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Patentability of Human-Animal Chimeras Ryan Hagglund
Santa Clara High Technology Law Journal Volume 25 | Issue 1 Article 4 2008 Patentability of Human-Animal Chimeras Ryan Hagglund Follow this and additional works at: http://digitalcommons.law.scu.edu/chtlj Part of the Law Commons Recommended Citation Ryan Hagglund, Patentability of Human-Animal Chimeras, 25 Santa Clara High Tech. L.J. 51 (2012). Available at: http://digitalcommons.law.scu.edu/chtlj/vol25/iss1/4 This Article is brought to you for free and open access by the Journals at Santa Clara Law Digital Commons. It has been accepted for inclusion in Santa Clara High Technology Law Journal by an authorized administrator of Santa Clara Law Digital Commons. For more information, please contact [email protected]. PATENTABILITY OF HUMAN-ANIMAL CHIMERAS Ryan Hagglundt Abstract The chimera was a mythological creature with a lion 's head, goat's body, and serpent's tail. Because of recent advances in biotechnology, such permutations on species are no longer the stuff of myth and legend The term "chimera " has come to describe a class of genetically engineered creatures composed of some cells from one species, which thus contain genetic material derived entirely from that species, and some cells from another species, containing only genetic material from that species. Scientists have created a goat- sheep chimera or "geep" which exhibits physical characteristicsof both animals. Likewise, scientists have also used the tools of modern molecular biology to create human-animal chimeras containing both human and animal cells. While none of the human-animal chimeras hitherto created have exhibited significant human characteristics,the synthesis of human-animal chimeras raises significant ethical concerns. -
The National Biodefense Analysis and Countermeasures Center: Issues
= -*=&9.43&1= .4)*+*38*=3&1>8.8=&3)= 4:39*72*&8:7*8=*39*7a=88:*8=+47=43,7*88= &3&=_=-*&= 5*(.&1.89=.3=(.*3(*=&3)=*(-3414,>=41.(>= :1>=+3`=,**1= 43,7*88.43&1= *8*&7(-=*7;.(*= 18/1**= <<<_(78_,4;= -,23+= =*5479=+47=43,7*88 Prepared for Members and Committees of Congress -*=&9.43&1= .4)*+*38*=3&1>8.8=&3)=4:39*72*&8:7*8=*39*7a=88:*8=+47=43,7*88= = :22&7>= The mission of the National Biodefense Analysis and Countermeasures Center (NBACC) is to understand current and future biological threats; assess vulnerabilities and determine potential consequences; and provide a national capability for conducting forensic analysis of evidence from bio-crimes and bio-terrorism. The NBACC is operational, with a program office and several component centers occupying interim facilities. A laboratory facility dedicated to executing the NBACC mission and to contain two NBACC component centers is being built at Fort Detrick, Maryland, as part of the National Interagency Biodefense Campus. The laboratory facility, with an estimated construction cost of $141 million, will be the first Department of Homeland Security laboratory specifically focused on biodefense. Its programmatic contents and component organization appear to be evolving, as conflicting information has been provided during previous budget cycles. Congressional oversight of programs, especially those performed in federal facilities for homeland security purposes, is considered key to maintaining transparency in biodefense. Policy issues that may interest Congress include the operation of the NBACC facility as a federally funded research and development center, transparency and oversight of research activities performed through the center, and the potential for duplication and coordination of research effort between the Department of Homeland Security and other federal agencies. -
Maximum Containment: the Most Controversial Labs in the World
Maximum Containment: The Most Controversial Labs in the World By Alison K. Bruzek B.A. Biological Sciences Northwestern University, 2010 SUBMITTED TO THE PROGRAM IN COMPARATIVE MEDIA STUDIES/WRITING IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN SCIENCE WRITING AT THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY MASSACHUSETTS IN'T-QUTE OF 7ECHNOLOqi September 2013 JUL 0 22013 @2013 Alison K. Bruzek. All rights reserved. Li__RARI ES The author hereby grants to MIT permission to reproduce and to distribute publicly paper and electronic copies of this thesis document in whole or in part in any medium now known or hereafter created. Signature of Author: -----.. Program in Con rativeMedia Studies/Writing June 10, 2013 Certified by: Philip Hilts Director, Knight Science Journalism Fellowships Thesis Supervisor Accepted by: Seth Mnookin Assistant Professor of Science Writing Director, Graduate Program in Science Writing 1 2 Maximum Containment: The Most Controversial Labs in the World By Alison K. Bruzek Submitted to the Program in Comparative Media Studies/Writing on June 10, 2013 in Partial Fulfillment of the Requirements for the Degree of Master of Science in Science Writing ABSTRACT In 2002, following the September 1 1 th attacks and the anthrax letters, the United States allocated money to build two maximum containment biology labs. Called Biosafety Level 4 (BSL-4) facilities, these labs were built to research new vaccines, diagnostics, and treatments for emerging infectious diseases, potential biological weapons, and to contribute to the nation's biodefense. These labs were not the first dramatic reaction to the threat of biowarfare and are in fact, one product of a long history of the country's contentious relationship with biological weapons. -
Responsible Life Sciences Research for Global Health Security a Guidance Document WHO/HSE/GAR/BDP/2010.2
Responsible life sciences research for global health security A GUIDANCE DOCUMENT WHO/HSE/GAR/BDP/2010.2 Responsible life sciences research for global health security A GUIDANCE DOCUMENT © World Health Organization 2010 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be ad- dressed to WHO Press, at the above address (fax: +41 22 791 4806; e-mail: [email protected]). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publica- tion. However, the published material is being distributed without warranty of any kind, either expressed or implied. -
High-Risk Human-Caused Pathogen Exposure Events from 1975-2016
F1000Research 2021, 10:752 Last updated: 04 AUG 2021 DATA NOTE High-risk human-caused pathogen exposure events from 1975-2016 [version 1; peer review: awaiting peer review] David Manheim 1, Gregory Lewis2 11DaySooner, Delaware, USA 2Future of Humanity Institute, University of Oxford, Oxford, UK v1 First published: 04 Aug 2021, 10:752 Open Peer Review https://doi.org/10.12688/f1000research.55114.1 Latest published: 04 Aug 2021, 10:752 https://doi.org/10.12688/f1000research.55114.1 Reviewer Status AWAITING PEER REVIEW Any reports and responses or comments on the Abstract article can be found at the end of the article. Biological agents and infectious pathogens have the potential to cause very significant harm, as the natural occurrence of disease and pandemics makes clear. As a way to better understand the risk of Global Catastrophic Biological Risks due to human activities, rather than natural sources, this paper reports on a dataset of 71 incidents involving either accidental or purposeful exposure to, or infection by, a highly infectious pathogenic agent. There has been significant effort put into both reducing the risk of purposeful spread of biological weapons, and biosafety intended to prevent the exposure to, or release of, dangerous pathogens in the course of research. Despite these efforts, there are incidents of various types that could potentially be controlled or eliminated by different lab and/or bioweapon research choices and safety procedures. The dataset of events presented here was compiled during a project conducted in 2019 to better understand biological risks from anthropic sources. The events which are listed are unrelated to clinical treatment of naturally occurring outbreaks, and are instead entirely the result of human decisions and mistakes. -
Molecular Phylogenetic Analysis
Assignment #2 Physics 498: Statistical Physics of Biological Complexity and Information Molecular Phylogenetic Analysis Date of Submission: 31th October, 2001 Rahul Roy Center for Biophysics and Computational Biology University of Illinois at Urbana-Champaign email: [email protected] Evolve by Borrowing ? Rahul Roy Center for Biophysics and Computational Biology University of Illinois at Urbana Champaign Introduction Molecular evolution over a period of four billion years has resulted in the development of present myriad of species from a hot soup of molecules. It has resulted in the evolution of complex multicellular organisms (Eukaryotes) along with single-celled organisms like prokaryotes at the same time. The question that has baffled scientists for long is: how did this incredible transition from a soup to this complex state take place? The discussion, that still continues, as how life started from the primordial soup is not the emphasis of the present debate, though Stanley Miller showed in, as back as 1950s, that organic chemicals can be synthesized from completely inorganic inputs. It has been proposed based on structural and functional complexity and fossil evidence that prokaryotes must have predated the eukaryotes by at least 1.0-2.0 billion years [Knoll, 1992]. This has led to the notion that eukaryotic cells have evolved from more simple prokaryotic organisms with which they share numerous common (or related) molecules [Margulis, 1970; Zillig, 1991]. Indeed, studies have shown that a number of eukaryotic organelles (namely mitochondria and chloroplasts) bear a close evolutionary relationship to specific groups of prokaryotes (namely α-proteobacteria and cyanobacteria, respectively) [Gray, 1992] So, how did the complex multicellular eukaryotes evolve from prokaryotes? To understand the origin of the eukaryotic cells a number of theories have been proposed. -
Studies of Military R&D and Weapons Development: Offensive/Defense
5. The Question of Offensive/Defensive Distinctions in Biological Weapons Related Research, and the Potential Stimulus to BW Proliferation by Expanded Research Programs The word "research," or any specific reference to "offensive" or "defensive" in a research context, does not appear in Article I of the Biological Weapons Convention. That reads as follows: "Each State Party to the Convention undertakes never in any circumstances to develop, produce, stockpile or otherwise acquire or retain: (1) Microbial or other biological agents, or toxins whatever their origin or method of production, of types and in quantities that have no justification for prophylactic, protective or other peaceful purposes; (2) Weapons, equipment or means of delivery designed to use such agents or toxins for hostile purposes or in armed conflict.,,1 However, the word research did appear in the provisional treaty draft that had been drawn up by the U.K. and that had been presented to the negotiating states on July 10, 1969. That draft required states signing or ratifying the treaty "not to conduct, assist or permit research aimed at production ... " of the agents or weapons forbidden by Article I (1) and (2) above. 2 Even earlier in a working paper on microbiological warfare that the U.K. submitted to the states negotiating in Geneva, the U.K. stated: The Convention would also need to deal with research work. It should impose a ban on research work aimed at production of the kind prohibited above, as regards both microbiological agents and ancillary equipment. It should also provide for the appropriate civil medical or health authorities to have access to all research work which might give rise to allegations that the obligations imposed by the Convention were not being fulfilled. -
The Sunshine Project
the sunshine project Key: High Containment Labs and Other Facilities of the US Biodefense Program This map shows existing biosafety level three and four facilities used in US biodefense research, as well as planned biodefense labs. It also shows important aerosol facilities and open air testing locations used in biodefense. BSL-3/4 facilities not known to be heavily dedicated to biodefense are not indicated here. Operational BSL-4 Facilities (Major) Planned / Under Construction BSL-3 Facilities USAMRIID Fort Detrick, Frederick, Maryland Tufts University, Grafton, Massachusetts DCLS "Biotech Six", Richmond, Virginia UMD of New Jersey, Newark Centers for Disease Control, Atlanta, Georgia (x2) University of Pittsburgh, Pennsylvania Univ. of Texas Medical Branch, Galveston University of Maryland, Baltimore Southwest Fdtn for Biomed. Res., San Antonio, TX George Mason University, Fairfax, Virginia University of Lousiville, Kentucky Planned / Under Construction BSL-4 Facilities Duke University, Durham, North Carolina Boston University, Boston, Massachusetts Medical University Of South Carolina, Charleston NIH Integrated Res. Fac., Frederick, Maryland University of Georgia, Athens DHS NBACC (Phase 1), Frederick, Maryland Scripps Institute, Palm Beach County, Florida USAMRIID (Phase 1), Frederick, Maryland University of Alabama at Birmingham USDA Planned Facility, Frederick, Maryland University of Tennessee at Memphis Univ. of Texas Medical Branch, Galveston Tulane Primate Center, Covington, Louisiana Rocky Mountain Labs, Hamilton, Montana University of Missouri, Columbia Operational BSL-3 Facilities University of Iowa, Iowa City (RCE planning) Harvard University, Cambridge, MA USDA / Iowa State University, Ames, IA Cornell University, Ithaca, New York Argonne National Lab, Argonne, Illinois DHS / USDA Plum Island, New York Agricultural Biosecurity Ctr., Manhattan, Kansas CALSPAN-UB, Buffalo, New York Univ. -
Biosecurity: a Comprehensive Action Plan Center for American Progress
Center for American Progress Biosecurity A Comprehensive Action Plan Andrew J. Grotto Jonathan B. Tucker Progressive Ideas for a Strong, Just, and Free America Biosecurity: A Comprehensive Action Plan Center for American Progress Biosecurity A Comprehensive Action Plan Andrew J. Grotto and Jonathan B. Tucker June 2006 After Guantanamo: A Special Tribunal for International Terrorist Suspects 1 Biosecurity: A Comprehensive Action Plan Center for American Progress Table of Contents EXECUTIVE SUMMARY i BIOLOGICAL THREATS FACING THE UNITED STATES 1 PREVENTING BIO-CATASTROPHES: THE NEED FOR A GLOBAL APPROACH 9 PREVENTING THE MISUSE OF THE LIFE SCIENCES 9 RECOMMENDATIONS STRENGTHENING BIOLOGICAL DISARMAMENT MEASURES 14 RECOMMENDATIONS 8 CONTAINING DISEASE OUTBREAKS: AN INTEGRATED PUBLIC HEALTH STRATEGY 21 TIMELY DETECTION OF OUTBREAKS 22 RECOMMENDATIONS 0 RAPID CONTAINMENT OF OUTBREAKS 32 RECOMMENDATIONS 5 DEFENDING AGAINST BIOLOGICAL THREATS: AN INTEGRATED RESEARCH STRATEGY 37 REFORMING THE DRUG DEVELOPMENT PROCESS 38 RECOMMENDATIONS 41 RATIONALIZING BIODEFENSE SPENDING 42 RECOMMENDATIONS 44 GLOSSARY 47 Biosecurity: A Comprehensive Action Plan ACKNOWLEDGMENTS The authors are deeply grateful to the following individuals for their valuable comments and criticisms on earlier drafts of this report: Bob Boorstin, Joseph Cirincione, P. J. Crowley, Richard Ebright, Gerald L. Epstein, Trevor Findlay, Brian Finlay, Elisa D. Harris, David Heyman, Ajey Lele, Dan Matro, Caitriona McLeish, Jonathan Moreno, Peter Ogden, Alan Pearson, Michael Schiffer, Laura Segal, and Bradley Smith. 4 Center for American Progress Executive Summary iological weapons and infectious diseases share several fundamental characteristics that the United States can leverage to counter both Bof these threats more effectively. Both a bioweapons attack and a natural pandemic, such as avian flu, can be detected in similar ways, and the effectiveness of any response to an outbreak of infectious disease, whether natural or caused deliberately by terrorists, hinges on the strength of the U.S. -
Pacific Forum Csis Young Leaders
The Biosecurity Lexicon Project: Breaking down the Complexities of Biosecurity Science for Policymakers PACIFIC FORUM CSIS YOUNG LEADERS Issues & Insights Vol. 12 – No. 11 Hanoi, Vietnam November 2012 Pacific Forum CSIS Based in Honolulu, the Pacific Forum CSIS (www.pacforum.org) operates as the autonomous Asia-Pacific arm of the Center for Strategic and International Studies in Washington, DC. The Forum’s programs encompass current and emerging political, security, economic, business, and oceans policy issues through analysis and dialogue undertaken with the region’s leaders in the academic, government, and corporate arenas. Founded in 1975, it collaborates with a broad network of research institutes from around the Pacific Rim, drawing on Asian perspectives and disseminating project findings and recommendations to opinion leaders, governments, and members of the public throughout the region. The Young Leaders Program The Young Leaders Program invites young professionals and scholars to join Pacific Forum policy dialogues and conferences. The program fosters education in the practical aspects of policy-making, generates an exchange of views between young and seasoned professionals, builds adaptive leadership capacity, promotes interaction among younger professionals from different cultures, and enriches dialogues with generational perspectives for all attendees. Participants must have a strong background in the area covered by the conference they are attending and an endorsement from respected experts in their field. Supplemental programs in conference host cities and mentoring sessions with senior officials and experts add to the Young Leader experience. The Young Leaders Program is possible with generous funding support by governments and philanthropic foundations, together with a growing number of universities, institutes, and organizations also helping to sponsor individual participants. -
Formation and Longevity of Chimeric and Duplicate Genes in Drosophila Melanogaster
Copyright Ó 2009 by the Genetics Society of America DOI: 10.1534/genetics.108.091538 Formation and Longevity of Chimeric and Duplicate Genes in Drosophila melanogaster Rebekah L. Rogers,1 Trevor Bedford2 and Daniel L. Hartl Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138 Manuscript received May 15, 2008 Accepted for publication November 11, 2008 ABSTRACT Historically, duplicate genes have been regarded as a major source of novel genetic material. However, recent work suggests that chimeric genes formed through the fusion of pieces of different genes may also contribute to the evolution of novel functions. To compare the contribution of chimeric and duplicate genes to genome evolution, we measured their prevalence and persistence within Drosophila melanogaster. We find that 80.4 duplicates form per million years, but most are rapidly eliminated from the genome, leaving only 4.1% to be preserved by natural selection. Chimeras form at a comparatively modest rate of 11.4 per million years but follow a similar pattern of decay, with ultimately only 1.4% of chimeras preserved. We propose two mechanisms of chimeric gene formation, which rely entirely on local, DNA-based mutations to explain the structure and placement of the youngest chimeric genes observed. One involves imprecise excision of an unpaired duplication during large-loop mismatch repair, while the other invokes a process akin to replication slippage to form a chimeric gene in a single event. Our results paint a dynamic picture of both chimeras and duplicate genes within the genome and suggest that chimeric genes contribute substantially to genomic novelty. -
Infectious Enveloped RNA Virus Antigenic Chimeras (Alphaviruses/Random Mutagenesis/Virus Vectors/Protein Engineering/Glycoproteins) STEVEN D
Proc. Natl. Acad. Sci. USA Vol. 89, pp. 207-211, January 1992 Biochemistry Infectious enveloped RNA virus antigenic chimeras (alphaviruses/random mutagenesis/virus vectors/protein engineering/glycoproteins) STEVEN D. LONDON*, ALAN L. SCHMAUOHNt, JOEL M. DALRYMPLEt, AND CHARLES M. RICE*t *Department of Molecular Microbiology, Washington University School of Medicine, 660 South Euclid Avenue, Box 8230, St. Louis, MO 63110-1093; and tUnited States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011 Communicated by Edwin D. Kilbourne, October 7, 1991 (receivedfor review August 26, 1991) ABSTRACT Random insertion mutagenesis has been used would allow recovery of infectious chimeric viruses. The to construct infectious Sindbis virus structural protein chime- insertional mutagen was an oligonucleotide encoding an ras containing a neutralization epitope from a heterologous 11-amino acid neutralization epitope (4D4) derived from the virus, Rift Valley fever virus. Insertion sites, permissive for external G2 glycoprotein of Rift Valley fever virus (RVFV). recovery of chimeric viruses with growth properties similar to Both a polyclonal anti-peptide antiserum and a monoclonal the parental virus, were found in the virion E2 glycoprotein and antibody (mAb), mAb 4D4, that react with this epitope on the secreted E3 glycoprotein. For the E2 chimeras, the epitope RVFV virions and also with denatured and reduced RVFV was expressed on the virion surface and stimulated a partially G2 (13, 14) are available. Thus,