Under the direction of Dr. John D. Altman, the mission of Core H, the Emory CFAR Immunology CoreLaboratory (ICL), is to provide the Emory community with the highest quality assessments of immunologicalfunction necessary for the study of the pathogenesis, treatment, and prevention of immunodeficiency virusinfections in humans and non-human primates. The ICL will achieve this mission through the followingSpecific Aims:1. Develop and perform optimized, standardized, and validated assays of cellular immune function invaccinated subjects, in HIV-infected humans, and in SIV-infected non-human primates (NHP);2. Create a repository of cryopreserved PBMC from naive (off-study) monkeys from the YerkesPrimate Research Center, thereby providing CFAR investigators with access to esse'ntial negative controlsamples for assay development and validation.3. Achieve economies of scale through the provision of immunological reagent resources shared bymultiple independent laboratories;4. Maintain a CFAR Flow Cytometry Core, for the purpose of providing members of the Emory CFAR, andthe larger AIDS research community, with the highest quality flow cytometry data and cell sortingservices available, including handling of biohazardous samples;5. Promote immunological assay education and training opportunities for CFAR investigators, theAIDS research community in Atlanta, and national and international AIDS investigators.Through these Aims, the ICL will enable all Emory CFAR investigators to take advantage of innovative andpowerful modern approaches to quantitative analysis of innate and acquired humoral and cell-mediatedimmunity that have been developed by individual Emory investigators and scientists elsewhere. Accuratecharacterization of cell-mediated immune responses is essential for guiding preclinical vaccine development,for determining possible correlates of vaccine efficacy in preclinical and clinical trials, and for betterunderstanding AIDS pathogenesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI050409-10
Application #
7667903
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2008-08-01
Project End
2012-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
10
Fiscal Year
2008
Total Cost
$380,685
Indirect Cost
Name
Emory University
Department
Type
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Dillard, Rebecca S; Hampton, Cheri M; Strauss, Joshua D et al. (2018) Biological Applications at the Cutting Edge of Cryo-Electron Microscopy. Microsc Microanal 24:406-419
Haas, David W; Bradford, Yuki; Verma, Anurag et al. (2018) Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events. Pharmacogenet Genomics 28:179-187
Ke, Zunlong; Dillard, Rebecca S; Chirkova, Tatiana et al. (2018) The Morphology and Assembly of Respiratory Syncytial Virus Revealed by Cryo-Electron Tomography. Viruses 10:
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Serota, David P; Rosenberg, Eli S; Lockard, Annie M et al. (2018) Beyond the Biomedical: Preexposure Prophylaxis Failures in a Cohort of Young Black Men Who Have Sex With Men in Atlanta, Georgia. Clin Infect Dis 67:965-970
Hightow-Weidman, Lisa B; Muessig, Kathryn; Rosenberg, Eli et al. (2018) University of North Carolina/Emory Center for Innovative Technology (iTech) for Addressing the HIV Epidemic Among Adolescents and Young Adults in the United States: Protocol and Rationale for Center Development. JMIR Res Protoc 7:e10365
Reyes-Robles, Tamara; Dillard, Rebecca S; Cairns, Lynne S et al. (2018) Vibrio cholerae outer membrane vesicles inhibit bacteriophage infection. J Bacteriol :

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