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 : A promising novel approach to DNA vaccines
Khursheed Anwer, IMUNON, United States
Title : Nanoscopic SubATVax™ adjuvanted vaccines against influenza A types H3N2, H1N1 and influenza type B for subcutaneous administration
David Craig Wright, D4 Labs, LLC, United States
Title : The importance of post-marketing surveillance and real-world data: For a product to be successful
Regina Au, BioMarketing Insight, 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 : 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 : Commensal bacteria drive B-cell lymphomagenesis in the setting of innate immunodeficiency
Ping Xie, Rutgers University, 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 : Establishing a platform method for physical appearance assessment of new parenteral pharmaceuticals
Ying Wan, Merck & Co., United States
Title : Tubercular disease in children: Optimizing treatment strategies through disease insights
Elena Chiappini, University of Florence, Italy