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Clinical Microbiology Reviews, April 2009, p. 274-290, Vol. 22, No. 2
0893-8512/09/$08.00+0 doi:10.1128/CMR.00040-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.
Division of Infectious Diseases and HIV Medicine, Department of Medicine, University Hospitals Case Medical Center and Case Western Reserve University, Cleveland, Ohio,1 Institute of Molecular Biology and Biotechnology, National Institutes of Health, University of the Philippines, Manila, Philippines,2 Section of Infectious Diseases, Department of Medicine, University of the Philippines College of Medicine and the Philippine General Hospital, Manila, Philippines3
Summary: Biologics are increasingly becoming part of routine disease management. As more agents are developed, the challenge of keeping track of indications and side effects is growing. While biologics represent a milestone in targeted and specific therapy, they are not without drawbacks, and the judicious use of these "magic bullets" is essential if their full potential is to be realized. Infectious complications in particular are not an uncommon side effect of therapy, whether as a direct consequence of the agent or because of the underlying disease process. With this in mind, we have reviewed and summarized the risks of infection and the infectious disease-related complications for all FDA-approved monoclonal antibodies and some related small molecules, and we discuss the probable mechanisms involved in immunosuppression as well as recommendations for prophylaxis and treatment of specific disease entities.
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