The primary mission of the Duke Center for AIDS Research (CFAR) is to promote and encourage activities that enhance collaboration and coordination of AIDS and AIDS-related research at Duke University, and serve the requirements of all AIDS investigators at Duke to meet these mission goals. This CFAR application proposes a series of core facilities to serve the entire AIDS research community and to foster rapid progress in the prevention and treatment of HIV infection. The Developmental Core will support a program of funding pilot innovative AIDS research, a program of funding fast-breaking HIV and HIV-related research, and a faculty recruitment program in partnership with the Duke University School of Medicine. The Proteomics Core will support CFAR investigators using Functional Proteomics to assist with ELISPOT assays, will provide surface plasmon resonance technology for study of protein-protein interactions, and will provide 2D-gel electrophoresis plus mass spectroscopy and expression proteomics to evaluate and develop new methodologies for human immune system monitoring. The Flow Cytometry Core will provide state-of-the- art flow cytometry capability for both HIV -infected and uninfected cell samples. Finally, the Clinical Research Core will provide the Duke HIV patient bank to CFAR investigators to facilitate insightful clinical research both in our local community and at our international collaborative sites. The permanent External Advisory Committee and an effective strategic planning process will ensure that the Duke CFAR continues to be a rich matrix of cores and programs that serves the entire Duke research community and provides the infrastructure that supports the development of new strategies to prevent and treat HIV and HIV -related diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI051445-02
Application #
6653968
Study Section
Special Emphasis Panel (ZAI1-HSD-A (J1))
Program Officer
Quill, Helen R
Project Start
2002-09-01
Project End
2007-06-30
Budget Start
2003-07-01
Budget End
2004-06-30
Support Year
2
Fiscal Year
2003
Total Cost
$2,164,111
Indirect Cost
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Bowles, R D; Karikari, I O; VanDerwerken, D N et al. (2016) In vivo luminescent imaging of NF-?B activity and NF-?B-related serum cytokine levels predict pain sensitivities in a rodent model of peripheral neuropathy. Eur J Pain 20:365-76
Mavura, Daudi R; Masenga, E John; Minja, Eli et al. (2015) Initiation of antiretroviral therapy in HIV-infected adults with skin complaints in northern Tanzania. Int J Dermatol 54:68-73
Perley, Casey C; Frahm, Marc; Click, Eva M et al. (2014) The human antibody response to the surface of Mycobacterium tuberculosis. PLoS One 9:e98938
Holmer, Stephanie M; Evans, Kathy S; Asfaw, Yohannes G et al. (2014) Impact of surfactant protein D, interleukin-5, and eosinophilia on Cryptococcosis. Infect Immun 82:683-93
Harmon, James L; Collins-Ogle, Michelle; Bartlett, John A et al. (2014) Integrating routine HIV screening into a primary care setting in rural North Carolina. J Assoc Nurses AIDS Care 25:70-82
Nyindo, Mramba; Kitau, Jovin; Lisasi, Esther et al. (2014) Introduction of team-based learning (TBL) at Kilimanjaro Christian Medical University College: experience with the ectoparasites module. Med Teach 36:308-13
Smith, Kristen L Jurcic; Saini, Divey; Bardarov, Svetoslav et al. (2014) Reduced virulence of an extensively drug-resistant outbreak strain of Mycobacterium tuberculosis in a murine model. PLoS One 9:e94953
Liao, Hua-Xin; Bonsignori, Mattia; Alam, S Munir et al. (2013) Vaccine induction of antibodies against a structurally heterogeneous site of immune pressure within HIV-1 envelope protein variable regions 1 and 2. Immunity 38:176-86
Buckley, Rebecca H; Win, Chan M; Moser, Barry K et al. (2013) Post-transplantation B cell function in different molecular types of SCID. J Clin Immunol 33:96-110
Cain, Derek W; O'Koren, Emily G; Kan, Matthew J et al. (2013) Identification of a tissue-specific, C/EBP*-dependent pathway of differentiation for murine peritoneal macrophages. J Immunol 191:4665-75

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