A Role for Immune Complexes in Enhanced Respiratory Syncytial Virus Disease

Author:

Polack Fernando P.123,Teng Michael N.4,L.Collins Peter4,Prince Gregory A.5,Exner Marcus6,Regele Heinz7,Lirman Dario D.13,Rabold Richard8,Hoffman Scott J.13,Karp Christopher L.9,Kleeberger Steven R.10,Wills-Karp Marsha11,Karron Ruth A.12

Affiliation:

1. Department of Pediatrics, School of Medicine

2. Department of International Health, Bloomberg School of Public Health at Johns Hopkins University, Baltimore, MD 21205

3. Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health at Johns Hopkins University, Baltimore, MD 21205

4. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892

5. Virion Systems Inc., Rockville, MD 20850

6. Department of Laboratory Medicine, University of Vienna, Vienna A-1090, Austria

7. Department of Clinical Pathology, University of Vienna, Vienna A-1090, Austria

8. Department of Environmental Health, Bloomberg School of Public Health at Johns Hopkins University, Baltimore, MD 21205

9. Division of Molecular Immunology, Children's Hospital Research Foundation, Cincinnati, OH 45229

10. National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle, NC 27709

11. Division of Immunobiology, Children's Hospital Research Foundation, Cincinnati, OH 45229

Abstract

Respiratory syncytial virus (RSV) is the leading cause of bronchiolitis and viral pneumonia in infants and young children. Administration of a formalin inactivated vaccine against RSV to children in the 1960s resulted in increased morbidity and mortality in vaccine recipients who subsequently contracted RSV. This incident precluded development of subunit RSV vaccines for infants for over 30 years, because the mechanism of illness was never clarified. An RSV vaccine for infants is still not available. Here, we demonstrate that enhanced RSV disease is mediated by immune complexes and abrogated in complement component C3 and B cell–deficient mice but not in controls. Further, we show correlation with the enhanced disease observed in children by providing evidence of complement activation in postmortem lung sections from children with enhanced RSV disease.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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