This program addresses the identification of antigens of leishmania which can induce and elicit T cell responses, including proliferation and cytokine production, and which can be used with specificity and sensitivity in serological tests. For evaluation of T cell responses, we will focus primarily on leishmania specific human T cell lines and clones. The phenotype of T cells responding to particular antigens will be emphasized. Candidate antigens will be cloned in E. coli. We will use conventional approaches as well as a novel approach for identifying cloned genes. The novel approach consists of screening transfected antigen presenting cells with leishmania-specific T cell lines, followed by isolation of the cloned cDNA of interest. For expression of antigen genes, we will emphasize yeast and mammalian cell systems. Cellular and molecular aspects of T cell responses are measured following stimulation with purified or recombinant proteins which we have produced. Peptide fragments of promising antigens will be similarly tested. Antigens which are effective in these assays will be tested in mice, in particular for their ability to protect against acute disease and to induce T cells capable of transferring similar protection to syngenic recipients. Finally, antigens will be evaluated as sero-diagnostics, using new methods which we have developed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI025038-08
Application #
2062860
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1993-11-01
Project End
1996-05-31
Budget Start
1994-06-01
Budget End
1995-05-31
Support Year
8
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Infectious Disease Research Institute
Department
Type
DUNS #
City
Seattle
State
WA
Country
United States
Zip Code
98102
Reed, Steven G; Carter, Darrick; Casper, Corey et al. (2018) Correlates of GLA family adjuvants' activities. Semin Immunol 39:22-29
Duthie, Malcolm S; Van Hoeven, Neal; MacMillen, Zachary et al. (2018) Heterologous Immunization With Defined RNA and Subunit Vaccines Enhances T Cell Responses That Protect Against Leishmania donovani. Front Immunol 9:2420
Duthie, Malcolm S; Lison, Aurore; Courtenay, Orin (2018) Advances toward Diagnostic Tools for Managing Zoonotic Visceral Leishmaniasis. Trends Parasitol 34:881-890
Duthie, Malcolm S; Reed, Steven G (2017) Not All Antigens Are Created Equally: Progress, Challenges, and Lessons Associated with Developing a Vaccine for Leishmaniasis. Clin Vaccine Immunol 24:
Sato, Camila Massae; Sanchez, Maria Carmen Arroyo; Celeste, Beatriz Julieta et al. (2017) Use of Recombinant Antigens for Sensitive Serodiagnosis of American Tegumentary Leishmaniasis Caused by Different Leishmania Species. J Clin Microbiol 55:495-503
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Duthie, Malcolm S; Favila, Michelle; Hofmeyer, Kimberley A et al. (2016) Strategic evaluation of vaccine candidate antigens for the prevention of Visceral Leishmaniasis. Vaccine 34:2779-86
Hofmeyer, Kimberly A; Duthie, Malcolm S; Laurance, John D et al. (2016) Optimizing Immunization Strategies for the Induction of Antigen-Specific CD4 and CD8 T Cell Responses for Protection against Intracellular Parasites. Clin Vaccine Immunol 23:785-94
Schaut, Robert G; Grinnage-Pulley, Tara L; Esch, Kevin J et al. (2016) Recovery of antigen-specific T cell responses from dogs infected with Leishmania (L.) infantum by use of vaccine associated TLR-agonist adjuvant. Vaccine 34:5225-5234
Carter, Darrick; Fox, Christopher B; Day, Tracey A et al. (2016) A structure-function approach to optimizing TLR4 ligands for human vaccines. Clin Transl Immunology 5:e108

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