immunogenicity of combined vaccines in infants helena käyhty, phd national public health institute...
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![Page 1: Immunogenicity of combined vaccines in infants Helena Käyhty, PhD National Public Health Institute Dept of Vaccines Helsinki, Finland](https://reader036.vdocuments.us/reader036/viewer/2022081603/56649f1e5503460f94c364ee/html5/thumbnails/1.jpg)
Immunogenicity of combined vaccines in infants
Helena Käyhty, PhDNational Public Health InstituteDept of VaccinesHelsinki, Finland
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Combined vs. reference administrationhexavalent vaccines
• Gylca et al. Vaccine 2001: DTaP-HBV-IPV / Hib vs. DTwP-IPV mixed with Hib +HBV at 6, 10, 14 weeks
• Schmitt et al. J Ped 2000: mixed vs. separate DTaP-HBV-IPV / Hib at 2, 3, 4 months
• Mallet et al. PIDJ 2000: DTaP-HBV-IPV-Hib vs. DTaP-IPV-Hib / HBV at 2, 4 and 6 months
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Combined vs. reference administration
0 1 2
D
T
HB
Polio 1
Polio 2
Polio 3
PTA
FHA
PRN
Hib Mallet ea
Schmitt ea
Gylca ea
fold difference
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Eskola et al. Lancet 1996Vaccinations at 4 and 6 mo
DTaP / Hib/ IPV
DTaP-IPV/ Hib
DTaP-Hib/ IPV
DTaP-Hib-IPV
GMC, g/ml 3.9 3.1 0.4 0.6
%>0.15 g/ml 93 93 78 79
% >1.0 g/ml 87 77 19 48
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Three doses, combined vs. separate administration in different studies
0
2
4
6
8
10
12
14
16
18combined
separate
Anti-Hib
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Mechanisms???
• Missing adjuvant effect of wP• Epitopic supression - antigenic competition• Physicochemical interference
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Immunogenicity trials in Sweden (3,5,12 mo) and Finland (4,6,14 mo)
0,9
9,8
2
15
1
12
5
35
0
5
10
15
20
25
30
35
40
6/7 mo 13/15 mo
An
ti-H
ibPRP-T/DT+IPV
PRP-T/DT/IPV
PRP-T/DT/IPV/aP
PRP-T+DTP, FIN
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T
B
B
B
B
HELP
Anti-CHO Ab
Anti-Tetanus Ab
CHO
Tet
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B
HELP
Anti-CHO Ab
Anti-Tetanus Ab
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PncT, PRP-T and T simultaneouslyDose of PncT and response to PRP-T and
Tetanus toxoid (Dagan et al. 1998)
0
2
4
6
8
10
12
Placebo PncT01 PncT03 PncT10
Hib
0
1
2
3
4
5
Placebo PncT01 PncT03 PncT10
Tetanus
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Concomitant administration 2 cm apart in the same leg at 2, 4 and 6 mo
Eskola et al.
0
2
4
6
8
10
12
mixed separate differentlegs
separate sameleg
2 mo
6 mo
7 mo
anti-Hib
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Clinical implications?
• Are the induced anti-Hib responses high enough for protection?
• Experience from Finland, Sweden, the UK and Germany
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Protective efficacy vs. antibody response
Study 1: PRP-D at 3, 4, 6 and 14 months
Anti-Hib 7 mo 14 moGMC, µg/ml 0.53 0.37% > 1 µg/ml 40 22% > 0.15 µg/ml 68 67% >0.06 µg /ml 85 85
Protection 90 (70-96) %
Eskola et al, 1990
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Protective efficacy vs. antibody response
Study 2: PRP-D at 4, 6 and 14 months
Anti-Hib 7 mo 14 moGMC, µg/ml 0.63 0.38% > 1 µg /ml 32 24% > 0.15 µg /ml 77 72% >0.06 µg/ml 86 90
Protection 87 (69-96) %
Peltola et al, 1994
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Immunogenicity trials in Sweden (3,5,12 mo) and Finland (4,6,14 mo)
0,9
9,8
2
15
1
12
5
35
0
5
10
15
20
25
30
35
40
6/7 mo 13/15 mo
An
ti-H
ibPRP-T/DT+IPV
PRP-T/DT/IPV
PRP-T/DT/IPV/aP
PRP-T+DTP, FIN
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Three doses, combined vs. separate administration in different studies
0
2
4
6
8
10
12
14
16
18combined
separate
Anti-Hib
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DTaP/Hib/(IPV) combinations in Germany Schmitt et al 2001
• 2 year follow up after the introduction of combined vaccines
• Overall VE 97.5 % (96.3-98.4)• 1 dose 88.6 % (76.1-94.3)• 2 doses 95.1 % (92.2-97.0)• 3 doses 98.8 % (98.2-99.3)
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Measurement of the immune response to vaccination
Vaccine Sample Antibody
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Capsular polysaccharides (PS)
• Antibodies protective• Poor and short lasting immune response in infants
and children• Long lasting antibody response in older children
and adults• TI-antigens -> no memory -> protection is based on
existing antibodies
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Conjugate vaccines????
• immunogenicity improved by conjugating PS to carrier proteins -> TD properties -> antibody response even in infancy
• development of memory• protection may last longer than detectable antibody• memory B cells triggered upon challenge -> high and
quick antibody response• increase in avidity -> antibodies may function better
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How to test development of memory
• Memory B cells• Priming with conjugate and booster with PS
– PS mimics contact with bacteria– more memory B cells to be triggered by PS– high antibody response of IgG isotype
• Avidity maturation
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Increasing Affinity / Avidity
104 108 1012
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Geometric mean titer (GMT) and GM avidity index (GMAI)
Goldblatt et al., JID 177, 1998, 1112-5
1.0
0.9
0.8
0.7
0.6
0.5
0.4
0.3
0.2
0.1
0.0
10.0
100.0
0.1
1.0
14121086420
Avi
dit
y In
dex
(G
MA
I)
An
ti-P
RP
Igg
(G
MT
µg
/ml)
Age (months)
AvidityTitre
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Poolman et al Vaccine 2001
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Avidity of anti-6B Pnc PS- primary seria at 2,4,6 mo with a conjugate - booster at 14 mo with conjugate or PS
30
35
40
45
50
55
60
65
70
75
80
5 10 15 20
Age, mo
AI
PncCRM
PncD
30
35
40
45
50
55
60
65
70
75
80
5 10 15 20
Age, mo
AI
PncCRM
PncD
PncT
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Laboratory surrogates for evaluation of new conjugates, modified from Frasch 1995
• antibody response in infancy• persistence of antibodies (up to booster dose)• induction of immunologic memory
• PS-vaccine• avidity
• isotype/subclass distribution and avidity of antibodies• functional activity of antibodies
(opsonic or bactericidal activity)
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Mucosal immune response
• is or may be important when• local mucosal infection• colonization precedes disease
• the role as a surrogate test unknown