The Penn CFAR Clinical Core (Core C) forms the central nexus for clinical, translational and patient sample-based interdisciplinary HIV research conducted by CFAR investigators. Its supports and encourages innovative HIV science conducted in multiple programmatic areas through quick access to a broad range of epidemiologic data and clinical material from HIV infected individuals characterized in detail, identification of HIV infected individuals for recruitment into cross sectional or longitudinal studies, and by providing education, mentoring and overall leadership. To carry out this mission the Clinical Core (1) Maintains an Adult/Adolescent Database comprised of over 3000 patients cared for at four adult HIV practices and one adolescent (behaviorally infected) practice, and a Pediatric Database including longitudinal data on 275 perinatally infected children;(2) Maintains both Adult/Adolescent and Pediatric Specimen Repositories linked to the Databases, and supplies investigators with fresh patient material, including large volumes of cells collected by phlebotomy or apheresis, genital secretions, gastrointestinal lymph tissue, peripheral adipose tissue biopsies and cerebrospinal fluid;(3) Provides consultation in design and execution of clinical/translational studies, and laboratory technician assistance with processing, storage, and shipment of clinical specimens;(4) Provides mentorship to trainees and junior faculty and directs educational activities. These services have evolved over the current funding cycle in response to changing scientific needs, opportunities and research priorities identified through proactive strategic planning, user feedback, and input from internal and external expert advisors. In the coming funding cycle we will further enhance support to HIV/AIDS investigators to meet current needs as well as lead the research agenda based on national and CFAR scientific priorities: We have (a) worked with the City of Philadelphia to make Department of Health data available to investigators to study linkage to and retention in care;(b) developed a web based interface so that CFAR investigators can independently access and download data in the Adult/Adolescent Database, and (c) enhanced the availability of large volumes of high-value PBMCs through procurement of apheresis products. Finally, we will support the CFAR Scientific Working Groups focused on HIV/Hepatitis Co-Infection, HIV/Substance Use and Eradication and Functional Cure through expansion and coordination of services responsive to their scientific agendas.

Public Health Relevance

The Clinical Core of the Penn Center for AIDS Research supports interdisciplinary HIV science by offering investigators access to data on a large cohort of patients with HIV infection, and to patient samples, including blood and other body tissues. The Clinical Core also supports investigators through consultation services, use of the CFAR Clinical Laboratory, and education and mentoring activities

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
2P30AI045008-16
Application #
8697302
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
16
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Kelly, Matthew S; Surette, Michael G; Smieja, Marek et al. (2018) Pneumococcal Colonization and the Nasopharyngeal Microbiota of Children in Botswana. Pediatr Infect Dis J 37:1176-1183
Fraietta, Joseph A; Nobles, Christopher L; Sammons, Morgan A et al. (2018) Disruption of TET2 promotes the therapeutic efficacy of CD19-targeted T cells. Nature 558:307-312
Milligan, Michael G; Bigger, Elizabeth; Abramson, Jeremy S et al. (2018) Impact of HIV Infection on the Clinical Presentation and Survival of Non-Hodgkin Lymphoma: A Prospective Observational Study From Botswana. J Glob Oncol :1-11
Chitre, Avantika S; Kattah, Michael G; Rosli, Yenny Y et al. (2018) A20 upregulation during treated HIV disease is associated with intestinal epithelial cell recovery and function. PLoS Pathog 14:e1006806
Washio, Yukiko; Novack Wright, Elizabeth; Davis-Vogel, Annet et al. (2018) Prior Exposure to Intimate Partner Violence Associated With Less HIV Testing Among Young Women. J Interpers Violence :886260518768564
Medvec, Andrew R; Ecker, Christopher; Kong, Hong et al. (2018) Improved Expansion and In Vivo Function of Patient T Cells by a Serum-free Medium. Mol Ther Methods Clin Dev 8:65-74
Uzzan, Mathieu; Tokuyama, Minami; Rosenstein, Adam K et al. (2018) Anti-?4?7 therapy targets lymphoid aggregates in the gastrointestinal tract of HIV-1-infected individuals. Sci Transl Med 10:
Wendel, Ben S; Del Alcazar, Daniel; He, Chenfeng et al. (2018) The receptor repertoire and functional profile of follicular T cells in HIV-infected lymph nodes. Sci Immunol 3:
Loy, Dorothy E; Plenderleith, Lindsey J; Sundararaman, Sesh A et al. (2018) Evolutionary history of human Plasmodium vivax revealed by genome-wide analyses of related ape parasites. Proc Natl Acad Sci U S A 115:E8450-E8459
Vadrevu, Surya Kumari; Trbojevic-Akmacic, Irena; Kossenkov, Andrew V et al. (2018) Frontline Science: Plasma and immunoglobulin G galactosylation associate with HIV persistence during antiretroviral therapy. J Leukoc Biol 104:461-471

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