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Post Docs: A postdoc position is available to study in Dr. Ceol's lab.Click here to apply.
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Post Docs: An entry level postdoctoral position is open immediately in the laboratory of Dr. Susan L. Swain to study the factors that control the development and survival of CD4 and CD8 T cell memory. Graduate student experience with tissue culture, in vitro assay, flow cytometry, experience in mouse models on infectious disease and a knowledge of cellular and molecular immunology are all strongly desired.
Rotation Projects: <p >Rotations: Projects in the following areas <p >CD4 T cell memory. We can generate in vitro CD4 T cells that are for all extents and purposes identical to the memory CD4 T cells observed in vivo. In situ memory CD4 T cells persist at very low frequency and in most instances it is difficult to analyze them thoroughly using tetramer or multimer reagents both because of their low frequency and the relatively low specific affinity of the Class II reagents for the TcR. Being able to generate “recent” memory cells in vitro gives us the opportunity to analyze in detail the mechanisms by which memory CD4 T cells may contribute to secondary immunity and immune protection. Once identified. will determine if particular pathways are relevant in situ. We have discovered that memory CD4 T cells are superior in protection to those from the primary response and that they display pleitropic functions that have not been previously identified. <p > Cytotoxic CD4 Effectors. One unexpected function of CD4 T cells we identified is robust, perforin-dependent cytotoxic activity (7, 16). Cytotoxic activity by CD4 T cells has been reported in response to several infections, but its significance has not heretofore been established. We find that “Th1 polarized” CD4 effectors and more relevantly the CD4 effectors found in the lung following influenza infection, are able to kill infected or peptide-pulsed Class II-bearing targets and we find that this perforin dependent activity can work together with antibody to provide protection against lethal influenza challenge in otherwise unprimed mice (17). We also will determine when memory CD4 T cells re-express cytotoxic activity following in vivo challenge and how cytotoxic killing contributes to the memory cell mediated protection. We want to analyze how the program of cytotoxicity is induced in these “ThCTL”. <p > Memory CD4 Cells Enhance an Innate Response. Memory cells can act by becoming secondary effectors but they are best characterized by …
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Rotation Projects: Rotations: Targeting the IFN-?-chemokine axis for treatment of vitiligo: We are using our newly developed mouse model and human tissues from patients with vitiligo to identify the cytokines and chemokines that are expressed within the depigmenting skin and which skin cells produce them. We are using genetically modified mouse strains (knockouts, conditional knockouts, fluorescent reporter strains), and cytokine and chemokine neutralizing antibodies to identify the key proteins required for disease. This data will permit us to rationally develop and test new therapeutic agents. Understanding the proinflammatory signals generated by melanocytes under cellular stress. Melanocytes from vitiligo patients have intrinsic abnormalities, including cellular stress evidenced by increased production of reactive oxygen species (ROS) and activation of the unfolded protein response (UPR). The immune system has evolved to recognize this stress as damage-associated molecular patterns (DAMPs), which activate innate immunity. We are using human cells and tissues to determine how cellular stress, innate immunity, and adaptive immunity cooperate to initiate and perpetuate depigmentation in vitiligo. Developing a humanized mouse model of immune-skin interactions to serve as a pre-clinical bridge to clinical studies: We are developing a humanized mouse model of skin disease that consists of an immunodeficient mouse strain as a host for an autologous human skin graft and immune reconstitution in order to study mechanisms of inflammation in the skin, including allergic contact dermatitis, response to infection, tumor immunotherapy, and autoimmunity, all within a fully human environment. This model system will act as a pre-clinical bridge between mouse models and human clinical trials, providing an opportunity to test new treatments on human cells and tissues prior to initiating trials on patients. Tracking real-time autoreactive T cell migration and interactions within the skin: We are usin…
Rotation Projects: Rotations: Targeting the IFN-g-chemokine axis for treatment of vitiligo: We are using our newly developed mouse model and human tissues from patients with vitiligo to identify the cytokines and chemokines that are expressed within the depigmenting skin and which skin cells produce them. We are using genetically modified mouse strains (knockouts, conditional knockouts, fluorescent reporter strains), and cytokine and chemokine neutralizing antibodies to identify the key proteins required for disease. This data will permit us to rationally develop and test new therapeutic agents. Understanding the proinflammatory signals generated by melanocytes under cellular stress. Melanocytes from vitiligo patients have intrinsic abnormalities, including cellular stress evidenced by increased production of reactive oxygen species (ROS) and activation of the unfolded protein response (UPR). The immune system has evolved to recognize this stress as damage-associated molecular patterns (DAMPs), which activate innate immunity. We are using human cells and tissues to determine how cellular stress, innate immunity, and adaptive immunity cooperate to initiate and perpetuate depigmentation in vitiligo. Developing a humanized mouse model of immune-skin interactions to serve as a pre-clinical bridge to clinical studies: We are developing a humanized mouse model of skin disease that consists of an immunodeficient mouse strain as a host for an autologous human skin graft and immune reconstitution in order to study mechanisms of inflammation in the skin, including allergic contact dermatitis, response to infection, tumor immunotherapy, and autoimmunity, all within a fully human environment. This model system will act as a pre-clinical bridge between mouse models and human clinical trials, providing an opportunity to test new treatments on human cells and tissues prior to initiating trials on patients. Tracking autoreactive T cell interactions within the skin: We are using fluorescently tagged C…
Summary: Interests: Vitiligo, autoimmunity, immunology, translational research
preferred title: Adjunct Professor

Wiss, Karen
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Person ID: 599
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Summary: Interests: Pediatric dermatology, epidermolysis bullosa, genodermatoses, midline developmental defects, childhood exanthems, medical education, pediatric laser
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Levin, Nikki
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Summary: Interests: Psoriasis, atopic dermatitis, acne vulgaris, perioral dermatitis, fungal infections, cutaneous malignancies, infectious diseases, medical education
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Lemon, Stephenie
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webpage: https://profiles.umassmed.edu/profile/28866492

Sullivan-Bolyai, Susan
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Goldberg, Robert
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Belazarian, Leah
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Person ID: 785
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Summary: Interests: Pediatric dermatology, psoriasis, genodermatoses, medical dermatology, inpatient dermatology
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Shaw, Leslie
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McManus, David
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Pediatric Genetics
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Research
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Friedmann, Peter
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UMass Chan – Baystate Regional Campus
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Goff, Sarah
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Mahmoud Abdallah, Bassel
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Summary: Interests: Mohs micrographic surgery for skin cancers, nail surgery, scar revision, lasers, vitiligo and cosmetic surgery
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Dermatology
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Singh, Sonal
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Person ID: 4649
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Lagu, Tara
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https://profiles.umassmed.edu/profile/16236502
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Lindenauer, Peter
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Gurwitz, Jerry
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Endowed Chair Honorary Title: Dr. John Meyers Professor in Primary Care Medicine
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Usmani, Saad
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Strauss, Kevin
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Population and Quantitative Health Sciences
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Schlaug, Gottfried
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Bokhour, Barbara
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Garg, Arvin
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Mulvaney, Patrick
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https://profiles.umassmed.edu/profile/28866492
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https://profiles.umassmed.edu/profile/28866558
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https://profiles.umassmed.edu/profile/28866602
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https://profiles.umassmed.edu/profile/28867032
ProfilesRNS Plugin Searchable Data: Tweets by @DrSherryPagoto
ProfilesRNS Plugin Searchable Data: Twitter Tweets Harvard Tweets

Healthcare Delivery and Population Sciences at UMass Chan - Baystate
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Medicine at UMass Chan - Baystate
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Neurology at UMass Chan - Baystate
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Adjunct Professor
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Professor
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Adjunct Professor
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Saranathan, Manojkumar
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full name: Manojkumar Saranathan PhD
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preferred title: Professor
webpage: https://profiles.umassmed.edu/profile/44403713

Parker, Margaret
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Weiss, Glen
first name: Glen
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Person ID: 10247163
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Svoboda, Ryan
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Sheldrick, Radley
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Adjunct Associate Professor
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Adjunct Professor
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Driban, Jeffrey
first name: Jeffrey
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Featured Videos: https://profiles.umassmed.edu/profile/40402890
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Dadras, Soheil
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Chair and Associate Professor
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Professor
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Associate Professor
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Professor
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Professor
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Associate Professor
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Assistant Professor
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Assistant Professor
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Walkey, Allan
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Professor
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Medicine at UMass Chan - Lahey
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Surgery at UMass Chan - Lahey
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https://profiles.umassmed.edu/profile/40402890
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Radiology at UMass Chan - Lahey
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Professor
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Professor
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Basic Pathology
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Health System Science
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Neurointerventional Radiology
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Pulmonary Medicine
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Professor
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Professor
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General Pediatrics
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Pediatric Neonatology
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Chair and Professor
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Tan Chingfen Graduate School of Nursing
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Professor Emeritus
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Professor Emeritus
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https://profiles.umassmed.edu/profile/44403713
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McAlindon, Timothy
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Martinez, Fernando
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Professor
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Professor Emeritus
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Krings, Timo
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Ghogawala, Zoher
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Professor
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Maron, Martin
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