? Immunology Core (Basic Science Core) The overall goal of the Immunology Core is to provide Duke HIV/AIDS scientists, clinicians, collaborators, and trainees access to an innovative, state-of-the-art, and standardized repertoire of immunologic assays that can comprehensively and deeply interrogate the immunologic space in response to HIV-1 infection, vaccination, co-infections, and cure strategies. The Immunology Core will continue to address gaps in the field. Three key examples of accomplishments to date are the following: 1) Provided implementation and training of standardized neutralization, binding, and cellular assays to national and international laboratories, such that diverse studies across multiple laboratories can now be directly and rigorously compared for advancing the science to the next phase. 2) Fostered innovation of new assay development and analysis for multiple simultaneous measurements, significantly advancing the depth and breadth of immunological information (i.e. global virus panels for neutralization breadth, immune monitoring assays for TB, flu, malaria, and typhoid, PK and functional ADA assays for broadly neutralizing antibodies, comprehensive array of Fc effector function assays, Env characterization on infected cells, novel analytical algorithms, and training for flow cytometric analyses (such as FLowPET) to integrate complex immunological data and multiplex binding breadth assays. 3) Provided scientific training and mentoring to Duke young investigators, resulting in R01 and P01 awards, high-impact publications, and career development opportunities. 4) Implemented a recharge system to provide services to the CFAR community. Thus, the Immunology Core investigators have a strong history together and are uniquely poised to tackle newly emerging gaps in the field of HIV-1 immunology. The Duke CFAR?s priority areas for innovative research at Duke are supported by the science and technology offered by the Immunology Core: 1) the ?Southern HIV Epidemic?, 2) HIV Co-Morbidities and Co-Infections, 3) Latency and Eradication, 4) Health Disparities, 5) Vaccine Design and Evaluation, 6) Mental Health and Substance Abuse, 7) the HIV Organ Policy Equity (HOPE) Act, and 8) Emerging Infections. The Immunology Core?s assay platform and commitment to innovation is ideally suited for support of the Duke CFAR priority areas and Specific Aims, as well as broadly covering the current and emerging needs of the Duke CFAR community of scientists and clinicians. As part of the overall Duke CFAR Aims, the Core will provide advanced assays and technologies to CFAR investigators, provide support and training for early stage investigators, and support NIH initiatives (PAVEG, HVTN, IMPAACT, HPTN, CHAVI-ID/CHAVD, MIG, CURE, EQAPOL) and collaborative partnerships with other CFARs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
2P30AI064518-16
Application #
9991042
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
16
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Watt, Melissa H; Cichowitz, Cody; Kisigo, Godfrey et al. (2018) Predictors of postpartum HIV care engagement for women enrolled in prevention of mother-to-child transmission (PMTCT) programs in Tanzania. AIDS Care :1-12
Itell, Hannah L; McGuire, Erin P; Muresan, Petronella et al. (2018) Development and application of a multiplex assay for the simultaneous measurement of antibody responses elicited by common childhood vaccines. Vaccine 36:5600-5608
Wiehe, Kevin; Bradley, Todd; Meyerhoff, R Ryan et al. (2018) Functional Relevance of Improbable Antibody Mutations for HIV Broadly Neutralizing Antibody Development. Cell Host Microbe 23:759-765.e6
McGuire, Erin P; Fong, Youyi; Toote, Christopher et al. (2018) HIV-Exposed Infants Vaccinated with an MF59/Recombinant gp120 Vaccine Have Higher-Magnitude Anti-V1V2 IgG Responses than Adults Immunized with the Same Vaccine. J Virol 92:
Skalski, Linda M; Towe, Sheri L; Sikkema, Kathleen J et al. (2018) Memory Impairment in HIV-Infected Individuals with Early and Late Initiation of Regular Marijuana Use. AIDS Behav 22:1596-1605
Mitchell, John T; LeGrand, Sara; Hightow-Weidman, Lisa B et al. (2018) Smartphone-Based Contingency Management Intervention to Improve Pre-Exposure Prophylaxis Adherence: Pilot Trial. JMIR Mhealth Uhealth 6:e10456
Okeke, Nwora Lance; Alenezi, Fawaz; Bloomfield, Gerald S et al. (2018) Determinants of Left Ventricular Hypertrophy and Diastolic Dysfunction in an HIV Clinical Cohort. J Card Fail 24:496-503
Clement, Meredith E; Seidelman, Jessica; Wu, Jiewei et al. (2018) An educational initiative in response to identified PrEP prescribing needs among PCPs in the Southern U.S. AIDS Care 30:650-655
Price, Alexander M; Messinger, Joshua E; Luftig, Micah A (2018) c-Myc Represses Transcription of Epstein-Barr Virus Latent Membrane Protein 1 Early after Primary B Cell Infection. J Virol 92:
Knettel, Brandon A; Cichowitz, Cody; Ngocho, James Samwel et al. (2018) Retention in HIV Care During Pregnancy and the Postpartum Period in the Option B+ Era: Systematic Review and Meta-Analysis of Studies in Africa. J Acquir Immune Defic Syndr 77:427-438

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