The Future of Respiratory Syncytial Virus Disease Prevention and Treatment

Joseph B Domachowske, Evan J Anderson, Mitchell Goldstein, Joseph B Domachowske, Evan J Anderson, Mitchell Goldstein

Abstract

Respiratory syncytial virus (RSV) is a major cause of respiratory tract infections in infants, young children, and older or immunocompromised adults. Although aerosolized ribavirin was licensed for RSV treatment on the basis of data demonstrating a reduced need for supplemental oxygen, ribavirin use is limited because of issues with efficacy, safety, and cost. Currently, the treatment of RSV is primarily supportive. New antiviral treatments for RSV are in the early stages of development, but it will be years until any of these may be licensed by the US Food and Drug Administration (FDA). Palivizumab, an RSV monoclonal antibody [immunoprophylaxis (IP)], has demonstrated effectiveness in disease prevention and is the only licensed IP for RSV disease in specific high-risk pediatric populations. Although its efficacy is well established, some challenges that may interfere with its clinical use include cost, need for monthly injections, and changing policy for use by the American Academy of Pediatrics (AAP). Preventing RSV disease would be possible through RSV vaccine development (e.g., live-attenuated, vector-based subunit, or particle-based). Alternatively, new long-acting monoclonal antibodies have demonstrated promising results in early clinical trials. Despite scientific advances, until new agents become available, palivizumab should continue to be used to reduce RSV disease burden in high-risk patients for whom it is indicated.

Keywords: American Academy of Pediatrics; High-risk preterm infants; Immunoprophylaxis; Monoclonal antibody; National Perinatal Association; Palivizumab; Respiratory syncytial virus; Treatment; Vaccine.

Figures

Fig. 1
Fig. 1
Targets of antiviral agents in phase 2/3 clinical development [, –29]. F fusion protein; G attachment glycoprotein; L large viral polymerase; M matrix protein; M2-1 protein, transcription factor; N nucleoprotein; P phosphoprotein
Fig. 2
Fig. 2
RSV antivirals, vaccines, and mAbs under phase 2/3 clinical development [37, 41]. E elderly; IP immunoprophylaxis; M maternal; mAb monoclonal antibody; P pediatric; RSV respiratory syncytial virus

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Source: PubMed

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