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National Hansen's Disease Program

Research Interests: Thomas P. Gillis

The major research focus of my lab is to better understand protective immunity in leprosy by studying immunological responses and their consequences in animal models of the disease with the ultimate aim of producing a vaccine capable of protecting humans against infection with Mycobacterium leprae. This research takes the form of designing, constructing and evaluating vaccines made from antigenic components of M. leprae and M. tuberculosis. Our current focus is on developing and testing DNA vaccines, recombinant BCG as well as auxotrophic mutants of M. tuberculosis.

Knowing who should receive a new leprosy vaccine requires a thorough understanding of the dynamics of leprosy within the community. To better understand this area we are working toward establishing a genotyping system for M. leprae that would allow tracking transmission of the bacteria. Short and intermediate length repeating DNA sequences, known as variable number tandem repeats, are being examined for their ability to differentiate strains of M. leprae with the goal of using these markers to define transmission patterns of leprosy in communities. Reaching the above goals will allow us to design better intervention strategies and tools for improving early diagnosis, minimizing transmission to individuals at risk for infection and provide reagents for vaccinating against infection.

 

Representative Publications

 

Gillis, T.P. Is there a role for a vaccine in leprosy control? Lepr Rev 78:1-5, 2007

Job, C.K., Jayakumar, J., Kearney, M., Gillis, T.P. Transmission of leprosy: a study of skin and nasal secretions of household contacts of leprosy patients using PCR. Am J Trop Med and Hyg 78 (3): 10-14, 2008.

Greenstein, RJ, Gillis, TP, Scollard, DS and ST Brown. Mycobacteria: Leprosy, a Battle Turned; Tuberculosis, a Battle Raging; Paratuberculosis, a Battle Ignored. in Sequelae and Long-Term Consequences of Infectious Diseases, Ed, Pina M. Fratamico, James L. Smith, and Kim A. Brogden; 2009 ASM Press, Washington, DC.

Raman, VS, O’Donnell, J, Bailor, HR, Goto, W Lahiri, R, Gillis, TP, Reed, SG and Duthie, MS.  ML0276 vaccination reduces local inflammation, but not bacterial burden, during experimental M. leprae infection. Infect and Immun 2009 September 28 [Epub ahead of print).

Williams, DL, Slayden RA, Amin, A, Martinez, AN, Pittman, T, Mira A, Mitra A, Nagaraja V, Morrison, NE, Moraes, M, Gillis, TP.  Implications of high level pseudogene transcription in Mycobacterium leprae.  BMC Genomics, 2009; 10(1):397.

Truman, RW, Andrews K, Robbins NY, Adams LB, Krahenbuhl, JL and Gillis TP.  Enumeration of Mycobacterium leprae using real-time PCR.  PLoS (Neglected Tropical Diseases), 2(11):e328. Epub 2008 Nov 4.


Thomas P. Gillis
 

Dr. Thomas Gillis

Chief, Laboratory Research Branch

Ph.D. 1978

Louisiana State University Medical Center,
New Orleans, LA

tgillis@lsu.edu

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