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Bacterial Respiratory Pathogens in Children With Inherited Immune and Airway Disorders: Nasopharyngeal Carriage and Disease Risk

Verhagen, Lilly M. MD; Luesink, Maaike MD; Warris, Adilia MD, PhD; de Groot, Ronald MD, PhD; Hermans, Peter W. M. PhD

Pediatric Infectious Disease Journal: April 2013 - Volume 32 - Issue 4 - p 399–404
doi: 10.1097/INF.0b013e31827db77a
Review Articles

Children with primary immunodeficiencies, sickle cell disease and cystic fibrosis are at risk to develop invasive bacterial infections caused by respiratory tract pathogens, in particular Streptococcus pneumoniae, Haemophilus influenzae and Staphylococcus aureus. This review article evaluates the role of nasopharyngeal colonization by these pathogens in the high prevalence of respiratory and invasive infections in children with inherited disorders affecting the immune system or the respiratory tract. We conclude that respiratory and invasive diseases that occur in children with primary immunodeficiencies or sickle cell disease are probably a result of increased nasopharyngeal colonization rates compared with healthy children. However, when the inherited disorder is characterized by local airway abnormalities such as in cystic fibrosis, enhanced nasopharyngeal colonization does not seem to play a major role in invasive disease risk. As the evidence for the role of nasopharyngeal colonization in disease risk in these specific patient groups partly comes from experimental studies and animal models, longitudinal studies in children are needed. Detailed understanding of the effect of colonization on the development of respiratory and invasive infections in children with primary immunodeficiencies, sickle cell disease or cystic fibrosis provides a justification for the selective introduction of vaccination and prophylactic antibiotic treatment. Recommendations for the use of (preventive) therapeutic strategies in these patient groups taking into account disease-specific immunologic mechanisms underlying colonization and disease are described.

From the Department of Pediatrics, Laboratory of Pediatric Infectious Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands.

Accepted for publication November 12, 2012.

L.M.V. and M.L. contributed equally.

The authors have no funding or conflicts of interest to disclose.

Address for correspondence: Peter W. M. Hermans, PhD, Laboratory of Pediatric Infectious Diseases, Radboud University Medical Centre, PO Box 9101 (internal post 224), 6500 HB Nijmegen, The Netherlands. E-mail: P.Hermans@cukz.umcn.nl.

© 2013 Lippincott Williams & Wilkins, Inc.