Brigitte Askonas 1923–2013
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The Story of César Milstein and Monoclonal Antibodies: Introduction Page 1 of 4
The Story of César Milstein and Monoclonal Antibodies: Introduction Page 1 of 4 Custom Search Search A HEALTHCARE REVOLUTION IN THE MAKING The Story of César Milstein and Monoclonal Antibodies Collated and written by Dr Lara Marks Today six out of ten of the best selling drugs in the world are monoclonal antibody therapeutics. One of these, Humira®, which is a treatment for rheumatoid arthritis and other autoimmune conditions, was listed as the top selling drug across the globe in 2012 with a revenue of US$9.3 billion. Based on its current performance many predict the annual sales of the drug will surpass the peak sales of Lipitor, a treatment for lowering cholesterol, that is the best selling therapeutic of all time. Currently monoclonal antibody drugs make up a third of all new medicines introduced worldwide. http://www.whatisbiotechnology.org/exhibitions/milstein 4/13/2017 PFIZER EX. 1524 Page 1 The Story of César Milstein and Monoclonal Antibodies: Introduction Page 2 of 4 Portrait of César Milstein. Photo credit: Godfrey Argent Studio Monoclonal antibodies are not only successful drugs, but are powerful tools for a wide range of medical applications. On the research front they are essential probes for determining the pathological pathway and cause of diseases like cancer and autoimmune and neurological disorders. They are also used for typing blood and tissue, a process that is vital to blood transfusion and organ transplants. In addition, monoclonal antibodies are critical components in diagnostics, having increased the speed and accuracy of tests. Today the antibodies are used for the detection of multiple conditions, ranging from pregnancy and heart attacks, to pandemic flu, AIDS and diseases like anthrax and smallpox released by biological weapons. -
Smutty Alchemy
University of Calgary PRISM: University of Calgary's Digital Repository Graduate Studies The Vault: Electronic Theses and Dissertations 2021-01-18 Smutty Alchemy Smith, Mallory E. Land Smith, M. E. L. (2021). Smutty Alchemy (Unpublished doctoral thesis). University of Calgary, Calgary, AB. http://hdl.handle.net/1880/113019 doctoral thesis University of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission. Downloaded from PRISM: https://prism.ucalgary.ca UNIVERSITY OF CALGARY Smutty Alchemy by Mallory E. Land Smith A THESIS SUBMITTED TO THE FACULTY OF GRADUATE STUDIES IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY GRADUATE PROGRAM IN ENGLISH CALGARY, ALBERTA JANUARY, 2021 © Mallory E. Land Smith 2021 MELS ii Abstract Sina Queyras, in the essay “Lyric Conceptualism: A Manifesto in Progress,” describes the Lyric Conceptualist as a poet capable of recognizing the effects of disparate movements and employing a variety of lyric, conceptual, and language poetry techniques to continue to innovate in poetry without dismissing the work of other schools of poetic thought. Queyras sees the lyric conceptualist as an artistic curator who collects, modifies, selects, synthesizes, and adapts, to create verse that is both conceptual and accessible, using relevant materials and techniques from the past and present. This dissertation responds to Queyras’s idea with a collection of original poems in the lyric conceptualist mode, supported by a critical exegesis of that work. -
Eulogy Professor Emeritus Brigitte A. Askonas You Have Doubtless Often
Eulogy Professor Emeritus Brigitte A. Askonas You have doubtless often heard it said that such a person needs no introduction. Well, I reckon the recipient of the 2007 Robert Koch Gold Medal deserves an introduction. I would like to introduce her, as she is not someone to blow her own trumpet. She would never describe herself as the grand dame of cellular immunology. She would never talk about the great influence she has had on immunology. She would never say that she has mentored countless outstanding scientists. She would never proudly list all her honorary memberships of scientific societies and academies and all her honorary professorships at top universities. Professor Brigitte Askonas is not very forthcoming about her successes, which is precisely why an introduction is necessary. We would like her to know how much we value her contributions to science and how impressed we are by the formative influence she has had on the biosciences in Europe and in particular on immunology. Ita Askonas started her scientific career as a biochemist. In 1944, she was awarded a bachelor’s degree in biochemistry from McGill University in Montreal, Canada. In 1952, she received her PhD from the Biochemistry Department of the University of Cambridge in the United Kingdom, where she served her scientific apprenticeship under Malcolm Dixon. She studied muscle enzymes, by no means the worst grounding for her subsequent research. After completing her doctorate, she became a member of the Scientific Staff at the National Institute of Medical Research in Mill Hill, London. There, she first continued with her enzyme studies and biochemical research. -
George D. Snell
NATIONAL ACADEMY OF SCIENCES GEORGE DAVIS SNELL 1903–1996 A Biographical Memoir by N. AVRION MITCHISON Any opinions expressed in this memoir are those of the author and do not necessarily reflect the views of the National Academy of Sciences. Biographical Memoirs, VOLUME 83 PUBLISHED 2003 BY THE NATIONAL ACADEMIES PRESS WASHINGTON, D.C. GEORGE DAVIS SNELL December 19, 1903–June 6, 1996 BY N. AVRION MITCHISON ENETICIST GEORGE SNELL is known principally for his part G in the discovery of H2, the major histocompatibility complex (MHC) of the mouse and the first known MHC. For this he shared the 1980 Nobel Prize in physiology or medicine. He was elected to the National Academy of Sci- ences in 1970. Most of his life was spent at Bar Harbor, Maine, where he worked in the Jackson Laboratory. George was proud of his New England roots, moral and intellectual. His life was passed in the northeast, apart from brief spells in Texas and the Midwest. He was born in Bradford, Massachusetts, and at the age of 19 went to Dartmouth College, where he obtained his B.S, degree in biology in 1926. He went on to Harvard University, where he obtained his D.Sc. four years later at the Bussey Institu- tion. During his last year he served as an instructor back at Dartmouth, and in the following year served again as an instructor at Brown University. He then obtained a National Research Council Fellowship to work at the University of Texas in the laboratory of H. J. Muller (1931-33) and re- turned there 20 years later to spend a sabbatical year read- ing up on ethics, as mentioned below. -
Oralhisttransretro00maririch.Pdf
University of California Berkeley of Regional Oral History Office University California The Bancroft Library Berkeley, California MARIAN E. KOSHLAND (1921-1997): RETROSPECTIVES ON A LIFE IN ACADEMIC SCIENCE, FAMILY, AND COMMUNITY ACTIVITIES James P. Allison Anne H. Good Catherine P. Koshland Daniel E. Koshland, Jr. Douglas E. Koshland James M. Koshland Hugh O. McDevitt Gail Koshland Wachtel Introduction by Daniel E. Koshland, Jr. Interviews Conducted by Sally Smith Hughes in 1999 and 2000 Copyright 2003 by The Regents of the University of California Since 1954 the Regional Oral History Office has been interviewing leading participants in or well-placed witnesses to major events in the development of northern California, the West, and the nation. Oral history is a method of collecting historical information through tape-recorded interviews between a narrator with firsthand knowledge of historically significant events and a well-informed interviewer, with the goal of preserving substantive additions to the historical record. The tape recording is transcribed, lightly edited for continuity and clarity, and reviewed by the interviewee. The corrected manuscript is indexed, bound with photographs and illustrative materials, and placed in The Bancroft Library at the University of California, Berkeley, and in other research collections for scholarly use. Because it is primary material, oral history is not intended to present the final, verified, or complete narrative of events. It is a spoken account, offered by the interviewee in response to questioning, and as such it is reflective, partisan, deeply involved, and irreplaceable. * * * * * if * * * * * * * * ** ** * * * ** * ** * * * * ** * * * * All uses of this manuscript are covered by a legal agreement between The Regents of the University of California and Daniel Koshland, December 14, 1998; Hugh McDevitt dated November 23, 1999; James M. -
Memory-Like CD8 and CD4 T Cells Cooperate to Break Peripheral
Memory-like CD8؉ and CD4؉ T cells cooperate to break peripheral tolerance under lymphopenic conditions Cecile Le Saout, Sandie Mennechet, Naomi Taylor, and Javier Hernandez1 Institut de Ge´ne´ tique Mole´culaire de Montpellier Unite´Mixte de Recherche 5535, Centre National de la Recherche Scientifique, Université de Montpellier 1 and 2, 34293 Montpellier, Cedex 5, France Edited by N. Avrion Mitchison, University College London, London, United Kingdom, and approved October 20, 2008 (received for review August 10, 2008) The onset of autoimmunity in experimental rodent models and established (9). In the case of naive T cells, T cell antigen receptor patients frequently correlates with a lymphopenic state. In this (TCR) interactions with MHC/self-peptide complexes (those that condition, the immune system has evolved compensatory homeo- mediate positive selection) and the IL-7 cytokine appear to be static mechanisms that induce quiescent naive T cells to proliferate required for this expansion (10–15). Recently, an IL-7 independent and differentiate into memory-like lymphocytes even in the apparent form of lymphopenia-driven proliferation has also been described absence of antigenic stimulation. Because memory T cells have less (16). However, in all these cases, proliferating cells differentiate and stringent requirements for activation than naive cells, we hypothe- acquire a memory-like phenotype and the ability to rapidly secrete sized that autoreactive T cells that arrive to secondary lymphoid effector cytokines (12, 17–19). Although memory-like T cells have organs in a lymphopenic environment could differentiate and bypass never been activated by cognate antigen, do not pass through an the mechanisms of peripheral tolerance such as those mediated by effector phase, and, as such, cannot be considered to be ‘‘true’’ self-antigen cross-presentation. -
General Kofi A. Annan the United Nations United Nations Plaza
MASSACHUSETTS INSTITUTE OF TECHNOLOGY DEPARTMENT OF PHYSICS CAMBRIDGE, MASSACHUSETTS O2 1 39 October 10, 1997 HENRY W. KENDALL ROOM 2.4-51 4 (617) 253-7584 JULIUS A. STRATTON PROFESSOR OF PHYSICS Secretary- General Kofi A. Annan The United Nations United Nations Plaza . ..\ U New York City NY Dear Mr. Secretary-General: I have received your letter of October 1 , which you sent to me and my fellow Nobel laureates, inquiring whetHeTrwould, from time to time, provide advice and ideas so as to aid your organization in becoming more effective and responsive in its global tasks. I am grateful to be asked to support you and the United Nations for the contributions you can make to resolving the problems that now face the world are great ones. I would be pleased to help in whatever ways that I can. ~~ I have been involved in many of the issues that you deal with for many years, both as Chairman of the Union of Concerne., Scientists and, more recently, as an advisor to the World Bank. On several occasions I have participated in or initiated activities that brought together numbers of Nobel laureates to lend their voices in support of important international changes. -* . I include several examples of such activities: copies of documents, stemming from the . r work, that set out our views. I initiated the World Bank and the Union of Concerned Scientists' examples but responded to President Clinton's Round Table initiative. Again, my appreciation for your request;' I look forward to opportunities to contribute usefully. Sincerely yours ; Henry; W. -
And STAT4–Dependent IL-33 Receptor Expression Directly Promotes Antiviral Th1 Cell Responses
T-bet– and STAT4–dependent IL-33 receptor expression directly promotes antiviral Th1 cell responses Claudia Baumanna,b,1, Weldy V. Bonillac,1, Anja Fröhlicha,b, Caroline Helmstettera,b, Michael Peinea,b, Ahmed N. Hegazyd, Daniel D. Pinschewerc,2,3, and Max Löhninga,b,2,3 aExperimental Immunology, Department of Rheumatology and Clinical Immunology, Charité–Universitätsmedizin Berlin, 10117 Berlin, Germany; bGerman Rheumatism Research Center Berlin, 10117 Berlin, Germany; cDivision of Experimental Virology, Department of Biomedicine, University of Basel, Basel, Switzerland; and dTranslational Gastroenterology Unit, Nuffield Department of Clinical Medicine, Experimental Medicine Division, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DU, United Kingdom Edited* by N. Avrion Mitchison, University College London Medical School, London, United Kingdom, and approved February 20, 2015 (received for review September 25, 2014) During infection, the release of damage-associated molecular associated transcription factors T-bet and STAT4 controlled patterns, so-called “alarmins,” orchestrates the immune response. ST2 expression in vivo and in vitro. ST2 deficiency of LCMV- + The alarmin IL-33 plays a role in a wide range of pathologies. Upon specific CD4 T cells resulted in impaired effector Th1 cell release, IL-33 signals through its receptor ST2, which reportedly is differentiation with substantially reduced cell expansion, im- + expressed only on CD4 T cells of the Th2 and regulatory subsets. paired antiviral cytokine production, and little virus-induced Here we show that Th1 effector cells also express ST2 upon differ- T-cell–mediated immunopathology. Thus, IL-33 acts directly + entiation in vitro and in vivo during lymphocytic choriomeningitis on CD4 T cells during infection to enhance antiviral effector virus (LCMV) infection. -
Spotlight on Graduation Behind the Scenes at the Postgraduate Awards Ceremonies Centre Pages
reporter www.imperial.ac.uk Issue 177 • 16 May 2007 Spotlight on Graduation Behind the scenes at the Postgraduate Awards Ceremonies centre pages Hot off the press Keeping in touch Hannah Gay’s Ambassadors visit official history of alumni around the globe Imperial launched PAGE 5 PAGE 3 in brief Caulcott to manage research Dr Celia Caulcott has joined the College as Research Manager on 3 May. Working to Celebrate in style the Deputy Rector, Professor Sir Leszek Borysiewicz, she will The Centenary Ball be responsible for the coordination of research Come celebrate 100 years of living activity between the science at the largest formal dinner faculties and for promoting the College’s central strategic research direction. Collaboration at the and party of the Centenary year. boundaries of faculties, departments and centres is With big name acts and DJs all night, plus an important area of growth and represents a major a fun fair, casino, big wheel, dodgems, opportunity for the College. Dr Caulcott’s role will be to facilitate the multi-dimensional and complex carousel, laser quest and giant table football! series of interactions that constitute modern Special VIP tickets are available: research and to ensure that external funders see Join over 2,000 staff, students, and alumni on to staff and alumni which grant access a ‘joined up’ approach by the various component to the VIP bar. The VIP bar will have Saturday 16 June 2007. Visit the website for complimentary champagne and parts of the College. full details and tickets. entertainment throughout the night and offers the perfect place to mingle McComb with friends. -
Brian B. Boycott 38
EDITORIAL ADVISORY COMMITTEE Marina Bentivoglio Duane E. Haines Edward A. Kravitz Louise H. Marshall Aryeh Routtenberg Thomas Woolsey Lawrence Kruger (Chairperson) The History of Neuroscience in Autobiography VOLUME 3 Edited by Larry R. Squire ACADEMIC PRESS A Harcourt Science and Technology Company San Diego San Francisco New York Boston London Sydney Tokyo This book is printed on acid-free paper. (~ Copyright © 2001 by The Society for Neuroscience All Rights Reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publisher. Requests for permission to make copies of any part of the work should be mailed to: Permissions Department, Harcourt Inc., 6277 Sea Harbor Drive, Orlando, Florida 32887-6777 Academic Press A Harcourt Science and Technology Company 525 B Street, Suite 1900, San Diego, California 92101-4495, USA http://www.academicpress.com Academic Press Harcourt Place, 32 Jamestown Road, London NW1 7BY, UK http://www.academicpress.com Library of Congress Catalog Card Number: 96-070950 International Standard Book Number: 0-12-660305-7 PRINTED IN THE UNITED STATES OF AMERICA 01 02 03 04 05 06 SB 9 8 7 6 5 4 3 2 1 Contents Morris H. Aprison 2 Brian B. Boycott 38 Vernon B. Brooks 76 Pierre Buser 118 Hsiang-Tung Chang 144 Augusto Claudio Guillermo Cuello 168 Robert W. Doty 214 Bernice Grafstein 246 Ainsley Iggo 284 Jennifer S. Lund 312 Patrick L. McGeer and Edith Graef McGeer 330 Edward R. -
Immune Privilege As an Intrinsic CNS Property: Astrocytes Protect the CNS Against T-Cell-Mediated Neuroinflammation
Hindawi Publishing Corporation Mediators of Inflammation Volume 2013, Article ID 320519, 11 pages http://dx.doi.org/10.1155/2013/320519 Review Article Immune Privilege as an Intrinsic CNS Property: Astrocytes Protect the CNS against T-Cell-Mediated Neuroinflammation Ulrike Gimsa,1 N. Avrion Mitchison,2 and Monika C. Brunner-Weinzierl3 1 Institute of Behavioural Physiology, Leibniz Institute for Farm Animal Biology, Wilhelm-Stahl-Allee 2, 18196 Dummerstorf, Germany 2 Division of Infection and Immunity, University College London, Cruciform Building, Gower Street, London WC1 6BT, UK 3 Experimental Pediatrics, University Hospital, Otto-von-Guericke University Magdeburg, Leipziger Straße 44, 39120Magdeburg,Germany Correspondence should be addressed to Monika C. Brunner-Weinzierl; [email protected] Received 21 February 2013; Accepted 9 July 2013 Academic Editor: Jonathan P. Godbout Copyright © 2013 Ulrike Gimsa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Astrocytes have many functions in the central nervous system (CNS). They support differentiation and homeostasis of neurons and influence synaptic activity. They are responsible for formation of the blood-brain barrier (BBB) and make up the glia limitans. Here, we review their contribution to neuroimmune interactions and in particular to those induced by the invasion of activated T cells. We discuss the mechanisms by which astrocytes regulate pro- and anti-inflammatory aspects of T-cell responses within the CNS. Depending on the microenvironment, they may become potent antigen-presenting cells for T cells and they may contribute to inflammatory processes. -
The Delayed Effects of Respiratory Syncytial Virus Infection
THE DELAYED EFFECTS OF RESPIRATORY SYNCYTIAL VIRUS INFECTION Thesis submitted for the degree of Doctor of Philosophy in the faculty of Clinical Sciences of the University of London by Diarmuid Rodney O’Donnell Respiratory Medicine St. Mary's Hospital Medical School at Imperial College Norfolk Place London August 1996 Abstract Respiratory Syncytial (RS) virus is the most important respiratory pathogen of infants. The role of RS virus, in the pathogenesis of wheezing and asthma has been a topic of medical interest for many years. Many questions about the pathogenesis of RS virus disease remain unanswered. With new techniques, answers to some of these questions can be attempted. In this thesis, novel techniques were used in studies of RS virus infected infants, children and adults, and mice. Using a nested reverse transcriptase polymerase chain reaction (RT-PCR), it was shown that cell associated viraemia occurs in some infants hospitalised with bronchiolitis but that RS virus cannot be detected in serum or cerebrospinal fluid. RT-PCR was also used to determine, first, the frequency of RS virus in nasopharyngeal aspirates from children admitted with respiratory illnesses, and, in bronchoalveolar lavage fluid from adults infected with human immunodeficiency virus being investigated for unexplained respiratory symptoms. In mice, RT-PCR showed that RS virus persists for at least 100 days after acute infection. Almost all the isolates sequenced from these mice contained an unchanged dominant epitope for cytotoxic lymphocyte (CTL) recognition and all the mice tested had vigorous CTL recognising this epitope. A mutant epitope was also detected, but extensive studies using synthetic peptides did not show interference or inhibition of CTL responses by this mutant.