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Research Laboratories at Penn Vet


Penn Vet faculty are engaged in ongoing groundbreaking research. Here are examples of faculty laboratories and the projects being investigated, both at our Philadelphia campus and at New Bolton Center.

Hunter Laboratory

T gondii in the retina, Hunter Lab

Dr. Christopher Hunter's research team has been working on various aspects of basic parasitology since 1984.

For nearly 25 years, Dr. Hunter's team has focused on understanding how the immune response to Toxoplasma gondii is regulated to allow the development of protective immunity as well as to limit T cell mediated pathology in multiple sites including the gut and brain.

Contact Information

Christopher Hunter, BSc, PhD

  • Professor and Chair, Pathobiology
  • Mindy Halikman Heyer President's Distinguished Chair, Pathobiology

University of Pennsylvania
School of Veterinary Medicine

Phone: 215-573-7772
Fax: 215-746-2295
Email: chunter@vet.upenn.edu

Research Overview

Dr. Hunter has been working on various aspects of basic parasitology since 1984 and for the last 25 years there has been a focus on understanding how the protective immune response to Toxoplasma gondii develops and how this relates to other parasitic infections.


CD8+T Cells Hunter Lab
Stylized images of CD8+ T cells looking at differential localization of the transcription factor T-bet in mouse cells after infection with the parasite Toxoplasma gondii, using the Amnis ImageStream. In the cell in the first and third box, T-bet (red) does not co-localize with DAPI (blue), indicating that it is cytoplasmic, whereas in the cell in the second and fourth box, T-bet does co-localize with DAPI, indicating that it is nuclear. Gretchen Harms and David Christian provided these images.

The Hunter Laboratory team has focused on the innate events that lead to the development of long term protective immunity mediated by T and B cells. These studies led us to develop expertise in cytokine biology and, while the focus has been in understanding their role in infectious disease, these findings are frequently relevant to cytokine function in autoimmunity and inflammatory processes associated with human disease.

For example, as part of studies to understand how IL-12 family members affect immunity to the T. gondii, we showed that IL-27 was important in limiting the T cell-mediated infection-induced inflammation. We have defined the mechanisms used by IL-27 to influence the immune system and our work has been shown to be relevant to inflammatory processes in multiple experimental systems that includes other infections as well as models of auto-immune inflammation, asthma and cancer.

Since toxoplasma causes a chronic infection in the brain there has been a long-term interest in the neuropathogenesis of infectious diseases and how lymphocytes access and operate in this immune privileged site.

In this laboratory we have developed all of the skills required for the routine analysis of multiple innate immune parameters and to quantify DC, macrophage, NK, T and B cell responses to infection.

We are also able to utilize different combinations of transgenic parasites (replication deficient, expressing fluorescent reporters, distinct model antigens OVA and E and the Cre recombinase) and TCR transgenic T cells to provide higher resolution analysis of individual parasite specific CD4 and CD8 T cell populations and apply multi-photon microscopy to image the innate and adaptive response to T. gondii.

As part of this research program Dr. Hunter has supervised more than 50 students from multiple programs that include Penn undergraduates, VMD summer students, graduate students from the Microbiology and Immunology graduate groups as well as combined degree (VMD/PhD and MD/PhD), and PhD candidates and undergraduates from the UK. He has been responsible for the training of 15 post-docs and 26 students (20 PhD, 3 Masters and 3 in training).

Almost all of these individuals are still in science with trainees in faculty positions at the University of Washington, UPenn, UVA, Columbia, Yale, UMass, UC Riverside, University of Arkansas and six in faculty positions in Canada, Brazil, Japan and Europe, with several in industry (Pfizer, Medimmune), Science policy at Stanford and a Program Advisor to the Malaria Vaccine Initiative.


STAT6 activation Hunter Lab
Image stream analysis of STAT6 activation in cells from infected mice. Zsgreen1+ macrophages that contain a single intracellular parasite (top row) or which are uninfected (lower row) are shown. Cells were stained with DAPI to identify the host cell nucleus as well as with a p-STAT6 antibody. The bright field overlay shows that in both cells the pSTAT6 is localized in the host nucleus.

  • University of Glasgow Cormie Prize in Neurology (1991)
  • Irvington Research Scholar (1993-1996),
  • Burroughs Wellcome Young Investigator Award (1996-1999)
  • Pfizer Award for Research Excellence, (1997)
  • Elected Fellow of the American Society of Microbiology (2009)
  • Elected Fellow of the Royal Society of Edinburgh (2011)
  • Senior Investigator American Asthma Foundation (2012-2015)
  • Elected to the Council of the Midwinter Conference of Immunologists
  • Visiting Professor University of Edinburgh, (2015)
  • External Reviewer for NCI Cancer and inflammation program and the UVA infectious disease T32 program
  • Journal Clinical Investigation (2010-2012)
  • Consulting Editor JCI (ongoing)
  • Journal Experimental Medicine (2008-present)
  • Infection and Immunity, (1996-present)
  • Current Reviews in Immunology (2004-present), Medical Immunology (2003)
  • Associate Editor, Journal of Immunology, (1999-2003)
  • Associate Editor PloS Pathogens (2006)
  • Section Editor, Journal of Immunology, (2003-2007)
  • Microbes and Infection (2003-2007)
  • Journal Biological Chemistry (2006-2008)
  • Guest Editor Parasite Immunology (2005, 2015)
  • Guest Editor Immunological Reviews (2008)
  • Guest Editor Current Opinions Immunology (2015)
  • Woods Hole Biology of Parasitism course Module (2004-2007) and Course Director (2006,2007)
  • Organizer Woods Hole Immunoparasitology meeting (2007-08)
  • International Cytokine Society Meeting (2007, 2011)
  • BWF Parasitology T32 meeting (2008, 2009, 2010)
  • AAI Program Committee, 2007-2010)
  • Keystone Biology of Cytokines (2012)
  • Organization of the American Society of Microbiology, Infection and Immunity Forum (1996-1998)
  • Selection Committee for the American Society of Tropical Medicine and Hygiene, Young Investigator Award (1999)
  • Admissions Review Committee Biology of Parasitism Course (2000, 2004-2006)
  • Asilomar Mid-Winter meeting co-organizer with Ananda Goldrath (2015)
  • Biannual Toxoplasma Meeting, Gettysburg, Co-organized with David Roos (2015)
Crossing the Blood-Brain Barrier.
Toxoplasma gondii infects up to 30 percent of the world's population. How does this parasite travel through the blood-brain barrier? Penn researchers, including the Hunter Lab at Penn Vet, find out. Video produced by University of Pennsylvania Communications.
Multi-photon image of T. gondii in the brain.
Intravital multi-photon imaging through an open skull window of CX3CR1-GFP reporter mouse infected with T. gondii strain expressing tdTomato 20 days post infection. Image shows CX3CR1-GFP+ cells (green) interacting with T. gondii cysts (red), Skull (blue). Vasculature (white). 
Multi-photon image of T. gondii in the bone marrow.
Intravital multi-photon imaging of the bone marrow of MHC II-GFP reporter mouse infected with T. gondii strain expressing tdTomato 10 days post infection. Image shows T. gondii (red) within the bone marrow of the skull (blue), MHC II-GFP+ cells (green). 
Multi-photon image of T. gondii in the brain.
Intravital multi-photon image through a thinned skull of a LysM-GFP reporter mouse infected i.v. with a T. gondii strain expressing tdTomato. Image shows the uptake of T. gondii (red) by LysM-GFP cells (green) in the vascular compartment. 
Multi-photon image of T. gondii in the brain.
Intravital multi-photon image through a thinned skull of a LysM-GFP reporter mouse infected with a T. gondii strain expressing tdTomato 15 days post infection. Image shows replicating T. gondii (red) in the meninges/ brain parenchyma. LysM-GFP+ cells (green), T. gondii (red), Skull (blue). 
Multi-photon image of T. gondii in the bone marrow.
Intravital multi-photon image through of the bone marrow of a LysM-GFP reporter mouse infected i.v. with a T. gondii strain expressing tdTomato. Image shows the arrival of T. gondii (red) in the bone marrow of the skull (blue). 
Multi-photon stack through the meninges and parenchyma of a CX3CR1-GFP reporter mouse, Skull (blue). Vasculature (red).