The place of accelerated schedules for hepatitis A and B vaccinations
- PMID: 12921484
- DOI: 10.2165/00003495-200363170-00001
The place of accelerated schedules for hepatitis A and B vaccinations
Abstract
The availability of accelerated schedules of vaccination, as well as the development of combination vaccines, has enhanced the methods of protection against infectious disease, in particular that of hepatitis A and B viruses. The benefits of using accelerated schedules include: (i) enhanced adherence to and subsequent completion of vaccine courses; (ii) convenience for the recipient of the vaccine; (iii) reduced administration costs of providing the vaccine; and, most importantly, (iv) the ability to provide protection against these serious infections to those who will be imminently exposed to the risk and so require protection as quickly as possible. Active immunisation against both hepatitis A and B viruses has only been recognised within the last 20 years. During this time clinical studies have demonstrated the safety and efficacy of administering the monovalent hepatitis B vaccine by way of accelerated schedules. There are now several accelerated schedules of administration of hepatitis B vaccine which can be tailored to the needs of the individual at risk of exposure to infection. One such schedule allows the primary course to be administered within a period of 1 month. This schedule of day 0, 7 and 21, with a booster at 12 months, is licensed for use with the recombinant hepatitis B vaccine Engerix B and results in a seroprotection rate of 65% at day 28 which increases to 99% at month 13. In more recent years, the development of a multivalent or combination vaccine against hepatitis A and B (Twinrix) has been a welcome advance in the protection against viral hepatitis, and has been of particular benefit to those who are at risk of infection with both viruses. The advantages of accelerated schedules have also been recognised with this combination vaccine. The primary course may be administered within a period of 1 month so providing protection for those at risk and, in particular, the last minute traveller.
Similar articles
-
Rapid and sustained immune response against hepatitis A and B achieved with combined vaccine using an accelerated administration schedule.J Travel Med. 2007 Jan-Feb;14(1):9-15. doi: 10.1111/j.1708-8305.2006.00106.x. J Travel Med. 2007. PMID: 17241248 Clinical Trial.
-
Immunogenicity of an accelerated vaccination regime with a combined hepatitis a/b vaccine in patients with chronic hepatitis C.Z Gastroenterol. 2003 Oct;41(10):983-90. doi: 10.1055/s-2003-42929. Z Gastroenterol. 2003. PMID: 14562195 Clinical Trial.
-
Rapid protection against hepatitis A and B using an accelerated vaccination schedule: comparison of combined vaccine, Twinrix, with separate vaccines.BioDrugs. 2003;17 Suppl 1:15-8. doi: 10.2165/00063030-200317001-00004. BioDrugs. 2003. PMID: 12785873 Clinical Trial. No abstract available.
-
Bivalent inactivated hepatitis A and recombinant hepatitis B vaccine.Expert Rev Vaccines. 2007 Dec;6(6):891-902. doi: 10.1586/14760584.6.6.891. Expert Rev Vaccines. 2007. PMID: 18377352 Review.
-
Accelerated vaccination schedules provide protection against hepatitis A and B in last-minute travelers.J Travel Med. 2004 Jul-Aug;11(4):260-1. doi: 10.2310/7060.2004.19013. J Travel Med. 2004. PMID: 15541232 Review. No abstract available.
Cited by
-
Short-term immunogenicity of standard and accelerated hepatitis B virus vaccination schedules in healthy adults: a comparative field study in China.Biosci Rep. 2018 Oct 17;38(5):BSR20180846. doi: 10.1042/BSR20180846. Print 2018 Oct 31. Biosci Rep. 2018. PMID: 30201691 Free PMC article.
-
Schedules for hepatitis B vaccination of risk groups: balancing immunogenicity and compliance.Sex Transm Infect. 2007 Oct;83(6):426-32. doi: 10.1136/sti.2006.022111. Sex Transm Infect. 2007. PMID: 17911142 Free PMC article. Review.
-
Combined hepatitis A and B vaccines: a review of their immunogenicity and tolerability.Drugs. 2003;63(23):2625-49. doi: 10.2165/00003495-200363230-00008. Drugs. 2003. PMID: 14636084 Review.
-
Old and new adjuvants for hepatitis B vaccines.Med Microbiol Immunol. 2015 Feb;204(1):69-78. doi: 10.1007/s00430-014-0375-9. Epub 2014 Dec 19. Med Microbiol Immunol. 2015. PMID: 25523196 Review.
-
Feasibility of completing an accelerated vaccine series for homeless adults.J Viral Hepat. 2009 Sep;16(9):666-73. doi: 10.1111/j.1365-2893.2009.01114.x. Epub 2009 Feb 24. J Viral Hepat. 2009. PMID: 19245384 Free PMC article. Clinical Trial.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources