Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/11224
Title: Studying the Potential of Poly (I:C) and R848 in Generation of B Cell Response and T Cells to Protein Antigen
Authors: Fultariya, Hirva
Jadeja, Mayurdhvajsinh
Mehta, Mili
Bhatt, Nishchay
Trivedi, Sakshi
Keywords: Biotechnology
Project Report
Project Report 2022
20MBC
20MBT
20MBC003
20MBT017
20MBT028
20MBC007
20MBT056
Issue Date: May-2022
Publisher: Institute of Science, Nirma University
Series/Report no.: ;SDR00442
Abstract: Our Immune system has its own blueprint to fight against various range of pathogen but there are certain microorganisms that escape our prompt immune system. With the advancements in technology, the interaction between host and pathogen has been well studied although the mechanism remains poorly understood. So, to combat this bleak situation, vaccination is the gold standard approach aiming to achieve protective and sterile immunity. However, activating and licensing the activity of both B and T cells is a major hurdle in successful vaccination. To enhance immune response, scientific community has tried using different adjuvants and at certain stage, success has been achieved, however, further validation is ongoing. With respect to this, here we are trying to explore the role of two different adjuvants: Poly(I:C) and R848, in line of sub-unit vaccine approach. Poly(I:C), a TLR 3 agonist, is well known for activating antigen-specific CMI response. On the other hand, R848, a TLR 7/8 agonist, is well investigated for its ability to generate high antibody titres. Moreover, protein antigen along with Poly (I:C), R848 and its combination shown the elevated antigen specific IgG levels and proliferative function of CD4+ and CD8+ T cells after in vitro peptide specific stimulation. In addition to that, repeated immunization has enhanced the production of cytotoxic T cells which may provide us protective immunity. In nutshell, both the adjuvant may aid in activating and boosting the immune system alongside protein antigen and could be the part of vaccination with prior detailed investigation.
Description: Guided by Prof. Sarat Dalai
URI: http://10.1.7.192:80/jspui/handle/123456789/11224
Appears in Collections:Dissertation, BT

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