DK2833909T3 - Pcv/mycoplasma hyopneumoniae/prrs-kombinationsvaccine - Google Patents

Pcv/mycoplasma hyopneumoniae/prrs-kombinationsvaccine Download PDF

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DK2833909T3
DK2833909T3 DK13717118.7T DK13717118T DK2833909T3 DK 2833909 T3 DK2833909 T3 DK 2833909T3 DK 13717118 T DK13717118 T DK 13717118T DK 2833909 T3 DK2833909 T3 DK 2833909T3
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hyo
pcv2
antigen
lys
composition
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DK13717118.7T
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Gregory P Nitzel
Jeffrey E Galvin
John Keith Garrett
James R Ii Kulawik
Tracy L Ricker
Megan Marie Smutzer
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Zoetis Services Llc
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    • C07K14/30Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Mycoplasmatales, e.g. Pleuropneumonia-like organisms [PPLO]
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    • AHUMAN NECESSITIES
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    • A61K2039/55511Organic adjuvants
    • A61K2039/55566Emulsions, e.g. Freund's adjuvant, MF59
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    • C12N2770/10034Use of virus or viral component as vaccine, e.g. live-attenuated or inactivated virus, VLP, viral protein

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Claims (16)

1. Trivalent immunogen sammensætning omfattende supernatanten afen Mycoplasma hyopneumoniae (M.hyo)-kultur; et porcint circovirus type 2 (PCV2) antigen; og et porcin reproduktions- og respirationssygdom (PRRS)-virusanti-gen, hvor supernatanten af M.hyo-kulturen er blevet separeret fra uopløseligt cellulært materiale ved centrifugering, filtrering eller udfældning og er fri for både (i) IgG og (ii) immunkomplekser bestående af antigen, der er bundet til immunglobulin.
2. Sammensætning ifølge krav 1, hvor supernatanten af M.hyo-kulturen er blevet behandlet med protein-A eller protein-G, før den blev tilsat til den immunogene sammensætning.
3. Sammensætning ifølge krav 1 eller 2, hvor PRRS-virusantigenet er et genmodificeret levende virus.
4. Sammensætning ifølge et hvilket som helst af kravene 1 til 3, hvor PCV2-antigenet er i form af et kimært type 1-type 2-circovirus, hvilket kimære virus omfatter et inaktiveret rekombinant porcint circovirus type 1, der eksprimerer det porcine circovirus type 2-ORF2-protein.
5. Sammensætning ifølge et hvilket som helst af kravene 1 til 4, hvor PCV2-antigenet er i form af et rekombinant ORF2-protein.
6. Sammensætning ifølge krav 5, hvor det rekombinante ORF2-protein ekspri-meres fra en baculovirusvektor.
7. Sammensætning ifølge et hvilket som helst af kravene 1 til 6, hvor sammensætningen yderligere omfatter en adjuvans.
8. Sammensætning ifølge krav 7, hvor adjuvansen er udvalgt fra gruppen bestående af en olie-i-vand-adjuvans, en polymer-og-vand-adjuvans, en vand-i-olie-adjuvans, en aluminiumhydroxid-adjuvans, en vitamin E-adjuvans og kombinationer deraf.
9. Sammensætning ifølge et hvilket som helst af kravene 1 til 8 til anvendelse ved immunisering afen gris imod M.hyo, PCV2 og PRRS-virus, som omfatter indgivelse af sammensætningen ifølge krav 1 til 8 til grisen.
10. Sammensætning til anvendelse ifølge krav 9, hvor sammensætningen indgives i en enkelt dosis.
11. Sammensætning til anvendelse ifølge krav 9 eller 10, hvor sammensætningen indgives til grise, som har maternelt afledte antistoffer mod mindst en af M.hyo, PCV2 og PRRS-virus.
12. Sammensætning til anvendelse ifølge et hvilket som helst af kravene 9 til 11, hvor sammensætningen indgives til grise, når de er er 3 uger gamle eller ældre.
13. Vaccinesammensætning omfattende en immunogen sammensætning ifølge et hvilket som helst af kravene 1 til 8, hvor sammensætningen yderligere omfatter en farmaceutisk acceptabel bærer.
14. Vaccinesammensætning ifølge krav 13 til anvendelse til beskyttelse af grise imod enzootisk pneumoni, PMWS (Post-weaning Multisystemic Wasting Syndrome) og porcin reproduktions- og respirationssygdom.
15. Kit omfattende en immunogen sammensætning eller vaccinesammensætning ifølge et hvilket som helst af kravene 1 til 14, hvor en første flaske omfatter både et PCV2-antigen og supernatanten af en Mycoplasma hyopneumoniae (M.hyo)-kultur, hvor supernatanten er fri for både (i) IgG og (ii) antigen/im-munglobulin-immunkomplekser, og en anden flaske omfatter PRRS-virusanti-gen; og eventuelt yderligere indbefattende en instruktionsmanual med anvisninger til kombinering af indholdet af den første flaske med indholdet af den anden flaske og til indgivelse af det kombinerede indhold af den første og anden flaske til en gris.
16. Fremgangsmåde til fremstilling af en immunogen sammensætning ifølge et hvilket som helst af kravene 1 til 14, hvilken fremgangsmåde omfatter: i) at dyrke M.hyo i et egnet medium overtidsrum på fra 18-144 timer; ii) efterfølgende at inaktivere M.hyo-kulturen; iii) at høste den inaktiverede kulturfluid, hvor den inaktiverede kulturfluid omfatter både en opløselig væskefraktion og uopløseligt cellulært materiale; iv) at separere den opløselige væskefraktion fra det uopløselige cellulære materiale ved filtrering, centrifugering eller udfældning; v) at fjerne både IgG og antigen/immunglobulin-immunkomplekserfra den fraseparerede væskefraktion til dannelse af M. hyo-kultur-supernatanten, der er fri for både (i) IgG og (ii) immunkomplekser bestående af antigen, der er bundet til immunglobulin; og vi) efterfølgende at kombinere supernatanten med et PCV2-antigen og PRRS-virusantigen.
DK13717118.7T 2012-04-04 2013-04-03 Pcv/mycoplasma hyopneumoniae/prrs-kombinationsvaccine DK2833909T3 (da)

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US201261620189P 2012-04-04 2012-04-04
PCT/US2013/035091 WO2013152086A1 (en) 2012-04-04 2013-04-03 Pcv/mycoplasma hyopneumoniae/prrs combination vaccine

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EP (2) EP3508217A1 (da)
JP (1) JP6271504B2 (da)
KR (1) KR101808903B1 (da)
AR (1) AR090614A1 (da)
AU (1) AU2013243540C1 (da)
BR (1) BR112014024775B1 (da)
CA (1) CA2869601C (da)
CL (1) CL2014002676A1 (da)
CO (1) CO7160027A2 (da)
CR (1) CR20140438A (da)
CY (1) CY1121578T1 (da)
DK (1) DK2833909T3 (da)
ES (1) ES2719483T3 (da)
GT (1) GT201400212A (da)
HK (1) HK1207283A1 (da)
HR (2) HRP20140956A2 (da)
HU (1) HUE042405T2 (da)
LT (1) LT2833909T (da)
MX (2) MX354773B (da)
MY (1) MY168549A (da)
NI (1) NI201400118A (da)
PH (1) PH12014502252A1 (da)
PL (1) PL2833909T3 (da)
PT (1) PT2833909T (da)
RS (1) RS58480B1 (da)
RU (1) RU2644256C2 (da)
SI (1) SI2833909T1 (da)
TR (1) TR201905176T4 (da)
TW (1) TWI504406B (da)
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