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Functionally Active HIV-Specific T Cells that Target Gag and Nef Can Be Expanded from Virus-Naïve Donors and Target a Range of Viral Epitopes: Implications for a Cure Strategy after Allogeneic Hematopoietic Stem Cell Transplantation.
Patel, Shabnum; Lam, Sharon; Cruz, Conrad Russell; Wright, Kaylor; Cochran, Christina; Ambinder, Richard F; Bollard, Catherine M.
Afiliação
  • Patel S; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and Center for Cancer and Immunology Research, Children's National Health System, Washington, DC; Department of Microbiology, Immunology, and Tropical Medicine, Institute for Bi
  • Lam S; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and Center for Cancer and Immunology Research, Children's National Health System, Washington, DC.
  • Cruz CR; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and Center for Cancer and Immunology Research, Children's National Health System, Washington, DC.
  • Wright K; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and Center for Cancer and Immunology Research, Children's National Health System, Washington, DC.
  • Cochran C; Department of Microbiology, Immunology, and Tropical Medicine, Institute for Biomedical Sciences, George Washington University, Washington, DC.
  • Ambinder RF; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Bollard CM; Program for Cell Enhancement and Technologies for Immunotherapy, Sheikh Zayed Institute for Pediatric Surgical Innovation, and Center for Cancer and Immunology Research, Children's National Health System, Washington, DC. Electronic address: cbollard@cnmc.org.
Biol Blood Marrow Transplant ; 22(3): 536-41, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26721209
ABSTRACT
Allogeneic hematopoietic stem cell transplantation (HSCT) can potentially cure human immunodeficiency virus (HIV) by eliminating infected recipient cells, particularly in the context of technologies that may confer HIV resistance to these stem cells. But, to date, the Berlin patient remains the only case of HIV cure despite multiple attempts to eradicate infection with HSCT. One approach to improve this is to administer virus-specific T cells, a strategy that has proven success in preventing other infections after transplantation. Although we have reported that broadly HIV-specific T cells can be expanded from HIV+ patients, allogeneic transplantations only contain virus-naïve T cells. Modifying this approach for the allogeneic setting requires a robust, reproducible platform that can expand HIV-specific cells from the naïve pool. Hence, we hypothesized that HIV-specific T cells could be primed ex vivo from seronegative individuals to effectively target HIV. Here, we show that ex vivo-primed and expanded HIV-specific T cells released IFNγ in response to HIV antigens and that these cells have enhanced ability to suppress replication in vitro. This is the first demonstration of ex vivo priming and expansion of functional, multi-HIV antigen-specific T cells from HIV-negative donors, which has implications for use of allogeneic HSCT as a functional HIV cure.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: HIV-1 / Transfusão de Linfócitos / Transplante de Células-Tronco Hematopoéticas / Epitopos de Linfócito T / Produtos do Gene gag do Vírus da Imunodeficiência Humana / Produtos do Gene nef do Vírus da Imunodeficiência Humana / Antígenos Virais Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: HIV-1 / Transfusão de Linfócitos / Transplante de Células-Tronco Hematopoéticas / Epitopos de Linfócito T / Produtos do Gene gag do Vírus da Imunodeficiência Humana / Produtos do Gene nef do Vírus da Imunodeficiência Humana / Antígenos Virais Idioma: En Ano de publicação: 2016 Tipo de documento: Article