Antibody Biology and Engineering play crucial roles in vaccine development, offering insights into how the immune system responds to pathogens and how antibodies can be harnessed to confer protection against infectious diseases. Antibodies, also known as immunoglobulins, are specialized proteins produced by the immune system in response to foreign substances, such as bacteria, viruses, and toxins. These proteins bind to specific antigens on the surface of pathogens, marking them for destruction by other immune cells or neutralizing their harmful effects.
In vaccine development, understanding the biology of antibodies is essential for identifying antigens that can elicit a robust immune response. Scientists study the structure and function of antibodies to design vaccines that mimic natural infection without causing illness. By targeting key antigens, vaccines can stimulate the production of protective antibodies, priming the immune system to recognize and combat future encounters with the pathogen. Recent advances in antibody engineering have revolutionized vaccine design and development. Techniques such as monoclonal antibody production, phage display, and recombinant DNA technology enable scientists to produce antibodies with specific properties tailored for therapeutic or prophylactic purposes.
Monoclonal antibodies, for example, are laboratory-made molecules that mimic the immune system's ability to fight off pathogens. These antibodies can be engineered to target specific antigens with high precision, making them valuable tools for treating infectious diseases and other medical conditions. Phage display is another powerful technique used in antibody engineering, allowing researchers to screen libraries of antibody fragments displayed on the surface of bacteriophages. This approach facilitates the identification of antibodies that bind to desired targets, paving the way for the development of novel vaccines and therapeutic agents.
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