Professor
E-mail: arup at rcb dot res dot in
The research in our lab is broadly directed at understanding the immune pathogenic mechanisms of vector-borne diseases caused by dengue and the Japanese encephalitis virus (JEV). The immunopathogenic mechanisms that drive disease progression are ill-understood. Among the immune cells, neutrophils are the body's first line of defense against infection and display plasticity, with the ability to adapt themselves in different inflammatory scenarios. Our recent studies showed that viral infection significantly impacts neutrophil biogenesis and phenotypes (J Leukocyte Biology, 2023a, b). However, there is a lack of in-depth knowledge of the phenotypic heterogeneity of immune cells that arise due to viral infection. Also, how these phenotypic changes are related to cell fate decisions in imparting adverse disease outcomes is unclear. In our lab, we use the JEV and dengue virus as prototype models to study the impact of neutrophil phenotypes on infection and immunity.
We are also interested in developing suitable models (small animal model, cell line, 3D organoid model) to study host-pathogen interaction at the interface of identifying immune modulators and antivirals.
Our lab is also interested in using extracellular vesicles to understand disease biology and novel interventions in viral infection.
Summary: Our lab has previously observed that neutrophil-associated genes are highly upregulated in severe dengue patients compared to mild symptoms. My research focuses on understanding neutrophils' role in the pathogenesis of dengue virus infection. I am trying to understand how the dengue virus modulates the functions of neutrophils that can increase inflammatory responses.
Hobby: Badminton and cricket.
Summary: We are focusing on the characterization of the exosomes in terms of their protein and cytokine content and their role in immune cell (CD4+ T cells) modulation. Our work suggests that surface proteins in EVs mediate immunomodulatory roles on CD4+ T cells.
Hobby: Reading books, Teaching and Dancing
Summary:Neutrophils, the first immune cells to respond to viral infection, can also modulate the adaptive immune response. Therefore, understanding neutrophil effector activities in disease pathology and immunity against infection are the major focus of my project.
Hobby: Motorbike riding/ Content creator
Summary: Neuroinflammation has emerged as a key factor contributing to neurological diseases and virus infections. NLRP3 inflammasome overactivation is one of the major contributors to neuroinflammation and neuronal death. This project focuses on engineering extracellular vesicles with overexpression of cytosolic and membrane-bound proteins, which can target the potent inducers of NLRP3 inflammasome formation and may help control neuroinflammation
Hobby:Listening to music
Summary: NLRC5 triggers inflammation and immune modulation in the central nervous system. Japanese Encephalitis virus causes inflammation in the brain. Therefore, studying the role of NLRC5 will provide mechanistic insights into JEV-induced inflammation and immune cell modulation in the brain.
Hobby:Binge-watching, Browsing, Adventurer
Summary: The balanced immune response determines the course of disease outcome. Various pathogens target the thymus and induce premature thymic atrophy in humans. Dengue virus infection induces thymic atrophy, conferring insufficient protection against the pathogen. I am working towards recognizing the mechanism involved in Thymic atrophy and addressing the clinical need to boost thymic function by reversing thymic involution in the modality of dengue.
Hobby:Dance, Drawing, Writing, Reading novel.
Dr. Arup Banerjee
Professor
Regional Centre for Biotechnology
NCR Biotech Science Cluster
3rd Milestone, Faridabad-Gurgaon Expressway
P.O. Box No. 3, Faridabad - 121 001
Haryana (NCR Delhi), India
E-mail: arup at rcb dot res dot in
Phone: 91 129-2848852