FREE ELECTRONIC LIBRARY - Books, dissertations, abstract

Pages:   || 2 |

«The Vaccines Oral poliovirus vaccine (OPV) Globally many manufacturers produce the trivalent OPV using Sabin vaccine seeds provided by the World ...»

-- [ Page 1 ] --



Global Vaccine Safety


Essential Medicines & Health Products

20, Avenue Appia, CH-1211 Geneva 27


May 2014

s & Health Product

20, avenue Appia, Ch-1211 Geneva 27 The Vaccines Oral poliovirus vaccine (OPV) Globally many manufacturers produce the trivalent OPV using Sabin vaccine seeds provided by the World Health Organization except for the Pfizer polio Sabin type 3. Most manufacturers grow the viruses in cultures containing monkey kidney cells and continuous cell lines (Vero or diploid cells). POLIO SABIN (oral) vaccine is a magnesium chloride stabilised preparation of live attenuated polio viruses of the Sabin strains type 1 (LS-c, 2ab), type 2 (P712, Ch, 2ab) and type 3 (Leon 12ab). Each dose of OPV contains residual amounts (less than 25 µg) of antibiotics including streptomycin and neomycin. No adjuvants or preservatives are used (Sutter et al., 1999).

Inactivated poliovirus vaccine (IPV) Like OPV, inactivated poliovirus vaccine contains three poliovirus strains, Mahoney type 1, MEF-1 (Middle East Forces) type 2 and Saukett type 3. The vaccine is administered via the injectable route. The viruses are grown either in Vero cells or human diploid (MRC-5) cells and then concentrated, purified and inactivated with formaldehyde (Plotkin, 1999).

Types of vaccines Route Vaccine antigens Excipients Oral Sabin polio strains - type 1, 2 and 3. The vaccine Streptomycin and neomycin, MgCl2 No adjuvants 5.9 5.0 contains 10 + 0.5 TCID 50 type1, 10 + or preservatives are used 5.7

0.5 TCID 50 type 2 and 10 + 0.5 TCID 50 type 3 Parenteral Polio strains (1, 2 and 3)- Each dose of vaccine Trace amounts of antibiotics (neomycin, contains 40 D antigen units of type 1, eight D streptomycin and polymyxin B). Some vaccines antigen units of type 2 and 32 D antigen units of contain 2-phenoxyethanol as a preservative.

type 3 Thiomersal cannot be used for IPV.

Adverse events following Oral Poliovirus Vaccine Mild adverse events In general, OPV is well tolerated by vaccine recipients.

Serious adverse events Despite its many advantages, OPV carries the risk of vaccine-associated paralytic poliomyelitis (VAPP) particularly among infants who receive the vaccine for the first time and their contacts. In addition, when polio vaccine coverage is low in the population, this live attenuated vaccine may revert its virulence and transmissibility and pose additional risk for emergence of vaccine-derived polioviruses (VDPVs), which have been associated with outbreaks. Because of these risks, OPV use will be discontinued worldwide once the goal of eradicating all wild poliovirus (WPV transmission) is achieved.

Vaccine-associated paralytic polio (VAPP) Reversion of the small number of substitutions conferring small genetic changes to the attenuated phenotype occurs during OPV replication in humans and is the underlying cause of the rare cases of VAPP in OPV recipients and their close contacts.

Observed Rate of Vaccine Reactions – Polio Vaccines Page 1 of 5 Sabin strains can replicate in the gut of vaccine recipients and poliovirus maybe excreted for 4 to 6 weeks. During this time, the few attenuating mutations present in the vaccine strains revert rapidly and the virus changes via several mechanisms. These include back mutations, site suppression mutations, recombination and a steady drift in molecular sequence. This reversion of the attenuating mutations during OPV replication in humans is the underlying cause of the rare cases of VAPP observed in OPV recipients and their close contacts.

The case definition for VAPP includes the following:

 A case of acute flaccid paralysis with residual weakness at 60 days after onset of symptoms;

 A negative stool sample for wild-type poliovirus but positive for vaccine virus as examined in a WHO accredited laboratory;

 Evaluation and confirmation of the case by an expert committee (WHO 1998).

The onset of symptoms with VAPP usually occurs 4–30 days following receipt of oral polio vaccine (OPV) or within 4–75 days after contact with a recipient of OPV. In immunodeficient individuals (especially those with low antibody – hypogammaglobulinemia) VAPP may occur outside these windows.

The precise rate of VAPP varies with the study and the methodology used to measure it. The rate of VAPP is higher for the first dose of OPV than for subsequent doses, ranging from one case per 700,000 to one case per 3.4 million first doses. The risk of VAPP among first dose recipients was estimated as 1 case per 2.8 million children in India compared with first dose recipient risk of 1 case per 1.4 million children in the United States. A 1969 WHO Collaborative study found a VAPP rate of one in every 5.9 million doses administered for vaccine recipients and one in every 6.7 million doses administered for contacts. Studies have found no significant differences in VAPP rates between developing and industrialized countries. In countries where wild poliovirus transmission has been extensive until recently, VAPP occurs more commonly in children and vaccine recipients than in adults and contacts. WHO estimates VAPP risk at 2-4 cases per million birth cohort. VAPP is more common in individuals who are immunocompromised. No study has demonstrated transmission from a VAPP case resulting in another VAPP case. (Varughese, 1989, Joce, 1991, Maass, 1987, Novello, 1987, Andrus, 1995, CDC, 1996, Esteves, 1988).


Vaccine-derived poliovirus (VDPV) On very rare occasions, the live, attenuated vaccine-virus can - over time and prolonged replication - genetically change. A vaccine-derived poliovirus (VDPV) is a live, attenuated strain of the virus contained in OPV, which has changed and reverted to a form that may be able to cause paralysis in humans and may develop the capacity for sustained circulation. VDPVs differ from the parental (original) Sabin strains found in the vaccine by 1 to 15% of VP1 nucleotides. This is a measurement of genetic change that is used to monitor the circulation of viruses. On rare occasions, in areas where populations are under-immunized, VDPVs can regain the ability to circulate in populations, and can occasionally cause paralysis. Most circulating VDPV are type 2 (between 2000 and 2011, there were 492 type 2, 79 type 1 and 9 type 3 VDPV reported). Oral polio vaccine protects against VDPVs and is used to contain outbreaks. Hence, the problem is not with the vaccine itself, but low vaccination coverage. If a population is fully immunized, they will be protected against both vaccine-derived and wild polioviruses.

Aseptic meningitis/encephalitis On rare occasions, particularly in immunodeficient infants, aseptic meningitis and encephalitis have been reported after OPV (Andronikou et al., 1998; Yeung et al., 1997; Rantala et al., 1989).

Other vaccine safety concerns Guillain–Barré syndrome (GBS) Current data do not indicate an increased risk of GBS following receipt of OPV (CDC, 1996). Research conducted in Finland during the 1980s had suggested an increased incidence of GBS following mass OPV vaccination (Kinnunen et al., 1989; CDC, 1997; Uhari et al., 1989). Since the findings which led the US Institute of Medicine to conclude that there was an association between OPV and GBS (Stratton et al., 1994), the Finland results have been reanalysed and other factors have been identified as having contributed to the increase in the incidence of GBS. These factors include an influenza epidemic and widespread circulation of wild type-3 poliovirus (Kinnunen et al., 1998). During this time period, another observational study was also completed in the United Stateswhich did not support a causal relationship between OPV and GBS (Rantala et al., 1994; CDC, 1996; Kinnunen et al., 1998).

Transverse myelitis (TM) There are case reports of transverse myelitis reported after OPV, but occurred following the administration of multiple vaccines.

TM was not observed in the clinical trials that occurred prior to licensure of the polio vaccine and no other controlled studies have been conducted. Therefore, the data is inadequate to determine whether a causal relationship exists between OPV and TM (Stratton et al., 1994, Heath K 2006).

Simultaneous administration OPV can be administered with other vaccines, with no evidence of increased rates of adverse events nor reduced immunogenicity. OPV is frequently administered simultaneously with diphtheria–tetanus–pertussis (DPT) vaccines and therefore side effects from the latter may often be falsely attributed to OPV. Rotavirus vaccines when administered simultaneously have not affected immune responses to OPV. However in general, the immune responses (i.e., antibody levels) to rotavirus vaccination were lower when rotavirus vaccines were co-administered with OPV. This is particularly greater after the first dose of OPV (M.

Patel et al. 2012).

Provocation poliomyelitis In persons incubating wild poliovirus infection, intramuscular injections (e.g. DTP) may provoke paralysis in the injected limb (Sutter et al.1992; Strebel, 1995).

Observed Rate of Vaccine Reactions – Polio Vaccine s Page 2 of 5 Simian papovavirus SV40 From 1954 to 1962, both the inactivated and live attenuated forms of polio vaccine were prepared in primary cultures of rhesus monkey kidney cells, some of which were derived from monkeys that were naturally infected with SV40. This is a live simian papovavirus 40 (SV-40) which may cause neural tumour in animals, and viruses from the same papovavirus family may cause neural tumours in human beings. Some studies tried to investigate possible causation between the receipt of polio vaccine and the development of tumours (Dittmann, 1992). Long-term follow-up studies do not support such an association (Butel & Lednicky, 1999). A meeting convened at the National Institute of Health in 1997 concluded, "No measurable increase in neoplastic diseases has occurred in humans exposed to SV40 contaminated polio vaccines" (Plotkin et al., 1999). All currently produced oral polio vaccine is now tested for SV40 and none has been found positive.

Adverse events following Inactivated Poliovirus Vaccine Mild adverse events Localized reactions are common with IPV and this includes injection site erythema (0.5-1%), induration (3-11%) and tenderness (14-29%) (WER 2003). These reactions are generally mild and transient. In most cases, they spontaneously resolve within two to three days and further medical attention is not required. Mild systemic reactions may also occur.

Serious adverse events Some formulations of IPV contain small amounts of streptomycin, polymyxin B and neomycin, which can theoretically cause reactions in persons allergic to these antibiotics – but no confirmation of such reactions has been found in post-marketing surveillance (Plotkin et al., 1999; CDC, 1997). No reports of anaphylaxis, thrombocytopenia or transverse myelitis (Stratton et al.,

1994) after IPV have been published.

Other safety issues Simultaneous administration IPV is frequently administered simultaneously with diphtheria–tetanus–pertussis (DTP) vaccines. The combination of IPV with other vaccines, including DPT and Hib, does not appear to increase adverse reactions (Murdin et al., 1996; Vidor et al., 1994).

Summary of mild and severe adverse events

–  –  –

Andrus JK, Strebel PM, de Quadros CA, et al. (1995). Risk of vaccine-associated paralytic poliomyelitis in Latin America, 1989–91.

Bulletin of the World Health Organization, 73(1):33–40.

Begg NT, Chamberlain R, Roebuck M (1987). Paralytic poliomyelitis in England and Wales 1970–84. Epidemic Infelligence, 99:97–106.

Butel J, Lednicky JA (1999). Cell and molecular biology of Simian Virus 40: Implications for human infections and disease. Journal of the National Cancer Institute, 91:119–34.

CDC (1996). Centers for Diseases Control and Prevention. Paralytic poliomyelitis 1980–94. MMWR: Morbidity and Mortality Weekly Report, 46:79–83.

CDC (1997). Centers for Diseases Control and Prevention. Poliomyelitis prevention in the United States: introduction of a sequential vaccination schedule of inactivated poliovirus vaccine followed by oral poliovirus vaccine: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR: Morbidity and Mortality Weekly Report, 46(RR-3):1-25.

Pages:   || 2 |

Similar works:

«This publication was produced for articulated rock truck owners and drivers as a guide to safetyrelated issues in their daily work environment. Interested stakeholders may also refer to or use the information contained in this document to assist them in carrying out their occupational health and safety roles and responsibilities. Health and Safety for WorkSafeBC makes no representations, warranties, or, condition, expressed or implied, Articulated Rock Truck that this document is and will...»

«Aus dem Institut für Parasitologie der Veterinärmedizinischen Fakultät der Universität Leipzig und dem Institut für Parasitologie und Zoologie der Veterinärmedizinischen Universität Wien Vitalitätsbestimmung von Cryptosporidium-parvum-Oozysten in einem Zellkultursystem mittels Immunfluoreszenztechnik und computergestützter Bildanalyse Inaugural-Dissertation zur Erlangung des Grades eines Doctor medicinae veterinariae (Dr. med. vet.) durch die Veterinärmedizinische Fakultät der...»

«Arthropod Containment Guidelines (Version 3.1) A project of the The American Committee of Medical Entomology of the American Society of Tropical Medicine and Hygiene Abbreviations INTRODUCTION Background Intent Field Sites Authorities RISK ASSESSMENT FOR ARTHROPOD VECTORS Principles of risk assessment Arthropods known to be free of specific pathogens Arthropods known to contain specific pathogens Arthropods containing unknown infectious agents or whose status is uncertain. 16 Vector Arthropods...»

«The Associate Psychologist: developing the graduate psychologist workforce Mark Burton and Christine Adcock, i Joint Learning Disability Service Mancunian Community Health (NHS) Trust and City of Manchester Social Services Department i Address for Corrrespondence: Joint Learning Disability Service Chapman Place Chapman St. Gorton Manchester M18 8UA We are grateful to (in no particular order) Mike Kellaway, Jean Jones, Godfrey Davis, Carolyn Kagan, Jean Lally, Jude Moss and Anne Necus for their...»

«DISABILITY-COMPETENT CARE SELF-ASSESSMENT TOOL INTRODUCTION Last modified 05/22/2013 1 Please submit feedback to sloehrer@ihi.org. Purpose The Disability-Competent Care Self-Assessment Tool was developed to help health plans and health systems evaluate their current ability to meet the needs of adults with functional limitations and to identify strategic opportunities for improvement. Serving Persons with Functional Limitations This Tool focuses primarily on persons with functional limitations,...»

«Walach, Harald (2011) Methodology Blog: Part 3 Translated from the original German online-course: http://harald-walach.de/methodenlehre-fuer-anfaenger/ Copyright © 2011 Harald Walach. Any further use in electronic or printed form is allowed only with the written consent of the author. Linking to this Article or to the category of this series is of course desired and permitted. A short methodology for Beginners Part 3: Consequences Prof. Dr. Harald Walach In this series of (blog-)articles I'll...»

«University of Pretoria.etd CHAPTER 3 3. SELECTION OF PLANTS 3.1 FAMILY COMBRETACEAE 3.1.1 Taxonomy The Combretaceae family belongs to the order Myrtales, which is sub-divided into two sub-families of which only the Combretoideae is of interest. Of the two tribes comprising this sub-family, only the Combreteae, which is further divided into three subtribes, is of relevance in Africa. The five genera from the three sub-tribes are Combretum, Terminalia, Pteleopsis, Quisqualis and Lumnitzera...»

«Aus der Klinik für Psychiatrie und Psychotherapie Fakultät 2, Klinische Medizin Der Universität des Saarlandes, Homburg/Saar Komm. Direktor: PD Dr. med. Günter Heinz Angstsensitivität und physiologische Stressreaktivität Dissertation zur Erlangung des Grades eines Doktors der Medizin Der Medizinischen Fakultät Der UNIVERSITÄT DES SAARLANDES Vorgelegt von Stefan Alexander Ruf Geb. am 21.02.1969 in Stuttgart Bad Cannstatt Inhaltsverzeichnis Zusammenfassung 5 Englische Zusammenfassung 6 1....»

«QUALITY ISSUES IN THE USE OF ADMINISTRATIVE DATA RECORDS Aileen Rothbard University of Pennsylvania 2 Quality Issues in the Use of Administrative Data Records   Contents  Introduction..   Secondary Data .. 5   Definition of Data Quality ..8    Components of Data Quality ..9    Addressing Data Quality Challenges in   Integrated data systems .. 15    Tools to Assess Data Quality ..20    Uses of Administrative Data in Research and Evaluation. 22   ...»

«Aus der Klinik für Innere Medizin / Kardiologie des Deutschen Herzzentrums Berlin Stiftung des Bürgerlichen Rechts DISSERTATION Die Bedeutung von Insulin-like Growth Factor-1 für die Integrinvermittelte Migration von humanen THP-1/Makrophagen zur Erlangung des akademischen Grades Doctor medicinae (Dr. med.) vorgelegt der Medizinischen Fakultät Charité – Universitätsmedizin Berlin von Jan Fritzsche aus Chemnitz Gutachter: 1. PD Dr. med. Philipp Stawowy 2. Prof. Dennis Bruemmer, M.D. 3....»

<<  HOME   |    CONTACTS
2016 www.book.dislib.info - Free e-library - Books, dissertations, abstract

Materials of this site are available for review, all rights belong to their respective owners.
If you do not agree with the fact that your material is placed on this site, please, email us, we will within 1-2 business days delete him.