Viral drug resistance refers to the ability of viruses to adapt and develop resistance to antiviral medications, diminishing the effectiveness of treatment. This phenomenon is a significant challenge in the management of viral infections, including HIV, hepatitis, influenza, and herpes viruses. The primary mechanism of viral drug resistance involves mutations in the viral genome, particularly in regions targeted by antiviral drugs. These mutations may confer a selective advantage to the virus, allowing it to evade the inhibitory effects of the medication. Continuous exposure to antiviral drugs, suboptimal treatment adherence, and inadequate drug concentrations in the body contribute to the development of resistance. Resistance can occur in individual patients, leading to treatment failure, and may also be transmitted to others. Monitoring viral drug resistance is critical in guiding treatment decisions, as it allows healthcare providers to choose effective antiviral regimens. Combination therapies, which target multiple steps in the viral life cycle, are employed to reduce the likelihood of resistance development. Ongoing research focuses on developing new antiviral drugs with higher barriers to resistance, improving treatment adherence strategies, and understanding the genetic factors influencing viral susceptibility to drugs. Addressing viral drug resistance is essential for ensuring the long-term efficacy of antiviral therapies and controlling the spread of resistant viral strains.
Title : The importance of post-marketing surveillance and real-world data: For a product to be successful
Regina Au, BioMarketing Insight, United States
Title : A promising novel approach to DNA vaccines
Khursheed Anwer, IMUNON, United States
Title : Prophylactic and molecular approaches for mitigating human influenza A viruses: i. Evaluating influenza vaccine effectiveness in the older population ii. Down-regulation of influenza virus genes with novel sirna-chimeric-ribozyme constructs
Madhu Khanna, University of Delhi, India
Title : Homology analysis of MPXV and VACV peptides underscores the need to consider both MPXV clades for vaccine development
Lara Isis Teodoro, Mayo Clinic, United States
Title : Development of a platform UPLC-CAD method for high-throughput lipid quantitation and characterization in novel mRNA LNPs
Janet Muzulu, Sanofi, United States
Title : Commensal bacteria drive B-cell lymphomagenesis in the setting of innate immunodeficiency
Ping Xie, Rutgers University, United States
Title : High seroprevalence of RSV antibodies in adults indicates potential undetected transmission and requires further public health assessment
Lara Isis Teodoro, Mayo Clinic, United States
Title : Establishing a platform method for physical appearance assessment of new parenteral pharmaceuticals
Ying Wan, Merck & Co., United States
Title : Post COVID-19 syndrome is associated with sex and severity of first COVID-19 episode in Honduras
Manuel Antonio Sierra Santos, Central American Technological University, Honduras
Title : Evaluating the immunogenic impact of process impurities in mRNA vaccine production: Establishing integrated control strategies and specifications
Jesse Kuiper, Merck Research Laboratories, United States