The primary mission of the Biosafety Core Support Facility (Core E) is to provide a fully manage, equipped and safe working environment where infectious pathogens, including (but not restricted to) HIV and Mycobacterium tuberculosis (M.tb) can be studied by investigators at CWRU and affiliated institutions, including the Cleveland Clinic Foundation. Dedicated BL-3 (approximately 1200 square foot) and BL-2 laboratories (approximately 150 square foot) including the Cleveland Clinic Foundation. Dedicated BL-3 (approximately 1200 square foot) and BL-2 laboratories (approximately 150 square foot), located immediately adjacent to each other on the 10th floor of the Biomedical Research Building in the Division of Infectious Diseases, are Available for Culture of HIV. The Core Support Facility provides state-of-the-art services to multiple CFAR investigators, permitting the culture and detection of both HIV and M.tb, thereby enhancing their research efforts. In addition to these services, Core personnel have assumed the responsibility of (a) familiarizing all BL-3 users in good laboratory practices and (b), pediatric retraining of all users to insure compliance with laboratory regulations. In addition to the Core Director (E.A. Rich), a 3-member Biosafety Committee (Drs. E.A. Rich, M.M. Lederman and Dr. S.F.J. Le Grice) meets on a periodic basis to supervise overall operational procedures. Since culture of an experimentation with biohazardous pathogens is a key element of AIDS research, this Facility constitutes an essential component of the CFAR. Key projects supported by Biosafety-3 Core Facility include: A human model of protective immunity (AI35207, J.J. Ellner); AIDS Clinical Trials Unit (AI25879, M.M. Lederman); Interaction of M.tb and HIV in the lung (HL51636, Z. Toosi); Expression of TB in the lung (HL-51630, E.A. Rich); Natural history of lymphocytic alveolitis in HIV disease (HL-53247, E.A. Rich); AIDS vaccine development-laboratory training (T2-00011, C. Whalen).

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI036219-07
Application #
6099827
Study Section
Project Start
1999-04-01
Project End
2000-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Type
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Silver, Nicholas; Paynter, Mary; McAllister, Georgina et al. (2018) Characterization of minority HIV-1 drug resistant variants in the United Kingdom following the verification of a deep sequencing-based HIV-1 genotyping and tropism assay. AIDS Res Ther 15:18
Jiang, Wei; Luo, Zhenwu; Martin, Lisa et al. (2018) Drug Use is Associated with Anti-CD4 IgG-mediated CD4+ T Cell Death and Poor CD4+ T Cell Recovery in Viral-suppressive HIV-infected Individuals Under Antiretroviral Therapy. Curr HIV Res 16:143-150
Martinez, Leonardo; Handel, Andreas; Shen, Ye et al. (2018) A Prospective Validation of a Clinical Algorithm to Detect Tuberculosis in Child Contacts. Am J Respir Crit Care Med 197:1214-1216
Fitzgerald, Wendy; Freeman, Michael L; Lederman, Michael M et al. (2018) A System of Cytokines Encapsulated in ExtraCellular Vesicles. Sci Rep 8:8973
Dazard, Jean-Eudes; Ishwaran, Hemant; Mehlotra, Rajeev et al. (2018) Ensemble survival tree models to reveal pairwise interactions of variables with time-to-events outcomes in low-dimensional setting. Stat Appl Genet Mol Biol 17:
Mukherjee, Pranab K; Chandra, Jyotsna; Retuerto, Mauricio et al. (2018) Dysbiosis in the oral bacterial and fungal microbiome of HIV-infected subjects is associated with clinical and immunologic variables of HIV infection. PLoS One 13:e0200285
Bengtson, Angela M; Pence, Brian W; Eaton, Ellen F et al. (2018) Patterns of efavirenz use as first-line antiretroviral therapy in the United States: 1999-2015. Antivir Ther 23:363-372
Tomalka, Amanda G; Resto-Garay, Ivelisse; Campbell, Kerry S et al. (2018) In vitro Evidence That Combination Therapy With CD16-Bearing NK-92 Cells and FDA-Approved Alefacept Can Selectively Target the Latent HIV Reservoir in CD4+ CD2hi Memory T Cells. Front Immunol 9:2552
Kalayjian, Robert C; Albert, Jeffrey M; Cremers, Serge et al. (2018) Women have enhanced bone loss associated with phosphaturia and CD4+ cell restoration during initial antiretroviral therapy. AIDS 32:2517-2524
AIDS-defining Cancer Project Working Group of IeDEA, COHERE in EuroCoord (2018) Non-Hodgkin lymphoma risk in adults living with HIV across five continents. AIDS 32:2777-2786

Showing the most recent 10 out of 539 publications