A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Total C4B deficiency due to gene deletion and gene conversion in a patient with severe infections
Tekijät: Jaatinen T, Lahti M, Ruuskanen O, Kinos R, Truedsson L, Lahesmaa R, Lokki ML
Kustantaja: AMER SOC MICROBIOLOGY
Julkaisuvuosi: 2003
Journal: Clinical and Diagnostic Laboratory Immunology
Tietokannassa oleva lehden nimi: CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
Lehden akronyymi: CLIN DIAGN LAB IMMUN
Vuosikerta: 10
Numero: 2
Aloitussivu: 195
Lopetussivu: 201
Sivujen määrä: 7
ISSN: 1071-412X
DOI: https://doi.org/10.1128/CDLI.10.2.195-201.2003
Tiivistelmä
Deficiencies of the early components of the classical complement pathway impair the actions of innate and humoral immunity and may lead to increased susceptibility to infections. We have studied the genetic basis of total C4B deficiency in a Finnish patient with recurrent meningitis, chronic fistulas and abscesses. The maternal chromosome carried a four-gene deletion including the C4B gene, and a conversion from C4B to C4A gene was found on the paternal chromosome resulting in complete deficiency of C4B. In the converted C4A gene, mutation screening did not reveal any amino acid changes or prominent mutations, yet a large number of nucleotide variations were found. Further, the patient was heterozygous for structural deficiency of mannan binding lectin (MBL) associating with medium levels of serum MBL. Our data provides new information on the genetic instability of the C4 gene region, and on the association of homozygous C4B deficiency and variant MBL genotype with increased susceptibility to recurrent and chronic infections. Importantly, plasma therapy induced a prompt clinical cure with long-term effects.
Deficiencies of the early components of the classical complement pathway impair the actions of innate and humoral immunity and may lead to increased susceptibility to infections. We have studied the genetic basis of total C4B deficiency in a Finnish patient with recurrent meningitis, chronic fistulas and abscesses. The maternal chromosome carried a four-gene deletion including the C4B gene, and a conversion from C4B to C4A gene was found on the paternal chromosome resulting in complete deficiency of C4B. In the converted C4A gene, mutation screening did not reveal any amino acid changes or prominent mutations, yet a large number of nucleotide variations were found. Further, the patient was heterozygous for structural deficiency of mannan binding lectin (MBL) associating with medium levels of serum MBL. Our data provides new information on the genetic instability of the C4 gene region, and on the association of homozygous C4B deficiency and variant MBL genotype with increased susceptibility to recurrent and chronic infections. Importantly, plasma therapy induced a prompt clinical cure with long-term effects.
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