KR101543623B1 - 종양-연관 항원을 발현하는 암에 대한 펩티드 백신 - Google Patents
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Abstract
Description
[도 1a] 도 1은 에피토프 펩티드의 스크리닝 결과, CDH3-A24-10-332(서열번호 34), CDH3-A24-10-470(서열번호 358), CDH3-A24-9-513(서열번호 19), CDH3-A24-9-406(서열번호 22), CDH3-A24-10-807(서열번호 30) 및 CDH3-A24-10-655(서열번호 344)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA-A*2402에 대한 결합 활성은 있지만, CTL-유도능은 검출될 수 없는 음성펩티드의 예를 나타낸다. "b"는 CDH3-A24-10-332(서열번호 34)의 CTL-유도능을 나타낸다. CDH3-A24-10-332(서열번호 34)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 4번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "c"는 CDH3-A24-10-470(서열번호 358)의 CTL-유도능을 나타낸다. CDH3-A24-10-470(서열번호 358)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 4번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "d"는 CDH3-A24-9-513(서열번호 19)의 CTL-유도능을 나타낸다. CDH3-A24-9-513(서열번호 19)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고. 왼쪽 패널의 박스 표시한 웰의 6번 웰에서 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 중간 패널의 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "e"는 CDH3-A24-9-406(서열번호 22)의 CTL-유도능을 나타낸다. CDH3-A24-9-406(서열번호 22)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다.
[도 1b] 도 1은 에피토프 펩티드의 스크리닝 결과, CDH3-A24-10-332(서열번호 34), CDH3-A24-10-470(서열번호 358), CDH3-A24-9-513(서열번호 19), CDH3-A24-9-406(서열번호 22), CDH3-A24-10-807(서열번호 30) 및 CDH3-A24-10-655(서열번호 344)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "f"는 CDH3-A24-10-807(서열번호 30)의 CTL-유도능을 나타낸다. CDH3-A24-10-807(서열번호 30)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 클론은 전장의 CDH3 유전자 및 HLA-A24 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다(하위 오른쪽 그래프). 한편, HLA-A24를 제외한 전장 CDH3만으로 형질도입된 COS7 및 전장 CDH3을 제외한 HLA-A24만으로 형질도입된 COS7을 음성 대조군으로 제조하였다. 상기에서 확립된 CTL 세포주는 전장 CDH3 유전자 및 HLA-A24 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성이 확인되었다. "g"는 CDH3-A24-10-655(서열번호 344)의 CTL-유도능을 나타낸다. CDH3-A24-10-655(서열번호 344)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 클론은 전장의 CDH3 유전자 및 HLA-A24 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다(하위 오른쪽 그래프). 한편, HLA-A24를 제외한 전장 CDH3만으로 형질도입된 COS7 및 전장 CDH3을 제외한 HLA-A24만으로 형질도입된 COS7을 음성 대조군으로 제조하였다. 상기 CTL 클론은 CDH3 및 HLA-A24로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보여주었다.
[도 2] 도 2는 에피토프 펩티드의 스크리닝 결과, Epha4-A24-9-453(서열번호 41), Epha4-A24-9-5(서열번호 44), Epha4-A24-9-420(서열번호 48), Epha4-A24-9-869(서열번호 46), Epha4-A24-10-24(서열번호 78) Epha4-A02-9-501(서열번호 376) 및 Epha4-A02-9-165(서열번호 379)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 Epha4-A24-9-453(서열번호 41)의 CTL-유도능을 나타낸다. Epha4-A24-9-453(서열번호 41)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "c"는 Epha4-A24-9-5(서열번호 44)의 CTL-유도능을 나타낸다. Epha4-A24-9-5(서열번호 44)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "d"는 Epha4-A24-9-420(서열번호 48)의 CTL-유도능을 나타낸다. Epha4-A24-9-420(서열번호 48)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고. 상위 패널의 박스 표시한 웰의 6번 웰에서 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 중간 패널의 박스 표시한 웰의 6번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "e"는 Epha4-A24-9-869(서열번호 46)의 CTL-유도능을 나타낸다. Epha4-A24-9-869(서열번호 46)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "f"는 Epha4-A24-10-24(서열번호 78)의 CTL-유도능을 나타낸다. Epha4-A24-10-24(서열번호 78)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 4번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "g"는 Epha4-A02-9-501(서열번호 376)의 CTL-유도능을 나타낸다. Epha4-A02-9-501(서열번호 376)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 8번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드로 펄스된 표적 세포에 대하여 상기에서 확립된 CTL 세포주의 세포독성 활성을 Cr-방출 분석(CRA)을 통하여 측정하였고(하위 그래프), 상기 CTL 세포주는 상기 펩티드로 펄스된 표적 세포에 대하여 매우 강력한 특이적 세포독성 활성을 가지고 있었다. "h"는 Epha4-A02-9-165(서열번호 379)의 CTL-유도능을 나타낸다. Epha4-A02-9-165(서열번호 379)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었으며. 상기 펩티드로 펄스된 표적 세포에 대한 상기에서 확립된 CTL 세포주의 세포독성 활성을 Cr-방출 분석을 통하여 측정하였고(오른쪽 그래프), 상기 CTL 세포주는 상기 펩티드로 펄스된 표적 세포에 대하여 매우 강력한 특이적 세포독성 활성을 가지고 있었다.
[도 3] 도 3은 에피토프 펩티드의 스크리닝 결과, ECT2-A24-9-515(서열번호 80), ECT2-A24-10-40(서열번호 100) 및 ECT2-A24-10-101(서열번호 101)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 ECT2-A24-9-515(서열번호 80)의 CTL-유도능을 나타낸다. ECT2-A24-9-515(서열번호 80)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고. 왼쪽 패널의 박스 표시한 웰의 5번 및 7번 웰에서 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 두 번 째 패널의 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 암 세포주에 대한 상기 CTL 세포주인 내재적으로 ECT2 및 HLA-A24를 발현하는 TE6의 세포독성 활성은 Cr-방출 분석(CRA)을 통하여 측정하였고, 상기 CTL 클론은 TE6에 대하여 매우 강력한 세포독성을 나타내었다. 한편, ECT2만을 발현하는 TE5 암 세포주에 대한 상기 CTL 세포주의 세포독성 활성이 작용 세포(effector cells)에서는 확인되지 않았다. "c"는 ECT2-A24-10-40(서열번호 100)의 CTL-유도능을 나타낸다. ECT2-A24-10-40(서열번호 100)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 클론은 전장의 ECT 유전자 및 HLA-A24 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다. 한편, HLA-A24를 제외한 전장 ECT2로 형질도입된 COS7, 전장 ECT2의 대용물로서 URLC10 유전자 및 HLA-A24로 형질도입된 COS7 및, HLA-A24로 형질도입되고 ECT2-10-101로 펄스된 COS7을 음성 대조군으로 제조하였다. 상기 CTL 클론은 ECT2 및 HLA-A24로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보여주었다. "d"는 ECT2-A24-10-101(서열번호 101)의 CTL-유도능을 나타낸다. ECT2-A24-10-101(서열번호 101)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 양성 웰로부터 CTL 세포주가 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 클론은 전장의 ECT2 유전자 및 HLA-A24 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다. HLA-A24를 제외한 전장 ECT2로 형질도입된 COS7, 전장 ECT2의 치환체로서 URLC10 유전자 및 HLA-A24로 형질도입된 COS7 및 HLA-A24로 형질도입되고 ECT2-10-40로 펄스된 COS7을 음성 대조군으로 제조하였다. 상기 CTL 클론은 ECT2 및 HLA-A24로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보여주었다.
[도 4a] 도 4는 에피토프 펩티드의 스크리닝 결과, HIG2-A24-9-19(서열번호 110), HIG2-A24-9-22(서열번호 111), HIG2-A24-9-8(서열번호 387) HIG2-A24-10-7(서열번호 112), HIG2-A24-10-18(서열번호 394) HIG2-A02-9-15(서열번호 116), HIG2-A02-9-4(서열번호 117) 및 HIG2-A02-10-8(서열번호 121)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 HIG2-A24-9-19(서열번호 110)의 CTL-유도능을 나타낸다. HIG2-A24-9-19(서열번호 110)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 6번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "c"는 HIG2-A24-9-22(서열번호 111)의 CTL-유도능을 나타낸다. HIG2-A24-9-22(서열번호 111)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "d"는 HIG2-A24-9-8(서열번호 387)의 CTL-유도능을 나타낸다. HIG2-A24-9-8(서열번호 387)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "e"는 HIG2-A02-9-8(서열번호 114)의 CTL-유도능을 나타낸다. HIG2-A02-9-8(서열번호 114)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 10번 양성 웰로부터 CTL 세포주가 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 세포주는 전장의 HIG2 유전자 및 HLA-A02 분자를 형질도입한 293T에 대해서 특이적 CTL 활성을 나타냈다. HLA-A02를 제외한 전장 HIG2로 형질도입된 293T, 전장 HIG2의 대용물로서 FoxP3 유전자 및 HLA-A02로 형질도입된 293T 및 HLA-A02로 형질도입되고 HIG2-9-15로 펄스된 293T를 음성 대조군으로 제조하였다. 상기 CTL 세포주가 상기 펩티드에 의해 전장 HIG2 유전자 및 HLA-A02 분자로 형질도입된 293T에 대한 높은 특이적 CTL 활성을 나타내었다.
[도 4b] 도 4는 에피토프 펩티드의 스크리닝 결과, HIG2-A24-9-19(서열번호 110), HIG2-A24-9-22(서열번호 111), HIG2-A24-9-8(서열번호 387) HIG2-A24-10-7(서열번호 112), HIG2-A24-10-18(서열번호 394) HIG2-A02-9-15(서열번호 116), HIG2-A02-9-4(서열번호 117) 및 HIG2-A02-10-8(서열번호 121)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "f"는 HIG2-A24-10-7(서열번호 112)의 CTL-유도능을 나타낸다. HIG2-A24-10-7(서열번호 112)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 및 7번 양성 웰로부터 CTL 세포주 및 클론이 확립되으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "g"는 HIG2-A24-10-18(서열번호 394)의 CTL-유도능을 나타낸다. HIG2-A24-10-18(서열번호 394)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "h"는 HIG2-A02-9-15(서열번호 116)의 CTL-유도능을 나타낸다. HIG2-A02-9-15(서열번호 116)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 10번 양성 웰로부터 CTL 세포주가 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 세포주는 전장의 HIG2 유전자 및 HLA-A02 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다. HLA-A02를 제외한 전장 HIG2로 형질도입된 COS7 및 HLA-A02로 형질도입되고 HIG2-9-8로 펄스된 COS7을 음성 대조군으로 제조하였다. 상기 CTL 세포주는 HIG2 유전자 및 HLA-A24 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보였다.
[도 4c]도 4는 에피토프 펩티드의 스크리닝 결과, HIG2-A24-9-19(서열번호 110), HIG2-A24-9-22(서열번호 111), HIG2-A24-9-8(서열번호 387) HIG2-A24-10-7(서열번호 112), HIG2-A24-10-18(서열번호 394) HIG2-A02-9-15(서열번호 116), HIG2-A02-9-4(서열번호 117) 및 HIG2-A02-10-8(서열번호 121)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "i"는 HIG2-A02-9-4(서열번호 117)의 CTL-유도능을 나타낸다. HIG2-A02-9-4(서열번호 117)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 10번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 세포주는 전장의 HIG2 유전자 및 HLA-A02 분자를 형질도입한 COS7에 대해서 특이적 CTL 활성을 나타냈다(중간 그래프). 또한, HLA-A02를 제외한 전장 HIG2로 형질도입된 COS7, 전장 HIG2의 치환체로서 TTK 유전자 및 HLA-A02로 형질도입된 COS7 및, HLA-A02로 형질도입되고 HIG2-9-8로 펄스된 COS7을 음성 대조군으로 제조하였다. 전장 HIG2 유전자 및 HLA-A02 분자로 형질도입된 293T 및 내재적으로 HIG2 및 HLA-A02를 발현하는 Caki-1 암 세포주에 대한 상기 CTL 클론의 세포독성 활성은 Cr-방출 분석을 통하여 측정하였고(하위 그래프), 상기 CTL 클론은 HIG2 유전자 및 HLA-A02의 형질도입체 및 Caki-1에 대하여 매우 강력한 세포독성 활성을 가지고 있었다. 한편, HIG2 또는 HLA-A02만으로 형질도입된 293T 및 HIG2만을 발현하는 A498 암 세포주에 대한 CTL 세포주의 세포독성 활성은 검출되지 않는 것이 작용세포에서는 확인되지 않았다. "j"는 HIG2-A02-10-8(서열번호 121)의 CTL-유도능을 나타낸다. HIG2-A02-10-8(서열번호 121)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 9번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다.
[도 5a]도 5는 에피토프 펩티드의 스크리닝 결과, INHBB-A24-9-180(서열번호 395) INHBB-A24-10-180(서열번호 133), INHBB-A24-10-305(서열번호 135), INHBB-A24-10-7(서열번호 137) 및 INHBB-A24-10-212(서열번호 426)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 INHBB-A24-9-180(서열번호 395)의 CTL-유도능을 나타낸다. INHBB-A24-9-180(서열번호 395)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. INHBB 및 HLA-A02 모두를 발현하는 Miapaca2 종양세포에 의해 유도된, 상기 확립된 CTL 클론의 세포독성 활성은 Cr-방출 분석(CRA)을 통하여 측정하였고, 작용세포는 Miapaca2에 대하여 높은 특이적 세포독성 활성을 보여주었다. 한편, INHBB는 발현하지만 HLA-A02는 발현하지 않는 Caki-1에 대해서는 유의한 특이적 세포독성 활성을 보이지 않았다. "c"는 INHBB-A24-10-180(서열번호 133)의 CTL-유도능을 나타낸다. INHBB-A24-10-180(서열번호 133)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 세포주는 전장의 INHBB 유전자 및 HLA-A24 분자를 형질도입한 293T에 대해서 특이적 CTL 활성을 나타냈다. 또한, HLA-A24를 제외한 전장 INHBB로 형질도입된 293T 및 HLA-A24로 형질도입되고 INHBB-10-305로 펄스된 293T를 음성 대조군으로 제조하였다.
[도 5b] 도 5는 에피토프 펩티드의 스크리닝 결과, INHBB-A24-9-180(서열번호 395) INHBB-A24-10-180(서열번호 133), INHBB-A24-10-305(서열번호 135), INHBB-A24-10-7(서열번호 137) 및 INHBB-A24-10-212(서열번호 426)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "d"는 INHBB-A24-10-305(서열번호 135)의 CTL-유도능을 나타낸다. INHBB-A24-10-305(서열번호 135)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 펩티드에 의해서 유도된, 상기 수립된 CTL 클론은 전장의 INHBB 유전자 및 HLA-A24 분자를 형질도입한 293T에 대해서 특이적 CTL 활성을 나타냈다. 또한, HLA-A24를 제외한 전장 INHBB로 형질도입된 293T 및 HLA-A24로 형질도입되고 INHBB-10-180로 펄스된 293T를 음성 대조군으로 제조하였다. "e"는 INHBB-A24-10-7(서열번호 137)의 CTL-유도능을 나타낸다. INHBB-A24-10-7(서열번호 137)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 상위 패널의 박스 표시한 웰의 8번 웰 및 하위 패널의 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주가 확립되었다. 8번 웰로부터 얻은 상기 CTL 세포주의 전장 INHBB 유전자 및 HLA-A24 분자로 형질도입된 293T에 대한 특이적 CTL 활성을 확인하였다. 또한, HLA-A24를 제외한 전장 INHBB로 형질도입된 293T 및 HLA-A24로 형질도입되고 INHBB-10-40로 펄스된 293T를 음성 대조군으로 제조하였다. "f"는 INHBB-A24-10-212(서열번호 426)의 CTL-유도능을 나타낸다. INHBB-A24-10-212(서열번호 426)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다.
[도 6a] 도 6은 에피토프 펩티드의 스크리닝 결과, KIF20A-A24-10-304(서열번호 186), KIF20A-A24-9-383(서열번호 178), KIF20A-A24-10-66(서열번호 194) 및 KIF20A-A24-9-305(서열번호 174)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 KIF20A-A24-10-304(서열번호 186)의 CTL-유도능을 나타낸다. KIF20A-A24-10-304(서열번호 186)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고. 하위 오른쪽 패널의 박스 표시한 웰의 5번 웰에서 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 상위 왼쪽 패널의 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 또한 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 상기에서 확립된 CTL 클론이 상기 펩티드에 의해 전장 KIF20A로 형질도입된 24-LCL에 대한 특이적 CTL 활성이 증가된 것을 확인하였다. 또한, 공벡터로 형질도입된 A24-LCL을 음성 대조군으로 제조하였다. KIF20A 및 HLA-A24를 발현하는 Miapaca2 종양세포에 대한 상기 CTL 세포주의 세포독성 활성은 Cr-방출 분석(CRA)을 통하여 측정하였고, 상기 CTL 클론은 Miapaca2에 대하여 매우 강력한 세포독성 활성을 가지고 있었다(하위 오른쪽 그래프). 한편, KIF20A는 발현하지만 HLA-A24는 발현하지 않는 PK59에 대한 유의한 특이적 세포독성 활성은 나타나지 않았다. "c"는 KIF20A-A24-9-383(서열번호 178)의 CTL-유도능을 나타낸다. KIF20A-A24-9-383(서열번호 178)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고. 오른쪽 패널의 박스 표시한 웰의 3번 및 4번 웰에서 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 왼쪽 패널의 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었으며, 또한 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 상기에서 확립된 CTL 세포주는 전장 KIF20A 유전자 및 HLA-A24 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성이 확인되었다. 또한, HLA-A24를 제외한 전장 KIF20A로 형질도입된 COS7 및 HLA-A24로 형질도입되고 HIG2-9-15로 펄스된 COS7을 음성 대조군으로 제조하였다.
[도 6b] 도 6은 에피토프 펩티드의 스크리닝 결과, KIF20A-A24-10-304(서열번호 186), KIF20A-A24-9-383(서열번호 178), KIF20A-A24-10-66(서열번호 194) 및 KIF20A-A24-9-305(서열번호 174)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "d"는 KIF20A-A24-10-66(서열번호 194)의 CTL-유도능을 나타낸다. KIF20A-A24-10-66(서열번호 194)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 상위 왼쪽 패널의 박스 표시한 웰의 6번 웰 및 하위 중간 패널의 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었으며 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 6번 웰의 CTL 세포주에서 한계 희석에 의해 선별된 CTL 클론은 표적 세포에 대한 특이적 CTL 활성을 나타내었다. 상기에서 확립된 CTL 클론이 전장 KIF20A 유전자 및 HLA-A24 분자로 형질도입된 COS7에 대한 특이적 CTL 활성이 증가된 것을 확인하였다. 또한, HLA-A24를 제외한 전장 KIF20A로 형질도입된 COS7, 전장 KIF20A의 대체물로서 URLC10 유전자 및 HLA-A24로 형질도입된 COS7 및, HLA-A24로 형질도입되고 KIF20A-10-308 펩티드로 펄스된 COS7을 음성 대조군으로 제조하였다. "e"는 KIF20A-A24-9-305(서열번호 174)의 CTL-유도능을 나타낸다. KIF20A-A24-9-305(서열번호 174)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 상위 왼쪽 패널의 박스 표시한 웰의 2번 웰 및 하위 중간 패널의 박스 표시한 웰의 6번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 2번 웰의 CTL 세포주로부터 한계 희석에 의해 선별된 CTL 클론도 표적 세포에 대한 특이적 CTL 활성을 확인하였다. KIF20A 및 HLA-A24를 발현하는 PK45P 종양세포에 대한 상기 CTL 세포주의 세포독성 활성은 Cr-방출 분석(CRA)을 통하여 측정하였고, 상기 CTL 클론은 PK45P에 대하여 매우 강력한 세포독성 활성을 가지고 있었다. 한편, KIF20A는 발현하지만 HLA-A24는 발현하지 않는 PK59에서는 유의한 특이적 세포독성이 나타나지 않았다.
[도 7a] 도 7은 에피토프 펩티드의 스크리닝 결과, KNTC2-A24-9-309(서열번호 196), KNTC2-A24-9-124(서열번호 202), KNTC2-A24-9-154(서열번호 210), KNTC2-A24-9-150(서열번호 213), KNTC2-A24-10-452(서열번호 214), KNTC2-A24-10-227(서열번호 217) 및 KNTC2-A24-10-273(서열번호 223)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 KNTC2-A24-9-309(서열번호 196)의 CTL-유도능을 나타낸다. KNTC2-A24-9-309(서열번호 196)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 8번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "c"는 KNTC2-A24-9-124(서열번호 202)의 CTL-유도능을 나타낸다. KNTC2-A24-9-124(서열번호 202)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "d"는 KNTC2-A24-9-154(서열번호 210)의 CTL-유도능을 나타낸다. KNTC2-A24-9-154(서열번호 210)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "e"는 KNTC2-A24-9-150(서열번호 213)의 CTL-유도능을 나타낸다. KNTC2-A24-9-150(서열번호 213)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다.
[도 7b] 도 7은 에피토프 펩티드의 스크리닝 결과, KNTC2-A24-9-309(서열번호 196) KNTC2-A24-9-124(서열번호 202) KNTC2-A24-9-154(서열번호 210) KNTC2-A24-9-150(서열번호 213), KNTC2-A24-10-452(서열번호 214), KNTC2-A24-10-227(서열번호 217) 및 KNTC2-A24-10-273(서열번호 223)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "f"는 KNTC2-A24-10-452(서열번호 214)의 CTL-유도능을 나타낸다. KNTC2-A24-10-452(서열번호 214)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 상위 왼쪽 패널의 박스 표시한 웰의 4번 웰 및 중간 패널의 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 또한, 5번 웰의 CTL 세포주로부터 한계 희석에 의해 선별된 CTL 클론은 표적 세포에 대한 특이적 CTL 활성을 나타내었다. 4번 웰로부터 확립된 CTL 세포주는 전장 KNTC2 유전자 및 HLA-A24 분자로 형질도입된 HEK293에 대하여 특이적 CTL 활성을 보였다. 또한, HLA-A24를 제외한 전장 KNTC2로 형질도입된 HEK293, 전장 KNTC2를 제외한 HLA-A24로 형질도입된 HEK293 및, HLA-A24로 형질도입되고 KNTC-9-309로 펄스된 HEK293을 음성 대조군으로 제조하였다. "g"는 KNTC2-A24-10-227(서열번호 217)의 CTL-유도능을 나타낸다. KNTC2-A24-10-227(서열번호 217)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "h"는 KNTC2-A24-10-273(서열번호 223)의 CTL-유도능을 나타낸다. KNTC2-A24-10-273(서열번호 223)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 8번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다.
[도 8a]도 8은 에피토프 펩티드의 스크리닝 결과, TTK-A02-9-462(서열번호 227), TTK-A02-9-719(서열번호 233), TTK-A02-9-547(서열번호 228) 및 TTK-A02-10-462(서열번호 254)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 TTK-A02-9-462(서열번호 227)의 CTL-유도능을 나타낸다. TTK-A02-9-462(서열번호 227)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 4번 양성 웰로부터 CTL 세포주 및 2개 클론이 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. 상기 확립된 CTL 클론은 전장 TTK 유전자 및 HLA-A02 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보였다. 또한, HLA-A02를 제외한 전장 TTK2로 형질도입된 COS7, 전장 TTK를 제외한 HLA-A02로 형질도입된 COS7 및, HLA-A02로 형질도입되고 TTK-9-547 펩티드로 펄스된 COS7을 음성 대조군으로 제조하였다. "c"는 TTK-A02-9-719(서열번호 233)의 CTL-유도능을 나타낸다. TTK-A02-9-719(서열번호 233)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 1번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 확립된 CTL 세포주는 전장 TTK 유전자 및 HLA-A02 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보였다. 또한, HLA-A02를 제외한 전장 TTK로 형질도입된 COS7 및 전장 TTK의 치환체로서 HIG2 유전자 및 HLA-A02로 형질도입된 COS7을 음성 대조군으로 제조하였다.
[도 8b] 도 8은 에피토프 펩티드의 스크리닝 결과, TTK-A02-9-462(서열번호 227), TTK-A02-9-719(서열번호 233), TTK-A02-9-547(서열번호 228) 및 TTK-A02-10-462(서열번호 254)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "d"는 TTK-A02-9-547(서열번호 228)의 CTL-유도능을 나타낸다. TTK-A02-9-547(서열번호 228)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 2번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다. 상기 확립된 CTL 세포주는 전장 TTK 유전자 및 HLA-A02 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보였다. 또한, HLA-A02를 제외한 전장 TTK로 형질도입된 COS7, 전장 TTK를 제외한 HLA-A02로 형질도입된 COS7 및 HLA-A02로 형질도입되고 TTK-10-462로 펄스된 COS7을 음성 대조군으로 제조하였다.
[도 8c] 도 8은 에피토프 펩티드의 스크리닝 결과, TTK-A02-9-462(서열번호 227), TTK-A02-9-719(서열번호 233), TTK-A02-9-547(서열번호 228) 및 TTK-A02-10-462(서열번호 254)가 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "e"는 TTK-A02-10-462(서열번호 254)의 CTL-유도능을 나타낸다. TTK-A02-10-462(서열번호 254)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 8번 양성 웰로부터 CTL 세포주 및 3개 클론이 확립되었다. 상기 확립된 CTL 클론은 전장 TTK 유전자 및 HLA-A02 분자로 형질도입된 COS7에 대하여 높은 특이적 CTL 활성을 보였다. 또한, HLA-A02를 제외한 전장 TTK로 형질도입된 COS7, 전장 TTK를 제외한 HLA-A02로 형질도입된 COS7 및 HLA-A02로 형질도입되고 TTK-9-547 펩티드로 펄스된 COS7을 음성 대조군으로 제조하였다.
[도 9a]도 9는 에피토프 펩티드의 스크리닝 결과, URLC10-A02-9-206(서열번호 271), URLC10-A02-9-212(서열번호 272) 및 URLC10-A02-10-211(서열번호 288)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "a"는 HLA에 대한 결합 활성은 있지만, CTL-유도능은 검출되지 않는 음성펩티드의 예를 나타낸다. "b"는 URLC10-A02-9-206(서열번호 271)의 CTL-유도능을 나타낸다. URLC10-A02-9-206(서열번호 271)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 7번 양성 웰로부터 CTL 세포주가 확립되었으며, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "c"는 URLC10-A02-9-212(서열번호 272)의 CTL-유도능을 나타낸다. URLC10-A02-9-212(서열번호 272)는 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 3번 양성 웰로부터 CTL 세포주가 확립되었다, 상기 에피토프 펩티드로 펄스된 표적 세포에 대한 특이적 반응을 확인하였다. "d"는 URLC10-A02-10-211(서열번호 288)의 CTL-유도능을 나타낸다. URLC10-A02-10-211(서열번호 288)은 IFN-감마 ELISPOT 분석에서 대조군에 비하여 강력한 IFN-감마 생성이 증명되었고, 박스 표시한 웰의 5번 양성 웰로부터 CTL 세포주 및 클론이 확립되었다.
[도 9b]도 9는 에피토프 펩티드의 스크리닝 결과, URLC10-A02-9-206(서열번호 271), URLC10-A02-9-212(서열번호 272) 및 URLC10-A02-10-211(서열번호 288)이 강력한 IFN-감마 생성을 보여주는 것을 차례로 증명한 것을 나타낸다. "d를 이어서" 상기 확립된 CTL 클론은 전장 URLC10 유전자 및 HLA-A02 분자로 형질도입된 COS7, HEK293 및 293T에 대하여 높은 특이적 CTL 활성을 보였다. 또한, HLA-A02를 제외한 전장 URLC10로 형질도입된 COS7, HEK293 또는 293T 및, HLA-A02로 형질도입되고 URLC10-10-64로 펄스된 COS7, HEK293 또는 293T를 음성 대조군으로 제조하였다.
여기서, "+"은 펩티드로 펄스된 표적, "-"은 펩티드로 펄스되지 않은 표적, "R"은 응답 세포(Responder), "S"는 자극 세포(Stimulator), "E"는 작용 세포(Effector), 및 "T"는 표적 세포를 의미한다.
Claims (29)
- 서열번호 114, 116, 117 또는 121로 기재되는 아미노산 서열을 포함하는 15개 아미노산 길이 이하의 정제된 펩티드.
- 하기의 군으로부터 선택되는 세포독성 T 세포의 유도능(inducibility)을 가지는 15개 아미노산 길이 이하의 펩티드:
(a) 서열번호 114, 116, 117 및 121로 구성되는 군으로부터 선택되는 어느 하나의 아미노산 서열에 있어서, N-말단으로부터 두 번째 아미노산이 루신(leucine) 또는 메티오닌(methionine)으로 치환된 서열을 포함하는 펩티드;
(b) 서열번호 114, 116, 117 및 121로 구성되는 군으로부터 선택되는 어느 하나의 아미노산 서열에 있어서, C-말단의 아미노산이 발린(valine) 또는 루신으로 치환된 서열을 포함하는 펩티드;
(c) 서열번호 114, 116, 117 및 121로 구성되는 군으로부터 선택되는 어느 하나의 아미노산 서열에 있어서, N-말단으로부터 두 번째 아미노산이 루신 또는 메티오닌으로 치환된 서열 및 C-말단의 아미노산이 발린 또는 루신으로 치환된 서열을 포함하는 펩티드.
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- 제 1항 또는 제 2항의 하나 이상의 펩티드, 또는 상기 펩티드를 암호화하는 폴리뉴클레오티드를 포함하는 암의 치료 또는 예방용 약학적 조성물.
- 제 11항에 있어서, 상기 암은 방광암, 유방암, 자궁경부암, 담관세포암, CML, 대장암, 자궁내막증, 식도암, 위암, 미만형 위암, 간암, NSCLC, 림프종, 골육종, 자궁암, 췌장암, 전립선암, 신장암, SCLC, 연조직 종양 및 고환종양으로 구성되는 군으로부터 선택되는 것을 특징으로 하는 약학적 조성물.
- 제 1항 또는 제 2항의 펩티드, 및 HLA를 포함하는 복합체를 표면에 제시하는 엑소솜(exosome).
- 제 13항에 있어서, 상기 HLA는 HLA-A2인 것을 특징으로 하는 엑소솜.
- 제 14항에 있어서, 상기 HLA는 HLA-A0201인 것을 특징으로 하는 엑소솜.
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- 하기 군으로부터 선택되는 단계를 포함하는, 실험관내(in vitro) 세포독성 T 세포 유도능을 가지는 항원 제시 세포 유도방법:
(a) 제 1항 또는 제 2항의 펩티드를 항원 제시 세포와 접촉시키는 단계; 및 (b) 제 1항 또는 제 2항의 펩티드를 암호화하는 폴리뉴클레오티드를 포함하는 유전자를 항원 제시 세포에 트랜스퍼(transfer)하는 단계.
- 하기 군으로부터 선택되는 단계를 포함하는 실험관내 세포독성 T 세포 유도방법:
(a) 제 1항 또는 제 2항의 펩티드를 항원 제시 세포와 접촉시키고, 상기 항원 제시 세포를 CD8+ T 세포와 혼합하여 이를 동시배양하는 단계; 및
(b) HLA2-A2와 관련하여 제 1항 또는 제 2항의 펩티드와 결합하는 TCR 서브유닛(subunit) 폴리펩티드를 암호화하는 핵산을 T 세포에 형질도입하는 단계.
- 제 20항의 방법으로 유도된, 정제된 세포독성 T 세포.
- HLA 및 제 1항 또는 제 2항의 펩티드 사이에서 형성된 복합체를 포함하는 항원 제시 세포.
- 제 19항의 방법으로 유도된, 항원 제시 세포.
- 제 1항 또는 제 2항의 펩티드를 유효 성분으로 포함하고, 서열번호 7로 기재되는 유전자를 발현하는 암세포의 증식을 억제하는 백신(vaccine).
- 제 24항에 있어서, 상기 암은 방광암, 유방암, 자궁경부암, 담관세포암, CML, 대장암, 자궁내막증, 식도암, 위암, 미만형 위암, 간암, NSCLC, 림프종, 골육종, 자궁암, 췌장암, 전립선암, 신장암, SCLC, 연조직 종양 및 고환종양으로 구성되는 군으로부터 선택되는 것을 특징으로 하는 백신.
- 제 24항에 있어서, HLA가 HLA-A2인 개체로 투여하기 위하여 조제되는 것을 특징으로 하는 백신.
- 제 1항 또는 제 2항의 펩티드 또는 상기 펩티드를 암호화하는 폴리뉴클레오티드를 포함하는, 개체 내 암의 치료 또는 예방용 백신.
- 제 27항에 있어서, 상기 암은 방광암, 유방암, 자궁경부암, 담관세포암, CML, 대장암, 자궁내막증, 식도암, 위암, 미만형 위암, 간암, NSCLC, 림프종, 골육종, 자궁암, 췌장암, 전립선암, 신장암, SCLC, 연조직 종양 및 고환종양으로 구성되는 군으로부터 선택되는 것을 특징으로 하는 백신.
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KR1020157026286A KR20150116463A (ko) | 2007-02-21 | 2008-02-21 | 종양-연관 항원을 발현하는 암에 대한 펩티드 백신 |
KR1020167010159A KR20160045939A (ko) | 2007-02-21 | 2008-02-21 | 종양-연관 항원을 발현하는 암에 대한 펩티드 백신 |
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JP (6) | JP5239103B2 (ko) |
KR (8) | KR101540000B1 (ko) |
CN (4) | CN102863514B (ko) |
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CA (3) | CA2678755C (ko) |
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SI (3) | SI2121731T1 (ko) |
TW (5) | TWI438207B (ko) |
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WO2006090810A2 (en) | 2005-02-25 | 2006-08-31 | Oncotherapy Science, Inc. | Peptide vaccines for lung cancers expressing ttk, urlc10 or koc1 polypeptides |
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