Association of mutations in mannose binding protein gene with childhood infection in consecutive hospital series
JA Summerfield, M Sumiya, M Levin, MW Turner - Bmj, 1997 - bmj.com
JA Summerfield, M Sumiya, M Levin, MW Turner
Bmj, 1997•bmj.comObjective: To determine the extent to which mutations in the mannose binding protein gene
predispose to childhood infection. Design: Clinical details and genotype of mannose binding
protein determined in consecutive children attending a paediatric department. Setting: Inner
city hospital paediatric service in London. Subjects: 617 children attending hospital between
October 1993 and August 1995. Main outcome measure: Infection as the cause for
attendance or admission in relation to mutations in the mannose binding protein gene …
predispose to childhood infection. Design: Clinical details and genotype of mannose binding
protein determined in consecutive children attending a paediatric department. Setting: Inner
city hospital paediatric service in London. Subjects: 617 children attending hospital between
October 1993 and August 1995. Main outcome measure: Infection as the cause for
attendance or admission in relation to mutations in the mannose binding protein gene …
Abstract
Objective: To determine the extent to which mutations in the mannose binding protein gene predispose to childhood infection.
Design: Clinical details and genotype of mannose binding protein determined in consecutive children attending a paediatric department.
Setting: Inner city hospital paediatric service in London.
Subjects: 617 children attending hospital between October 1993 and August 1995.
Main outcome measure: Infection as the cause for attendance or admission in relation to mutations in the mannose binding protein gene.
Results: The prevalence of mutations in the mannose binding protein gene in children with infection (146/345) was about twice that in children without infection (64/272) (P<0.0001). Increased susceptibility to infection was found in both heterozygotic and homozygotic children. 13 out of 17 children homozygotic for variant alleles presented with strikingly severe infections, including 6 with septicaemia.
Conclusions: The findings suggest that mutations in the mannose binding protein gene are an important risk factor for infections in children. Screening for such mutations should be included in the investigation of severe or frequent infections.
Key messages
Mutations in the mannose binding protein gene, which cause a common opsonic defect, are strongly associated with children presenting to hospital with infection
The mutations increase susceptibility to infection in children who are heterozygotic or homozygotic for the mutations
Children homozygotic for mannose binding protein gene mutations usually present with severe infections
Investigation of severe or frequent infections should include screening for mannose binding protein gene mutations
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