Viral Vectors are a type of delivery system used in vaccine development to deliver genetic material from a pathogen into host cells, stimulating an immune response against the target pathogen. They are derived from viruses that have been genetically modified to carry and express antigens from the target pathogen without causing disease. Viral vectors work by infecting host cells and introducing the genetic material encoding specific antigens. Once inside the host cell, the viral vector hijacks the cell's machinery to produce the target antigens, which are then recognized by the immune system as foreign. This triggers an immune response, leading to the production of antibodies and memory cells that provide protection against future infections by the target pathogen.
There are several types of viral vectors commonly used in vaccine development, including adenoviruses, lentiviruses, retroviruses, and poxviruses. Each type of viral vector has its own advantages and limitations, depending on factors such as safety, immunogenicity, and scalability. Adenoviral vectors, for example, are efficient at delivering genetic material into host cells and inducing strong immune responses. They are particularly useful for generating rapid and robust immune responses against infectious diseases such as COVID-19, Ebola, and HIV. However, adenoviral vectors may be limited by pre-existing immunity in the population, which can reduce their effectiveness. Lentiviral vectors, derived from HIV, are another type of viral vector used in vaccine development. They have the advantage of being able to infect both dividing and non-dividing cells, making them suitable for targeting a wide range of cell types. Lentiviral vectors have been investigated for use in vaccines against HIV, cancer, and genetic disorders.
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 novel multi-component vaccine to address the burden of otitis media in high-risk populations
Ayesha Zahid, Griffith University, Australia
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 : 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 : New biomarkers in leishmania major vaccine development
Negar Seyed, Pasteur Institute of Iran, Iran (Islamic Republic of)
Title : Tubercular disease in children: Optimizing treatment strategies through disease insights
Elena Chiappini, University of Florence, Italy
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
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 : Capillary electrophoresis for adjuvanted multivalent recombinant vaccine purity determination
Ashley Prout, Merck, United States