Respiratory syncytial virus (RSV) is a common cause of
respiratory tract infections. In severely immunosuppressed patients RSV can cause significant morbidity and mortality. The only FDA-approved
drug for RSV is aerosolized
ribavirin. Given the high morbidity and mortality in high-risk populations and inconsistent results with aerosolized
ribavirin, new strategies for prevention and treatment of RSV are being sought.
Palivizumab is an RSV-specific
monoclonal antibody. A randomized, double-blind, placebo-controlled multicenter study showed significant reduction in hospitalization rates among children at high risk of
RSV infection who had been given prophylactic
palivizumab; these findings led to
palivizumab's approval by the FDA in June 1998.
Palivizumab also has a role in prevention of severe
respiratory tract infections in high-risk infants. In immunocompromised patients,
palivizumab has an excellent safety profile and may be beneficial in the prevention and treatment of
RSV infections; however, clinical trials are needed to determine its effectiveness. In this article, we review the role of
palivizumab in prevention and treatment of
RSV infections in immunocompetent and immunocompromised patients.