An inactivated yellow fever 17DD vaccine cultivated in Vero cell cultures. Issue 35 (20th August 2015)
- Record Type:
- Journal Article
- Title:
- An inactivated yellow fever 17DD vaccine cultivated in Vero cell cultures. Issue 35 (20th August 2015)
- Main Title:
- An inactivated yellow fever 17DD vaccine cultivated in Vero cell cultures
- Authors:
- Pereira, Renata C.
Silva, Andrea N.M.R.
Souza, Marta Cristina O.
Silva, Marlon V.
Neves, Patrícia P.C.C.
Silva, Andrea A.M.V.
Matos, Denise D.C.S.
Herrera, Miguel A.O.
Yamamura, Anna M.Y.
Freire, Marcos S.
Gaspar, Luciane P.
Caride, Elena - Abstract:
- <abstract abstract-type="author" id="abs0005"> <title id="sect0005">Abstract</title> <sec> <p id="spar0005">Yellow fever is an acute infectious disease caused by prototype virus of the genus <italic>Flavivirus</italic>. It is endemic in Africa and South America where it represents a serious public health problem causing epidemics of hemorrhagic fever with mortality rates ranging from 20% to 50%. There is no available antiviral therapy and vaccination is the primary method of disease control. Although the attenuated vaccines for yellow fever show safety and efficacy it became necessary to develop a new yellow fever vaccine due to the occurrence of rare serious adverse events, which include visceral and neurotropic diseases. The new inactivated vaccine should be safer and effective as the existing attenuated one. In the present study, the immunogenicity of an inactivated 17DD vaccine in C57BL/6 mice was evaluated. The yellow fever virus was produced by cultivation of Vero cells in bioreactors, inactivated with β-propiolactone, and adsorbed to aluminum hydroxide (alum). Mice were inoculated with inactivated 17DD vaccine containing alum adjuvant and followed by intracerebral challenge with 17DD virus. The results showed that animals receiving 3 doses of the inactivated vaccine (2 μg/dose) with alum adjuvant had neutralizing antibody titers above the cut-off of PRNT<sub>50</sub> (Plaque Reduction Neutralization Test). In addition, animals immunized with inactivated vaccine showed<abstract abstract-type="author" id="abs0005"> <title id="sect0005">Abstract</title> <sec> <p id="spar0005">Yellow fever is an acute infectious disease caused by prototype virus of the genus <italic>Flavivirus</italic>. It is endemic in Africa and South America where it represents a serious public health problem causing epidemics of hemorrhagic fever with mortality rates ranging from 20% to 50%. There is no available antiviral therapy and vaccination is the primary method of disease control. Although the attenuated vaccines for yellow fever show safety and efficacy it became necessary to develop a new yellow fever vaccine due to the occurrence of rare serious adverse events, which include visceral and neurotropic diseases. The new inactivated vaccine should be safer and effective as the existing attenuated one. In the present study, the immunogenicity of an inactivated 17DD vaccine in C57BL/6 mice was evaluated. The yellow fever virus was produced by cultivation of Vero cells in bioreactors, inactivated with β-propiolactone, and adsorbed to aluminum hydroxide (alum). Mice were inoculated with inactivated 17DD vaccine containing alum adjuvant and followed by intracerebral challenge with 17DD virus. The results showed that animals receiving 3 doses of the inactivated vaccine (2 μg/dose) with alum adjuvant had neutralizing antibody titers above the cut-off of PRNT<sub>50</sub> (Plaque Reduction Neutralization Test). In addition, animals immunized with inactivated vaccine showed survival rate of 100% after the challenge as well as animals immunized with commercial attenuated 17DD vaccine.</p> </sec> </abstract> … (more)
- Is Part Of:
- Vaccine. Volume 33:Issue 35(2015)
- Journal:
- Vaccine
- Issue:
- Volume 33:Issue 35(2015)
- Issue Display:
- Volume 33, Issue 35 (2015)
- Year:
- 2015
- Volume:
- 33
- Issue:
- 35
- Issue Sort Value:
- 2015-0033-0035-0000
- Page Start:
- 4261
- Page End:
- 4268
- Publication Date:
- 2015-08-20
- Subjects:
- Vaccines -- Periodicals
615.372 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0264410X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/0264410X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/0264410X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.vaccine.2015.03.077 ↗
- Languages:
- English
- ISSNs:
- 0264-410X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9138.628000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4332.xml