• No results found

Towards a blood stage malaria vaccine, dealing with allelic polymorphism in the vaccine candidate apical membrane antihen 1

N/A
N/A
Protected

Academic year: 2021

Share "Towards a blood stage malaria vaccine, dealing with allelic polymorphism in the vaccine candidate apical membrane antihen 1"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

Towards a blood stage malaria vaccine, dealing with allelic

polymorphism in the vaccine candidate apical membrane antihen 1

Kusi, K.A.

Citation

Kusi, K. A. (2012, January 18). Towards a blood stage malaria vaccine, dealing with allelic polymorphism in the vaccine candidate apical membrane antihen 1. Retrieved from

https://hdl.handle.net/1887/18387

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/18387

Note: To cite this publication please use the final published version (if applicable).

(2)

Propositions (stellingen) of the thesis

“Towards a blood stage malaria vaccine; dealing with allelic polymorphism in the vaccine candidate apical membrane antigen 1”

1. Despite the many allelic variants found in nature, PfAMA1 antigens do have common epitopes, which enable the induction of broad protective responses (this thesis).

2. Multi-allele vaccines incorporating three PfAMA1 alleles elicit the broadest possible proportion of cross-strain anti-AMA1 antibodies (this thesis).

3. Individuals exposed naturally to variant malaria parasites are likely to accumulate a strain-transcending repertoire of protective antibodies against polymorphic vaccine targets with time (this thesis).

4. The polymorphic nature of PfAMA1 does not necessarily mean it will fail as a vaccine candidate (this thesis).

5. An effective subunit malaria vaccine would ultimately be one with a mixture of individually proven immunogens from multiple stages of the parasite’s life cycle.

6. The most advanced malaria vaccine to date (RTS,S) has been shown to have 50%

efficacy over the first 8 months of study follow-up and protection that persists for up to 15 months after vaccination of 5 – 17 month old children in two

malaria-endemic areas (Bejon et al., N Engl J Med (2008). 359: 2521–2532; Olotu et al., Lancet Infect Dis (2011). 11: 102–109). Though modest, this is an

encouraging prospect for malaria vaccine development.

7. The pace of current vaccine development efforts would be greatly enhanced by the availability of non-proprietary, highly potent adjuvants.

8. The global fight against some infectious diseases can be won with a little science and much more commitment.

9. Africa’s stagnated development is mainly due to a lack of adequate investment in science and technology.

10. All of mankind inherently look up to a higher being; for some it is God, for others it is themselves.

11. The quest for knowledge has but one purpose; to enable us make an informed choice.

12. Wisdom is like a baobab tree; no one individual can embrace it. ~ A Ghanaian proverb

Referenties

GERELATEERDE DOCUMENTEN

For each policy (defined by vaccine valency, coverage level, and strength of cross-immunity), a point (X,Y) on the graph suggests that for the proportion X of simulated epidemics

The thesis investigates multi-allele vaccine formulation as a strategy for overcoming the effect of allelic polymorphism on immune responses to Plasmodium falciparum

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden Downloaded.

Towards a blood stage malaria vaccine, dealing with allelic polymorphism in the vaccine candidate apical membrane antihen 1..

knowlesi (24 hours) being exceptions.. Life cycle of the human Plasmodium species. Source: http://www.uni-tuebingen.de/modeling/Mod_Malaria_Cycle_en.html, with

The assay was independent of the specific antibody source (serum or purified IgG) and the antibody dilution factor when the working OD values fell within the

Specificity profiles of antibodies from rabbit immunisations with the three- antigen (DiCo mix, Gp 2) and seven-antigen (DiCo mix + AMA1 alleles from FVO, HB3, 3D7 and

Sequential exposure to the different PfAMA1 allelic variants induced immunological recall of responses to previous alleles and yielded functional cross-strain