Detection of heterozygous C8β deficiency by PCR in a healthy Italian population

D. Bellavia, P. M. Schneider, C. Rittner, G. Malfitano, T. J. Kaufmann, M. Brai

Research output: Contribution to journalArticle

Abstract

In Italy a rather high number of homozygotes with late complement component defects has been found among patients with meningococcal disease. It seems that clinical manifestations of meningococcal disease are less severe in patients with complement deficiency than in normal individuals. This situation could even be more evident in the heterozygous carriers for whom a selective advantage is discussed. In this study we have screened a cohort of 527 Italian blood donors from western Sicily for the presence of C8B mutated allele. Heterozygotes for C8β deficiency were identified using a specific PCR assay to detect a C → T transition in exon 9 of the C8B gene. This mutation represents the most frequent genetic mechanism for C8β deficiency in Caucasians. A rapid PCR screening test was performed on DNA extracted from pooled blood samples of up to 8 individuals. A single male individual with heterozygous C8β deficiency was detected. In the family studies it was shown that his two brothers and the mother were heterozygous carriers too. Functional activity of the classical and alternative complement pathways were normal. No neisserial infections or inflammatory diseases were found in the family history. It was shown that the allele-specific PCR is a sensitive and rapid method to examine large numbers of DNA samples. It permitted to assess the real prevalence of the C8B mutated null allele in the general population free of ascertainment bias.

Original languageEnglish
Pages (from-to)173-180
Number of pages8
JournalExperimental and Clinical Immunogenetics
Volume13
Issue number3-4
Publication statusPublished - Apr 1997

Fingerprint

Alleles
Polymerase Chain Reaction
Sicily
Classical Complement Pathway
Population
Alternative Complement Pathway
DNA
Homozygote
Heterozygote
Blood Donors
Italy
Siblings
Exons
Mothers
Mutation
Infection
Genes

Keywords

  • C8β deficiency
  • Complement
  • Heterozygous
  • PCR methods
  • Population frequency

ASJC Scopus subject areas

  • Immunology
  • Genetics(clinical)
  • Genetics

Cite this

Bellavia, D., Schneider, P. M., Rittner, C., Malfitano, G., Kaufmann, T. J., & Brai, M. (1997). Detection of heterozygous C8β deficiency by PCR in a healthy Italian population. Experimental and Clinical Immunogenetics, 13(3-4), 173-180.

Detection of heterozygous C8β deficiency by PCR in a healthy Italian population. / Bellavia, D.; Schneider, P. M.; Rittner, C.; Malfitano, G.; Kaufmann, T. J.; Brai, M.

In: Experimental and Clinical Immunogenetics, Vol. 13, No. 3-4, 04.1997, p. 173-180.

Research output: Contribution to journalArticle

Bellavia, D, Schneider, PM, Rittner, C, Malfitano, G, Kaufmann, TJ & Brai, M 1997, 'Detection of heterozygous C8β deficiency by PCR in a healthy Italian population', Experimental and Clinical Immunogenetics, vol. 13, no. 3-4, pp. 173-180.
Bellavia D, Schneider PM, Rittner C, Malfitano G, Kaufmann TJ, Brai M. Detection of heterozygous C8β deficiency by PCR in a healthy Italian population. Experimental and Clinical Immunogenetics. 1997 Apr;13(3-4):173-180.
Bellavia, D. ; Schneider, P. M. ; Rittner, C. ; Malfitano, G. ; Kaufmann, T. J. ; Brai, M. / Detection of heterozygous C8β deficiency by PCR in a healthy Italian population. In: Experimental and Clinical Immunogenetics. 1997 ; Vol. 13, No. 3-4. pp. 173-180.
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