Improving the duration of immunity for FMD vaccines€¦ · Killed inactivated oil adjuvanted...
Transcript of Improving the duration of immunity for FMD vaccines€¦ · Killed inactivated oil adjuvanted...
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Improving the duration of
immunity for FMD vaccines
Satya Parida
The Pirbright Institute
Oxford, University
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Challenges for FMD control
in endemic settings through vaccination
Killed inactivated oil adjuvanted vaccines are in use.
Biannual vaccinations (3 PD50 vaccines) are practised to control the disease in endemic settings
One of the major challenges- short lived immunity (~3 to 4 months max) which allows at least 2 month window for bringing back the disease before 2nd vaccination.
Main aim: To increase the duration of immunity, at least to cover the window between biannual vaccination
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VNT and IFN-γ responses in serotype A and
SAT2 vaccinated cattle on 21dpv
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A Malaysia 97 (IFN-γ) SAT2 Eritrea (IFN-γ)
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How does the new generation
adjuvants help?
• Activate the innate
immune system
via ligand binding
to PRR
• Enhance the anti-
viral environment
• Enhance the
adaptive response
(CMI and humoral)
• Improve memory
responses
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Screening of potent adjuvants-I
Type O antigen (sub-optimal dose) in
cattleGroups No of
animals Details of vaccine FMD
antigen Adjuvant/ISA
206 Protected/Total Percent
protection
1 4* FMD antigen + Abisco 300 + ISA 206
5 µg 1 mg + 1 ml 3/3 100
2 4* FMD antigen + CpG + Emulsigen + ISA 206
5 µg 0.25 mg + 1 ml + 1ml
1/3 33
3 4 FMD antigen + ISA 70V 5 µg 1 ml 2/4 50
4 4 FMD antigen + ISA 206 + Poly I:C
5 µg 1 ml + 0.4 mg 3/4 75
5 4 FMD antigen + ISA 206 + Imiquimod
5 µg 1 ml + 0.4 mg 3/4 75
6 4 FMD antigen + ISA 206 + MPL-A
5 µg 1 ml + 0.4 mg 3/4 75
7 4 FMD antigen + Liposome
5 µg 0.2 ml 1/4 25
8 4 FMD antigen + ISA 206 5 µg 1 ml 2/4 50
9 4 FMD antigen + ISA 206 10 µg 1 ml 4/4 100
10 2 PBS alone without FMD antigens
Nil Nil 0/2 0
*
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*
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Screening of potent adjuvants- II
Type O antigen (sub-optimal dose):
cattle
Groups No of animals
Details of vaccine FMD antigen
Adjuvant/ISA 206
Protected/Total Percent protection
1 4* FMD antigen + Abisco 300 + ISA 206
5 µg 1 mg + 1 ml 3/3 100
2 4* FMD antigen + CpG + Emulsigen + ISA 206
5 µg 0.25 mg + 1 ml + 1ml
1/3 33
3 4 FMD antigen + ISA 70V 5 µg 1 ml 2/4 50
4 4 FMD antigen + ISA 206 + Poly I:C
5 µg 1 ml + 0.4 mg 3/4 75
5 4 FMD antigen + ISA 206 + Imiquimod
5 µg 1 ml + 0.4 mg 3/4 75
6 4 FMD antigen + ISA 206 + MPL-A
5 µg 1 ml + 0.4 mg 3/4 75
7 4 FMD antigen + Liposome
5 µg 0.2 ml 1/4 25
8 4 FMD antigen + ISA 206 5 µg 1 ml 2/4 50
9 4 FMD antigen + ISA 206 10 µg 1 ml 4/4 100
10 2 PBS alone without FMD antigens
Nil Nil 0/2 0
*,one animal died (non- specific) before the day of challenge (21 dpv). Animals were vaccinated intramuscularly on one occasion and
challenged by the intradermolingual route with log104 CCID50 dose of FMDV O/IND/R2/75, 3 weeks later.
Groups No of animals
Details of vaccine FMD antigen
Adjuvant/ISA 206
Protected/Total Percent protection
1 4* FMD antigen + Abisco 300 + ISA 206
5 µg 1 mg + 1 ml 3/3 100
2 4* FMD antigen + CpG + Emulsigen + ISA 206
5 µg 0.25 mg + 1 ml + 1ml
1/3 33
3 4 FMD antigen + ISA 70V 5 µg 1 ml 2/4 50
4 4 FMD antigen + ISA 206 + Poly I:C
5 µg 1 ml + 0.4 mg 3/4 75
5 4 FMD antigen + ISA 206 + Imiquimod
5 µg 1 ml + 0.4 mg 3/4 75
6 4 FMD antigen + ISA 206 + MPL-A
5 µg 1 ml + 0.4 mg 3/4 75
7 4 FMD antigen + Liposome
5 µg 0.2 ml 1/4 25
8 4 FMD antigen + ISA 206 5 µg 1 ml 2/4 50
9 4 FMD antigen + ISA 206 10 µg 1 ml 4/4 100
10 2 PBS alone without FMD antigens
Nil Nil 0/2 0
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Final screening of potent adjuvants
using Type A antigen (sub-optimal
dose) in cattle
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Non-Vaccinates control
A22 Iraq+ ISA-206 control
A22 Iraq+ ISA-206 + poly (I:C) adjuvant
A22 Iraq+ ISA-206 + AbISCO adjuvant
A22 Iraq+ ISA-206 + R848 adjuvant
A22 Iraq+ ISA-206 + MPLA adjuvant
A22 Iraq+ ISA-206 + R848+ MPLA adjuvant
Serotype A Vaccine Trial Design
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A22 Iraq Vaccination
(sub-optimal dose)
7 14 21 28
A22 Iraq Challenge
Cull
30140 7 21 28
SamplingDaily Rectal TempSwabsClotted bloodHeparinized blood
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All calves had viraemia and sub-
clinical infection
Genome copy in nasal secretions
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FACS analysis- IFN-γ from CD4+ and
CD8+ cells
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Poly (I:C) and AbISCO had significantly increased neutralizing antibodies on 28dpv
compared to the ISA-206 control group
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• Achieved an increased potency as indicated by
lack of clinical symptoms in Poly I:C and AbISCO groups
(although not able to prevent sub-clinical infection)
• Significantly elevated neutralizing antibodies in Abisco
and Poly I:C group cattle
• Some indication of IFN-g upregulation by CD4+ and
CD8+ cells
Summary-1
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ISA 206 + Poly I:C 11 cattle
ISA 206 11 cattle
Type O antigen full dose- 10 microgram
Vaccinated cattle were monitored for 225 days (7.5 months) at Indian Immunologicals
Serum, PBMC and antigen specfic stimulated whole blood plasma were transported to Pirbright for analysis
Longer duration of immunity study
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Virus neutralisation titres• Titres significantly higher in cattle when vaccinated with poly
I:C (blue) compared with conventional adjuvant (red)
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Whole blood Interferon-γ• Significantly higher levels in cattle when vaccinated with poly
I:C (blue) compared with conventional adjuvant (red)
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Gr-1 Conv. vaccine Gr-2 Poly:IC vaccine
Mean-CD4-IFNg+
Mean-CD8-IFNg+
IFN-γ production -flow cytometry on 120 dpv
% I
FN
-γ+
cells
% of CD4 or CD8 cells from the total live population showing antigen specific IFNγ expression
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• Significantly higher VN titre in cattle vaccinated with poly I:C compared with conventional adjuvant
• By 4th month many of the conventional vaccinated animals lost the protective level of antibody titre
• IFNγ levels significantly higher in cattle when vaccinated with poly I:C when compared with conventional adjuvant
• Indication of IFN-gamma upregulationby CD4+ and CD8+ cells were observed in Poly I:C group in FACS analysis.
• Duration of immunity can be enhanced up to 6 months post-vaccination that covers the window of susceptibility before 2nd vaccination
Summary-2
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Acknowledgements
The Pirbright campus is being redeveloped
Katie Lloyds-Jones
Mana Mahapatra
Krupali Parekh
Katy Moffat
Becky Herbert
Aravindh Babu
Simon Gubbins
David Paton
Geraldine Taylor
Funding:
BBSRC
DFID, UK
Oxford, University
Indian Immunological
Dr V.A Srinivasan
Dr S B NagendraKumar
Dr M Madhanmohan
Dr R Lingala