The UAB Center for AIDS Research (CFAR) is a designated University-wide Center, a department-level status, and is concerned by a Constitution and By-Laws. The overall research goals of investigators in the UAB CFAR are to understand at the molecular level, and at the level of the infected individual, the pathogenesis of HIV infection and to utilize this information in conjunction with investigators pursuing experimental therapeutics, vaccine development, and behavioral modification to interfere with this pathogenic process. The multidisciplinary base of the Center ensures the rapid translation of fundamental knowledge about AIDS and its related disorders into these clinical treatment and prevention programs. In order to facilitate this process, the major objectives of the Center for AIDS Research are threefold. 1. To enhance ongoing outstanding research programs by facilitating interdisciplinary interactions, providing critical shared resource facilities, and providing administrative and fiscal management support mechanisms for Center investigators. 2. To stimulate participation of existing junior and established faculty in research programs aimed at AIDS-related subjects. This will be through the continued administration of a peer-reviewed competitive Developmental Grant Program that will provide funding for both developmental and pilot grants. 3. To stimulate recruitment and program developmental efforts in AIDS- related areas. The Center has identified new program areas and will assist Departments and Divisions in the process of investigator recruitment. Thus we anticipate continued growth and development of AIDS-related research in the CFAR. The Center will be led Dr. Eric Hunter (Director) and by an Executive Steering Committee consisting of Dr. George Shaw (Deputy Director) and seven Associate Directors, Drs. Beatrice Hahn (Basic Sciences and Program Development), Laura Leviton (Prevention Sciences), Jiri Mestecky (Vaccine Development), Michael Saag (Clinical Care and Experimental Therapeutics), John-Pierre Sommadossi (Pre-Clinical Therapeutics Development), Richard Whitley (Clinical Sciences) and Sten Vermund (Epidemiology). The Center is comprised of 120 Center members from 24 Divisions and Departments within the University funded by more than 100 AIDS-related grants and contracts totalling more than $35 million in research support. Eleven Core Facilities are proposed (Clinical, Biostatistics, Central Virus, Molecular Biology, DNA Sequence, Flow Cytometry, SCID-hu Mouse, International Research, and Behavioral Science, as well as Developmental and Administrative) that will provide key support for this funded research base. From its inception, the UAB CFAR has played a pivotal role in stimulating and supporting basic and clinical AIDS research and linking the two through interdisciplinary research programs. This has been most evident in the Center's principal thematic areas of viral pathogenesis, experimental therapeutics, and vaccine development. The success of the UAB CFAR is reflected in the growth in extramural funding for AIDS-related research from $4.0 million in 1988 (annual costs) to greater than $35.o million in 1997 (annual costs), the increase in number of R01-type AIDS-related grants from 5 to 50 during this same period, and the large number (>1,000) of AIDS-related publications by Center members in peer-reviewed scientific journals between 1993 and 1997. All of the major research efforts within the Center link basic and clinical/behavioral research and together they utilize every shared facility supported by the CFAR Core grant.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI027767-12
Application #
2882155
Study Section
Special Emphasis Panel (ZAI1-SCO-A (J1))
Program Officer
Plaeger, Susan F
Project Start
1988-03-30
Project End
2003-02-28
Budget Start
1999-03-01
Budget End
2000-02-29
Support Year
12
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Bilal, Usama; McCaul, Mary E; Crane, Heidi M et al. (2018) Predictors of Longitudinal Trajectories of Alcohol Consumption in People with HIV. Alcohol Clin Exp Res 42:561-570
Bekhbat, Mandakh; Mehta, C Christina; Kelly, Sean D et al. (2018) HIV and symptoms of depression are independently associated with impaired glucocorticoid signaling. Psychoneuroendocrinology 96:118-125
Payne, Emily H; Ramalingam, Dhivya; Fox, Donald T et al. (2018) Polyploidy and Mitotic Cell Death Are Two Distinct HIV-1 Vpr-Driven Outcomes in Renal Tubule Epithelial Cells. J Virol 92:
Nag, Mukta; Wang, Yan; De Paris, Kristina et al. (2018) Histone Modulation Blocks Treg-Induced Foxp3 Binding to the IL-2 Promoter of Virus-Specific CD8? T Cells from Feline Immunodeficiency Virus-Infected Cats. Viruses 10:
Turan, Bulent; Crockett, Kaylee B; Buyukcan-Tetik, Asuman et al. (2018) Buffering Internalization of HIV-Stigma: Implications for Treatment Adherence and Depression. J Acquir Immune Defic Syndr :
Frugé, Andrew D; Ptacek, Travis; Tsuruta, Yuko et al. (2018) Dietary Changes Impact the Gut Microbe Composition in Overweight and Obese Men with Prostate Cancer Undergoing Radical Prostatectomy. J Acad Nutr Diet 118:714-723.e1
Friedman, Gregory K; Bernstock, Joshua D; Chen, Dongquan et al. (2018) Enhanced Sensitivity of Patient-Derived Pediatric High-Grade Brain Tumor Xenografts to Oncolytic HSV-1 Virotherapy Correlates with Nectin-1 Expression. Sci Rep 8:13930
Si, Ying; Cui, Xianqin; Crossman, David K et al. (2018) Muscle microRNA signatures as biomarkers of disease progression in amyotrophic lateral sclerosis. Neurobiol Dis 114:85-94
Yanik, Elizabeth L; Hernández-Ramírez, Raúl U; Qin, Li et al. (2018) Brief Report: Cutaneous Melanoma Risk Among People With HIV in the United States and Canada. J Acquir Immune Defic Syndr 78:499-504
Park, Sang Hyun; Zhang, Yong; Kwon, Dongjin et al. (2018) Alcohol use effects on adolescent brain development revealed by simultaneously removing confounding factors, identifying morphometric patterns, and classifying individuals. Sci Rep 8:8297

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