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Comparable Antigenicity and Immunogenicity of Oligomeric Forms of a Novel, Acute HIV-1 Subtype C gp145 Envelope for Use in Preclinical and Clinical Vaccine Research.
Wieczorek, Lindsay; Krebs, Shelly J; Kalyanaraman, Vaniambadi; Whitney, Stephen; Tovanabutra, Sodsai; Moscoso, Carlos G; Sanders-Buell, Eric; Williams, Constance; Slike, Bonnie; Molnar, Sebastian; Dussupt, Vincent; Alam, S Munir; Chenine, Agnes-Laurence; Tong, Tina; Hill, Edgar L; Liao, Hua-Xin; Hoelscher, Michael; Maboko, Leonard; Zolla-Pazner, Susan; Haynes, Barton F; Pensiero, Michael; McCutchan, Francine; Malek-Salehi, Shawyon; Cheng, R Holland; Robb, Merlin L; VanCott, Thomas; Michael, Nelson L; Marovich, Mary A; Alving, Carl R; Matyas, Gary R; Rao, Mangala; Polonis, Victoria R.
Afiliação
  • Wieczorek L; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Krebs SJ; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Kalyanaraman V; Advanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
  • Whitney S; Advanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
  • Tovanabutra S; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Moscoso CG; University of California, Davis, California, USA.
  • Sanders-Buell E; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Williams C; New York University School of Medicine and Veterans Affairs Medical Center, New York, New York, USA.
  • Slike B; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Molnar S; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Dussupt V; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Alam SM; Duke University, Durham, North Carolina, USA.
  • Chenine AL; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Tong T; HJF-DAIDS, Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Hill EL; HJF-DAIDS, Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Liao HX; Duke University, Durham, North Carolina, USA.
  • Hoelscher M; Klinikum of the University of Munich, Department of Infectious Diseases and Tropical Medicine, Munich, Germany German Center for Infection Research (DZIF), Munich, Germany.
  • Maboko L; National Institute for Medical Research-Mbeya Medical Research Center, Mbeya, Tanzania.
  • Zolla-Pazner S; New York University School of Medicine and Veterans Affairs Medical Center, New York, New York, USA.
  • Haynes BF; Duke University, Durham, North Carolina, USA.
  • Pensiero M; Division of AIDS, NIH, Bethesda, Maryland, USA.
  • McCutchan F; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • Malek-Salehi S; University of California, Davis, California, USA.
  • Cheng RH; University of California, Davis, California, USA.
  • Robb ML; Military HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
  • VanCott T; Advanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
  • Michael NL; Military HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Marovich MA; Military HIV Research Program, Bethesda, Maryland, USA Division of AIDS, NIH, Bethesda, Maryland, USA.
  • Alving CR; Military HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Matyas GR; Military HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Rao M; Military HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Polonis VR; Military HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA vpolonis@hivresearch.org.
J Virol ; 89(15): 7478-93, 2015 Aug.
Article em En | MEDLINE | ID: mdl-25972551
ABSTRACT
UNLABELLED Eliciting broadly reactive functional antibodies remains a challenge in human immunodeficiency virus type 1 (HIV-1) vaccine development that is complicated by variations in envelope (Env) subtype and structure. The majority of new global HIV-1 infections are subtype C, and novel antigenic properties have been described for subtype C Env proteins. Thus, an HIV-1 subtype C Env protein (CO6980v0c22) from an infected person in the acute phase (Fiebig stage I/II) was developed as a research reagent and candidate immunogen. The gp145 envelope is a novel immunogen with a fully intact membrane-proximal external region (MPER), extended by a polylysine tail. Soluble gp145 was enriched for trimers that yielded the expected "fan blade" motifs when visualized by cryoelectron microscopy. CO6980v0c22 gp145 reacts with the 4E10, PG9, PG16, and VRC01 HIV-1 neutralizing monoclonal antibodies (MAbs), as well as the V1/V2-specific PGT121, 697, 2158, and 2297 MAbs. Different gp145 oligomers were tested for immunogenicity in rabbits, and purified dimers, trimers, and larger multimers elicited similar levels of cross-subtype binding and neutralizing antibodies to tier 1 and some tier 2 viruses. Immunized rabbit sera did not neutralize the highly resistant CO6980v0c22 pseudovirus but did inhibit the homologous infectious molecular clone in a peripheral blood mononuclear cell (PBMC) assay. This Env is currently in good manufacturing practice (GMP) production to be made available for use as a clinical research tool and further evaluation as a candidate vaccine. IMPORTANCE At present, the product pipeline for HIV vaccines is insufficient and is limited by inadequate capacity to produce large quantities of vaccine to standards required for human clinical trials. Such products are required to evaluate critical questions of vaccine formulation, route, dosing, and schedule, as well as to establish vaccine efficacy. The gp145 Env protein presented in this study forms physical trimers, binds to many of the well-characterized broad neutralizing MAbs that target conserved Env epitopes, and induce cross-subtype neutralizing antibodies as measured in both cell line and primary cell assays. This subtype C Env gp145 protein is currently undergoing good manufacturing practice production for use as a reagent for preclinical studies and for human clinical research. This product will serve as a reagent for comparative studies and may represent a next-generation candidate HIV immunogen.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Vacinas contra a AIDS / Produtos do Gene env do Vírus da Imunodeficiência Humana Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 / Vacinas contra a AIDS / Produtos do Gene env do Vírus da Imunodeficiência Humana Idioma: En Ano de publicação: 2015 Tipo de documento: Article