Title: Vaksienes: opgedateerde weergawe
1Vaksienes opgedateerde weergawe
- Dr Lynne Webber
- Maart 2008
2Lewende vaksienes en tyd
- Pokke
- Antraks
- Hondsdolheid
- BCG
- Geelkoors
- OPV
- Masels
- adenovirusse
- 1798
- 1881
- 1885
- 1927
- 1935
- 1962
- 1963
- 1971
3Lewende vaksienes en tyd
- Waterpokkies
- Rotavirus
- Duitse masels
- Lewende griep
- Onaktiewe griep
- Lewende griep
- Rotavirus koei-mens stam
- 1995
- 2005
- 1969
- 2003
- 1970s
- 2003
- 2005
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5 1950s The cell-culture revolution
- Mass production of virus followed by complete
inactivation. Virus grown in - Eggs (influenza type A B)
- Continuous monkey kidney cell lines
(poliovirus 1,2 3) IPV (Salk) - Human diploid fibroblasts (rabies,
HAV) - Mouse brain (JEV)
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71900s Viral subunit vaccines
- Virus is inactivated with a chemical such as
formalin and/or disrupted with a detergent e.g.
Influenza vaccines
81986 Recombinant subunit vaccines
- Construction of inactivated antigens e.g.
- Hepatitis B vaccine manufactured in a yeast
recombinant carrying the gene for the S protein - Insertion of genes into yeast, Escherichia coli
or Chinese hamster ovary cells enabled production
of a variety of recombinant proteins in
development - Lyme OspA, cytomegalovirus gB, pertussis toxin
92006 Recombinant subunit vaccines- Virus-like
particles (VLPs)
- Capsid proteins of nonenveloped viruses the
nucleocapsid of some enveloped viruses can
self-assemble into VLPs - VLPs consist of capsid proteins assembled into a
similar shell like structure, but viral nucleic
acid is not present within the shell
- These shells can display conformational epitopes
that are not present on individual purified
capsid proteins
10Nie-lewende vaksienes
- Tifoied, cholera en plaag
- Heel-sel pertussis
- Griep
- IPV
- Hepatitis A
- Japanese enkefalities
- 1896 7
- 1926
- 1938
- 1955
- 1995
- 1944
11Nie-lewende vaksienes
- Meningokokaal
- Pneumokokaal
- Tifoied
- H. influenza b
- Staphylokokaal
- Hepatitis B
- Menslike papiloomvirus
- 1974
- 1977
- 1995
- 1987
- Future
- 1986
- 2006-2007
12Recombinant vector vaccines
13Replication-competent vectors (recombinant live
attenuated virus vaccines)
- Molecular technologies are used to construct
viable recombinants
- Possess
- surface proteins of a virus against which the
vaccine is directed plus - the remaining coding noncoding regions of
another related virus that bears attenuating
mutations
14Immunology finally helps vaccinology
- Most successes in immunization have been mediated
through the induction of protective antibodies - Major challenge induction of T cell immunity
- Several of the new strategies, incl. vectors,
plasmid DNA lipidated peptides, are capable of
inducing both CD4 CD8 cellular responses - Stimulation of innate adaptive immune responses
can be accomplished by the choice of proper
adjuvants - Adjuvants for vaccines
- until recently essentially limited to aluminum
salts (alum) that stimulate a T helper type 2
(Th2) response - creation of new oil-in-water emulsions,
liposomes, Toll-like receptor (TLR) agonists,
cytokines other substances that push the immune
system in a T helper type 1 (Th1) direction
15Nuwe gedagtes!
16Enlargement of routes of immunization need for
mucosal immune responses
- Transdermal application deliver Ag across the
skin - Closest to actual use e.g. Hepatitis B, anthrax
- Many devices have been developed e.g.
- patches applied to lightly abraded skin
- microneedles to pierce the stratum corneum
- Once past the superficial layer the Ag comes in
contact with DCs ? travel to LN initiate immune
responses - If transdermal immunization works well,
vaccination practice could be revolutionized
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19SA Childhood EPI schedule
20Recommended immunization schedule for ages 0 to 6
years, US 2007
http//www.cdc.gov/vaccines/recs/schedules/downloa
ds/child/2007/child-schedule-color-print.pdf
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22HPV vaccines
- Gardasil (Merck) was FDA EU approved in 2006
- VLPs from HPV types 6, 11, 16 18 manufactured
in a yeast system with alum as adjuvant - Cervarix (GSK) are pending FDA approval
- VLPs from HPV types 16 18 manufactured in a
baculovirus system - Three-doses regimen 0-, 2-, 6-months
- Efficacy safety
- 99.7 of those vaccinated developed an Ab
response - In 16-23 year old ? HPV 16 naïve at baseline
100 effective - No serious vaccine-related adverse events
- CDC recommendations
- 11-26 year old females regardless of whether or
not they have had prior gynaecological or Pap
screening even with a history of having an
abnormal Pap examination - Ideal 9-15 years old before sexual debut
- NOT a therapeutic vaccine
23A vast array of vaccinations
- By the age of 18 children in the US will have
received up to 44 vaccine injections - Excl. rotavirus (oral) HPV
24New combination approaches
- Co delivery of multivalent vaccines
- Co delivery by different routes
- Sequential combination of vaccines
- (Prime-boost strategies)
25Co delivery of multivalent vaccines Combination
vaccines
- Hexavalent combinations (Hib/DTaP/IPV/HBV)
- used in Europe
- Pentavalent combinations (Hib/DTaP/IPV)
- used in many parts of the world
- Pentacel pending FDA licensure in the US
- Varicella vaccine has been incorporated into
measles-mumps-rubella vaccines (MMR-V) - ProQuad FDA licensure 2005
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27New population target groups for vaccination
28Herpes zoster vaccine for prevention of zoster
- 2 new vaccine formulations have been evaluated
- Heat inactivated Oka/Merck vaccine preparation
was associated with a reduced incidence of zoster
to 13 during the first year after autologous
hematopoeitic cell transplantation when given as
1 dose before and 3 doses after transplantation - Higher potency live attenuated Oka vaccines were
developed evaluated for their potential to
increase VZV cellular immunity in healthy older
adults (gt60 years) - Zostavax FDA licensed in 2006
- VZV-specific memory T cells decline with age
- The administration of zoster vaccine to older
persons may prevent VZV-specific T cells from
dropping below the threshold for zoster occurrence
29Dankie en sterkte vir die res van die dag!