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Archives of Disease in Childhood 2002;86:426; doi:10.1136/adc.86.6.426
Copyright © 2002 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Archives of Disease in Childhood 2002;86:426
© 2002 Archives of Disease in Childhood

ORIGINAL ARTICLE

No association between asthma or allergy and the CCR5{Delta} 32 mutation

A Nagy1, G T Kozma2, Á Bojszkó3, D Krikovszky2, A Falus4, C Szalai4

1 Budai Children's Hospital, Hungary
2 Semmelweis University Budapest, Hungary
3 Heim Pál Pediatric Hospital, Hungary
4 Section of Molecular Immunology, Hungarian Academy of Sciences

Correspondence to:
Correspondence to:
Dr C Szalai, Heim Pál Pediatric Hospital Budapest, Hungary, PO Box 66, H-1958;
szalai{at}heim.sote.hu

Aims: To investigate whether the presence of the CCR5{Delta}32 allele was associated with atopy or asthma.

Methods: A total of 118 children with asthma, 145 children with non-asthmatic, but allergic phenotype, and 303 children without allergic or asthmatic disorders were studied.

Results: There were no significant differences in the frequency of CCR5{Delta}32, or in the distributions of genotypes between the groups. The relative eosinophil blood count was slightly lower in patients with heterozygous genotype, than in patients with wild type genotype.

Conclusion: No association was found between the susceptibility of allergy or asthma and the functional deficient CCR5{Delta}32 allele.

Keywords: asthma; allergy; chemokine


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This article has been cited by other articles:

  • Batra, J, Sharma, M, Chatterjee, R, Sharma, S, Mabalirajan, U, Ghosh, B (2005). CCR5 {Delta}32 deletion and atopic asthma in India. Thorax 60: 85-85 [Full Text]  

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