HIV Vaccines. Join Keystone Symposia for the 2016 conference on: March 20 24, 2016 Resort at Squaw Creek Olympic Valley, California USA

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Join Keystone Symposia for the 2016 conference on: HIV Vaccines March 20 24, 2016 Resort at Squaw Creek Olympic Valley, California Scientific Organizers: David C. Montefiori and Mario Roederer Joint with the conference on: HIV Persistence Pathogenesis and Eradication Evidence from multiple passive transfer experiments in non-human primates, as well as from studies of immunologic correlates of modest efficacy in the RV144 Thai trial, support the notion that both neutralizing and non-neutralizing antibodies have potential to prevent infection. Major advances have been made in understanding the epitopes, structures and evolutionary pathways of broadly neutralizing antibodies, leading to new avenues to pursue for vaccine design. The extraordinary breadth and potency of some recently discovered neutralizing antibodies has generated additional interest in potential therapeutic applications, including cure strategies. There has also been a steady increase in knowledge of other types of antiviral antibodies and their effector functions that may be important for vaccines. This meeting aims to cover a range of topics including: 1) Initial virus transmission events for vaccine intervention, 2) Non-neutralizing antibody correlates of sterilizing immunity; 3) Epitopes, structures and ontogeny of broadly neutralizing antibodies; 4) Novel vaccine concepts for broadly neutralizing antibody induction; and 5) Immunotherapy. Emphasis will be placed on recent unpublished findings in key areas that hold the greatest promise for rapid progress toward an effective vaccine. Session Topics: Acute HIV Infection and Initial Transmission Events (Joint) Immunologic Correlates of Sterilizing Immunity Epitopes, Structures and Ontogeny of Broadly Neutralizing Antibodies Vaccine Concepts I & II Pathways Leading to Long-Term Protective Immunity Against HIV-1 Immunotherapy (Joint) Bridging Innate and Acquired Immunity Submitting an abstract is a great way of participating in the conference through poster presentation and possible selection for a short talk. Scholarship & Discounted Abstract Deadline: Nov 19, 2015 Abstract Deadline: Dec 17, 2015 Discounted Registration Deadline: Jan 21, 2016 For additional details, visit www.keystonesymposia.org/16x8. www.keystonesymposia.org/meetings 1.800.253.0685 1.970.262.1230 a 501(c)(3) nonprofit educational organization

Part of the Keystone Symposia Global March 20-24, 2016 Resort at Squaw Creek Olympic Valley, California, SUNDAY, MARCH 20 Arrival and Registration MONDAY, MARCH 21 Welcome and Keynote Address (Joint) *David M. Margolis, University of North Carolina at Chapel Hill, *Carl W. Dieffenbach, NIAID, National Institutes of Health, Anthony S. Fauci, NIAID, National Institutes of Health, Recorded Presentation: Ending the HIV/AIDS Pandemic: Follow the Science Acute HIV Infection and Initial Transmission Events (Joint) *Nilu Goonetilleke, University of North Carolina at Chapel Hill, George M. Shaw, University of Pennsylvania, Novel SHIV Design to Recapitulate HIV-1 Transmission, Persistence and Pathogenesis and as a Guide for Vaccine and Cure Research Joseph Eron, University of North Carolina School of Medicine, Acute HIV Infection: Antiretroviral Therapy and Persistence Giuseppe Pantaleo, Centre Hospitalier Universitaire Vaudois, Switzerland Novel Therapeutic Interventions in the Targeting of the HIV Cell Reservoir Zachary S. Ende, Emory University, Short Talk: Heterosexual Transmission of Subtype C HIV-1 Does Not Require Increased Replicative Capacity or Interferon Resistance Shilpa Iyer, University of Pennsylvania, Short Talk: Mucosal Transmission of HIV-1 Selects for Variants with Enhanced Infectivity, Replication Fitness and Interferon Resistance DAIDS Programmatic Agendas, Recent Review Policy Updates, and Grantsmanship Advice (Joint) Workshop 1: Requirements for bnab Induction (X8) *Pamela J. Bjorkman, California Institute of Technology, Matthew D. Gray, Fred Hutchinson Cancer Research Center, Self-assembling HIV Envelope Nanoparticles Increase Antibody Binding, Membrane Dynamics and B-cell Activation Christina Guzzo, NIAID, National Institutes of Health, Critical Role of V2 Sulfotyrosines in Stabilizing the HIV-1 Envelope Trimer in Its Closed, Antibody-Protected Conformation Colin Havenar-Daughton, La Jolla Institute of Allergy and Immunology, Virtual Immunization with eod-gt8: Probing the Human Naive B Cell Repertoire to a Candidate HIV Vaccine Immunogen Cassandra Simonich, Fred Hutchinson Cancer Research Center, An Infant bnab with Low Somatic Hypermutation Contributes to Polyclonal Breadth Lorena S. Ver, IAVI, International Aids Vaccine Initiative, Characterization of Neutralizing Antibody Responses to the N332 Site of Vulnerability on HIV Env in IAVI Protocol C Cohort Amelia Escolano, Rockefeller University, Sequential Immunization Strategies to Elicit HIV-1 bnabs in Human Ig Knock-in Mice Daniela Fera, Boston Children's Hospital, Harvard Medical School, Structural Analysis of an HIV-1 Broadly Neutralizing B-Cell Lineage Targeting the Env N332 Glycan Immunologic Correlates of Sterilizing Immunity (X8) *Mark Connors, NIAID, National Institutes of Health, Merlin L. Robb, Walter Reed Army Institute of Research, Optimizing Quality and Durability of Immune Responses: Insights from RV 144 Follow-up Studies Genoveffa Franchini, NCI, National Institutes of Health, Activated RAS in PBMCs and Extracellular Vesicle, Mucosal Envelope Antibody to V2, and Innate Lymphoid Cells are Associated with Vaccine-Mediated Reduced Risk of SIVmac251 Acquisition Georgia D. Tomaras, Duke University Medical Center, HIV-1 Vaccine Humoral Immunity, Immune Correlates and Mechanistic Insights Genevieve Fouda, Duke University Medical Center, Short Talk: HIV Exposed Infants Vaccinated with a rgp120/mf59 Vaccine have Higher Magnitude anti-v1v2 IgG Responses than Adults Immunized with the Same Vaccine Thomas Musich, DHHS, National Institutes of Health, Short Talk: Vaccine-Induced Effects on Neutrophils in Rhesus Macaques Mechanisms of Persistent Infection (X7) *Steven G. Deeks, University of California, San Francisco, Jonathan Karn, Case Western Reserve University, Epigenetic Control of HIV Latency Melanie M. Ott, University of California, San Francisco, Epigenetic Regulation of HIV Latency Susana T. Valente, Scripps Florida, Eradication without Reactivation Andrew P. Rice, Baylor College of Medicine, Regulation of P-TEFb and HIV Latency Poster Session 1 TUESDAY, MARCH 22

Part of the Keystone Symposia Global March 20-24, 2016 Resort at Squaw Creek Olympic Valley, California, Epitopes, Structures and Ontogeny of Broadly Neutralizing Antibodies (X8) *Rogier W. Sanders, Weill Medical College of Cornell University, Pamela J. Bjorkman, California Institute of Technology, Structure-Based Design of Improved Antibodies Against HIV Sasha Murrell, The Scripps Research Institute, Short Talk: Crystal Structures of Two Related Broadly Neutralizing Antibodies against the N332 Supersite in HIV Env Marit van Gils, University of Amsterdam, Netherlands Short Talk: Broadly Neutralizing Antibodies from an Elite Neutralizer Target a Novel Site at the gp120-gp41 Interface Dennis R. Burton, The Scripps Research Institute, Broadly Neutralizing Antibodies to Guide HIV Vaccine Design Jinal Nomathemba Bhiman, The Scripps Research Institute, Viral Variants that Initiate and Drive Maturation of Broadly Neutralizing Antibodies William Schief, IAVI and The Scripps Research Institute, Epitope-Focused HIV Vaccine Design Christina Yacoob, Fred Hutchinson Cancer Research Center, Short Talk: Selective Allelic Expansion of HIV-1 Immunized Rhesus Macaques Based on Different Antigenic Properties of Env Immunogens Reservoirs and Persistence I (X7) *Susana T. Valente, Scripps Florida, Janice E. Clements, Johns Hopkins University, Tissue Reservoirs of CD4+T Cells and Macrophages in ART Suppressed SIV-Infected Macaques Satya Dandekar, University of California, Davis, Early Establishment of HIV Reservoirs John M. Coffin, Tufts University, Mechanism of HIV Persistence despite Suppressive Antiretroviral Therapy J. Victor Garcia-Martinez, University of North Carolina at Chapel Hill, In vivo Analysis of HIV Persistence Sara Ferrando-Martinez, NIAID, National Institutes of Health, Short Talk: Immune Activation Drives Accumulation of Follicular CTL during Chronic HIV/SIV Infection Binhua Ling, Tulane National Primate Research Center, Short Talk: Gut Viral Reservoirs in SIV-Infected Long-Term Nonprogressing Chinese Rhesus Macaques on Antiretroviral Therapy Hands-On Computer Session on Los Alamos Sequence Database (X8) Workshop 1: Challenges of Persistent HIV Infection (X7) *Romas Geleziunas, Gilead Sciences, Inc., Kirston M. Barton, University of Sydney, Australia HIV-1 in the Blood and Intestine Contribute to Viremia During Treatment Interruption Ya-Chi Ho, Yale School of Medicine, Activation of Novel Splice Donor Sites Allows Production of tat and rev Transcripts in Defective Patient-Derived HIV-1 Proviruses Lillian B. Cohn, Rockefeller University, HIV DNA Integration Site Selection in Productive Infection Allison Thomas, George Washington University, After Long-Term ART, T-cell Responses Targeting Early HIV Proteins Uniquely Correlate with Infected Cell Frequencies Luca Micci, Emory University, YNPRC, Determinants of Viral Control following ART-interruption in SIV-infected Rhesus Macaques James L. Riley, University of Pennsylvania, Engineering Chimeric Antigen Receptors for Durable Control over HIV-1 Replication Maud Mavigner, Emory University, Reducing HIV Persistence by Targeting Stem Cell Properties of Memory CD4+ T-cells Angela Wahl, University of North Carolina at Chapel Hill, CD4+ Tissue-Resident Memory T Cells are an Important Reservoir for HIV Persistence Vaccine Concepts I (X8) David C. Montefiori, Duke University Medical Center, Standardized Assessments of HIV Vaccine-Elicited Neutralizing Antibodies *Mario Roederer, NIAID, National Institutes of Health, The SIV Model to Evaluate Antibody-Based Intervention Bette Tina Marie Korber, Los Alamos National Laboratory, Using Neutralization Resistance/Sensitivity Signatures to Inform Vaccine Design Javier Guenaga, IAVI Neutralizing Antibody Center at TSRI, Short Talk: Display of the HIV-1 Env MPER in the Context of a Well-ordered Soluble Uncleaved (NFL) Trimer James Mark Binley, San Diego Biomedical Research Institute, Short Talk: Eliciting Tier 2 anti-hiv-1 NAbs using Native, Membrane Trimers Auxillary Genes and Host Restriction Factors (X7) *J. Victor Garcia-Martinez, University of North Carolina at Chapel Hill, Alan N. Engelman, Dana-Farber Cancer Institute, CPSF6 Regulates HIV-1 Integration into Active Chromatin

Part of the Keystone Symposia Global March 20-24, 2016 Resort at Squaw Creek Olympic Valley, California, Stephen P. Goff, Columbia University, Retroviral Silencing: Transcriptional and Post-Transcriptional Regulation Michael Emerman, Fred Hutchinson Cancer Research Center, Evolution of Host Antiviral Restriction Factors Richard Apps, NCI, National institutes of Health, Short Talk: HIV-1 Immune Evasion by Downregulation of HLA-C Poster Session 2 WEDNESDAY, MARCH 23 Pathways Leading to Long-Term Protective Immunity Against HIV-1 (X8) *Jay A. Berzofsky, NCI, National Institutes of Health, Bali Pulendran, Stanford University School of Medicine, Signaling Mechanisms W. Ripley Ballou, GlaxoSmithKline Vaccines, Inducing Long-Term Protection with Vaccines Richard A. Koup, NIAID, National Institutes of Health, T Cell Help Maria Blasi, Duke University Medical Center, Use of Integrase Defective Lentiviral Vectors Expressing HIV-Envs to Induce Durable Immune Responses Jinghe Huang, NIAID, National Institutes of Health, Short Talk: Intranasal Replication Competent Adenovirus Type 4-Influenza-H5 (Ad4-H5-Vtn) Vaccine Induces Durable Neutralizing Antibody Responses in Humans Konstantin Virnik, Food and Drug Administration, Short Talk: Expression of HIV and SIV Env Proteins in a Highly Immunogenic Rubella Vaccine Platform Antiviral Host Response and Inflammation (X7) *Satya Dandekar, University of California, Davis, Nicolas Chomont, Université de Montréal, Canada Immune Checkpoint Molecules and HIV Persistence during ART Alberto Bosque, George Washington University, Short Talk: Targeting Pathogen Recognition Receptors to Reactivate Latent HIV-1 Ivona Pandrea, University of Pittsburgh, Nonhuman Primate Studies with Relevance for Cure Research David Favre, GlaxoSmithKline, Immune Modulation as a Strategy to Clear Persistent Infection Heinrich Gottlinger, University of Massachusetts Medical School, Short Talk: SERINC3 and SERINC5 Synergistically Inhibit HIV-1 Infectivity and are Antagonized by Nef Catherine A. Blish, Stanford University School of Medicine, Short Talk: NK Cell Response Hands-On Computer Session on Los Alamos Immunology Database (X8) Workshop 2: New Technologies and Approaches (X7) *Karl Salzwedel, NIAID, National Institutes of Health, Collin Kieffer, California Institute of Technology, Longitudinal Imaging of Early HIV infection in Humanized Mice with Parallel 3D Immunofluorescence and Electron Microscopy Bonnie J. Howell, Merck, Ultrasensitive Detection of Viral p24 following Reactivation of Latent HIV Tram N.Q. Pham, Institut de Recherches Cliniques de Montreal, Canada Enhancing Tethering of HIV Virions by BST2/Tetherin Augments the Susceptibility of Productively and Latently Infected T Cells to ADCC Mediated by Broadly Neutralizing Anti-HIV Antibodies Yik Lim Kok, University Hospital Zurich, Switzerland A Novel HIV-1-Based Vector that Reproduces Features of Productive and Latent HIV-1 Infections Julia Sung, University of North Carolina, HIV specific Ex vivo Expanded T Cell (HXTC) Therapy to Target the Latent Reservoir Kenneth M. Law, Icahn School of Medicine at Mount Sinai, Cell-to-cell HIV-1 Transmission Promotes Multicopy Micro-Compartmentalized Infection in Humanized Mice Lydie Trautmann, US Military HIV Research Program, Differentiation of Effector CD8 T Cells Toward Short Lived Cells Lacking Memory Potential During Acute HIV Infection Sarah DiNapoli, NIAID, National Institutes of Health, Lymphoid Tissue-Resident Myeloid Cells Contain Replication-Competent Virus that is Genetically Similar to Virus from CD4+ T Cells in ARV-Naïve Asian Macaques Vaccine Concepts II (X8) *Bette Tina Marie Korber, Los Alamos National Laboratory, John P. Moore, Weill Medical College of Cornell University, How to Make and Use Multiple Native-Like SOSIP Trimers for Vaccine and Structural Studies Barton F. Haynes, Duke University Medical Center, B Cell Lineage Immunogen Design Approach to Elicit HIV Broadly Neutralizing Antibodies Peter D. Kwong, NIAID, National Institutes of Health, Structure-Based Immunogen Design Marzena Pazgier, Institute of Human Virology, Short Talk: Paring down HIV-1 Env: Design and Structure of an Independent Inner Domain of gp120 Stably Expressing the A32 ADCC Epitope Sub-region

Part of the Keystone Symposia Global March 20-24, 2016 Resort at Squaw Creek Olympic Valley, California, Talar Tokatlian, Massachusetts Institute of Technology, Short Talk: Design and Characterization of gp140 Envelope Trimer-Coupled Liposomes for an HIV Vaccine Cure Studies in Models and Man (X7) *Carl W. Dieffenbach, NIAID, National Institutes of Health, Daria J. Hazuda, Merck Research Laboratories, HIV Latency Drug Discovery: Optimizing Drugs to Induce Latent HIV Expression John W. Mellors, University of Pittsburgh School of Medicine, Biomarkers of HIV Persistence and Response to Therapeutic Interventions Jerome A. Zack, University of California, Los Angeles, Synthetic PKC Modulators as HIV Latency Reversing Agents Lucy Dorrell, University of Oxford, UK Short Talk: Elimination of HIV-1 Reservoir Cells from Antiretroviral Therapy-Suppressed Subjects by Engineered Immune-Mobilising Dual Affinity T cell Receptors Poster Session 3 THURSDAY, MARCH 24 Keynote Address (Joint) *David C. Montefiori, Duke University Medical Center, John R. Mascola, NIAID, National Institutes of Health, Active and Passive Antibody-Based Immunity to HIV-1 Immunotherapy (Joint) *Michael Seaman, Beth Israel Deaconess Medical Center-Harvard Medical School, David D. Ho, Aaron Diamond AIDS Research Center, Bispecific Antibodies Michael Farzan, The Scripps Research Institute, AAV-Expressed ecd4-ig as an Alternative HIV-1 Vaccine David M. Margolis, University of North Carolina at Chapel Hill, Enlisting Effector Cells to Clear Latent HIV Infection Louis J. Picker, Oregon Health & Science University, CMV-Based HIV Vaccines for HIV Prevention and Clearance Poster Session 4 Workshop 2: NHP Models for *Diane L. Bolton, US Military HIV Research Program, WRAIR, Nina Rafterman Derby, Population Council, HSV-2 Infection Increases Rectal SIV?Nef Infection and May Reduce Vaccine Effect Shelby O'Connor, University of Wisconson-Madison, Tracking SIV Infection and Viral Evolution in vivo using a Barcoded Virus Stock Hadia Mohammad Abdelaal, University of Minnesota, CTL-Based Vaccine-Induced Protection is Associated with Induction of High Follicular to Extra-Follicular Ratios of Virus-Specific CD8 T Cells Namal Liyanage, Ohio State University, College of Medicine, Recruitment of Vaccine Induced MMucosal IL17+NKp44+Innate Lymphoid Cells (ILCs) to Decrease the Risk of SIVmac251 Acquisition in Macaques M. Anthony Moody, Duke University Medical Center, Vaccine-Induced Anatomic Distribution of Env-Specific B Cell Repertoires: Implications for the Genesis of Induced Mucosal Antibodies in Rhesus Macaques George M. Shaw, University of Pennsylvania, Jay A. Berzofsky, NCI, National Institutes of Health, Immune Activation and the Microbiome in Mucosal Transmission of SHIV Donald Forthal, University of California, Irvine, Non-Neutralizing Antibodies Reduce the Rate of SIVmac251 Infection Following Low-Dose Repeated Penile Challenge Bridging Innate and Acquired Immunity (X8) *Nicole Frahm, Fred Hutchinson Cancer Research Center, Stylianos Bournazos, Rockefeller University, Optimizing Antibody-FcR Interactions Margaret Ellen Ackerman, Dartmouth College, Profiling Protective Antibody Responses George K. Lewis, University of Maryland, Qualitative and Quantitative Variables that Contribute to Fc-mediated Protection Against HIV-1 Reservoirs and Persistence II (X7) *Douglas D. Richman, University of California, San Diego, Sarah E. Palmer, University of Sydney, Australia Characterizing the HIV-1 Reservoir During Long-Term Therapy Vicente Planelles, University of Utah, Novel Classes of HIV Latency-Reversing Agents Nancie M. Archin, University of North Carolina, Chapel Hill, Updates on in vivo Administration of Vorinostat Meeting Wrap-Up: Outcomes and Future Directions (Organizers) (X8) Meeting Wrap-Up: Outcomes and Future Directions (Organizers) (X7) FRIDAY, MARCH 25 Departure