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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.
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Thomas P. Gillis
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Chief, Laboratory Research Branch
Ph.D. 1978
Louisiana State University Medical Center,
New Orleans, LA
tgillis@lsu.edu
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