Janice Telfer

Janice Telfer, PhD

Department of Veterinary and Animal Sciences
427D Integrated Science Building
661 North Pleasant Street
Amherst, MA 01003

(413) 545-5564
telfer@vasci.umass.edu
https://www.umass.edu/veterinary-animal-sciences/about/directory/janice…

Professor of Veterinary and Animal Sciences

Research areas include all of the cells of the blood descend from the progeny of hematopoietic stem cells resident in the bone marrow. Hematopoietic stem cells are very long-lived: they survive and divide for the life of the organism. Their daughter cells go through a period of development in which they become more and more specialized, turning on and off the expression of specific genes, until they are fully differentiated. The subversion of this process of normal development often results in cancer or myelodysplasia. My laboratory is interested in how the regulation of gene expression by the RUNX family of transcription factors influences the development and cancerous transformation of cells of the immune system. Using retroviral transduction and membrane soluble protein delivery, we have shown that normal Runx transcription factors repress the expression of the transcription factor Myc, one of the most potent oncogenes known.

We are also interested in the characterization of an ancient and conserved SRCR family of immune receptors known as WC1 in cattle, present in multiple copies in the genomes of organisms ranging from sea urchins, chickens, duck-billed platypus, cattle to humans. WC1 acts as a co-activator and determiner of the response of gamma delta T cells to bacterial pathogens such as Leptospira and Anaplasma, which infect both animals and humans. Activation of gamma delta T cells is important to the design of vaccines and to cancer therapy, since they act much earlier in immune response and can catch pathogens and cancer cells that evade the antibody producing B cells and conventional alpha beta T cells.

Current Research
We are examining how Runx transcription factors regulate gene targets by modifying packaging of DNA so that it is more or less accessible to being transcribed, using lentiviral transduction and protein delivery though the membrane. We are also characterizing WC1 binding specificity for pathogens, such as Leptospira and Mycobacterium tuberculosis and Mycobacterium bovis, the causative agents of tuberculosis, and working to define WC1’s bacterial ligands. It is estimated that Leptospira infects 7-10 million people per year; Mycobacterium spp. Infects one-third of the world’s population. Identification of bacteria-derived molecules that stimulate a memory gamma delta T cell response will be of potentially large impact towards the design of better vaccines against these zoonotic pathogens.

Academic Background

PhD Harvard University, 1995
Postdoctoral Training: California Institute of Technology

  • Center for Bioactive Delivery 
  • Models to Medicine Center 
  • Infection & Immunity 
  • Antimicrobials and Drug Resistance 
  • Vaccine Development