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- Introduction to Vaccines
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1. History of vaccines
- Prof. Stanley Plotkin
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2. The science of vaccine adjuvants
- Dr. Derek O'Hagan
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3. Vaccine preclinical studies 1
- Dr. Rebecca Sheets
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4. Vaccine preclinical studies 2
- Dr. Rebecca Sheets
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5. Vaccine manufacturing 1
- Dr. Don Gerson
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6. Vaccine manufacturing 2
- Dr. Don Gerson
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10. Recommendations of the U.S. advisory committee on immunization practices
- Prof. Jonathan Temte
- Vaccines in Development
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11. HIV vaccine development
- Dr. Patricia Fast
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12. Developing tuberculosis vaccines - challenges and strategies 1
- Dr. Thomas Evans
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13. Developing tuberculosis vaccines - challenges and strategies 2
- Dr. Thomas Evans
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14. Malaria vaccine development 1
- Dr. Ashley Birkett
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15. Malaria vaccine development 2
- Dr. Ashley Birkett
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16. Dengue vaccine development: l. status
- Prof. Scott Halstead
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17. Dengue vaccine development: II. problems to be solved
- Prof. Scott Halstead
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18. Respiratory syncytial virus vaccination
- Prof. Peter Openshaw
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19. Herpes simplex virus vaccines
- Prof. Lawrence Stanberry
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20. Bacterial vaccines in development 1
- Dr. Kathrin Jansen
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21. Bacterial vaccines in development 2
- Dr. Kathrin Jansen
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22. Biodefense and special pathogen vaccines in development 1
- Dr. Gerald Kovacs
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23. Biodefense and special pathogen vaccines in development 2
- Dr. Gerald Kovacs
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24. Cancer vaccines 1
- Prof. Cornelis Melief
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25. Cancer vaccines 2
- Prof. Cornelis Melief
- Future Directions for Vaccine Development
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26. Replication-competent viral vectors
- Dr. Farshad Guirakhoo
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27. Vector mediated immunoprophylaxis
- Dr. Bruce Schnepp
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28. Future directions for vaccine discovery 1
- Dr. Chris Wilson
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29. Future directions for vaccine discovery 2
- Dr. Chris Wilson
- Archived Lectures *These may not cover the latest advances in the field
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30. Vaccine adjuvants 1
- Dr. Derek O'Hagan
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31. Vaccine adjuvants 2
- Dr. Derek O'Hagan
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32. Respiratory syncytial virus vaccine development
- Prof. Peter Openshaw
Printable Handouts
Navigable Slide Index
- Introduction
- Novel vaccines for Gram+ pathogens
- Medical need for an S. aureus vaccine
- S. aureus is a challenging vaccine target
- Vaccine approach for S. aureus infections
- Learning from past failures
- Design of next generation S. aureus vaccines
- S. aureus capsular polysaccharides as targets
- S. aureus opsonophagocytic assay (OPA)
- CP5/CP8 polysaccharide conjugates OPA titers
- S. aureus antigens associated with virulence
- Clumping factor A: an important virulence factor
- FBI assay
- Manganese transporter C and S. aureus virulence
- Pfizer’s SA4AG vaccine - Phase 2 clinical study
- Novel vaccines for Gram- pathogens
- N. meningitidis serogroup B: unmet medical need
- Novel approaches to identify MnB antigens (1)
- Novel approaches to identify MnB antigens (2)
- Assessing MnB vaccine immunogenicity/efficacy
- Recently licensed MnB vaccines in the US
- Trumenba and Bexsero vaccines approaches
- Summary
Topics Covered
- Novel vaccines for Gram+ pathogens: S. aureus
- Novel vaccines for Gram- pathogens N. meningitides serogroup B
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Jansen, K. (2015, September 30). Bacterial vaccines in development 2 [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved March 13, 2025, from https://doi.org/10.69645/SIXG4791.Export Citation (RIS)
Publication History
- Published on September 30, 2015
Financial Disclosures
- Dr. Kathrin Jansen, Dr. Jansen is an employee and shareholder of Pfizer Inc
Bacterial vaccines in development 2
Published on September 30, 2015
38 min
A selection of talks on Vaccines
Transcript
Please wait while the transcript is being prepared...
0:04
Now, we'll move on to describe vaccines and development against
a highly complex pathogen, Staphylococcus aureus.
This pathogen causes disease by expressing a number of virulence factors.
0:22
S.aureus causes a wide spectrum of diseases ranging from
relatively mild skin infections to life-threatening wound and bloodstream infections.
It is a leading cause of morbidity and mortality
in both healthcare-associated and community settings.
In surgical patients, S.aureus infections
are associated with high morbidity and mortality,
prolongation of hospital stays and an increase in healthcare costs.
We also noted increases in antibiotic resistance,
most notably, methicillin resistance.
There is an alarming increase in community-acquired infections as
well in many settings, including pediatric populations.
I also listed on the slide,
populations that are at high risk of S.aureus infection.
1:20
Now, Staphylococcus aureus is a challenging vaccine target.
It's a highly successful commensal organism,
and about 30 percent of humans are colonized with Staph aureus.
Staph aureus exhibits a diverse array of
virulence factors that facilitate colonization and evasion of host immune responses,
such as toxins and adhesion factors;
it is a master in scavenging nutrients from the host,
it exhibits capsular polysaccharides to evade phagocytosis,
and it also has a number of virulence factors that
interfere with appropriate immune host-mediated immune response.
Staph aureus shows extensive strain diversity.
Most humans actually fail to generate
functional antibodies against S. aureus following natural exposure,
be it by colonization or infection.
The importance of this,
I will describe it a little bit later on.