Biosynthetic pathways for vaccine production involve using biological systems, such as bacteria, yeast, or mammalian cells, to synthesize components required for vaccine formulations. These pathways allow for the mass production of antigens, proteins, or other biologically active substances that are key ingredients in vaccines. Advances in biotechnology have made it possible to engineer microorganisms or cells to produce large quantities of vaccine components quickly and efficiently. For instance, recombinant DNA technology can be used to introduce genes that code for antigens from a pathogen into a host cell, prompting it to produce the antigen for vaccine use. This method is not only cost-effective but also reduces the need for traditional methods like growing pathogens in culture, ensuring both safety and scalability. Biosynthetic pathways continue to evolve, providing more sustainable, rapid, and flexible options for vaccine production, particularly in response to emerging infectious diseases.
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 : 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 : A promising novel approach to DNA vaccines
Khursheed Anwer, IMUNON, United States
Title : The role of immunity in the pathogenesis of SARS-COV-2 and in the protection generated by COVID-19 in different age groups
Ahmed Abdulazeez, BHRUT Trust, United Kingdom
Title : Development of a novel multi-component vaccine to address the burden of otitis media in high-risk populations
Ayesha Zahid, Griffith University, Australia
Title : Tubercular disease in children: Optimizing treatment strategies through disease insights
Elena Chiappini, University of Florence, Italy
Title : New biomarkers in leishmania major vaccine development
Negar Seyed, Pasteur Institute of Iran, Iran (Islamic Republic of)
Title : Racial disparities in pediatric pneumonia in Brazil: The role of structural racism forging inequalities in acess to vaccines
Livia Daflon Silva, Federal University of State of Rio de Janeiro, Brazil
Title : Approaches towards developing and establishing a biomanufacturing research & development, and manufacturing industry in Zimbabwe: A review of the need, potential funding sources, policy development and implementation
Elliot Nyagumbo, Midlands State University, Zimbabwe