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   Molecular and Human Genetics Department in Varanasi, Molecular and Human Genetics Department in Banaras Hindu University Varanasi, Molecular and Human Genetics Department in Uttar Pradesh, Immunology, Immunogenetics, Systemic Lupus Erythematosus, SLE, Netosis, 
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                                        <h3>
                                            Geeta Rai, Ph.D, MNASI, FSAB</h3>
                                        <p>
                                            <strong>Associate Professor</strong><br />
                                            <strong>Department of Molecular & Human Genetics</strong><br />
                                            <strong>Institute of Science</strong><br />
                                            <strong>Banaras Hindu University,Varanasi- 221005 (India)</strong></p>
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                                                Welcome to the Immunogenetics laboratory of Geeta Rai, PhD.</h3>
                                            <p>
                                                Our current research program comprises of several independent but synergistically
                                                interacting projects with major focus in three domains:</p>
                                            <ul class="list-unstyled">
                                                <li><i class="fa fa-star"></i><span>Autoimmune disease Systemic Lupus Erythematosus
                                                    (SLE).</span></li>
                                                <li><i class="fa fa-star"></i><span>Defective mechanisms of the innate immunity in low
                                                    birth weight (LBW) newborns. </span></li>
                                                <li><i class="fa fa-star"></i><span>Stem cell studies to develop better tools for regenerative
                                                    medicine.</span></li>
                                                <li><i class="fa fa-star"></i><span>Biosimilar/Monoclonal Antibodies development</span></li>
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                                            <ul class="list-unstyled">
                                                <li><i>1.</i><span>My research contribution in SLE initiates from development of a novel
                                                    disease model and extends to identification, optimization and evaluation of disease
                                                    processes aimed at amelioration of the disease state in human beings. The salient
                                                    research outputs have been, elucidation of role of Toll like Receptors in paradigm
                                                    of diverse clinical manifestations in SLE (Patent, 2013(a)., best oral presentation
                                                    award, Immunocon 2012). Significant efforts have led to successful characterization
                                                    of novel markers in SLE using genomic and proteomic approaches. Results of miRNA
                                                    and global transcriptome sequencing studies have helped provide a strong basis for
                                                    dintinguishing SLE in 3 distinct subgroups with a potential of impacting treatment
                                                    modality.</span></li>
                                                <li><i>2.</i><span>Transcriptomic and proteomic studies involving newborns have resulted
                                                    in identification of defective immune pathways responsible for increased susceptibility
                                                    of LBW newborns towards life threatening infections and mortality (GP Talwar young
                                                    scientist award, Immunocon 2013). Our observations on impaired Neutrophil Extra
                                                    trap (NET) formation in LBW newborns (Best oral presentation award, Immunocon 2013’)
                                                    led to development of novel formulation to improve immune efficiency and NET formation
                                                    (Patent 2013(b)).</span></li>
                                                <li><i>3.</i><span>Our recent research focus in stem cells, has identified defective
                                                    differentiation of cord blood hematopoetic stem cells in specific group of newborns.</span></li>
                                                <li><i>4.</i><span>Development of Biosimilars for various Immunopathologies.</span></li><br />
                                                <li><span>In addition, we are involved in development of monoclonal Abs and biosimilars
                                                    and our efforts to manage Dengue fever through immunomodulation have resulted in
                                                    a novel formulation (Patent 2016). Development of biogenic silver nanoparticles
                                                    which target and destroy cancer cells has been our most recent research effort (Patent
                                                    2017).</span></li>
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                                    <p class="text-justify">
                                        <strong><i class="fa fa-star"></i></strong><strong>Post Doctoral Fellow</strong><i
                                            class="glyphicon glyphicon-arrow-right"></i>Lab of Immunology, NIAID, National
                                        Institute of Health, Bethesda, USA 2003-2006.</p>
                                    <p class="text-justify">
                                        <strong><i class="fa fa-star"></i></strong><strong>Ph.D.</strong> (Immunology)<i
                                            class="glyphicon glyphicon-arrow-right"></i>Sanjay Gandhi Post Graduate Institute
                                        of Medical Sciences (SGPGIMS), Lucknow, India (2002).
                                    </p>
                                    <p class="text-justify">
                                        <strong><i class="fa fa-star"></i></strong><strong>Master of Science</strong> (Biochemistry
                                        and Biotechnology)<i class="glyphicon glyphicon-arrow-right"></i>Govind Ballabh
                                        Pant University of Agriculture and Technology, Pantnagar, India (1997).
                                    </p>
                                    <p class="text-justify">
                                        <strong><i class="fa fa-star"></i></strong><strong>Bachelor of Science</strong>
                                        (Botany, Zoology, Chemistry)<i class="glyphicon glyphicon-arrow-right"></i>Banaras
                                        Hindu University, Varanasi, India (1995).
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				 	<p class="text-justify"><strong><i class="fa fa-star"></i></strong><strong>G.P. Talwar Young scientist award(Immunocon 2013)<i class="glyphicon glyphicon-arrow-right"></i></strong>Singh VV, Chauhan SK, Rai R, Soni UK, Ashok Kumar, Rai G. Impaired Genetic Mechanisms of Innate Immunity in Low Birth Weight Newborns. 40th Ann. Conf. of Indian Immunology Society, University of Delhi, North Campus, New Delhi, November 15 -17, 2013; P-30. </p>
                    <p class="text-justify"><strong><i class="fa fa-star"></i></strong><strong>Firstprize in oral presentation (Immunocon 2013)<i class="glyphicon glyphicon-arrow-right"></i></strong>	Soni UK, Singh VV, Chauhan SK, Rai R, Ashok Kumar, Rai G. Leukotriene B4 receptor regulates Neutrophil Extracellular Trap formation by activation of Gas/Rap1/b-Raf/ERK1/2 signaling pathway. 40th Ann. Conf. of Indian Immunology Society, University of Delhi, North Campus, New Delhi, November 15 -17, 2013; P-60. </p>
                    <p class="text-justify"><strong><i class="fa fa-star"></i></strong><strong>Firstprize in oral presentation  (Immunocon 2012)<i class="glyphicon glyphicon-arrow-right"></i></strong>	Chauhan SK, Singh VV, Rai R, Rai M, Rai G. TLR7 and TLR9 upregulation associates    with autoantibodies against specific nuclear targets in systemic lupus erythematosus. 39th Ann. Conf. of Indian Immunology Society, Banaras Hindu University, Varanasi, November 9-11, 2012; P-40. </p>
                    <p class="text-justify"><strong><i class="fa fa-star"></i></strong><strong>Secondprize in oral presentation (Immunocon 2012)<i class="glyphicon glyphicon-arrow-right"></i></strong>	Soni UK, Singh VV, Chauhan SK, Rai R, Kumar A, Rai G. HL60 differentiation: Highest ROS activity with maximum survivability of neutrophil-like cells achieved after 120 hrs by All Trans Retinoic Acid (ATRA) induction. 39th Ann. Conf. of Indian Immunol.Soc., BHU, Varanasi, November 9-11, 2012; P-59. </p>
                    
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                                <h3>
                                    Systemic Lupus Erythematosus</h3>
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                                    <p class="text-justify">
                                        SLE(Systemic Lupus Erythematosus) is a complex, chronic autoimmune disease with
                                        significant mortality and morbidity. It is characterized by a diverse range of autoantibodies
                                        against nuclear/ cytoplasmic components.<span class="text-justify moretext" style="display: none;">The
                                            clinical manifestations of SLE are highly variable with multiple organs and organ
                                            systems affected; these include skin joints, heart, kidney, and the nervous. Presence
                                            of autoantibodies, to RNA spliceosomalribonucleoproteins and dsDNA are characteristic
                                            in this disease. We in our lab identified differential Toll-like receptors (TLRs)
                                            expression in different subsets of SLE patients based on autoantibodies present
                                            in their sera . In a rabbit model of neuropsychiatric lupus, we have also established
                                            a link between different autoantibody repertoires with differential gene expression
                                            in SLE. We aim to understand different genetic and epigenetic regulatory mechanisms
                                            operative in different SLE subsets. Our goal is to uncover the molecular basis for
                                            such tremendous heterogeneity and differential response to the therapies observed
                                            in SLE patients. Further, the identification of these biomarkers which can help
                                            the clinicians in characterizing the patients into appropriate groups and planning
                                            a more targeted treatment strategy.</span>
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                                    Immunity in Neonates</h3>
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                                    <p class="text-justify">
                                        Due to immuno-compromised status of low birth weight (LBW) newborns and inefficient
                                        immune responses they are highly susceptible to various infections resulting into
                                        sepsis, and have high morbidity and mortality rates.<span class="text-justify moretext"
                                            style="display: none;">Netosis is a unique antimicrobial function of the neutrophils
                                            in which neutrophil cells are activated in response to pathogenic infection, and
                                            release their chromatin outside the cell membrane along with antimicrobial peptides
                                            such as neutrophil elastase, Myeloperoxidase, Defensin 1 and 2, Cathepsin G. This
                                            histone mixed DNA make a net-like structure termed as NET which is employed in trapping
                                            and killing of the pathogens. In our earlier studies we have found poor NETs formation
                                            in LBW newborns.</span>
                                    </p>
                                    <p class="text-justify moretext" style="display: none;">
                                        Our aim is to investigate novel genes and protein molecules not known earlier to
                                        be involved in netosis which is a marker of innate immunity in newborns and toboost
                                        up the NETosis in LBW newborns to protect them from infection.</p>
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                                    Stem cells</h3>
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                                    <p class="text-justify">
                                        Cord blood is conventionally known to contain stem cells that are easily accessible
                                        at birth and also capable of differentiating into various cell types and therefore
                                        considered as relevant source of stem cells especially for the treatment of neonatal
                                        diseases.
                                    </p>
                                    <p class="text-justify moretext" style="display: none;">
                                        Our laboratory has been working on understanding the role of immunological responses
                                        in outcome of life threatening infections in low birth weight (LBW) newborns (birth
                                        weight < 2.5 Kg) for the past few years. The LBW newborns have long been known to
                                        have significantly lesser number of immune cells makes them highly susceptible for
                                        microbial infections. Since all blood cells are generated through hematopoiesis.
                                        This prompted us to focus our investigation on evaluating hemotopoeisis and differentiation
                                        occurring at the hematopoietic stem cell level in these newborns. Our stem cell
                                        research will eventually make great contributions to the development of safe, efficacious
                                        and a novel therapeutic intervention against life threatening microbial infections
                                        and resulting mortality.</p>
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