JPWO2021094562A5 - - Google Patents

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JPWO2021094562A5
JPWO2021094562A5 JP2022525171A JP2022525171A JPWO2021094562A5 JP WO2021094562 A5 JPWO2021094562 A5 JP WO2021094562A5 JP 2022525171 A JP2022525171 A JP 2022525171A JP 2022525171 A JP2022525171 A JP 2022525171A JP WO2021094562 A5 JPWO2021094562 A5 JP WO2021094562A5
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antigenic peptide
cell
antigenic
treatment
amino acid
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Priority claimed from PCT/EP2020/082101 external-priority patent/WO2021094562A2/en
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配列番号1~257及び476~500のいずれかで表されるアミノ酸配列を含む又はからなる抗原性ペプチドであって、任意に、1個又は2個のアミノ酸残基が、置換、欠失、又は付加されていてもよいことを特徴とする、B細胞悪性腫瘍の治療のための抗原性ペプチド。An antigenic peptide comprising or consisting of an amino acid sequence represented by any of SEQ ID NOs: 1 to 257 and 476 to 500, optionally with one or two amino acid residues substituted, deleted, or An antigenic peptide for the treatment of B cell malignant tumors, which may optionally have an antigenic peptide added thereto. 前記抗原性ペプチドが、配列番号114で表されるアミノ酸配列を含む又はからなる、請求項1に記載の抗原性ペプチド。The antigenic peptide according to claim 1, wherein the antigenic peptide comprises or consists of the amino acid sequence represented by SEQ ID NO: 114. 前記抗原性ペプチドが、配列番号110で表されるアミノ酸配列を含む又はからなる、請求項1に記載の抗原性ペプチド。The antigenic peptide according to claim 1, wherein the antigenic peptide comprises or consists of the amino acid sequence represented by SEQ ID NO: 110. 前記抗原性ペプチドが、配列番号220で表されるアミノ酸配列を含む又はからなる、請求項1に記載の抗原性ペプチド。The antigenic peptide according to claim 1, wherein the antigenic peptide comprises or consists of the amino acid sequence represented by SEQ ID NO: 220. 前記抗原性ペプチドが、配列番号65で表されるアミノ酸配列を含む又はからなる、請求項1に記載の抗原性ペプチド。The antigenic peptide according to claim 1, wherein the antigenic peptide comprises or consists of the amino acid sequence represented by SEQ ID NO: 65. 前記抗原性ペプチドの長さが、30アミノ酸を超えない、請求項1から5のいずれかに記載の抗原性ペプチド。The antigenic peptide according to any of claims 1 to 5, wherein the length of the antigenic peptide does not exceed 30 amino acids. 前記抗原性ペプチドの長さが、25アミノ酸を超えない、請求項1から6のいずれかに記載の抗原性ペプチド。Antigenic peptide according to any of claims 1 to 6, wherein the length of the antigenic peptide does not exceed 25 amino acids. 前記抗原性ペプチドの長さが、20アミノ酸を超えない、請求項1から7のいずれかに記載の抗原性ペプチド。Antigenic peptide according to any of claims 1 to 7, wherein the length of the antigenic peptide does not exceed 20 amino acids. 前記抗原性ペプチドの長さが、15アミノ酸を超えない、請求項1から8のいずれかに記載の抗原性ペプチド。Antigenic peptide according to any of claims 1 to 8, wherein the length of the antigenic peptide does not exceed 15 amino acids. 前記抗原性ペプチドの長さが、10アミノ酸を超えない、請求項1から9のいずれかに記載の抗原性ペプチド。Antigenic peptide according to any of claims 1 to 9, wherein the length of the antigenic peptide does not exceed 10 amino acids. 前記抗原性ペプチドが、完全長(マイクロバイオータ)タンパク質ではない、請求項1から10のいずれかに記載の抗原性ペプチド。11. Antigenic peptide according to any of claims 1 to 10, wherein the antigenic peptide is not a full-length (microbiota) protein. 請求項1から11のいずれかに記載の抗原性ペプチドを含むことを特徴とする、B細胞悪性腫瘍の治療のための免疫原性化合物。An immunogenic compound for the treatment of B-cell malignancies, characterized in that it comprises an antigenic peptide according to any one of claims 1 to 11. 前記抗原性ペプチドが、担体分子に結合されている、請求項12に記載の免疫原性化合物。13. The immunogenic compound of claim 12, wherein the antigenic peptide is conjugated to a carrier molecule. 前記担体分子が、担体タンパク質又は担体ペプチドである請求項13に記載の免疫原性化合物。14. The immunogenic compound according to claim 13, wherein the carrier molecule is a carrier protein or a carrier peptide. 式(I)のポリペプチドを含む又はからなる、請求項12から14のいずれかに記載の免疫原性化合物。15. An immunogenic compound according to any of claims 12 to 14, comprising or consisting of a polypeptide of formula (I).
PepNt-CORE-PepCt (I)PepNt-CORE-PepCt (I)
(式中、(In the formula,
-「PepNt」は、0~500個のアミノ酸残基の長さを有するポリペプチドからなり、前記式(I)のポリペプチドのN末端に位置し、- "PepNt" consists of a polypeptide having a length of 0 to 500 amino acid residues and is located at the N-terminus of the polypeptide of formula (I),
-COREは、請求項1から11のいずれかに定義される抗原性ペプチドからなり、- the CORE consists of an antigenic peptide as defined in any of claims 1 to 11;
-「PepCt」は、0~500個のアミノ酸残基の長さを有するポリペプチドからなり、前記式(I)のポリペプチドのC末端に位置する。)- "PepCt" consists of a polypeptide having a length of 0 to 500 amino acid residues and is located at the C-terminus of the polypeptide of formula (I) above. )
請求項1から11のいずれかに記載の抗原性ペプチド又は請求項12から15のいずれかに記載の免疫原性化合物がロードされたことを特徴とする、B細胞悪性腫瘍の治療のための抗原提示細胞。Antigen for the treatment of B-cell malignancies, characterized in that it is loaded with an antigenic peptide according to any one of claims 1 to 11 or an immunogenic compound according to any one of claims 12 to 15. Presenting cells. 前記抗原提示細胞が、樹状細胞である、請求項16に記載の抗原提示細胞。The antigen-presenting cell according to claim 16, wherein the antigen-presenting cell is a dendritic cell. 請求項1から11のいずれかに記載の抗原性ペプチド又は請求項12から15のいずれかに記載の免疫原性化合物をコードし、前記免疫原性化合物がペプチド又はタンパク質であることを特徴とする、B細胞悪性腫瘍の治療のための核酸。Encoding an antigenic peptide according to any one of claims 1 to 11 or an immunogenic compound according to any one of claims 12 to 15, characterized in that the immunogenic compound is a peptide or a protein. , Nucleic acids for the treatment of B-cell malignancies. 前記核酸が、DNA分子又はRNA分子であり、好ましくはゲノムDNA;cDNA;mRNA;アンチセンスDNA;アンチセンスRNA;相補的RNA及び/又はDNA配列;及びそれらの組合せから選択される、請求項18に記載の核酸。18. The nucleic acid is a DNA or RNA molecule, preferably selected from genomic DNA; cDNA; mRNA; antisense DNA; antisense RNA; complementary RNA and/or DNA sequences; and combinations thereof. Nucleic acid described in. 請求項18又は19に記載の核酸を含むことを特徴とする、B細胞悪性腫瘍の治療のための宿主細胞。A host cell for the treatment of B cell malignancy, characterized in that it contains the nucleic acid according to claim 18 or 19. 請求項1から11のいずれかに記載の抗原性ペプチドに特異的であることを特徴とする、B細胞悪性腫瘍の治療のための細胞傷害性Tリンパ球(CTL)。Cytotoxic T lymphocytes (CTL) for the treatment of B cell malignancies, characterized in that they are specific for the antigenic peptide according to any of claims 1 to 11. 有効成分として、As an active ingredient,
-請求項1から11のいずれかに記載の抗原性ペプチド、- an antigenic peptide according to any one of claims 1 to 11;
-請求項12から15のいずれかに記載の免疫原性化合物、- an immunogenic compound according to any of claims 12 to 15,
-請求項16又は17に記載の抗原提示細胞、- the antigen presenting cell according to claim 16 or 17;
-請求項18又は19に記載の核酸、- the nucleic acid according to claim 18 or 19,
-請求項20に記載の宿主細胞、及び/又は- a host cell according to claim 20, and/or
-請求項21に記載の細胞傷害性Tリンパ球、- cytotoxic T lymphocytes according to claim 21;
を含むことを特徴とする、B細胞悪性腫瘍の治療用医薬組成物。A pharmaceutical composition for treating B-cell malignant tumor, comprising:
1つ以上の免疫刺激剤をさらに含む、請求項22に記載のB細胞悪性腫瘍の治療用医薬組成物。23. A pharmaceutical composition for the treatment of B-cell malignancies according to claim 22, further comprising one or more immunostimulatory agents. 前記免疫刺激剤が、免疫アジュバントおよび抗原提示細胞からなる群から選択される、請求項23に記載のB細胞悪性腫瘍の治療用医薬組成物。24. The pharmaceutical composition for the treatment of B cell malignancy according to claim 23, wherein the immunostimulatory agent is selected from the group consisting of immune adjuvants and antigen presenting cells. (i)請求項1から11のいずれかに記載の抗原性ペプチドである少なくとも2つの異なる抗原性ペプチド;(i) at least two different antigenic peptides which are antigenic peptides according to any of claims 1 to 11;
(ii)請求項12から15のいずれかに記載の免疫原性化合物である少なくとも2つの異なる免疫原性化合物;(ii) at least two different immunogenic compounds which are immunogenic compounds according to any of claims 12 to 15;
(iii)請求項16又は17に記載の抗原提示細胞である少なくとも2つの異なる抗原提示細胞;(iii) at least two different antigen presenting cells which are antigen presenting cells according to claim 16 or 17;
(iv)請求項18又は19に記載の核酸である少なくとも2つの異なる核酸;(iv) at least two different nucleic acids which are the nucleic acids of claim 18 or 19;
(v)請求項20に記載の宿主細胞である少なくとも2つの異なる宿主細胞;又は(v) at least two different host cells which are host cells according to claim 20; or
(vi)請求項21に記載の細胞傷害性Tリンパ球である少なくとも2つの異なる細胞傷害性Tリンパ球、(vi) at least two different cytotoxic T lymphocytes, which are the cytotoxic T lymphocytes of claim 21;
を含む、請求項22に記載のB細胞悪性腫瘍の治療用医薬組成物。The pharmaceutical composition for treating B cell malignancy according to claim 22, comprising:
(i)~(vi)のいずれかに記載の少なくとも3つ又は4つの異なる成分、好ましくは3つ又は4つの異なる抗原性ペプチドを含む、請求項25に記載のB細胞悪性腫瘍の治療用医薬組成物。A medicament for the treatment of B-cell malignancies according to claim 25, comprising at least three or four different components according to any of (i) to (vi), preferably three or four different antigenic peptides. Composition. 前記少なくとも3つ又は4つの異なる活性成分が、The at least three or four different active ingredients are
-配列番号110で表されるアミノ酸配列を含む又はからなる抗原性ペプチド;- an antigenic peptide comprising or consisting of the amino acid sequence represented by SEQ ID NO: 110;
-配列番号114で表されるアミノ酸配列を含む又はからなる抗原性ペプチド;- an antigenic peptide comprising or consisting of the amino acid sequence represented by SEQ ID NO: 114;
-配列番号220で表されるアミノ酸配列を含む又はからなる抗原性ペプチド;及び- an antigenic peptide comprising or consisting of the amino acid sequence represented by SEQ ID NO: 220; and
-任意に、配列番号65で表されるアミノ酸配列を含む又はからなる抗原性ペプチド、- optionally an antigenic peptide comprising or consisting of the amino acid sequence represented by SEQ ID NO: 65,
に関する、請求項26に記載のB細胞悪性腫瘍の治療用医薬組成物。27. The pharmaceutical composition for the treatment of B cell malignancy according to claim 26.
ヘルパーペプチド、好ましくは、配列番号475で表されるアミノ酸配列を含む又はからなるペプチドを更に含む、請求項22又は23に記載のB細胞悪性腫瘍の治療用医薬組成物。The pharmaceutical composition for treating B cell malignancy according to claim 22 or 23, further comprising a helper peptide, preferably a peptide comprising or consisting of the amino acid sequence represented by SEQ ID NO: 475. 請求項1から11のいずれかに記載の抗原性ペプチドである少なくとも2つの異なる抗原性ペプチドの、B細胞悪性腫瘍の治療のための組合せ。A combination of at least two different antigenic peptides, which are antigenic peptides according to any of claims 1 to 11, for the treatment of B cell malignancies. 請求項1から11のいずれかに記載の抗原性ペプチドである、1つの抗原性ペプチド又は2以上の異なる抗原性ペプチドを含む、請求項22に記載のB細胞悪性腫瘍の治療用医薬組成物。23. The pharmaceutical composition for the treatment of B cell malignancy according to claim 22, comprising one antigenic peptide or two or more different antigenic peptides, which are the antigenic peptides according to any of claims 1 to 11. 前記B細胞悪性腫瘍が、非ホジキンリンパ腫(NHL)、びまん性大細胞型B細胞リンパ腫(DLBCL)、NOS(低悪性度リンパ腫から新たに形質転換したもの(de novo and transformed from indolent))、原発性縦隔大細胞型B細胞リンパ腫(PMBCL)、T細胞/組織球豊富型大細胞型B細胞リンパ腫(TCHRBCL)、バーキットリンパ腫、マントル細胞リンパ腫(MCL)、及び濾胞性リンパ腫(FL)からなる群から選択されるB細胞リンパ腫である、請求項22に記載のB細胞悪性腫瘍の治療用医薬組成物。The B-cell malignant tumor may be non-Hodgkin lymphoma (NHL), diffuse large B-cell lymphoma (DLBCL), NOS (de novo and transformed from indolent low-grade lymphoma), or primary tumor. consisting of mediastinal large B-cell lymphoma (PMBCL), T-cell/histiocyte-rich large B-cell lymphoma (TCHRBCL), Burkitt lymphoma, mantle cell lymphoma (MCL), and follicular lymphoma (FL). 23. The pharmaceutical composition for the treatment of B-cell malignancy according to claim 22, which is a B-cell lymphoma selected from the group. 請求項1から11のいずれかに記載の抗原性ペプチドを含むことを特徴とする、抗原特異的T細胞検出用のペプチド-MHC(pMHC)マルチマー。A peptide-MHC (pMHC) multimer for detecting antigen-specific T cells, comprising the antigenic peptide according to any one of claims 1 to 11.
JP2022525171A 2019-11-15 2020-11-13 Antigenic peptides for the prevention and treatment of B-cell malignancies Pending JP2023501204A (en)

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EP19306475 2019-11-15
EP19306475.5 2019-11-15
EPPCT/EP2020/079257 2020-10-16
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PCT/EP2020/082101 WO2021094562A2 (en) 2019-11-15 2020-11-13 Antigenic peptides for prevention and treatment of b-cell malignancy

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