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David Koelle, MD

We are building knowledge of the immune system's response to the herpes virus; one day a vaccine may be developed using our research on skin-homing molecules.

Office: 
750 Republican St. CERID Room E651 Box 358061 Seattle, WA 98109

Lab Staff

Chris McClurken
Nancy Hosken
Lichen Jung
Kerry Laing
Lichun Dong
Ronnie Russell
Tran Tran
Meena Ramchandani
Cosmas Okaru
David Koelle, MD
Professor, Division of Allergy and Infectious Diseases Adjunct Professor, Global Health and Laboratory Medicine, University of Washington. Affiliate Investigator, Fred Hutchinson Cancer Research Center.

Herpesviruses are a family of viruses that produce a variety of complications for patients. Some of these viruses can be very dangerous for immunocompromised patients and even promote the development of cancers.

The laboratory studies immune responses to infections, pathogen genetic variation, and the relationship between host genomics and infection severity. Pathogens of interest include herpes simplex viruses types 1 and 2, varicella zoster virus, vaccinia (the vaccine agent for smallpox), Merkel cell polyoma virus (MCPyV), and Mycobacterium tuberculosis (MTB). These agents mostly have large genomes, so determination of the antigens that drive T-cell responses is a non-trivial problem. Their specific technical expertise is in the use of genomic libraries and genome-spanning ORF sets to interrogate CD8 and CD4 T-cell responses to a very high level of definition. A suite of modern immunology tools such as intracellular cytokine cytometry, tetramers, cell killing assays, etc. are used in this work. Candidate HSV-1 and HSV-2 vaccine candidates have been identified, and some have been studied in mice and are poised to enter phase I trials. The laboratory is decoding the T cell response to MCPyV to assist cancer therapy.

A specific focus of the lab has been measuring cellular immunity at sites of infection, such as skin, the female genital tract, the cornea, trigeminal ganglia, and tumor biopsies. Homing markers identified with this approach are being studied at the mechanistic level to understand how virus-specific T-cells are programmed to rapidly return to these sites. Newer initiatives include studies of T-cell diversity using regular and deep sequencing of TCR hypervariable regions, studies of HSV-1 and HSV-2 diversity at the DNA level, and detailed study of long-term T-cell memory decades after pathogen exposure. Large numbers of T-cell tests for MTB exposure are being run in the clinical lab and epitope discovery has begun for MTB. 

Image courtesy of DNA Illustrated