HRP20211443T1 - Izbor neoepitopa kao ciljeva specifičnih za bolest za trerapiju sa povećanom efikasnošću - Google Patents

Izbor neoepitopa kao ciljeva specifičnih za bolest za trerapiju sa povećanom efikasnošću Download PDF

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HRP20211443T1
HRP20211443T1 HRP20211443TT HRP20211443T HRP20211443T1 HR P20211443 T1 HRP20211443 T1 HR P20211443T1 HR P20211443T T HRP20211443T T HR P20211443TT HR P20211443 T HRP20211443 T HR P20211443T HR P20211443 T1 HRP20211443 T1 HR P20211443T1
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disease
neoepitope
gene
copies
mutated allele
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HRP20211443TT
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Arbel D. Tadmor
Ugur Sahin
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BioNTech SE
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Claims (11)

1. Postupak za određivanje podobnosti neoepitopa koji je rezultat mutacije specifične za bolest na alelu u genu (mutirani alel) kao cilja specifičnog za bolest, naznačen time, što uključuje određivanje, u oboljeloj stanici ili populaciji oboljelih stanica, broja kopija mutiranog alela koji kodira neoepitop, pri čemu broj kopija mutiranog alela koji je veći od 2 ukazuje na podobnost neoepitopa kao cilja specifičnog za bolest, pri čemu je bolest rak i pri čemu što je viši broj kopija mutiranog alela, viša je podobnost neoepitopa kao cilja specifičnog za bolest.
2. Postupak prema patentnom zahtjevu 1, naznačen time, što broj kopija mutiranog alela koji je veći od 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, ili veći od 100 ukazuje na podobnost neoepitopa kao cilja specifičnog za bolest.
3. Postupak prema patentnim zahtjevima 1 ili 2, naznačen time, što je odnos broja kopija mutiranog alela prema ukupnom broju kopija nukleotidnog mjesta na kojem se mutacija mapira veći od 0.5, pri čemu, poželjno, odnos iznosi 1.
4. Postupak prema patentnom zahtjevu 3, naznačen time, da što je viši odnos broja kopija mutiranog alela prema ukupnom broju kopija nukleotidnog mjesta na kojem se mutacija mapira, viša je podobnost neoepitopa kao cilja specifičnog za bolest.
5. Postupak prema bilo kojem od patentnih zahtjeva 1 do 4, naznačen time, što je gen vodeći gen čija ekspresija rezultira transformacijom stanice u kancerogeni fenotip ili čiji izostanak ekspresije rezultira time da kancerogena stanica izgubi svoj kancerogeni fenotip.
6. Postupak prema bilo kojem od patentnih zahtjeva 1 do 5, naznačen time, što je gen esencijalni gen, pri čemu, poželjno, esencijalni gen je gen koji, kada je utišan ili je njegova ekspresija smanjena, rezultira bar ometenim rastom ili smanjenim fitnesom stanice u kojoj se esencijalni gen eksprimira, poželjno oboljeloj stanici; ili se esencijalni gen eksprimira u velikom broju različitih tkiva i eksprimira se sa minimalnim RPKM pragom većim od 0.
7. Postupak prema bilo kojem od patentnih zahtjeva 1 do 6, naznačen time, što je mutacija specifična za bolest varijacija pojedinačnog nukleotida.
8. Postupak prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time, što je neoepitop identificiran postupkom koji uključuje sekvenciranje genoma oboljele stanice ili njegovog dijela.
9. Postupak za davanje cjepiva, naznačen time, što uključuje identificiranje podobnog neoepitopa ili kombinacije podobnih neoepitopa prema postupku iz bilo kojeg od patentnih zahtjeva 1 do 8.
10. Postupak prema patentnom zahtjevu 9, naznačen time, što cjepivo uključuje peptid ili polipeptid koji sadrže jedan ili više podobnih neoepitopa ili kombinaciju podobnih neoepitopa, ili nukleinsku kiselinu koja kodira navedeni peptid ili polipeptid.
11. Postupak prema patentnom zahtjevu 10, naznačen time, što je nukleinska kiselina RNK.
HRP20211443TT 2016-07-20 2017-07-19 Izbor neoepitopa kao ciljeva specifičnih za bolest za trerapiju sa povećanom efikasnošću HRP20211443T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP2016067348 2016-07-20
PCT/EP2017/068226 WO2018015433A2 (en) 2016-07-20 2017-07-19 Selecting neoepitopes as disease-specific targets for therapy with enhanced efficacy
EP17743311.7A EP3488443B8 (en) 2016-07-20 2017-07-19 Selecting neoepitopes as disease-specific targets for therapy with enhanced efficacy

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US (1) US20190189241A1 (hr)
EP (2) EP3967324A1 (hr)
JP (2) JP7171543B2 (hr)
KR (2) KR20230019223A (hr)
CN (2) CN109477149A (hr)
BR (1) BR112018077122A8 (hr)
CA (1) CA3031003A1 (hr)
CY (1) CY1124551T1 (hr)
DK (1) DK3488443T3 (hr)
ES (1) ES2890424T3 (hr)
HR (1) HRP20211443T1 (hr)
HU (1) HUE056660T2 (hr)
IL (2) IL311369A (hr)
LT (1) LT3488443T (hr)
MX (4) MX2019000733A (hr)
PL (1) PL3488443T3 (hr)
PT (1) PT3488443T (hr)
RS (1) RS62390B1 (hr)
SG (2) SG10201912678QA (hr)
SI (1) SI3488443T1 (hr)
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JP2023009120A (ja) 2023-01-19
ES2890424T3 (es) 2022-01-19
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WO2018015433A2 (en) 2018-01-25
PT3488443T (pt) 2021-09-24
WO2018015433A3 (en) 2018-03-01
MX2019000733A (es) 2019-05-02
JP7171543B2 (ja) 2022-11-15
DK3488443T3 (da) 2021-09-27
KR20190027832A (ko) 2019-03-15
MX2023009371A (es) 2023-08-16
IL264203A (en) 2019-02-28
AU2017299162A1 (en) 2019-02-07
CY1124551T1 (el) 2022-07-22
US20190189241A1 (en) 2019-06-20
LT3488443T (lt) 2021-10-25
IL264203B2 (en) 2024-08-01
PL3488443T3 (pl) 2021-12-20
CN117757931A (zh) 2024-03-26
JP2019524106A (ja) 2019-09-05
MX2023009370A (es) 2023-08-16
KR20230019223A (ko) 2023-02-07
EP3488443B8 (en) 2021-09-29
EP3488443B1 (en) 2021-08-18
CN109477149A (zh) 2019-03-15
SG11201900132QA (en) 2019-02-27
EP3967324A1 (en) 2022-03-16
RS62390B1 (sr) 2021-10-29
SG10201912678QA (en) 2020-02-27
CA3031003A1 (en) 2018-01-25
IL264203B1 (en) 2024-04-01
SI3488443T1 (sl) 2021-11-30
BR112018077122A8 (pt) 2023-01-31
KR102516166B1 (ko) 2023-03-31
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EP3488443A2 (en) 2019-05-29
BR112018077122A2 (pt) 2019-04-30

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