Animal Models of Alzheimer's Disease and Drug Development

Total Page:16

File Type:pdf, Size:1020Kb

Animal Models of Alzheimer's Disease and Drug Development Vol. 10, No. 3 2013 Drug Discovery Today: Technologies Editors-in-Chief Kelvin Lam – Simplex Pharma Advisors, Inc., Arlington, MA, USA Henk Timmerman – Vrije Universiteit, The Netherlands DRUG DISCOVERY TODAY TECHNOLOGIES Translational pharmacology Animal models of Alzheimer’s disease and drug development 1, 2 2 Bart Laurijssens *, Fabienne Aujard , Anisur Rahman 1 BEL Pharm Consulting, Moulin d’Ozil, 07140 Chambonas, France 2 CNRS UMR 7179, MNHN, 1 Av du Petit Chaˆteau, 91800 Brunoy, France Animal disease models are considered important in the Section editor: development of drugs for Alzheimer’s disease. This Oscar Della Pasqua – Leiden/Amsterdam Center for Drug brief review will discuss possible reasons why their Research, Leiden, The Netherlands. success in identifying efficacious treatments has been limited, and will provide some thoughts on the role of loss in brain regions involved in learning and memory pro- animal experimentation in drug development. Specifi- cesses (http://www.alz.org/) [1]. cally, none of the current models of Alzheimer’s dis- The interest in finding a cure or prevention for AD is ease have either construct or predictive validity, and no understandably great. Proper animal models of human AD are considered desirable if not essential in this process and model probably ever will. Clearly, specific animal much research effort has been put into that effect. As no experiments contribute to our understanding of the perfect model exists, the question becomes whether ‘the best disease and generate hypotheses. Ultimately, however, models available’ are good enough. What exactly can be the hypothesis can only be tested in human patients inferred from the results and what not? Or, differently put, how do they contribute to our understanding and decision- and only with the proper tools. These tools are a making. pharmacologically active intervention (in humans) The objective, therefore, of this brief review is to discuss the and a clinical trial suited to evaluate the mechanism potential role of the current animal disease models for AD in of action. Integration of knowledge in quantitative drug development. Specifically, the aim is to discuss why the (sub) models is considered important if not essential animal models of AD should have such a limited success in predicting successful treatments in the clinic (or rather, in this process. clinical trials), and to provide some thoughts on how to use animal experiments in drug development. Introduction Alzheimer’s disease (AD) is a neurodegenerative disease Animal models of Alzheimer’s disease affecting an estimated 5.4 million people globally, mainly The aetiology of AD is unknown, but there is still a general the elderly. There is currently no cure for AD, but some consensus in favour of the ‘amyloid hypothesis’ [1,2], even if symptomatic treatments are available. The disease is charac- it has been questioned [3]. A wide range of animal models terized by its hallmark histopathological findings of extra- have been developed to mimic the human context of the cellular b-amyloid (Ab) plaques and intracellular disease for the purpose of developing therapeutics or disease neurofibrillary tangles of tau and by neuronal and synaptic modifying agents. In fact, in most of the animal models the *Corresponding author.: B. Laurijssens ([email protected]) first goal is to simulate the neuropathological findings of AD 1740-6749/$ ß 2012 Elsevier Ltd. All rights reserved. http://dx.doi.org/10.1016/j.ddtec.2012.04.001 e319 Drug Discovery Today: Technologies | Translational pharmacology Vol. 10, No. 3 2013 followed by the correlation of cognitive function without animal models reviewed in this section either show major knowing whether the neuropathological agents have similar AD-related neuropathology or are in close phylogenetic biological consequences in humans and in animal models. It proximity to humans. In recent years dogs have been con- is beyond the scope of this review to discuss all the different sidered as a useful animal model for AD due to the close models. Here we will briefly summarize some potential ani- proximity of canine and human brain aging. Dogs develop mal models and their translation towards the clinical settings extensive Ab and diffuse plaque deposition and the extent of (Table 1). Animal models used in AD can be broadly divided Ab deposition correlates with the decline of some measures of into three categories: Natural models, Genetic models and cognitive function in the absence of neurofibrillary tangles Interventional models. (NFTs). Moreover, the amino acid sequence of Ab is fully conserved between dogs and humans [5]. Because of sponta- Natural models neous age-related Ab deposition and relative ease of cognitive Several animals including polar bears, dogs, cats, goats and function assessment, aged dogs were used to evaluate inter- sheep and some non-human primates spontaneously develop ventions with the aim of reduction of Ab load and subsequent some AD-related neuropathological features [4]. The few cognitive improvement (Table 1). Table 1. Some animal models of AD and clinical trials Model Treatment active in model Clinical trial Natural models Dog Active immunization with Ab1-42 [49] Trial stopped due to CNS side effects [50] Antioxidant [49] No effects [51] Rhesus monkey Acetylcholinesterase inhibitor, Donepezil [14] Approved for AD Nicotinic receptor agonist ABT-418 [14] Discontinued for side effects Glutamate receptor blocker Memantine [14] Approved for AD Mouse lemur, Octodon, No pharmacological trial has been reported yet. Chimpanzees, Orang-utans, Polar bear, Cat, Sheep, Goat, Wolverine a Genetic models PDAPP mice Active immunization with aggregated Ab1–42 [52] Trial stopped due to CNS side effects [50] Passive immunization with IgG [53] Vasogenic oedema and microhaemorrhage in some patients, no significant cognitive benefit, Phase-III trials underway [53] APP mice b-Secretase inhibitor [54] Reduce plasma Ab significantly, Under phase-III clinical trial [62] Tg2576 mice g-Secretase inhibitors [55] Trial halted because the drug failed to stop disease progression, associated with worsening cognitive function and increased risk of skin cancer [63] g-Secretase modulators [56] No benefit, trial discontinued [62] Acetylcholinesterase inhibitor [57] Approved for AD Cognitive decline cannot be prevented, cognitive benefits with treatment associated adverse effects reported [64] PSAPP mice Non-steroidal anti-inflammatory drugs [58] Negative results [65] Tg-tau mice Simvastatin [59] No cognitive benefit [66] À/À Ttpa APPsw mice a-tocopherol [60] No efficacy [67] Fruit-fly Doxycycline [61] Together with Rifampin. Some positive effect on cognitive performance [68] Interventional models Rat Intrahippocampal amyloid infusion model Curcumin [69] In Phase-II [4] Intracerebroventricular Ab infusion model GSK3 inhibitor [70] Marginal benefits, larger trial ongoing [71] a PDAPP mice: Mutation of human APP with valine at residue 717 substituted by phenylalanine under the control of human platelet derived growth factor promoter. APP mice: Mutation of three isoforms [695, 751 and 770] of human APP under the control of various promoters. Tg2576 mice: Swedish double mutation [K670N/M671L] on the 695 human APP under the control of hamster prion protein promoter. PSAPP mice: Swedish double mutation [K670N/M671L] plus Presenilin 1 exon 9 deleted. Tg-tau mice: Human À/À normal shortest 3R tau isoform inserted into the mouse genome under the promoter. Ttpa APPsw mice: Tg2576 mice crossed with a-tocopherol transfer protein knockout mice [31,60]. e320 www.drugdiscoverytoday.com Vol. 10, No. 3 2013 Drug Discovery Today: Technologies | Translational pharmacology Among the non-human primate models, mouse lemurs Another interesting finding is the presence of extensive astro- seem to be a potential animal model that exhibit amyloid gliosis in the aged octodon brain, which is a characteristic plaque, NFTs and some other AD related neuropathology [6]. feature of human AD brain. It has been hypothesized that This small prosimian primate lives 8–10 years in captivity and high homology (97.5%) of octodon Ab and human Ab might shows age-related changes similar to those of aging humans be an important factor in the appearance of AD markers in [6]. About 20% of mouse lemurs aged five years or older show this rodent. Breeding difficulty and comparatively longer life- significant brain atrophy [7], extensive accumulation of amy- span are limitations of this rodent model [16,17]. loid plaques, neurodegeneration [8] and/or loss of cholinergic neurons [9]. The genes responsible for the formation of senile Genetic models plaques are highly similar between mouse lemurs and Transgenic technology provides unique opportunity to repro- humans [8]. The presence of amyloid deposition has been duce the cause of familial AD by transfecting a mutant human recently linked to cerebral atrophy in aged individuals, giving amyloid precursor protein (APP). Mice have extensively been new insight into the understanding of pathological aging in used as transgenic models and facilitated our understanding of this non-human primate species [10]. Moreover, a compar- the molecular mechanisms associated with Ab-production, able decline in declarative memory and executive function deposition and clearance and the effects of Ab on neuronal has been reported in both aged human and aged mouse lemur network and synapses that play important role in cognitive whereas procedural memory appears to be conserved in both function. The
Recommended publications
  • Exosome TDP-43 Profile in Canine Model of ALS: a Preliminary Study in Developing Surrogate Biomarker
    bioRxiv preprint doi: https://doi.org/10.1101/2021.06.17.448876; this version posted June 18, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Exosome TDP-43 profile in canine model of ALS: A preliminary study in developing surrogate biomarker Penelope Pfeiffer 1, Joan R. Coates 2, Andrew Kennedy3, Kyleigh Getchell3, Edina Kosa3, Abdulbaki Agbas 3, 4* 1 Mount Sinai Hospital, Chicago IL; [email protected] 2 University of Missouri-Columbia, MO; [email protected] 3 Kansas City University, Kansas City MO; [email protected]; [email protected]; [email protected]; [email protected] 4 Heartland Center for Mitochondrial Medicine, Kansas City KS * Correspondence: [email protected]; Tel.: +1 816-654-7614 Abstract: Blood-based biomarkers are much-needed diagnostic and prognostic tools for ALS. Canine degenerative myelopathy (DM) is recognized animal disease model to study the biology of human ALS. Serum derived exosomes are potential carrier that transport intercellular hormone-like messengers, together with their stability as carrier of proteins and RNA, make them ideal as biomarkers for a variety of diseases and biological processes. We study exosomal TDP-43 pattern as a surrogate biomarker that reflects biochemical changes in central nervous system. We isolated exosomes from canine serum using commercial exosome isolation reagents. TDP-43 and SOD1 profile in spinal cord homogenate lysate and that of serum-derived exosomes were found elevated in dogs with DM.
    [Show full text]
  • The Good and the Bad of CRISPR/Cas9 Genome Editing
    Replicating human disease in rodents: the good and the bad of CRISPR/Cas9 genome editing Guillaume Pavlovic, PhD Head of Unit at PHENOMIN ‐ Institut Clinique de la Souris email: [email protected] CMC Strategy Forum Europe linkedIn: http://bit.ly/2VMLoJ9 Understanding Human disease with rodents: three challenges phenotypes of protein Some failure of mice and other coding genes in Mouse model organisms studies to be replicated or translated to humans Multiple phenotypes No known Knowledge Translation phenotype on disease from rodent One genes to Human phenotype Probability of success Reproducibility of preclinical studies https://www.mousephenotype.org/ 50% of preclinical data are irreproducible CRISPR/Cas9 genome editing in rodents THE GOOD What new possibilities does CRISPR open to better mimic human diseases ? – The genetic context (background) is not adapted – The designed mutation does not mimic the Human pathology With CRISPR/Cas9 new types of mutations can be easily engineered THE BAD There is more than off targets ! Understanding CRISPR/Cas9 genome editing to reduce lack of reproducibility – You are facing experimental variability, poor experimental design or bad reproducibility why do the results discovered using in vivo models sometimes fail to translate to human disease? Plenty of literature showing that the inbred genetic background has an effect on the phenotype Cerebellar phenotype of En1Hd/Hd mutants on 129/Sv and C57BL/6J backgrounds. deletion of the cerebellum 129/Sv—En1Hd/Hd C57BL/6J—En1Hd/Hd Bilovocky et al. J. Neurosci. 2003 why do the results discovered using in vivo models sometimes fail to translate to human disease? Plenty of literature showing that the inbred genetic background has an effect on the phenotype genetic background limits generalizability of genotype-phenotype relationships Sittig et al.
    [Show full text]
  • Current and Emerging Treatment Options for Endometriosis
    Expert Opinion on Pharmacotherapy ISSN: 1465-6566 (Print) 1744-7666 (Online) Journal homepage: http://www.tandfonline.com/loi/ieop20 Current and emerging treatment options for endometriosis Simone Ferrero, Giulio Evangelisti & Fabio Barra To cite this article: Simone Ferrero, Giulio Evangelisti & Fabio Barra (2018): Current and emerging treatment options for endometriosis, Expert Opinion on Pharmacotherapy, DOI: 10.1080/14656566.2018.1494154 To link to this article: https://doi.org/10.1080/14656566.2018.1494154 Published online: 05 Jul 2018. Submit your article to this journal View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=ieop20 EXPERT OPINION ON PHARMACOTHERAPY https://doi.org/10.1080/14656566.2018.1494154 REVIEW Current and emerging treatment options for endometriosis Simone Ferrero a,b, Giulio Evangelistia,b and Fabio Barra a,b aAcademic Unit of Obstetrics and Gynecology, Ospedale Policlinico San Martino, Genoa, Italy; bDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy ABSTRACT ARTICLE HISTORY Introduction: Pharmacotherapy has a pivotal role in the management of endometriosis with long-term Received 8 June 2018 treatments balancing clinical efficacy (control of pain symptoms and prevention of recurrence of the Accepted 25 June 2018 disease after surgery) with an acceptable safety profile. Treatment choice is based on several factors KEYWORDS including age and patient preference, reproductive plans, intensity of pain, severity of disease and Endometriosis; combined incidence of adverse effects. oral contraceptives; Areas covered: The aim of this review is to provide the reader with a complete overview of drugs that progestins; gonadotropin- are currently available or are under investigation for the treatment of endometriosis highlighting on- releasing hormone agonist; going clinical trials.
    [Show full text]
  • Lancl1 Promotes Motor Neuron Survival and Extends the Lifespan of Amyotrophic Lateral Sclerosis Mice
    Cell Death & Differentiation (2020) 27:1369–1382 https://doi.org/10.1038/s41418-019-0422-6 ARTICLE LanCL1 promotes motor neuron survival and extends the lifespan of amyotrophic lateral sclerosis mice 1 1 1 1 1 1 1 Honglin Tan ● Mina Chen ● Dejiang Pang ● Xiaoqiang Xia ● Chongyangzi Du ● Wanchun Yang ● Yiyuan Cui ● 1,2 1 1,3 4 4 3 1,5 Chao Huang ● Wanxiang Jiang ● Dandan Bi ● Chunyu Li ● Huifang Shang ● Paul F. Worley ● Bo Xiao Received: 19 November 2018 / Revised: 3 September 2019 / Accepted: 6 September 2019 / Published online: 30 September 2019 © The Author(s) 2019. This article is published with open access Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive loss of motor neurons. Improving neuronal survival in ALS remains a significant challenge. Previously, we identified Lanthionine synthetase C-like protein 1 (LanCL1) as a neuronal antioxidant defense gene, the genetic deletion of which causes apoptotic neurodegeneration in the brain. Here, we report in vivo data using the transgenic SOD1G93A mouse model of ALS indicating that CNS-specific expression of LanCL1 transgene extends lifespan, delays disease onset, decelerates symptomatic progression, and improves motor performance of SOD1G93A mice. Conversely, CNS-specific deletion of fl 1234567890();,: 1234567890();,: LanCL1 leads to neurodegenerative phenotypes, including motor neuron loss, neuroin ammation, and oxidative damage. Analysis reveals that LanCL1 is a positive regulator of AKT activity, and LanCL1 overexpression restores the impaired AKT activity in ALS model mice. These findings indicate that LanCL1 regulates neuronal survival through an alternative mechanism, and suggest a new therapeutic target in ALS.
    [Show full text]
  • Preliminary Evidence for an Influence of Exposure to Polycyclic Aromatic
    Zhang et al. BMC Pediatrics (2021) 21:86 https://doi.org/10.1186/s12887-021-02539-w RESEARCH ARTICLE Open Access Preliminary evidence for an influence of exposure to polycyclic aromatic hydrocarbons on the composition of the gut microbiota and neurodevelopment in three-year-old healthy children Wei Zhang1†, Zhongqing Sun2†,QianZhang3†,ZhitaoSun4,YaSu4,JiahuiSong1,BinglingWang4* and Ruqin Gao4* Abstract Background: During the second and third year after birth the gut microbiota (GM) is subjected to important development. The polycyclic aromatic hydrocarbon (PAH) exposure could influence the GM in animal and early postnatal exposure is associated with neurodevelopment disorder in children. This study was designed to explore the possible influence of the polycyclic aromatic hydrocarbons (PAHs) on the composition of the gut microbiota (GM) and neurodevelopment in a sample of 38 healthy children at the age of 3 years. Methods: A brief development (Gesell Development Inventory, GDI) and behavior test (Child Behavior Checklist, CBCL) were completed on 3-yr-olds and stool samples were collected for 16S rRNA V4-V5 sequencing. The PAH- DNA adduct in the umbilical cord blood and the urinary hydroxyl PAHs (OH-PAHs) at the age of 12 months were measured as pre- and postnatal PAH exposure, respectively. Results: The most abundant two phyla were Bacteroidetes (68.6%) and Firmicutes (24.2%). The phyla Firmicutes, Actinobacteria, Proteobacteria, Tenericutes, and Lentisphaerae were positively correlated with most domain behaviors of the GDI, whereas the Bacteroidetes, Cyanobacteria, and Fusobacteria were negatively correlated. Correspondingly, the phyla Bacteroidetes, Actinobacteria, and Fusobacteria showed positive correlations with most CBCL core and broadband syndromes, whereas the Firmicutes, Verrucomicrobia, Synergistetes, Proteobacteria and Tenericules were negatively correlated.
    [Show full text]
  • Pathophysiology and Treatment of Stroke: Present Status and Future Perspectives
    International Journal of Molecular Sciences Review Pathophysiology and Treatment of Stroke: Present Status and Future Perspectives Diji Kuriakose and Zhicheng Xiao * Development and Stem Cells Program, Monash Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Melbourne, VIC 3800, Australia; [email protected] * Correspondence: [email protected] Received: 29 September 2020; Accepted: 13 October 2020; Published: 15 October 2020 Abstract: Stroke is the second leading cause of death and a major contributor to disability worldwide. The prevalence of stroke is highest in developing countries, with ischemic stroke being the most common type. Considerable progress has been made in our understanding of the pathophysiology of stroke and the underlying mechanisms leading to ischemic insult. Stroke therapy primarily focuses on restoring blood flow to the brain and treating stroke-induced neurological damage. Lack of success in recent clinical trials has led to significant refinement of animal models, focus-driven study design and use of new technologies in stroke research. Simultaneously, despite progress in stroke management, post-stroke care exerts a substantial impact on families, the healthcare system and the economy. Improvements in pre-clinical and clinical care are likely to underpin successful stroke treatment, recovery, rehabilitation and prevention. In this review, we focus on the pathophysiology of stroke, major advances in the identification of therapeutic targets and recent trends in stroke research. Keywords: stroke; pathophysiology; treatment; neurological deficit; recovery; rehabilitation 1. Introduction Stroke is a neurological disorder characterized by blockage of blood vessels. Clots form in the brain and interrupt blood flow, clogging arteries and causing blood vessels to break, leading to bleeding.
    [Show full text]
  • Stem Cell Trials Using Companion Animal Disease Models
    TRANSLATIONAL AND CLINICAL RESEARCH Concise Review: Stem Cell Trials Using Companion Animal Disease Models a b ANDREW M. HOFFMAN, STEVEN W. DOW Key Words. Companion animal disease models • Naturally occurring disease • Spontaneous disease models • Canine stem cells • Feline stem cells • Adipose tissue-derived mesen- chymal stem cells • Bone marrow mesenchymal stem cells • Olfactory ensheathing cells • Mesenchymal stem cell neural lineage • Osteoarthritis • Intervertebral disc degeneration • Spinal disc herniation • Spinal cord injury • Dilated cardiomyopathy • Atopic dermatitis • Inflammatory bowel disease • Lymphocytic-plasmocytic colitis • Keratoconjunctivitis sicca • Sjogren’s syndrome • Multiple sclerosis • Meningoencepha- litis of unknown origin • Granulomatous meningoencephalomyelitis • Canine furuncu- losis • Canine perianal fistulas • Crohn’s fistulitis • Rectocutaneous fistulas • End stage renal disease • Feline chronic kidney disease • One Health • Investigational new ani- mal drug aRegenerative Medicine ABSTRACT Laboratory, Department of Studies to evaluate the therapeutic potential of stem cells in humans would benefit from more Clinical Sciences, Cummings realistic animal models. In veterinary medicine, companion animals naturally develop many dis- School of Veterinary eases that resemble human conditions, therefore, representing a novel source of preclinical Medicine, Tufts University, models. To understand how companion animal disease models are being studied for this pur- Grafton, Massachusetts, USA; pose, we reviewed the literature
    [Show full text]
  • Veklury: Assessment Report
    25 June 2020 EMA/357513/2020 Committee for Medicinal Products for Human Use (CHMP) Assessment report Veklury International non-proprietary name: remdesivir Procedure No. EMEA/H/C/005622/0000 Note Assessment report as adopted by the CHMP with all information of a commercially confidential nature deleted. Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 An agency of the European Union Table of contents 1. Background information on the procedure .............................................. 7 1.1. Submission of the dossier ..................................................................................... 7 1.2. Steps taken for the assessment of the product ........................................................ 8 2. Scientific discussion ................................................................................ 9 2.1. Problem statement ............................................................................................... 9 2.1.1. Disease or condition .......................................................................................... 9 2.1.2. Epidemiology .................................................................................................. 10 2.1.3. Biologic features, aetiology and pathogenesis ..................................................... 11 2.1.4. Clinical presentation, diagnosis ........................................................................
    [Show full text]
  • Predictive Validity of Animal Pain Models? a Comparison of the Pharmacokineticepharmacodynamic Relationship for Pain Drugs in Rats and Humans
    Available online at www.sciencedirect.com Neuropharmacology 54 (2008) 767e775 www.elsevier.com/locate/neuropharm Mini-review Predictive validity of animal pain models? A comparison of the pharmacokineticepharmacodynamic relationship for pain drugs in rats and humans G.T. Whiteside a,*, A. Adedoyin b, L. Leventhal a a Neuroscience Discovery Research, Wyeth Research, CN 8000, Princeton, NJ 08543, USA b Drug Safety and Metabolism, 500 Arcola Road, Collegeville, PA 19426, USA Received 8 August 2007; received in revised form 3 January 2008; accepted 7 January 2008 Abstract A number of previous reviews have very eloquently summarized pain models and endpoints in animals. Many of these reviews also discuss how animal models have enhanced our understanding of pain mechanisms and make forward-looking statements as to our proximity to the de- velopment of effective mechanism-based treatments. While a number of reports cite failures of animal pain models to predict efficacy in humans, few have actually analyzed where these models have been successful. This review gives a brief overview of those successes, both backward, providing validation of the models, and forward, predicting clinical efficacy. While the largest dataset is presented on treatments for neuropathic pain, this review also discusses acute and inflammatory pain models. Key to prediction of clinical efficacy is a lack of side effects, which may incorrectly suggest efficacy in animals and an understanding of how pharmacokinetic parameters translate from animals to man. As such, this review focuses on a description of the pharmacokineticepharmacodynamic relationship for a number of pain treatments that are effective in both animals and humans. Finally we discuss where and why animal pain models have failed and summarize improvements to pain models that should expand and improve their predictive power.
    [Show full text]
  • Animal Infection Models for Vaccine Development
    ChapterClinical Title Studies Animal Infection Models for Vaccine Development Abstract stringent in terms of requirements for the qualitative and Animal health is considered one of the cornerstones of quantitative composition, the tests to be carried out, and the “One Health” concept, which includes the interaction substances and materials used in their production. and fight against human, animal and wildlife pathogens able to cause disease. Moreover, reduction of antibiotic Efficacy and safety are two of the requirements to use is nowadays a compulsory future direction both in license a vaccine. There are a number of methods able to animals and humans. In these scenarios, the control of test those two aspects during the product development, diseases through vaccination is considered of paramount but in most cases animal models are used. This review aims importance. This review aims to discuss the need, design, to discuss the need, design, use and benefit of utilising use and benefit of utilising animal infection models animal infection models to develop vaccine products to develop vaccine products able to reduce the impact able to prevent not only human diseases and zoonotic not only of human diseases and zoonotic pathogens pathogens transmitted by animals, but also diseases transmitted by animals, but also diseases causing causing significant economic problems in livestock. significant economic problems in livestock. Animal Disease Model Considerations Introduction Translational medicine is often described as an effort A vaccine is a biological preparation that improves to carry scientific knowledge “from bench to bedside”, adaptive immunity to a particular disease (WHO). representing the process by which the laboratory research The vaccine product contains a killed or attenuated results are directly used to develop new ways to treat/ disease-causing microorganism, its toxins, one or prevent illness/cure patients (Cohrs et al., 2015).
    [Show full text]
  • National Center for Advancing Translational Sciences 2014 Report
    National Center for Advancing Translational Sciences 2014 REPORT NCATS’ Definitions of Translation and Translational Science: Translation is the process of turning observations in the laboratory, clinic and community into interventions that improve the health of individuals and the public — from diagnostics and therapeutics to medical procedures and behavioral changes. Translational science is the field of investigation focused on understanding the scientific and operational principles underlying each step of the translational process. NCATS studies translation on a system-wide level as a scientific and operational problem. Table of Contents Director’s Message . 1 Pre-Clinical Innovation . 3 Improving the Drug Development Process . 4 Assay Development and Screening Technology . 4 NCATS Chemical Genomics Center . 5 Bridging Interventional Development Gaps (BrIDGs) . 6 Repurposing Drugs . 7 NCATS Pharmaceutical Collection (NPC) . 7 New Therapeutic Uses . 8 Testing and Predictive Models . 10 Tissue Chip for Drug Screening . 10 Toxicology in the 21st Century (Tox21) . .11 RNA Interference (RNAi) . 13 Clinical Innovation . 14 Clinical and Translational Science Awards (CTSA) Program . 14 Accelerating Rare Diseases Research . 16 SM NIH/NCATS Global Rare Diseases Patient Registry Data Repository/GRDR . 16 Rare Diseases Clinical Research Network (RDCRN) . 17 Therapeutics for Rare and Neglected Diseases (TRND) . 18 Patient/Community Engagement and Health Information . 19 Partnerships and Collaborations . 22 Resources for Small Businesses . 24 Tools for Accelerating Translational Science . 25 Enabling Public Access to Data . 25 Appendix: Therapeutics for Rare and Neglected Diseases (TRND) Program 2013–2014 Annual Reports . 27 Front cover, left: The Biorepository at the Einstein-Montefiore Institute for Clinical and Translational Research is a quality-assured facility for acquisition, processing, storage and secure distribution of specimens with patient-specific annotations from the electronic medical record (Courtesy of Albert Einstein College of Medicine).
    [Show full text]
  • DEXEDRINE® (Dextroamphetamine Sulfate) SPANSULE® Sustained-Release Capsules and Tablets
    DX:L58 PRESCRIBING INFORMATION DEXEDRINE® (dextroamphetamine sulfate) SPANSULE® sustained-release capsules and Tablets WARNING AMPHETAMINES HAVE A HIGH POTENTIAL FOR ABUSE. ADMINISTRATION OF AMPHETAMINES FOR PROLONGED PERIODS OF TIME MAY LEAD TO DRUG DEPENDENCE AND MUST BE AVOIDED. PARTICULAR ATTENTION SHOULD BE PAID TO THE POSSIBILITY OF SUBJECTS OBTAINING AMPHETAMINES FOR NON-THERAPEUTIC USE OR DISTRIBUTION TO OTHERS, AND THE DRUGS SHOULD BE PRESCRIBED OR DISPENSED SPARINGLY. MISUSE OF AMPHETAMINES MAY CAUSE SUDDEN DEATH AND SERIOUS CARDIOVASCULAR ADVERSE EVENTS. DESCRIPTION DEXEDRINE (dextroamphetamine sulfate) is the dextro isomer of the compound d,l-amphetamine sulfate, a sympathomimetic amine of the amphetamine group. Chemically, dextroamphetamine is d-alpha-methylphenethylamine, and is present in all forms of DEXEDRINE as the neutral sulfate. Structural formula: SPANSULE capsules: Each SPANSULE sustained-release capsule is so prepared that an initial dose is released promptly and the remaining medication is released gradually over a prolonged period. Each capsule, with brown cap and clear body, contains dextroamphetamine sulfate. The 5-mg capsule is imprinted 5 mg and 3512 on the brown cap and is imprinted 5 mg and SB on the clear body. The 10-mg capsule is imprinted 10 mg—3513—on the brown cap and is imprinted 10 mg—SB—on the clear body. The 15-mg capsule is imprinted 15 mg and 3514 on the brown cap and is imprinted 15 mg and SB on the clear body. A narrow bar appears above and below 15 mg and 3514. Product reformulation in 1996 has caused a minor change in the color of the time-released pellets within each capsule.
    [Show full text]