ANNUAL REPORT 2019 Unding Brave and Bold
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
18Th World Vaccine Congress Agenda: Day 1 – Tuesday 10Th October 2017
18th World Vaccine Congress Agenda: Day 1 – Tuesday 10th October 2017 Plenary Session ROOM: RUBI/ZAFIR 08:50 Chair’s opening remarks Dr Gregory Poland, Director, Mayo Clinic 09:00 Opening plenary discussion: Creating a new strategy - How does the current global outbreak response system need to change? Moderator: Dr Gregory Poland, Director, Mayo Clinic Speakers: Dr Marie-Paule Kieny, Former Assistant Director-General - Health Systems and Innovation, WHO Richard Hatchett, CEO, CEPI Prof Helen Rees, Chair and Executive Director, Wits Reproductive Health and HIV Institute 10:00 Maternal immunisation: Where do we stand and how do we use vaccines, antivirals and antibodies – What’s the strategy? Francesca Ceddia, VP, Head Global Medical Affairs Vaccines, GSK Vaccines 10:30 Break the ice with your peers and exchange business cards in the conference room 10:40 Morning Networking Break Therapeutic Vaccines Track Respiratory Vaccines Track ONE HEALTH with ROOM: RUBI ROOM: ZAFIR ROOM: ROSSINI 11:40 Chair’s opening remarks Chair’s opening remarks Chair’s opening remarks Dr Emmett V. Schmidt, Exec Director, Clinical Dr Gregory Poland, Director, Mayo Clinic Nathalie Garcon, CEO/CSO, BIOASTER Research, Merck Research Laboratories - Oncology Therapeutic & Immunotherapy Vaccines Influenza Vaccines Discovery and Drivers for Emerging Diseases 11:45 Why haven't Alzheimer's vaccines succeeded yet? Clinical development of a nasal inactivated influenza Bringing together experts in human and animal health Professor Nikolai Petrovsky, Flinders University vaccine -
EMBO Facts & Figures
excellence in life sciences Reykjavik Helsinki Oslo Stockholm Tallinn EMBO facts & figures & EMBO facts Copenhagen Dublin Amsterdam Berlin Warsaw London Brussels Prague Luxembourg Paris Vienna Bratislava Budapest Bern Ljubljana Zagreb Rome Madrid Ankara Lisbon Athens Jerusalem EMBO facts & figures HIGHLIGHTS CONTACT EMBO & EMBC EMBO Long-Term Fellowships Five Advanced Fellows are selected (page ). Long-Term and Short-Term Fellowships are awarded. The Fellows’ EMBO Young Investigators Meeting is held in Heidelberg in June . EMBO Installation Grants New EMBO Members & EMBO elects new members (page ), selects Young EMBO Women in Science Young Investigators Investigators (page ) and eight Installation Grantees Gerlind Wallon EMBO Scientific Publications (page ). Programme Manager Bernd Pulverer S Maria Leptin Deputy Director Head A EMBO Science Policy Issues report on quotas in academia to assure gender balance. R EMBO Director + + A Conducts workshops on emerging biotechnologies and on H T cognitive genomics. Gives invited talks at US National Academy E IC of Sciences, International Summit on Human Genome Editing, I H 5 D MAN 201 O N Washington, DC.; World Congress on Research Integrity, Rio de A M Janeiro; International Scienti c Advisory Board for the Centre for Eilish Craddock IT 2 015 Mammalian Synthetic Biology, Edinburgh. Personal Assistant to EMBO Fellowships EMBO Scientific Publications EMBO Gold Medal Sarah Teichmann and Ido Amit receive the EMBO Gold the EMBO Director David del Álamo Thomas Lemberger Medal (page ). + Programme Manager Deputy Head EMBO Global Activities India and Singapore sign agreements to become EMBC Associate + + Member States. EMBO Courses & Workshops More than , participants from countries attend 6th scienti c events (page ); participants attend EMBO Laboratory Management Courses (page ); rst online course EMBO Courses & Workshops recorded in collaboration with iBiology. -
PDCD5 Interacts with P53 and Functions As a Regulator of P53 Dynamics in the DNA Damage Response
i \Zhuge-BJ" | 2018/6/13 | 5:45 | page 1 | #1 i i i Biophysical Journal Volume: 00 Month Year 1{12 1 PDCD5 interacts with p53 and functions as a regulator of p53 dynamics in the DNA damage response Changjing Zhugea, Xiaojuan Sunb, Yingyu Chenc, Jinzhi Leid a College of Sciences, Beijing Forestry University, 35 Tsinghua East Road, Beijing 100083, China; b School of Science, Beijing University of Posts and Telecommunications, 10 Xitucheng Road, Beijing 100876, China; c Laboratory of Medical Immunology, School of Basic Medical Science, Peking University, 38 Xueyuan Road, Beijing 100083, China; d MOE Key Laboratory of Bioinformatics, Zhou Pei-Yuan Center for Applied Mathematics, Tsinghua University, Beijing 100084, China Abstract The tumor suppressor p53 plays a central role in cell fate decisions after DNA damage. Programmed Cell Death 5 (PDCD5) is known to interact with the p53 pathway to promote cell apoptosis. Recombinant human PDCD5 can significantly sensitize different cancers to chemotherapies. In the present paper, we construct a computational model that includes PDCD5 interactions in the p53 signaling network and study the effects of PDCD5 on p53- mediated cell fate decisions during the DNA damage response. Our results revealed that PDCD5 functions as a co-activator of p53 that regulates p53-dependent cell fate decisions via the mediation of p53 dynamics. The effects of PDCD5 are dose-dependent such that p53 can display either sustained or pulsed dynamics at different PDCD5 levels. Moreover, PDCD5 regulates caspase-3 activation via two mechanisms during the two phases of sustained and pulsed p53 dynamics. This study provides insights regarding how PDCD5 functions as a regulator of the p53 pathway and might be helpful for increasing our understanding of the molecular mechanisms by which PDCD5 can be used to treat cancers. -
2020 Stanford Bio-X Fellowship Brochure
STANFORD BIO-X PHD FELLOWSHIPS 2020 Stanford Bio-X Fellows Group Photo 2019 The Stanford Bio-X Graduate Fellowships The mission of the Stanford Bio-X Program is to catalyze discovery by crossing the boundaries between disciplines to bring interdisciplinary solutions, to create new knowl- edge of biological systems, and to benefit human health. Since it was established in 1998, Stanford Bio-X has charted a new approach to life science research by bringing together clinical experts, life scientists, engineers, and others to tackle the complexity of the human body. Currently over 980 Stanford Faculty and over 8,000 students, postdocs, researchers, etc. are affiliated with Stanford Bio-X. The generous support from donors, including the Bowes Foundation, enables the program to remain successful—at any given time, Stanford Bio-X is training at least 60 Ph.D fellows, and Fall 2020 brings 21 new fellows to the program. The Stanford Bio-X Graduate Fellowship Program was started to answer the need for training a new breed of visionary science leaders capable of crossing the bound- aries between disciplines in order to bring novel research endeavors to fruition. Since its inception in 2004, the three-year fellowships, including the Stanford Bio-X Bowes Fellowships and the Bio-X Stanford Interdisciplinary Graduate Fellowships (Bio-X SIGFs), have provided 318 graduate students with awards to pursue interdisciplinary research and to collaborate with multiple mentors, enhancing their potential to gen- erate profound transformative discoveries. Stanford Bio-X Fellows become part of a larger Stanford Bio-X community of learning that encourages their further networking and development. -
Synthetic Immunology: Hacking Immune Cells to Expand Their Access Provided by University of California - San Francisco UCSF on 10/10/18
IY35CH09-Lim ARI 6 April 2017 15:15 ANNUAL REVIEWS Further Click here to view this article's online features: • Download figures as PPT slides • Navigate linked references • Download citations Synthetic Immunology: • Explore related articles • Search keywords Hacking Immune Cells to Expand Their Therapeutic Capabilities Kole T. Roybal1 and Wendell A. Lim2 1Parker Institute for Cancer Immunotherapy, Department of Microbiology and Immunology, University of California, San Francisco, California 94143; email: [email protected] 2Howard Hughes Medical Institute, Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94158; email: [email protected] Annu. Rev. Immunol. 2017. 35:229–53 Keywords The Annual Review of Immunology is online at synthetic biology, immunotherapy, engineered immune cells, T cells, immunol.annualreviews.org synthetic Notch, chimeric antigen receptors https://doi.org/10.1146/annurev-immunol- 051116-052302 Abstract Copyright c 2017 by Annual Reviews. The ability of immune cells to survey tissues and sense pathologic insults All rights reserved and deviations makes them a unique platform for interfacing with the body Annu. Rev. Immunol. 2017.35:229-253. Downloaded from www.annualreviews.org and disease. With the rapid advancement of synthetic biology, we can now engineer and equip immune cells with new sensors and controllable thera- peutic response programs to sense and treat diseases that our natural immune Access provided by University of California - San Francisco UCSF on 10/10/18. For personal use only. system cannot normally handle. Here we review the current state of engi- neered immune cell therapeutics and their unique capabilities compared to small molecules and biologics. -
The Pseudo-Caspase FLIP(L) Regulates Cell Fate Following P53 Activation
The pseudo-caspase FLIP(L) regulates cell fate following p53 activation Andrea Leesa,1, Alexander J. McIntyrea,1, Nyree T. Crawforda, Fiammetta Falconea, Christopher McCanna, Caitriona Holohana, Gerard P. Quinna, Jamie Z. Robertsa, Tamas Sesslera, Peter F. Gallaghera, Gemma M. A. Gregga, Katherine McAllistera, Kirsty M. McLaughlina, Wendy L. Allena, Laurence J. Eganb, Aideen E. Ryanb,c, Melissa J. Labonte-Wilsona, Philip D. Dunnea, Mark Wappetta, Vicky M. Coylea, Patrick G. Johnstona, Emma M. Kerra, Daniel B. Longleya,2,3, and Simon S. McDadea,2,3 aPatrick G Johnston Centre for Cancer Research, Queen’s University Belfast, Belfast, Northern Ireland BT9 7BL, United Kingdom; bDiscipline of Pharmacology & Therapeutics, Lambe Institute for Translational Research, School of Medicine, College of Medicine, Nursing and Health Sciences, National University of Ireland Galway, Galway, Ireland; and cRegenerative Medicine Institute, College of Medicine, Nursing and Health Sciences, National University of Ireland Galway, Galway, Ireland Edited by Karen H. Vousden, Francis Crick Institute, London, United Kingdom, and approved June 8, 2020 (received for review February 12, 2020) p53 is the most frequently mutated, well-studied tumor-suppressor switch from cell-cycle arrest to cell death induction remain gene, yet the molecular basis of the switch from p53-induced cell- poorly understood, although p53-mediated transcriptional up- cycle arrest to apoptosis remains poorly understood. Using a combi- regulation of PUMA has been suggested to be crucial in a nation of transcriptomics and functional genomics, we unexpectedly number of studies (10, 11). identified a nodal role for the caspase-8 paralog and only human Despite p53/TP53 being the most frequently mutated gene in pseudo-caspase, FLIP(L), in regulating this switch. -
The Puzzling Interplay Between P53 and Sp1 - Full Text
7/20/2021 Aging | The puzzling interplay between p53 and Sp1 - Full Text Editorial Volume 9, Issue 5 pp 1355—1356 The puzzling interplay between p53 and Sp1 Ariella Oppenheim1 , Galit Lahav2 1 Department of Hematology, Hebrew University Faculty of Medicine, Jerusalem 91120, Israel 2 Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA Received: May 4, 2017 Published: May 9, 2017 https://doi.org/10.18632/aging.101238 How to Cite Copyright: Oppenheim and Lahav. This is an open‐access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited The paradigm tumor suppressor protein p53 was initially discovered in the Seventies by a number of investigators as a protein that was tightly bound to SV40 large T-antigen, a “contaminant” during T-antigen purification [1]. Its role as a tumor suppressor was realized only a few years later, when it was found that it is absent or mutated in many tumors. Since then p53 has been described as the “guardian of the genome”, due to its central role in keeping genome integrity in response to genotoxic stress as well as many other insults [2]. Specificity Factor 1, Sp1, was the first mammalian transcription factor to be purified and characterized by Dynan and Tjian in the early Eighties. Sp1 is overexpressed in many types of cancer, including those carrying wild-type p53. Sp1 therefore is considered as a ‘hallmark of cancer’ and a candidate target for cancer therapy [3]. -
Andreas Zingg – Curriculum Vitae
Andreas Zingg Curriculum Vitae Education 2011–2013 Basic Studies in Biology, University of Zurich, Zurich 2013–2015 Bachelor of Science ETH in Biotechnology, ETH Zurich, Basel 2015–2017 Master of Science ETH in Biotechnology, ETH Zurich, Basel Research Experience 06/2020 Doctoral Student - present University Hospital, Basel Cancer Immunotherapy, Prof. Dr. Heinz Läubli Project Titel: Redirection of immune cells to glycan antigens on tumour cells In the scope of this project, CAR-T cells will be developed that target the Sialyl-Thomsen-Nouveau antigen which is expressed on the majority of tumours. Various strategies will be evaluated to counteract the immunosuppressive tumour environment. Finally, this project should pave the way towards clinical trials with anti-STn directed, armored fourth generation CAR-T cells. 03/2019 Research Associate - 05/2020 Memo Therapeutics AG, Schlieren MTx is an ETH spin-off with 10 employees. It is an innovator in the field of antibody discovery based on microfluidics and its program includes targets in infectious diseases and immuno- oncology. I was responsible for most cell culture related experiments such as antibody library screening, assay development and routine cell culture but also supported the team in various molecular biological tasks. Specifically, I was trained in operating the company’s proprietary microfluidic system for emulsion PCR, cell-encapsulation and droplet sorting. Furthermore, for MTx’ screening project for SARS-CoV-2 neutralizing antibodies, I developed a pseudovirus assay to evaluate promising antibody candidates. 02/2018 Internship: Discovery of cell-penetrating antibodies - 12/2018 UCB Celltech, Slough UCB is multinational biopharmaceutical company with roughly 8’000 employees and a revenue of almost 5 billion euro. -
The Ups and Downs of P53: Proc
PERSPECTIVES 155. Akira, S. & Takeda, K. Toll-like receptor signalling. Nature Rev. Immunol. 4, 499–511 (2004). OPINION 156. Tsenova, L., Bergtold, A., Freedman, V. H., Young, R. A. & Kaplan, G. Tumour necrosis factor α is a determinant of pathogenesis and disease progression in mycobacterial infection in the central nervous system. The ups and downs of p53: Proc. Natl Acad. Sci. USA 96, 5657–5662 (1999). 157. Schluter, D. et al. Both lymphotoxin-α and TNF are crucial for control of Toxoplasma gondii in the central nervous system. J. Immunol. 170, 6172–6182 (2003). understanding protein dynamics 158. Pasparakis, M. et al. Peyer’s patch organogenesis is intact yet formation of B lymphocyte follicles is defective in peripheral lymphoid organs of mice deficient for in single cells tumor necrosis factor and its 55-kDa receptor. Proc. Natl Acad. Sci. USA 94, 6319–6323 (1997). 159. Kuprash, D. V. et al. Novel tumor necrosis factor- Eric Batchelor, Alexander Loewer and Galit Lahav knockout mice that lack Peyer’s patches. Eur. J. Immunol. 35, 1592–1600 (2005). 160. Grivennikov, S. I. et al. Distinct and nonredundant Abstract | Cells living in a complex environment must constantly detect, process in vivo functions of TNF produced by T cells and macrophages/neutrophils: protective and deleterious and appropriately respond to changing signals. Therefore, all cellular information effects. Immunity 22, 93–104 (2005). 161. Beutler, B. et al. Identity of tumour necrosis factor and processing is dynamic in nature. As a consequence, understanding the process of the macrophage-secreted factor cachetin. Nature 316, signal transduction often requires detailed quantitative analysis of dynamic 552–554 (1985). -
R E P Or T in G S C Ien C E & T E C Hn O Log Y F O R H E a Lt H
| MARCH 2015 MISROCK FOUNDATION FOR HEALTH ETH ZÜRICH FOUNDATION SCIENCE & TECHNOLOGY SCIENCE & TECHNOLOGY REPORTING Professor Sai Reddy is one of 17 professors at the D-BSSE in Basel. HIGHLIGHT PROFESSOR SAI REDDY IS A PROJECT LEADER AT THE NCCR MOLECULAR ENGINEERING Molecular Systems Engineering is a National Centre of Competence in Research (NCCR) funded by the Swiss National Science Foundation (SNSF) and headed by the University of Basel and ETH Zürich. This particular NCCR combines the disciplines biology, chemistry and physics with bioinformatic and engineering. The goal is to engineer and to combine molecular modules to design “molecular factories”. These molecular factories will be used for industrial production or to control cellular systems in health and disease. Professor Reddy is one of 17 professors at the Department of Biosystems Science & Engineering (D-BSSE) in Basel, Switzerland and one of the project leaders at the NCCR Molecular Engineering. He teaches Master students in Biomolecular Engineering & Immunotechnology and PhD students assigned to the joint ETH – University of Zurich Graduate Programme on Microbology & Immunology. ACKNOWLEDGING OUR PARTNERS The Laboratory for Systems and Synthetic Immunology and the professorship of Sai Reddy is made possible by the generous endowment of the S. Leslie Misrock Foundation. 02 ETH ZÜRICH FOUNDATION | MARCH 2015 The new president: The new rector: The new vice president of Lino Guzzella Sarah Springman research and corporate rela- tions: Detlef Günther Lino Guzzella, former rector of ETH Sarah Springman succeeds Lino Detlef Günther will be responsible Zurich (2012–2014) is Ralph Eichler’s Guzzella as rector. After Heidi Wun- for strategic research supervision successor. -
International RCI Symposium
Speakers / Sponsors General Information / Registration SPITZE IN DER MEDIZIN. MENSCHLICH IN DER BEGEGNUNG. Speakers Program Committee Hinrich Abken Hinrich Abken Genetic Immunotherapy Chair for Genetic Immunotherapy RCI Regensburg Center for Interventional Immunology RCI Regensburg Center for Interventional Immunology c/o University Hospital Regensburg, Germany c/o University Hospital Regensburg, Germany Benedikt Brors Applied Bioinformatics Philipp Beckhove Deutsches Krebsforschungszentrum, Heidelberg Chair for Interventional Immunology Matthias Edinger RCI Regensburg Center for Interventional Immunology Department of Internal Medicine III c/o University Hospital Regensburg, Germany University Hospital Regensburg, Germany Matthias Edinger Markus Feuerer Department of Internal Medicine III Immunology University Hospital Regensburg, Germany RCI Regensburg Center for Interventional Immunology c/o University Hospital Regensburg, Germany Markus Feuerer Tudor Fulga Chair for Immunology Genome Engineering and Synthetic Biology RCI Regensburg Center for Interventional Immunology University of Oxford, Oxford c/o University Hospital Regensburg, Germany Luca Gattinoni Venue Experimental Transplantation and Immunology National Cancer Institute, Bethesda Thon-Dittmer-Palais, Haidplatz 8, Florent Ginhoux 93047 Regensburg, Germany Ontogeny and Differentiation of Macrophages Cells Suggested hotels Singapore Immunology Network (SLgN), Singapore Achat Plaza Hotel Thomas Höfer www.achat-hotels.de | Phone: +49 (0)941 58400 0 Theoretical Systems Biology (B086) -
Engineered Th17 Cell Differentiation Using a Photo-Activatable Immune Modulator
bioRxiv preprint doi: https://doi.org/10.1101/719021; this version posted July 30, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Engineered Th17 cell differentiation using a photo-activatable immune modulator Bibudha Parasar1 and Pamela V. Chang*2,3,4 1Department of Chemistry and Chemical Biology; 2Department of Microbiology and Immunology, 3Center for Immunology, 4Cornell Institute of Host-Microbe Interactions & Disease, Cornell University, Ithaca, NY 14853 * Correspondence: [email protected] Abstract T helper 17 (Th17) cells, an important subset of CD4+ T cells, help to eliminate extracellular infectious pathogens that have invaded our tissues. Despite the critical roles of Th17 cells in immunity, how the immune system regulates the production and maintenance of this cell type remains poorly understood. In particular, the plasticity of these cells, or their dynamic ability to trans-differentiate into other CD4+ T cell subsets, remains mostly uncharacterized. Here, we report a synthetic immunology approach using a photo-activatable immune modulator (PIM) to increase Th17 cell differentiation on demand with spatial and temporal precision to help elucidate this important and dynamic process. In this chemical strategy, we developed a latent agonist that, upon photochemical activation, releases a small-molecule ligand that targets the aryl hydrocarbon receptor (AhR) and ultimately induces Th17 cell differentiation. We used this chemical tool to control AhR activation with spatiotemporal precision within cells and to modulate Th17 cell differentiation on demand by using UV light illumination. We envision that this approach will enable an understanding of the dynamic functions and behaviors of Th17 cells in vivo during immune responses and in mouse models of inflammatory disease.