Immunology and Immunotherapy Faculty

Margaret E. Ackerman, Ph.D.

Professor of Engineering, and Microbiology and Immunology

Thayer School of Engineering

Office: 119B Cummings Hall

Phone: 603-646-9922

The Ackerman laboratory conducts interdisciplinary research at the interface of biomedical and engineering sciences: developing high throughput tools to evaluate the antibody response in disease states ranging from infection to cancer in order to aid in therapeutic antibody and vaccine design and development, and to understand the protective mechanism of antibodies using approaches grounded in fundamental engineering principles utilizing protein evolution, molecular biology, and mathematical modeling.

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James B. Bliska, Ph.D.

Distinguished Professor of Microbiology and Immunology

Office: 524A Remsen


My long-term research focus is to understand how bacterial toxins interact with the immune system to trigger pathogenesis or host protection. At Dartmouth, I will expand my research to investigate opportunistic bacterial pathogens that produce toxins and cause mucosal infections, such as those that occur in the lungs of Cystic Fibrosis patients. I will also be using synthetic immunology to develop novel therapeutics to combat opportunistic mucosal pathogens.

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David J. Bzik, Ph.D.

Professor of Microbiology and Immunology

Office: 654E Borwell

Phone: 603-650-7951

We are interested in understanding how the obligate intracellular parasite Toxoplasma gondii manipulates the mammalian host cell to ensure it's successful replication and triggering of host responses required for development and transmission. Our interests are the biological intersections of host-parasite interaction, pathogenesis, and immunity, while our goals are the development new drug therapies and vaccines against infectious diseases and cancer.

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Robert A. Cramer, Ph.D.

Professor of Microbiology and Immunology

Office: 213 Remsen

Phone: 603-650-1040

Our research group investigates the molecular mechanisms through which the human fungal pathogen Aspergillus fumigatus causes disease in diverse patient populations. We utilize molecular genetics, genomics, biochemistry, microscopy, immunology, and animal model approaches to develop, explore, and test our clinically relevant questions and hypotheses regarding these too often lethal infections.
 Our long-term goal is to translate results from these studies into novel therapeutic advances.

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Steven N. Fiering, Ph.D.

Professor of Microbiology and Immunology, and Molecular and Systems Biology

Office: 622 Rubin

Phone: 603-653-9966

My lab is working on novel approaches to detection and treatment of cancer. These approaches center on developing antitumor immune responses using nanoparticles and microorganisms. We are also generating novel mouse models of cancer and other diseases using genetically engineering mice.

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William R. Green, Ph.D.

Elmer R. Pfefferkorn Professor of Microbiology and Immunology

Office: 603W Borwell

Phone: 603-650-8607

Our research focuses on the T-cell immune responses to retroviruses.

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Karl E. Griswold, Ph.D.

Associate Professor of Engineering, and Biological Sciences

Office: 128E Cummings Hall

Phone: 603-646-2127

The Griswold research group develops performance-enhanced biomolecules through the application of protein engineering technologies. Current projects are focused on biotherapeutic agents.

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Paul M. Guyre, Ph.D.

Active Emeritus Professor of Microbiology and Immunology

Office: 646W Borwell

Phone: 603-650-7924

Dr. Guyre's principal research interests  to date have been: (i) Cancer immunotherapy; (ii) understanding the regulation and function of IgG Fc receptors on phagocytes, and (iii) how hormones and cytokines regulate the functional activity of white blood cells including monocytes, macrophages, dendritic cells, and neutrophils. The Guyre lab team is currently focused on finding biomarkers for the neuroimmune related disease, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and the tick-induced mammalian meat allergy Alpha Gal Syndrome. Vastly underdiagnosed, IgE anti-alpha gal (a sugar found on all mammals except humans) can induce life threatening anaphylaxis to not only meals of beef and pork, but to medications contained in gelatin capsules.


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Yina H. Huang, Ph.D.

Associate Professor of Microbiology and Immunology, and Pathology and Lab Medicine, Chair of the MCB Program

Office: 604E Borwell

Phone: 603-650-7545 

We investigate how T cells traffic and respond to infections and tumors. In particular, we study the signals that regulate differentiation and migration of effector and memory T cell and are exploring methods to manipulate their activity to ensure protective and durable immune protection. 

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Claudia Jakubzick, Ph.D.

Associate Professor of Microbiology and Immunology

Office:  628W Borwell

Phone:  603-650-2829

My lab primarily focuses on understanding the functional role of mononuclear phagocytes (i.e., macrophages, monocytes, and dendritic cells) in homeostasis and inflammation. Current projects include 1- The regulation of the adaptive immune response by dendritic cells and monocytes, 2- The role of interstitial macrophages during inflammation, 3- The role of B cells and mononuclear phagocytes in transplant rejection and early-stage cancer recognition, and 4- Defining the human and mouse mononuclear phagocyte counterparts in the lung, skin and draining lymph nodes.




Jiwon Lee, Ph.D.

Ralph and Marjorie Crump Assistant Professor of Engineering

Thayer School of Engineering

Office:  751 Williamson Translational Research Building

Phone:  603-646-3485

The Lee Lab studies the dynamics of antibody repertoires in infectious disease, autoimmune disease, and cancer using high-throughput sequencing of B cell transcripts and high-resolution mass spectrometry. The repertoire of antibody molecules circulating in blood or coating mucosal surfaces is the basis for protective immunity, and we employ machine learning frameworks, big data analytics tools, proteomic analytical methods, and data modeling to gain clinically relevant insights regarding protective mechanisms at unprecedented details. Leveraging this knowledge, we aim to design next-generation therapeutics and vaccines precisely tailored to maximize effectiveness in the context of particular diseases and/or patients (i.e.personalized/precision medicine).

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David A. Leib, Ph.D.

Professor and Chair of Microbiology and Immunology

Office: 630E Borwell

Phone: 603-650-8616

We study the molecular pathogenesis of herpes simplex virus (HSV). In particular, we are interested in ways that viruses evade both innate and adaptive immune responses.
We also study maternal immunity to HSV infections and how it shapes the pathogenesis of neonatal HSV – a rare yet devastating manifestation of HSV infection.

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David W. Mullins, Ph.D.

Associate Professor of Medical Education, and Microbiology and Immunology

Office:  232 Remsen

Phone:  603-650-1208

Our lab studies the molecular mechanisms that govern T cell infiltration of metastatic cancers. We translate our basic research findings into novel therapies that induce or augment immune cell infiltration of refractory tumors, thereby enhancing the clinical efficacy of immunotherapy.

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Randolph J. Noelle, Ph.D.

Thomas S. Kosasa Professor of Microbiology and Immunology

Office: 702 Rubin

Phone: 603-653-9908

We study mediators that control the development of adaptive immunity. Our current focus is on the role of retinoic acid in controlling immunity, elements of the immune microenvironment that control allograft tolerance and tumor immunity, and new members of the PD-L family that govern how monocytes regulate T cell responses.

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Josh Obar, Ph.D MCB'06

Associate Professor of Microbiology and Immunology

Office: 650W Borwell

Phone: 603-650-6858

Research in the Obar lab investigates the mechanisms by which inflammatory leukocytes are recruited to the lungs during infections. Specifically, we are interested in viral infections, such as influenza A virus, and fungal infection, such as Aspergillus fumigatus. 

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Patricia A. Pioli, Ph.D. MCB'01

Associate Professor of Microbiology and Immunology

Office: 644E Borwell Building

Phone: 603-650-2584 

Research in our laboratory is focused on identifying the molecular mechanisms that regulate macrophage activation in the context of both autoimmunity and cancer. Taking advantage of macrophage plasticity, we then use this information to determine how macrophage activation can be altered for maximal therapeutic benefit.


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William F.C. Rigby, M.D.

Professor of Medicine, and Microbiology and Immunology

Office: 608W Borwell

Phone: 603-646-7912

Dr. Rigby is examining the changes that accompany clinical responses in patients with rheumatoid arthritis treated with biologics.

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Pamela Rosato, Ph.D., MCB'15

Pamela Rosato, Ph.D.

Assistant Professor, Microbiology and Immunology

Office:  732 Rubin Building


Our research focuses on understanding the function and regulation of virus-specific resident memory T cells (TRM). Using mouse and human tissue explant models, we seek to develop a foundational understanding of TRMbiology in distinct tissues to be able to contextualize the role of TRMin pathologic and protective settings. Our current focuses are on the functions of anti-viral TRMin the brain, repurposing virus-specific TRMas a brain tumor immunotherapy, and investigating the role of TRMwithin tumors during oncolytic viral therapy.

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Rahul Sarpeshkar, Ph.D.

Thomas E Kurtz Professor, Professor of Engineering, Microbiology and Immunology, Physics, Molecular and Systems Biology

Office: 507A Vail

Phone: 603-646-6821

Synthetic analog and digital biological circuits in electri-cigenic and other microbes; Applications of synthetic and systems biology to immunology, infectious disease, and cancer; Precision measurement, electronic circuit modeling, and feedback control of living cells at the fundamental limits set by physics.

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Charles L. Sentman, Ph.D.

Professor of Microbiology and Immunology, Director for Synthetic Immunity

Office: 640W Borwell

Phone: 603-650-8007

My laboratory is interested in innate immunity and how it regulates adaptive immunity in response to cancer and infectious disease. We focus our work on NK cells and CD8 T cells, and we are using innate immune receptors as a means to develop therapeutics for cancer.

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Bruce Stanton, Ph.D.

Andrew C. Vail Memorial Professor

Professor of Microbiology and Immunology, and of Physiology

Office: 615 Remsen

Phone: 603-650-1775

Our laboratory studies the genetic disease Cystic Fibrosis. In particular we study host pathogen interactions between bacteria and human airway epithelial cells and the interactome of CFTR and how interacting proteins regulate CFTR trafficking. We also examine how environmental toxins, in particular arsenic, cause and contribute to respiratory and diseases and inflammation.

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Mary Jo Turk, Ph.D.

O. Ross McIntyre, M.D. Endowed Professor of Microbiology and Immunology, Co-Director, Immunology and Cancer Immunotherapy Program

Office: 732 Rubin

Phone: 603-653-3549

Our research focuses on understanding how the immune system responds to cancer, with an emphasis on T cell memory. We are also interested in learning how autoimmunity influences anti-tumor immunity.

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Edward J. Usherwood, Ph.D.

Professor of Microbiology and Immunology

Office: 608E Borwell

Phone: 603-650-7730

Research in the Usherwood lab focuses on T cell-mediated immune surveillance to virus infections and cancer. We are interested in factors that regulate T cell memory and immune surveillance. A major goal is to exploit these findings to develop novel immunotherapies for cancer and persistent virus infections.

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Michael L. Whitfield, Ph.D.

Professor of Molecular and Systems Biology

Chair of Biomedical Data Sciences

Office: 705A Remsen

Phone: 603-650-1105 

The complexities of biological systems can now be studied with genome-wide approaches that take a global view of the underlaying biology. 

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