Literature DB >> 8854020

Stability of yellow fever vaccine.

T P Monath1.   

Abstract

Yellow fever, an acute mosquito-borne viral haemorrhagic fever, is preventable by use of the live, attenuated 17D vaccine. The vaccine is used principally in tropical climates and is subject to potentially adverse conditions. Lyophilized vaccine without stabilizers deteriorates rapidly when exposed to temperatures above -20 degrees C. In 1987, the WHO recommended that each lot of vaccine meet the following stability test: maintenance of potency (> 1,000 mouse i.c.LD50/human dose) with mean loss of titre < 1.0 log10 after being held at 37 degrees C for 14 days. In 1987, only 5 out of 12 yellow fever vaccines produced worldwide met the stability standards. To improve stability of the vaccine, a number of additives have been systematically investigated. A successful formulation, now used by a number of manufacturers, employs sugars, amino acids, and divalent cations [lactose (4%), sorbitol (2%), histidine (0.01 M), alanine (0.01 M), in phosphate buffered saline with Ca2+ and Mg2+]. As opposed to vaccine produced without stabilizers, which loses 1.5-2.5 log10/dose, stabilized vaccines lose only 0.3-0.5 log10 after being held at 37 degrees C for 14 days. The vaccine is stable after storage for > or = two years at 4 degrees C and 22 degrees C, and has a stability profile as good or better than many other live and inactivated vaccines currently used in the EPI, including measles, pertussis, oral and inactivated poliomyelitis vaccines. WHO is taking steps to enssure that all 11 current YF vaccine manufacturers produce vaccines that meet accepted stability standards. The principal rationale for increasing 17D vaccine stability beyond that achieved with the present stabilizers would be the improvement in stability of other EPI vaccines, to the point where yellow fever vaccine was the most sensitive vaccine among those deployed. The acceptable characteristics of current stabilized 17D vaccines and the high cost of changing and validating new vaccine formulations precludes a major investment at this time. Despite its stability when freeze dried, yellow fever 17D vaccine is quite unstable after reconstitution and must be discarded after one hour. Improvement in vaccine stability after reconstitution would thus reduce cost, stretch supplies of vaccine, and ensure against vaccine failures due to use of degraded vaccine. This is an area for future research.

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Year:  1996        PMID: 8854020

Source DB:  PubMed          Journal:  Dev Biol Stand        ISSN: 0301-5149


  8 in total

1.  Novel formulations enhance the thermal stability of live-attenuated flavivirus vaccines.

Authors:  O'Neil Wiggan; Jill A Livengood; Shawn J Silengo; Richard M Kinney; Jorge E Osorio; Claire Y-H Huang; Dan T Stinchcomb
Journal:  Vaccine       Date:  2011-07-29       Impact factor: 3.641

Review 2.  Advances and controversies in yellow fever vaccination.

Authors:  Emile F F Jonker; Leonardus G Visser; Anna H Roukens
Journal:  Ther Adv Vaccines       Date:  2013-11

3.  The yellow fever vaccine: a history.

Authors:  J Gordon Frierson
Journal:  Yale J Biol Med       Date:  2010-06

4.  Synthetic rabbit-human antibody conjugate as a control in immunoassays for immunoglobulin M specific to hepatitis E virus.

Authors:  Kuo Zhang; Lunan Wang; Min Liu; Rui Zhang; Jinming Li
Journal:  Virol J       Date:  2010-05-20       Impact factor: 4.099

5.  A lyophilized formulation of RiVax, a recombinant ricin subunit vaccine, retains immunogenicity.

Authors:  Joan E Smallshaw; Ellen S Vitetta
Journal:  Vaccine       Date:  2010-01-12       Impact factor: 3.641

6.  Effect of chemical stabilizers on the thermostability and infectivity of a representative panel of freeze dried viruses.

Authors:  Boris Pastorino; Cecile Baronti; Ernest A Gould; Remi N Charrel; Xavier de Lamballerie
Journal:  PLoS One       Date:  2015-04-29       Impact factor: 3.240

7.  Randomized, double-blinded, controlled non-inferiority trials evaluating the immunogenicity and safety of fractional doses of Yellow Fever vaccines in Kenya and Uganda.

Authors:  Derick Kimathi; Aitana Juan; Philip Bejon; Rebecca F Grais; George M Warimwe
Journal:  Wellcome Open Res       Date:  2019-11-20

8.  Intradermally administered yellow fever vaccine at reduced dose induces a protective immune response: a randomized controlled non-inferiority trial.

Authors:  Anna H Roukens; Ann C Vossen; Peter J Bredenbeek; Jaap T van Dissel; Leo G Visser
Journal:  PLoS One       Date:  2008-04-23       Impact factor: 3.240

  8 in total

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