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Challenges and Approaches for the Development of Safer Immunomodulatory Biologics
REVIEWS Challenges and approaches for the development of safer immunomodulatory biologics Jean G. Sathish1*, Swaminathan Sethu1*, Marie-Christine Bielsky2, Lolke de Haan3, Neil S. French1, Karthik Govindappa1, James Green4, Christopher E. M. Griffiths5, Stephen Holgate6, David Jones2, Ian Kimber7, Jonathan Moggs8, Dean J. Naisbitt1, Munir Pirmohamed1, Gabriele Reichmann9, Jennifer Sims10, Meena Subramanyam11, Marque D. Todd12, Jan Willem Van Der Laan13, Richard J. Weaver14 and B. Kevin Park1 Abstract | Immunomodulatory biologics, which render their therapeutic effects by modulating or harnessing immune responses, have proven their therapeutic utility in several complex conditions including cancer and autoimmune diseases. However, unwanted adverse reactions — including serious infections, malignancy, cytokine release syndrome, anaphylaxis and hypersensitivity as well as immunogenicity — pose a challenge to the development of new (and safer) immunomodulatory biologics. In this article, we assess the safety issues associated with immunomodulatory biologics and discuss the current approaches for predicting and mitigating adverse reactions associated with their use. We also outline how these approaches can inform the development of safer immunomodulatory biologics. Immunomodulatory Biologics currently represent more than 30% of licensed The high specificity of the interactions of immu- biologics pharmaceutical products and have expanded the thera- nomodulatory biologics with their relevant immune Biotechnology-derived peutic options available -
This Thesis Has Been Submitted in Fulfilment of the Requirements for a Postgraduate Degree (E.G
This thesis has been submitted in fulfilment of the requirements for a postgraduate degree (e.g. PhD, MPhil, DClinPsychol) at the University of Edinburgh. Please note the following terms and conditions of use: • This work is protected by copyright and other intellectual property rights, which are retained by the thesis author, unless otherwise stated. • A copy can be downloaded for personal non-commercial research or study, without prior permission or charge. • This thesis cannot be reproduced or quoted extensively from without first obtaining permission in writing from the author. • The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the author. • When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given. Bio-Oligomers as Antibacterial Agents and Strategies for Bacterial Detection Jagath C. Kasturiarachchi Ph.D. The University of Edinburgh College of Medicine & Veterinary Medicine 2014 i Declaration This thesis represents my own work. All of the experiments described herein were performed by me. I received technical assistance to perform flow cytometry and confocal analysis as declared in the acknowledgements. All chemical .entities were synthesised by the Department of Chemistry at University of Edinburgh. …………………………………………. J C Kasturiarachchi ii Acknowledgements I am very grateful to Dr Kev Dhaliwal, Professor Mark Bradley and Professor Chris Haslett for their supervision and support. I would like to thank Dr Jeff Walton and Dr Nicos Avlonitis designing and synthesis of peptoid library. I would like to thank Dr Nicos Avlonitis, Dr Marc Vendrell and Miss Alize Marangoz for their support for the synthesis of peptide probes. -
The Nuremberg Code Subverts Human Health and Safety by Requiring Animal Modeling
UC San Diego UC San Diego Previously Published Works Title The Nuremberg Code subverts human health and safety by requiring animal modeling Permalink https://escholarship.org/uc/item/2947x3sq Journal BMC Medical Ethics, 13(1) ISSN 1472-6939 Authors Greek, Ray Pippus, Annalea Hansen, Lawrence A Publication Date 2012-07-08 DOI http://dx.doi.org/10.1186/1472-6939-13-16 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Greek et al. BMC Medical Ethics 2012, 13:16 http://www.biomedcentral.com/1472-6939/13/16 DEBATE Open Access The Nuremberg Code subverts human health and safety by requiring animal modeling Ray Greek1*, Annalea Pippus1 and Lawrence A Hansen2 Abstract Background: The requirement that animals be used in research and testing in order to protect humans was formalized in the Nuremberg Code and subsequent national and international laws, codes, and declarations. Discussion: We review the history of these requirements and contrast what was known via science about animal models then with what is known now. We further analyze the predictive value of animal models when used as test subjects for human response to drugs and disease. We explore the use of animals for models in toxicity testing as an example of the problem with using animal models. Summary: We conclude that the requirements for animal testing found in the Nuremberg Code were based on scientifically outdated principles, compromised by people with a vested interest in animal experimentation, serve no useful function, increase the cost of drug development, and prevent otherwise safe and efficacious drugs and therapies from being implemented. -
Pharmacokinetics and Bioavailability of the Gnrh Analogs in the Form of Solution and Zn2+-Suspension After Single Subcutaneous Injection in Female Rats
Eur J Drug Metab Pharmacokinet (2017) 42:251–259 DOI 10.1007/s13318-016-0342-5 ORIGINAL RESEARCH ARTICLE Pharmacokinetics and Bioavailability of the GnRH Analogs in the Form of Solution and Zn2+-Suspension After Single Subcutaneous Injection in Female Rats 1 2 3 Aleksandra Suszka-S´witek • Florian Ryszka • Barbara Dolin´ska • 4 5 1 1 Renata Dec • Alojzy Danch • Łukasz Filipczyk • Ryszard Wiaderkiewicz Published online: 14 May 2016 Ó The Author(s) 2016. This article is published with open access at Springerlink.com Abstract Follicle-stimulating hormone (FSH) and 17b-estradiol in the Background and Objectives Although many synthetic serum was measured by radioimmunological method. gonadoliberin analogs have been developed, only a few of Results The Extent of Biological Availability (EBA), calcu- them, including buserelin, were introduced into clinical lated on the base of AUC0-?, showed that in the form of practice. Dalarelin, which differs from buserelin by just solution buserelin and dalarelin display, respectively, only 13 one aminoacid in the position 6 (D-Ala), is not widely used and 8 % of biological availability of their suspension coun- so far. Gonadotropin-releasing hormone (GnRH) analogs terparts. Comparing both analogs, the EBA of dalarelin was are used to treat many different illnesses and are available half (53 %) that of buserelin delivered in the form of solution in different forms like solution for injection, nasal spray, and 83 % when they were delivered in the form of suspension. microspheres, etc. Unfortunately, none of the above drug The injection of buserelin or dalarelin, in the form of solution formulations can release the hormones for 24 h. -
Half 1 3:50PM — 4:50PM in Vivo and in Vitro Activities of Auranofin Against Vancomycin-Resistant Enterococci
Half 1 3:50PM — 4:50PM In vivo and in vitro activities of auranofin against vancomycin-resistant enterococci 1 1 1 Nader S. Abutaleb , Marwa Alhashimi , Ahmed Elkashif , and Mohamed N. Seleem1 1 Department of Comparative Pathobiology, Purdue University, WL, IN, 47905, US Vancomycin-resistant enterococci (VRE) are the second-most common cause of nosocomial infections causing more than 5% of all deaths attributed to antibiotic-resistant infections in USA. VRE acquired resistance to all antibiotics used for treatment, severely limiting the number of available effective therapeutic options. Consequently, novel antimicrobials are urgently needed. However, new antimicrobials are becoming difficult to develop. Repurposing FDA-approved drugs, with well-characterized toxicology and pharmacology, to find new applications outside the scope of their original medical indication is a novel way to reduce time and cost associated with antimicrobial innovation. In an intensive search for antimicrobial activity among FDA approved drugs, we identified auranofin as a potent drug against VRE. It demonstrated a potent activity against 30 clinical drug-resistant VRE isolates with MIC90(1μg/mL) Additionally, no enterococci resistant mutants could be developed against auranofin after 14 passages. It also, inhibited highly resistant stationary phase cells, biofilm formation on urinary catheters, protease, lipase and haemagglutinins production at sub-inhibitory concentrations. The promising features and the potent antimicrobial activity of auranofin prompted us to evaluate its in vivo efficacy against drug-of-choice, linezolid, in our established lethal VRE septicemia mouse model. Both drugs protected 100% of mice against a lethal VRE dose. However, auranofin was superior to linezolid in reducing the bacterial load in internal organs (liver, kidney and spleen). -
Measuring Ligand Efficacy at the Mu- Opioid Receptor Using A
RESEARCH ARTICLE Measuring ligand efficacy at the mu- opioid receptor using a conformational biosensor Kathryn E Livingston1,2, Jacob P Mahoney1,2, Aashish Manglik3, Roger K Sunahara4, John R Traynor1,2* 1Department of Pharmacology, University of Michigan Medical School, Ann Arbor, United States; 2Edward F Domino Research Center, University of Michigan, Ann Arbor, United States; 3Department of Pharmaceutical Chemistry, School of Pharmacy, University of California San Francisco, San Francisco, United States; 4Department of Pharmacology, University of California San Diego School of Medicine, La Jolla, United States Abstract The intrinsic efficacy of orthosteric ligands acting at G-protein-coupled receptors (GPCRs) reflects their ability to stabilize active receptor states (R*) and is a major determinant of their physiological effects. Here, we present a direct way to quantify the efficacy of ligands by measuring the binding of a R*-specific biosensor to purified receptor employing interferometry. As an example, we use the mu-opioid receptor (m-OR), a prototypic class A GPCR, and its active state sensor, nanobody-39 (Nb39). We demonstrate that ligands vary in their ability to recruit Nb39 to m- OR and describe methadone, loperamide, and PZM21 as ligands that support unique R* conformation(s) of m-OR. We further show that positive allosteric modulators of m-OR promote formation of R* in addition to enhancing promotion by orthosteric agonists. Finally, we demonstrate that the technique can be utilized with heterotrimeric G protein. The method is cell- free, signal transduction-independent and is generally applicable to GPCRs. DOI: https://doi.org/10.7554/eLife.32499.001 *For correspondence: [email protected] Competing interests: The authors declare that no Introduction competing interests exist. -
Toolkit: Emergency Department Management of Sepsis in Adults and Young People Over 12 Years- 2016
Toolkit: Emergency Department management of Sepsis in adults and young people over 12 years- 2016 This clinical toolkit has been developed in partnership with the Royal College of Emergency Medicine and in full communication with the National Institute for Health and Care Excellence (NICE). It is designed to provide operational solutions to the complexities challenging the reliable identification and management of sepsis which are compatible with the 2016 NICE Clinical Guideline on Sepsis (NG51), and complements clinical toolkits designed for other clinical areas. Produced for the UK Sepsis Trust by: Dr Tim Nutbeam Dr Ron Daniels Dr Jeff Keep UKST EM TOOLKIT 2016 1 Staff working in Emergency Departments (ED) should be familiar with the significant morbidity and mortality associated with sepsis and possess the knowledge and skills to recognize it early and initiate resuscitation and treatment. The ED provides a key role in identifying patients at risk of sepsis, followed by risk stratification for sepsis and septic shock, initiating resuscitation and treatment, and ensuring the correct onward management of patients identified with sepsis. EDs are vital to the success of collaborative care pathways for the seamless management of patients with sepsis from the prehospital environment, through the ED, and to admission in either a ward bed or the Critical Care Unit. Sepsis responds well to early treatment and, if required, rapid escalation of therapy. 1 Background The UK mortality rate for patients admitted with sepsis is 30%1 - approximately 5 times higher than for ST elevation myocardial infarction and stroke - and is responsible for approximately 44,000 deaths and 150,000 hospital admissions in the United Kingdom (UK) per year2. -
IL15RA and SMAD3 Genetic Variants Predict Overall Survival in Metastatic Colorectal Cancer Patients Treated with FOLFIRI Therapy: a New Paradigm
cancers Article IL15RA and SMAD3 Genetic Variants Predict Overall Survival in Metastatic Colorectal Cancer Patients Treated with FOLFIRI Therapy: A New Paradigm Elena De Mattia 1 , Jerry Polesel 2 , Rossana Roncato 1 , Adrien Labriet 3, Alessia Bignucolo 1 , Sara Gagno 1, Angela Buonadonna 4, Mario D’Andrea 5, Eric Lévesque 6, Derek Jonker 7,Félix Couture 6, Chantal Guillemette 3 , Erika Cecchin 1,* and Giuseppe Toffoli 1 1 Experimental and Clinical Pharmacology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, via Franco Gallini n. 2, 33081 Aviano, Italy; [email protected] (E.D.M.); [email protected] (R.R.); [email protected] (A.B.); [email protected] (S.G.); [email protected] (G.T.) 2 Unit of Cancer Epidemiology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, via Franco Gallini n. 2, 33081 Aviano, Italy; [email protected] 3 Pharmacogenomics Laboratory, Centre Hospitalier Universitaire de Québec (CHU de Québec) Research Center and Faculty of Pharmacy, Laval University, Québec, QC G1V 4G2, Canada; [email protected] (A.L.); [email protected] (C.G.) 4 Medical Oncology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, via Franco Gallini n. 2, 33081 Aviano, Italy; [email protected] 5 Medical Oncology Unit, “San Filippo Neri Hospital”, Via Giovanni Martinotti, 20, 00135 Rome, Italy; Citation: De Mattia, E.; Polesel, J.; [email protected] 6 CHU de Québec Research Center and Faculty of Medicine, Laval University, Québec, QC G1V 4G2, Canada; Roncato, R.; Labriet, A.; Bignucolo, [email protected] (E.L.); [email protected] (F.C.) A.; Gagno, S.; Buonadonna, A.; 7 Division of Medical Oncology, Ottawa Hospital Research Institute, University of Ottawa, 501 Smyth Road, D’Andrea, M.; Lévesque, E.; Jonker, Ottawa, ON K1H 8L6, Canada; [email protected] D.; et al. -
Hemorrhagic Shock: the “Physiology Approach”
Review Article Hemorrhagic shock: The “physiology approach” Fabrizio Giuseppe Bonanno Trauma Directorate, Chris Hani Baragwanath Hospital, Johannesburg, South Africa ABSTRACT A shift of approach from ‘clinics trying to fit physiology’ to the one of ‘physiology to clinics’, with interpretation of the clinical phenomena from their physiological bases to the tip of the clinical iceberg, and a management exclusively based on modulation of physiology, is finally surging as the safest and most efficacious philosophy in hemorrhagic shock. ATLS® classification and recommendations on hemorrhagic shock are not helpful because antiphysiological and potentially misleading. Hemorrhagic shock needs to be reclassified in the direction of usefulness and timing of intervention: in particular its assessment and management need to be tailored to physiology. Key Words: Classification, hemorrhagic shock, management INTRODUCTION management of a scenario or of a problem [Table 1]. ATLS® classification of hemorrhagic shock (HS)[1] is not sensitive It has always been puzzling trying to understand and accept the and specific enough to help decision-making in reference to rationale and benefits of the ATLS classification[1] especially after the timing of management, being based only on the amount having replaced Holcroft more sensible classification,[2] as for the of blood loss that may or may not be rightly estimated, and difficulty of practical implementation with reference to timing and it is unhelpful and difficult to apply too.[9] The previous optimal management. -
Severe Sepsis, Cryptic Shock, Vasoplegic
ORIGINAL ARTICLE Otavio Tavares Ranzani1,2, Mariana Barbosa Monteiro1, Elaine Maria Ferreira3, Sergio Reclassifying the spectrum of septic patients using Ricardo Santos1, Flavia Ribeiro Machado3,4, Danilo Teixeira Noritomi1, on behalf of “Grupo de lactate: severe sepsis, cryptic shock, vasoplegic Cuidados Críticos Amil” shock and dysoxic shock Reclassificando o espectro de pacientes sépticos com o uso do lactato: sepse grave, choque críptico, choque vasoplégico e choque disóxico 1. Intensive Care Unit, Hospital Paulistano - São ABSTRACT Results: In total, 1,948 patients were Paulo (SP), Brazil. analyzed, and the sepsis group represented 2. Intensive Care Unit, Discipline of Clinical Objective: The current definition of 52% of the patients, followed by 28% Emergency, Hospital das Clínicas, Universidade severe sepsis and septic shock includes de São Paulo - USP - São Paulo (SP), Brazil. with vasoplegic shock, 12% with dysoxic 3. Latin American Sepsis Institute - São Paulo a heterogeneous profile of patients. shock and 8% with cryptic shock. Survival (SP), Brazil. Although the prognostic value of at 28 days differed among the groups 4. Discipline of Anesthesiology, Pain and hyperlactatemia is well established, (p<0.001). Survival was highest among Intensive Care, Escola Paulista de Medicina, hyperlactatemia is observed in patients the severe sepsis group (69%, p<0.001 Universidade Federal de São Paulo - UNIFESP - with and without shock. The present São Paulo (SP), Brazil. versus others), similar in the cryptic study aimed to compare the prognosis and vasoplegic shock groups (53%, of septic patients by stratifying them p=0.39), and lowest in the dysoxic shock according to two factors: hyperlactatemia group (38%, p<0.001 versus others). -
Ion Channels
UC Davis UC Davis Previously Published Works Title THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels. Permalink https://escholarship.org/uc/item/1442g5hg Journal British journal of pharmacology, 176 Suppl 1(S1) ISSN 0007-1188 Authors Alexander, Stephen PH Mathie, Alistair Peters, John A et al. Publication Date 2019-12-01 DOI 10.1111/bph.14749 License https://creativecommons.org/licenses/by/4.0/ 4.0 Peer reviewed eScholarship.org Powered by the California Digital Library University of California S.P.H. Alexander et al. The Concise Guide to PHARMACOLOGY 2019/20: Ion channels. British Journal of Pharmacology (2019) 176, S142–S228 THE CONCISE GUIDE TO PHARMACOLOGY 2019/20: Ion channels Stephen PH Alexander1 , Alistair Mathie2 ,JohnAPeters3 , Emma L Veale2 , Jörg Striessnig4 , Eamonn Kelly5, Jane F Armstrong6 , Elena Faccenda6 ,SimonDHarding6 ,AdamJPawson6 , Joanna L Sharman6 , Christopher Southan6 , Jamie A Davies6 and CGTP Collaborators 1School of Life Sciences, University of Nottingham Medical School, Nottingham, NG7 2UH, UK 2Medway School of Pharmacy, The Universities of Greenwich and Kent at Medway, Anson Building, Central Avenue, Chatham Maritime, Chatham, Kent, ME4 4TB, UK 3Neuroscience Division, Medical Education Institute, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY, UK 4Pharmacology and Toxicology, Institute of Pharmacy, University of Innsbruck, A-6020 Innsbruck, Austria 5School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, UK 6Centre for Discovery Brain Science, University of Edinburgh, Edinburgh, EH8 9XD, UK Abstract The Concise Guide to PHARMACOLOGY 2019/20 is the fourth in this series of biennial publications. The Concise Guide provides concise overviews of the key properties of nearly 1800 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. -
IL-15 Superagonist Expands Mcd8+ T, NK and NKT Cells After Burn
RESEARCH ARTICLE IL-15 Superagonist Expands mCD8+T, NK and NKT Cells after Burn Injury but Fails to Improve Outcome during Burn Wound Infection Naeem K. Patil1, Liming Luan1, Julia K. Bohannon1, Yin Guo2, Antonio Hernandez1, Benjamin Fensterheim2, Edward R. Sherwood1,2* 1 Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN, United States of America, 2 Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, United States of America * [email protected] Abstract OPEN ACCESS Background Citation: Patil NK, Luan L, Bohannon JK, Guo Y, Severely burned patients are highly susceptible to opportunistic infections and sepsis, Hernandez A, Fensterheim B, et al. (2016) IL-15 Superagonist Expands mCD8+T, NK and NKT Cells owing to the loss of the protective skin barrier and immunological dysfunction. Interleukin- after Burn Injury but Fails to Improve Outcome during 15 (IL-15) belongs to the IL-2 family of common gamma chain cytokines and stimulates the Burn Wound Infection. PLoS ONE 11(2): e0148452. proliferation and activation of T (specifically memory CD8), NK and NKT cells. It has been doi:10.1371/journal.pone.0148452 shown to preserve T cell function and improve survival during cecal ligation and puncture Editor: Fabrizio Mattei, Istituto Superiore di Sanità, (CLP)-induced sepsis in mice. However, the therapeutic efficacy of IL-15 or IL-15 superago- ITALY nist (SA) during infection after burn injury has not been evaluated. Moreover, very few, if Received: November 8, 2015 any, studies have examined, in detail, the effect of burn injury and infection on the adaptive Accepted: January 18, 2016 immune system.