Infection with HIV leads to widespread immunosuppression as well as immune activation. Among the sequelae of HIV infection are disorders of the central nervous system, known as neuroAIDS. Studies on the pathogenesis and therapy of neuroAIDS could be greatly enhanced by the availability of appropriate immunological assays, many of which are not readily available within most laboratories. The Immunological Assay Core will be active in implementing the objectives of the Center, which are to further the understanding, mechanisms, prevention, and treatment for the neurological effects of HIV. The overall goal of the Immunological Assay Core is to perform the highest quality immunologically-based assays for SNAPS investigators with the Center. The core will provide technical expertise, advise, perform assays, and make available state of the art technology to the center investigators. The activities to be performed by the core include T cell proliferation, cytotoxicity, leukocyte purification, cytokine and chemokine detection, T cell hybridoma production, flow cytometry, tetramer production/usage, and BIAcore measurements. Trained personnel within the core will perform these techniques for center investigators. The Core will participate in all SNAPS activities, demonstrate excellence in laboratory quality assurance, and maintain a high standard of performance. Additionally, the core will provide technical advice and training in the appropriate use and critical assessment of these methodologies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Center Core Grants (P30)
Project #
5P30MH062261-02
Application #
6504177
Study Section
Special Emphasis Panel (ZMH1)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Sil, Susmita; Niu, Fang; Tom, Eric et al. (2018) Cocaine Mediated Neuroinflammation: Role of Dysregulated Autophagy in Pericytes. Mol Neurobiol :
Olson, Katherine E; Bade, Aditya N; Namminga, Krista L et al. (2018) Persistent EcoHIV infection induces nigral degeneration in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated mice. J Neurovirol 24:398-410
Hu, Guoku; Liao, Ke; Niu, Fang et al. (2018) Astrocyte EV-Induced lincRNA-Cox2 Regulates Microglial Phagocytosis: Implications for Morphine-Mediated Neurodegeneration. Mol Ther Nucleic Acids 13:450-463
Schutt, Charles R; Gendelman, Howard E; Mosley, R Lee (2018) Tolerogenic bone marrow-derived dendritic cells induce neuroprotective regulatory T cells in a model of Parkinson's disease. Mol Neurodegener 13:26
Sillman, Brady; Bade, Aditya N; Dash, Prasanta K et al. (2018) Creation of a long-acting nanoformulated dolutegravir. Nat Commun 9:443
Domingo-Almenara, Xavier; Montenegro-Burke, J Rafael; Benton, H Paul et al. (2018) Annotation: A Computational Solution for Streamlining Metabolomics Analysis. Anal Chem 90:480-489
Thomas, Midhun B; Gnanadhas, Divya Prakash; Dash, Prasanta K et al. (2018) Modulating cellular autophagy for controlled antiretroviral drug release. Nanomedicine (Lond) 13:2139-2154
Spooner, Rachel K; Wiesman, Alex I; Mills, Mackenzie S et al. (2018) Aberrant oscillatory dynamics during somatosensory processing in HIV-infected adults. Neuroimage Clin 20:85-91
Kiyota, Tomomi; Machhi, Jatin; Lu, Yaman et al. (2018) URMC-099 facilitates amyloid-? clearance in a murine model of Alzheimer's disease. J Neuroinflammation 15:137
Guijas, Carlos; Montenegro-Burke, J Rafael; Warth, Benedikt et al. (2018) Metabolomics activity screening for identifying metabolites that modulate phenotype. Nat Biotechnol 36:316-320

Showing the most recent 10 out of 374 publications