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Updated: Jun 8, 2026

Generation, Amplification, and Titration of Recombinant Respiratory Syncytial Viruses
Published on: April 4, 2019
Therapeutic targeting of respiratory syncytial virus G-protein
Lawrence M Kauvar1, Jennifer L Harcourt, Lia M Haynes
1Trellis Bioscience, 2-B Corporate Drive, South San Francisco, CA 94080, USA. lkauvar@trellisbio.com
Insights
New treatments targeting the Respiratory Syncytial Virus (RSV) G-protein show promise. Monoclonal antibodies offer a dual mechanism for therapeutic intervention against RSV infections in vulnerable populations.
Area of Science:
- Virology
- Immunology
- Infectious Diseases
Background:
- Respiratory Syncytial Virus (RSV) is a major cause of severe respiratory illness in infants, the elderly, and immunocompromised individuals.
- Current interventions, like fusion protein monoclonal antibodies, are mainly prophylactic and lack post-infection therapeutic efficacy.
- There is a significant unmet need for effective treatments against RSV in susceptible populations.
Purpose of the Study:
- To evaluate the therapeutic potential of targeting the RSV G-protein using monoclonal antibodies.
- To investigate the dual mechanism of action: modulating host innate immune response and direct antiviral activity.
Main Methods:
- Investigated monoclonal antibody targeting of the RSV G-protein.
- Assessed the antibody's ability to reduce G-protein-mediated distortion of the innate immune response.
- Evaluated direct complement-mediated antiviral activity.
Main Results:
- Recent findings support the use of monoclonal antibodies against the RSV G-protein for therapeutic purposes.
- The proposed dual mechanism offers a novel therapeutic strategy against RSV.
Conclusions:
- Monoclonal antibody targeting of the RSV G-protein presents a promising therapeutic approach.
- This strategy addresses the limitations of current RSV interventions by offering post-infection efficacy.
- The dual mechanism provides a robust framework for developing new RSV treatments.
Abstract:
Respiratory syncytial virus (RSV) is a leading cause of pneumonia and bronchiolitis in infants and young children and an important pathogen of the elderly and immune suppressed. The only intervention currently available is a monoclonal antibody against the RSV fusion protein, which has shown utility as a prophylactic for high-risk premature infants, but which has not shown postinfection therapeutic efficacy in the specific RSV-infected populations studied. Thus, for the major susceptible populations, there remains a great need for effective treatment. Recent results support monoclonal antibody targeting of the RSV G-protein for therapeutic use. This objective encompasses a dual mechanism: reduction in the ability of RSV G-protein to distort the host innate immune response, and direct complement-mediated antiviral activity.
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