Rabies Immune Globulin and Vaccine What Are Rabies Immune Globulin and Into the Area(S) Surrounding the Wound
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RNA-Based Adjuvant CV8102 Enhances the Immunogenicity of a Licensed Rabies Vaccine in a first-In-Human Trial
Vaccine 37 (2019) 1819–1826 Contents lists available at ScienceDirect Vaccine journal homepage: www.elsevier.com/locate/vaccine RNA-based adjuvant CV8102 enhances the immunogenicity of a licensed rabies vaccine in a first-in-human trial Fatma Doener a,1, Henoch S. Hong a,1, Ingo Meyer b,1, Keyvan Tadjalli-Mehr c, Angelika Daehling c, ⇑ Regina Heidenreich a, Sven D. Koch a, Mariola Fotin-Mleczek a, Ulrike Gnad-Vogt c, a Curevac AG, Paul-Ehrlich-Strasse 15, 72076 Tübingen, Germany b CRS Clinical Research Services Mönchengladbach GmbH, 41061 Mönchengladbach, Germany c Curevac AG, Schumannstrasse 27, 60325 Frankfurt, Germany article info abstract Article history: Background: We report the first-in-concept human trial of the safety, tolerability and immunogenicity Received 27 September 2018 when a novel TLR 7/8/RIG I agonist RNA-based adjuvant, CV8102, was administered alone or mixed with Received in revised form 30 January 2019 fractional doses of a licensed rabies vaccine (RabipurÒ) as model antigen. Accepted 3 February 2019 Methods: The primary objective was to assess the safety and reactogenicity of various dose levels of Available online 21 February 2019 CV8102 alone or mixed with RabipurÒ in healthy 18–40 year-old male volunteers. A secondary objective was to assess the immune-enhancing potential of bedside-mixes of CV8102 with fractional doses of Keywords: Ò Rabipur by measuring induction of rabies virus neutralising titres (VNTs). Adjuvant Results: Fifty-six volunteers received 50–100 lg CV8102 alone (n = 11), bedside-mixed CV8102 and RNA Ò Ò Ò Rabies Rabipur (n = 20), or Rabipur alone (n = 25; control). -
Antibody-Mediated Enhancement of Rabies Virus
542 Nature Vol. 290 16 April 1981 rearranged, K-chain gene, for example; region than the salivary gland mRNA. It is Are these findings at all relevant to the only one of these is destined to appear in possible that this affects the translation rabies 'early death' effect? Rabies viruses the mRNA, the remainder being removed efficiences of the mRNA (see 'Discussion' were thought to be serologically identical, by differential splicing. in Young et al.). Although the explanation but a number of rabies-related viruses are Why does the mouse go to all this for this fascinating genetic mechanism is now knownl2 , and antigenic variation trouble? Any explanation should consider the subject of future work, it is, of course, between rabies virus strains has been estab the fact that a-amylase mRNA accounts likely to be tied up with the primary lished I3 • Mice inoculated with Lagos Bat or for 2 per cent of the cytoplasmic mRNA in question - what determines the different Mokola viruses, two of the rabies-related the salivary gland, but only 0.02 per cent in level of a-amylase in two different tissues? viruses, and subsequently challenged with liver. This level may reflect the transcrip In the rat (and other mammals) the rabies virus, also died more quicklyl4. tion rate from the two genes; the 'salivary situation may be even more complicated. These findings suggest that it is not gland' promoter would then be consider MacDonald and his co-workers (Nature essential to have homologous neutralizing ably stronger than the 'liver' promoter. 287, 17; 1980) have analysed the rat antibodies to produce the rabies 'early Alternatively, the rate of RNA processing a-amylase genes and these studies point to death' effect, but that cross-reacting sera andlor export to the cytoplasm may be at least five non-allelic a-amylase genes or may also be active in this system as in the different for the two mRNAs. -
USDA-Approved Animal Rabies Vaccines
United States Department of Agriculture (USDA) Approved Animal Rabies Vaccines Table 1. Rabies Vaccines Licensed and Marketed in the United States, 2016 Age at For use Route of Product Name Produced by Marketed by Dose primary Booster vaccination in inoculation vaccination* A) MONOVALENT (Inactivated) RAB RABVAC 1 Boehringer Boehringer Dogs 1 ml 3 months Annually IM or SC Ingelheim Ingelheim Vetmedica Cats 1 ml 3 months Annually IM or SC Vetmedica Inc Inc License No. 124 RABVAC 3 Boehringer Boehringer Dogs 1 ml 3 months 1 year later & triennially IM or SC Ingelheim Ingelheim Vetmedica Cats 1 ml 3 months 1 year later & triennially IM or SC Vetmedica Inc Inc Horses 2 ml 3 months Annually IM License No. 124 EQUIRAB with Merck Animal Merck Animal Health Horses 1 ml 4 months Annually IM Havlogen Health License No. 165A DEFENSOR 1 Zoetis Zoetis Dogs 1 ml 3 months Annually IM or SC License No. 190 Cats 1 ml 3 months Annually SC DEFENSOR 3 Zoetis Zoetis Dogs 1 ml 3 months 1 year later & triennially IM or SC License No. 190 Cats 1 ml 3 months 1 year later & triennially SC Sheep 2 ml 3 months Annually IM Cattle 2 ml 3 months Annually IM NOBIVAC: 1- Zoetis Merck Animal Health Dogs 1 ml 3 months Annually IM or SC Rabies License No. 190 Cats 1 ml 3 months Annually SC NOBIVAC: 3- Zoetis Merck Animal Health Dogs 1 ml 3 months 1 year later & triennially IM or SC Rabies and 3- License No. 190 Cats 1 ml 3 months 1 year later & triennially SC Rabies CA Sheep 2 ml 3 months Annually IM Cattle 2 ml 3 months Annually IM IMRAB 1 Merial, Inc Merial, Inc Dogs 1 ml 3 months Annually SC License No. -
A Guide to Vaccinations for Parents
A GUIDE TO VACCINATIONS FOR PARENTS What are vaccines? When should my child be vaccinated? Why does my child need the HPV vaccine? HISTORY OF VACCINATIONS Smallpox is a serious infectious disease that causes fever and a distinctive, progressive 600 1796 skin rash. years ago Edward Jenner developed Variolation, intentionally a vaccine against smallpox. Cases of paralysis from polio in the U.S. exposing an individual to Almost 200 years later, in 1980, in the early 1950s: smallpox material, traces back the World Health Organization more than to 16th-century China. This declared that smallpox process resulted in a milder had been eradicated, 15,000 form of the disease. or wiped out. In the year 2017: Childhood vaccines can prevent 14 potentially serious 0 diseases or conditions throughout your child’s lifetime. 1955 1940s 1885 Jonas Salk’s polio vaccine The routine immunization Louis Pasteur developed a was proven safe and effective. schedule included vaccines vaccine against rabies. The Polio has now been eliminated against four potentially serious rabies vaccine series, which in the U.S., and organizations diseases (smallpox, diphtheria, can be given to people who are currently working tetanus, and pertussis). may have been exposed to to eradicate polio Now the schedule includes the virus, has made rabies worldwide. vaccines to prevent a total infection very rare in the of 14 conditions. United States. In the U.S., vaccines go through three phases of clinical trials to make sure they are safe and effective before they are licensed. 2006 Today The HPV vaccine was Vaccine research licensed in the U.S. -
Characterizing and Evaluating the Zoonotic Potential of Novel Viruses Discovered in Vampire Bats
viruses Article Characterizing and Evaluating the Zoonotic Potential of Novel Viruses Discovered in Vampire Bats Laura M. Bergner 1,2,* , Nardus Mollentze 1,2 , Richard J. Orton 2 , Carlos Tello 3,4, Alice Broos 2, Roman Biek 1 and Daniel G. Streicker 1,2 1 Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK; [email protected] (N.M.); [email protected] (R.B.); [email protected] (D.G.S.) 2 MRC–University of Glasgow Centre for Virus Research, Glasgow G61 1QH, UK; [email protected] (R.J.O.); [email protected] (A.B.) 3 Association for the Conservation and Development of Natural Resources, Lima 15037, Peru; [email protected] 4 Yunkawasi, Lima 15049, Peru * Correspondence: [email protected] Abstract: The contemporary surge in metagenomic sequencing has transformed knowledge of viral diversity in wildlife. However, evaluating which newly discovered viruses pose sufficient risk of infecting humans to merit detailed laboratory characterization and surveillance remains largely speculative. Machine learning algorithms have been developed to address this imbalance by ranking the relative likelihood of human infection based on viral genome sequences, but are not yet routinely Citation: Bergner, L.M.; Mollentze, applied to viruses at the time of their discovery. Here, we characterized viral genomes detected N.; Orton, R.J.; Tello, C.; Broos, A.; through metagenomic sequencing of feces and saliva from common vampire bats (Desmodus rotundus) Biek, R.; Streicker, D.G. and used these data as a case study in evaluating zoonotic potential using molecular sequencing Characterizing and Evaluating the data. -
Rabies Information for Dog Owners
Rabies Information for Dog Owners Key Facts Disease in dogs: • During initial days of illness, signs can be nonspecific, such as fever, anxiety and consumption of foreign items (e.g. blankets) • Progresses to more severe signs, such as: • Behavioral change (e.g. aggression, excitability) • Incoordination, loss of balance, disorientation, weakness • Hypersalivation • Seizures • Death results within 10 days of first signs of illness Rabies in dogs is not treatable. Vaccination is key to prevention: • Rabies vaccines are protective if given before exposure to the rabies virus. • Proof of dog vaccination is mandated by many jurisdictions and required for international travel. • Dogs not current on vaccination that are likely exposed to the rabies virus may be required to be euthanized or undergo a long and expensive quarantine. What is it? Rabies is caused by infection with the rabies virus. In North America, the most common wildlife rabies The virus lives in various species of mammals and species (termed reservoirs) vary regionally and is most commonly spread through bites from one include raccoons, skunks, foxes, coyotes, and animal to another or to a human (i.e. in an infected bats. Each year in the United States over 4,000 animal’s saliva). rabid animals are reported, including several Disease in dogs may begin with vague signs of hundred rabid dogs and cats, other domestic illness, but rapidly progresses to severe neurologic species (e.g., horses, cattle, sheep, goats) and signs (e.g. aggression, incoordination). Typically, thousands of wildlife animals. death occurs within 10 days of the first signs of illness. Where is it? The rabies virus is present in nearly all parts of the world. -
Everything You Always Wanted to Know About Rabies Virus ♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣♣ (But Were Afraid to Ask) Benjamin M
ANNUAL REVIEWS Further Click here to view this article's online features: t%PXOMPBEmHVSFTBT115TMJEFT t/BWJHBUFMJOLFESFGFSFODFT t%PXOMPBEDJUBUJPOT Everything You Always Wanted t&YQMPSFSFMBUFEBSUJDMFT t4FBSDILFZXPSET to Know About Rabies Virus (But Were Afraid to Ask) Benjamin M. Davis,1 Glenn F. Rall,2 and Matthias J. Schnell1,2,3 1Department of Microbiology and Immunology and 3Jefferson Vaccine Center, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, 19107; email: [email protected] 2Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111 Annu. Rev. Virol. 2015. 2:451–71 Keywords First published online as a Review in Advance on rabies virus, lyssaviruses, neurotropic virus, neuroinvasive virus, viral June 24, 2015 transport The Annual Review of Virology is online at virology.annualreviews.org Abstract This article’s doi: The cultural impact of rabies, the fatal neurological disease caused by in- 10.1146/annurev-virology-100114-055157 fection with rabies virus, registers throughout recorded history. Although Copyright c 2015 by Annual Reviews. ⃝ rabies has been the subject of large-scale public health interventions, chiefly All rights reserved through vaccination efforts, the disease continues to take the lives of about 40,000–70,000 people per year, roughly 40% of whom are children. Most of Access provided by Thomas Jefferson University on 11/13/15. For personal use only. Annual Review of Virology 2015.2:451-471. Downloaded from www.annualreviews.org these deaths occur in resource-poor countries, where lack of infrastructure prevents timely reporting and postexposure prophylaxis and the ubiquity of domestic and wild animal hosts makes eradication unlikely. Moreover, al- though the disease is rarer than other human infections such as influenza, the prognosis following a bite from a rabid animal is poor: There is cur- rently no effective treatment that will save the life of a symptomatic rabies patient. -
Mm7002e1 Allergic Reactions Including Anaphylaxis After Receipt
Morbidity and Mortality Weekly Report Early Release / Vol. 70 January 6, 2021 Allergic Reactions Including Anaphylaxis After Receipt of the First Dose of Pfizer-BioNTech COVID-19 Vaccine — United States, December 14–23, 2020 CDC COVID-19 Response Team; Food and Drug Administration As of January 3, 2021, a total of 20,346,372 cases of were determined not to be anaphylaxis, 86 were judged to coronavirus disease 2019 (COVID-19) and 349,246 associ- be nonanaphylaxis allergic reactions, and 61 were considered ated deaths have been reported in the United States. Long- nonallergic adverse events. Seven case reports were still under term sequalae of COVID-19 over the course of a lifetime investigation. This report summarizes the clinical and epide- currently are unknown; however, persistent symptoms and miologic characteristics of case reports of allergic reactions, serious complications are being reported among COVID-19 including anaphylaxis and nonanaphylaxis allergic reactions, survivors, including persons who initially experience a mild after receipt of the first dose of Pfizer-BioNTech COVID-19 acute illness.* On December 11, 2020, the Food and Drug vaccine during December 14–23, 2020, in the United States. Administration (FDA) issued an Emergency Use Authorization CDC has issued updated interim clinical considerations for (EUA) for Pfizer-BioNTech COVID-19 vaccine to prevent use of mRNA COVID-19 vaccines currently authorized in the COVID-19, administered as 2 doses separated by 21 days. On United States (4) and interim considerations for preparing for December 12, 2020, the Advisory Committee on Immunization the potential management of anaphylaxis (5). In addition to Practices (ACIP) issued an interim recommendation for use screening for contraindications and precautions before admin- of Pfizer-BioNTech COVID-19 vaccine (1); initial doses were istering COVID-19 vaccines, vaccine locations should have recommended for health care personnel and long-term care the necessary supplies available to manage anaphylaxis, should facility residents (2). -
Eye-Opening Approach to Norovirus Surveillance
LETTERS Rapid collaboration between pub- DOI: 10.3201/eid1608.091380 of norovirus infections in society. lic health authorities in the Philippines We therefore present a new approach and Finland led to appropriate action References to estimate the number of cases and at the site of origin of the rabies case spread of norovirus infections in the 1. Meslin FX. Rabies as a traveler’s risk, es- within a few days. In a country in pecially in high-endemicity areas. J Travel community. which rabies is not endemic, diagnos- Med. 2005;Suppl 1:S30–40. We plotted the number of queries ing rabies and implementing control 2. Srinivasan A, Burton EC, Kuehnert MJ, for *vomit* (asterisks denote any pre- measures in healthcare settings are of- Rupprecht C, Sutker WL, Ksiazek TG, et fi x or suffi x) submitted to the search al. Rabies in Transplant Recipients Inves- ten diffi cult because of limited experi- tigation Team. Transmission of rabies vi- engine on a medical website in Swe- ence with this disease. The last human rus from an organ donor to four transplant den (www.vardguiden.se). This num- rabies case in Finland was diagnosed recipients. N Engl J Med. 2005;352:1103– ber was normalized to account for in 1985, when a bat researcher died 11. DOI: 10.1056/NEJMoa043018 the increasing use of the website over 3. Metlin AE, Rybakov SS, Gruzdev KN, after being bitten by bats abroad and Neuvonen E, Cox J, Huovilainen A. An- time and aggregated by week, starting in Finland (5). For imported cases, pa- tigenic and molecular characterization of with week 40 in 2005. -
Overview, Prevention, and Treatment of Rabies
Overview, Prevention, and Treatment of Rabies Andrea Julia Nigg, Pharm.D., and Pamela L. Walker, Pharm.D. Each year, approximately 55,000 individuals worldwide die from an infection due to the rabies virus. Rabies is a life-threatening disease caused by an RNA virus that is usually transmitted to humans through bites from rabid animals. More recently, reports of transmission by means of organ transplantation have been reported. Since human rabies is nearly 100% fatal if prophylactic measures are not followed, an increased awareness of who should receive prophylaxis and when prophylaxis should be administered is necessary. Preexposure prophylaxis entails the administration of the rabies vaccine to individuals at high risk for exposure to rabies viruses (e.g., laboratory workers who handle infected specimens, diagnosticians, veterinarians, animal control workers, rabies researchers, cave explorers). Preexposure prophylaxis involves a three-dose series of the rabies vaccine that may confer some protection from the virus while simplifying postexposure prophylaxis regimens. Postexposure prophylaxis consists of a multimodal approach to decrease an individual’s likelihood of developing clinical rabies after a possible exposure to the virus. Regimens depend on the vaccination status of the victim and involve a combination of wound cleansing, administration of the rabies vaccine, and administration of human rabies immune globulin. If used in a timely and accurate fashion, postexposure prophylaxis is nearly 100% effective. Once clinical manifestations of rabies have developed, however, treatment options for rabies are limited, and to date, only seven individuals have survived rabies virus infection. Treatment of clinical rabies consists of medical support in an intensive care unit, using a multifaceted approach that includes supportive care, heavy sedation, analgesics, anticonvulsants, and antivirals. -
A Scoping Review of Viral Diseases in African Ungulates
veterinary sciences Review A Scoping Review of Viral Diseases in African Ungulates Hendrik Swanepoel 1,2, Jan Crafford 1 and Melvyn Quan 1,* 1 Vectors and Vector-Borne Diseases Research Programme, Department of Veterinary Tropical Disease, Faculty of Veterinary Science, University of Pretoria, Pretoria 0110, South Africa; [email protected] (H.S.); [email protected] (J.C.) 2 Department of Biomedical Sciences, Institute of Tropical Medicine, 2000 Antwerp, Belgium * Correspondence: [email protected]; Tel.: +27-12-529-8142 Abstract: (1) Background: Viral diseases are important as they can cause significant clinical disease in both wild and domestic animals, as well as in humans. They also make up a large proportion of emerging infectious diseases. (2) Methods: A scoping review of peer-reviewed publications was performed and based on the guidelines set out in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) extension for scoping reviews. (3) Results: The final set of publications consisted of 145 publications. Thirty-two viruses were identified in the publications and 50 African ungulates were reported/diagnosed with viral infections. Eighteen countries had viruses diagnosed in wild ungulates reported in the literature. (4) Conclusions: A comprehensive review identified several areas where little information was available and recommendations were made. It is recommended that governments and research institutions offer more funding to investigate and report viral diseases of greater clinical and zoonotic significance. A further recommendation is for appropriate One Health approaches to be adopted for investigating, controlling, managing and preventing diseases. Diseases which may threaten the conservation of certain wildlife species also require focused attention. -
Morbillivirus Experimental Animal Models: Measles Virus Pathogenesis Insights from Canine Distemper Virus
viruses Review Morbillivirus Experimental Animal Models: Measles Virus Pathogenesis Insights from Canine Distemper Virus Renata da Fontoura Budaszewski 1,2 and Veronika von Messling 2,* 1 Laboratório de Virologia, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Porto Alegre 91540-000, Brazil; [email protected] 2 Veterinary Medicine Division, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen 63225, Germany * Correspondence: [email protected]; Tel.: +49-6103-777-400 Academic Editor: Richard K. Plemper Received: 11 August 2016; Accepted: 30 September 2016; Published: 11 October 2016 Abstract: Morbilliviruses share considerable structural and functional similarities. Even though disease severity varies among the respective host species, the underlying pathogenesis and the clinical signs are comparable. Thus, insights gained with one morbillivirus often apply to the other members of the genus. Since the Canine distemper virus (CDV) causes severe and often lethal disease in dogs and ferrets, it is an attractive model to characterize morbillivirus pathogenesis mechanisms and to evaluate the efficacy of new prophylactic and therapeutic approaches. This review compares the cellular tropism, pathogenesis, mechanisms of persistence and immunosuppression of the Measles virus (MeV) and CDV. It then summarizes the contributions made by studies on the CDV in dogs and ferrets to our understanding of MeV pathogenesis and to vaccine and drugs development. Keywords: morbillivirus genus; canine distemper virus; animal models; pathogenesis 1. Introduction Morbilliviruses are enveloped, negative-stranded RNA viruses which cause a moderate to severe respiratory and gastrointestinal disease and long-lasting immunosuppression in their respective hosts. Despite the availability of a safe and cost-effective vaccine, the Measles virus (MeV) remains one of the leading causes of death among young children in developing countries [1].