The goal of this proposal is to explain the role of TH1-type and TH2- type cytokine profiles in disease progression for the pathogens human immunodeficiency virus type 1 (HIV-1) and Mycobacterium tuberculosis. We investigate the following hypotheses: (1) The progression of disease during the pathogenesis of HIV infection is dependent upon a long-term shift of TH1- and TH2-type cytokines that are expressed during the evolution of the disease. This paradigm would predict that a dominant phenotype characterized by TH2-type cytokines is present in end-stage disease. (2) The establishment and maintenance of latency in infection with Mycobacterium tuberculosis may be predicted based on the cytokine profiles, balancing the tissue damaging response with resolution. The three specific aims are to formulate mathematical models based on the complex cytokine network in the cellular immune response to disease to: (1) Determine the predictive role of a TH1/TH2 cytokine balance in differentiating the disease outcomes in infection with Mycobacterium tuberculosis. Specifically, we will investigate why most individuals develop latent TB infection, yet others progress to disease, via either a fast or slow progression. (2) Explore the role of a long-term TH1/TH2 cytokine shift expressed during HIV-1 disease progression and to determine the predictive role of a TH1/TH2 cytokine imbalance in that progression. (3) Investigate the use of cytokines as therapeutic strategies as agents of immunotherapy, either alone or in conjunction with chemotherapy, for both latent and progressive disease for both drug-resistant and drug-sensitive HIV-1 and M. tuberculosis. These results are also expected to lead to a greater understanding of co- infections with HIV-1 and TB. Mathematical models will be developed that reflect the dynamics of the different diseases as well as disease states. These models include experimental data and will be analyzed using mathematical approaches for characterizing nonlinear dynamical systems. The interaction of multiple factors that control, activate or facilitate the cellular-immune response to the pathogens will be defined. Key parameters governing these interactions will be identified through mathematical sensitivity analyses. These results will incorporate, and be tested against, known clinical and experimental data.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL062119-05
Application #
6527437
Study Section
Special Emphasis Panel (ZHL1-CSR-N (S2))
Program Officer
Peavy, Hannah H
Project Start
1998-09-30
Project End
2003-12-31
Budget Start
2002-09-01
Budget End
2003-12-31
Support Year
5
Fiscal Year
2002
Total Cost
$200,115
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Hogue, Ian B; Bajaria, Seema H; Fallert, Beth A et al. (2008) The dual role of dendritic cells in the immune response to human immunodeficiency virus type 1 infection. J Gen Virol 89:2228-39
Sud, Dhruv; Bigbee, Carolyn; Flynn, Joanne L et al. (2006) Contribution of CD8+ T cells to control of Mycobacterium tuberculosis infection. J Immunol 176:4296-314
Ye, Ping; Kazanjian, Powel; Kunkel, Steven L et al. (2004) Lack of good correlation of serum CC-chemokine levels with human immunodeficiency virus-1 disease stage and response to treatment. J Lab Clin Med 143:310-9
Bajaria, Seema H; Webb, Glenn; Kirschner, Denise E (2004) Predicting differential responses to structured treatment interruptions during HAART. Bull Math Biol 66:1093-118
Joseph, Ian M; Kirschner, Denise (2004) A model for the study of Helicobacter pylori interaction with human gastric acid secretion. J Theor Biol 228:55-80
Marino, Simeone; Pawar, Santosh; Fuller, Craig L et al. (2004) Dendritic cell trafficking and antigen presentation in the human immune response to Mycobacterium tuberculosis. J Immunol 173:494-506
Ye, Ping; Kourtis, Athena P; Kirschner, Denise E (2003) Reconstitution of thymic function in HIV-1 patients treated with highly active antiretroviral therapy. Clin Immunol 106:95-105
Joseph, Ian M P; Zavros, Yana; Merchant, Juanita L et al. (2003) A model for integrative study of human gastric acid secretion. J Appl Physiol 94:1602-18
Murphy, Brian M; Singer, Benjamin H; Kirschner, Denise (2003) On treatment of tuberculosis in heterogeneous populations. J Theor Biol 223:391-404
Bajaria, Seema H; Webb, Glenn; Cloyd, Miles et al. (2002) Dynamics of naive and memory CD4+ T lymphocytes in HIV-1 disease progression. J Acquir Immune Defic Syndr 30:41-58

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