-Ludwig Stein, PhD candidate, Research Assistant, Institut für Klinische Immunologie und Transfusionsmedizin.

Search for more papers by this author
Sentot Santoso

Sentot Santoso

Sentot Santoso, PhD, Research Assistant, Institut für Klinische Immunologie und Transfusionsmedizin.

Search for more papers by this author
Christian Mueller-Eckhardt

Christian Mueller-Eckhardt

Christian Mueller-Eckhardt, MD, Professor and Director, Institut für Klinische Immunologie und Transfusionsmedizin.

Search for more papers by this author
First published: January 1995
Citations: 113

Abstract

BACKGROUND: The granulocyte antigens NA1 and NA2 are often targets of granulocyte antibodies causing immune neutropenia. Currently, NA typing relies on the properties of the typing sera or antibodies and the techniques used. Therefore, the technique of polymerase chain reaction with sequence-specific primers (PCR-SSP) was adapted for DNA-based NA typing and was used for determining the NA gene frequencies in the German population. STUDY DESIGN AND METHODS: The genomic DNA of 160 unrelated healthy individuals was typed for NA1 and NA2 by PCR-SSP. In 60 granulocyte samples, the NA phenotype was additionally determined by the antigen capture assay and the granulocyte immunofluorescence test (GIFT) and correlated with the genotyping results. RESULTS: Results of the antigen capture assay and PCR-SSP correlated precisely, whereas nine individuals were typed heterozygous only by GIFT. The gene frequencies were 0.35 for NA1 and 0.65 for NA2. CONCLUSION: The NA2 gene is more frequent in the German population than the NA1 gene, as determined by genotyping using PCR-SSP. In contrast to GIFT, which showed an error rate for NA typing of 15 percent, PCR-SSP and the antigen-capture assay are more reliable methods of NA typing of granulocytes.

Abbreviations:

  • bp =
  • base pairs;
  • FcRIII =
  • Fc-γ-receptor III;
  • GIFT =
  • granulocyte Immunofluorescence test;
  • HGH =
  • human growth hormone;
  • MAIGA =
  • monoclonal antibody-specific Immobilization of granulocyte antigens (assay);
  • PCR-SSP =
  • polymerase chain reaction with sequence-specific primers.
    • The full text of this article hosted at iucr.org is unavailable due to technical difficulties.