mRNA Vaccines represent a groundbreaking approach to vaccination that harnesses the body's own cellular machinery to produce a protective immune response against infectious diseases. Unlike traditional vaccines, which contain either weakened or inactivated forms of a virus, mRNA vaccines work by delivering synthetic strands of messenger RNA (mRNA) encoding specific viral proteins into the body. Once inside the body, the mRNA molecules instruct cells to produce the viral protein, such as the spike protein of the target virus, which triggers an immune response. This immune response includes the production of antibodies and the activation of T cells, which work together to recognize and neutralize the virus if the person is exposed to it in the future.
One of the key advantages of mRNA vaccines is their speed and flexibility in development. Traditional vaccine production methods often involve growing large quantities of the virus in cell cultures, which can be time-consuming and labor-intensive. In contrast, mRNA vaccines can be designed and manufactured relatively quickly using synthetic biology techniques. The rapid development of mRNA vaccines was demonstrated during the COVID-19 pandemic, where multiple mRNA vaccines were developed and authorized for emergency use within record time. The Pfizer-BioNTech and Moderna COVID-19 vaccines, for example, were developed in less than a year and have been highly effective in preventing COVID-19 illness.
In addition to their speed, mRNA vaccines offer several other advantages. They do not contain live virus, so there is no risk of causing the disease they are designed to prevent. They are also highly specific, targeting only the viral proteins encoded by the mRNA, which reduces the risk of unwanted side effects. Despite their promise, mRNA vaccines also pose some challenges. They require cold storage and transportation to maintain their stability, which can complicate distribution in resource-limited settings. Additionally, their long-term safety profile is still being studied, although extensive clinical trials have demonstrated their safety and efficacy in preventing COVID-19.
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Madhu Khanna, University of Delhi, India
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Title : Development of a novel multi-component vaccine to address the burden of otitis media in high-risk populations
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Title : The role of immunity in the pathogenesis of SARS-COV-2 and in the protection generated by COVID-19 in different age groups
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Title : Tubercular disease in children: Optimizing treatment strategies through disease insights
Elena Chiappini, University of Florence, Italy
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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
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