HIV Envelope gp120-induced immunosuppression

HIV包膜gp120诱导的免疫抑制

• 批准号: 8321780
• 负责人: Catarina E Hioe
• 金额: $ 42.25万
• 依托单位: NEW YORK UNIVERSITY SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-01 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8321780
• 关键词: Address; Adenoviruses; Adhesions; Affect; Antibody Formation; Antigen-Presenting Cells; Antigens; Apoptosis; Binding; CD3 Antigens; CD4 Positive T Lymphocytes; Cell Communication; Cell physiology; Cells; Characteristics; Collaborations; Cytotoxic T-Lymphocytes; DNA; DNA Sequence Rearrangement; DNA Viruses; Data; Development; Disease; Elements; Epidemic; Event; Fluorescence Microscopy; Glass; Goals; HIV; HIV Antibodies; HIV Envelope Protein gp120; HIV Infections; HIV vaccine; HIV-1; Helper-Inducer T-Lymphocyte; Hour; Image; Immune; Immune response; Immunosuppression; Immunosuppressive Agents; Induction of Apoptosis; Institutes; Intercellular adhesion molecule 1; Intercept; Letters; Ligands; Literature; MHC Interaction; Maintenance; Mediating; Membrane; Modeling; Molecular; Morphology; Natural Killer Cells; Pathway interactions; Pattern; Peptide/MHC Complex; Peripheral; Physiological; Preventive; Production; Reading; Regulatory T-Lymphocyte; Reporting; Resolution; Signal Transduction; Signaling Molecule; Surface; System; T cell differentiation; T cell response; T-Cell Activation; T-Cell Receptor; T-Lymphocyte; Testing; Therapeutic; Up-Regulation; Vaccines; Viral; Viral Tumor Antigens; Viral Vector; Virus; Virus Diseases; base; cell type; chemokine receptor; crosslink; cytokine; cytotoxicity; design; env Gene Products; immunological synapse; immunological synapse formation; innovative technologies; memory CD4 T lymphocyte; receptor; response; spatiotemporal; vaccinia virus vector; vector vaccine; virus envelope