JP6274542B2 - 抗cd4抗体を有効成分とする抗がん剤の治療効果を判定する方法 - Google Patents
抗cd4抗体を有効成分とする抗がん剤の治療効果を判定する方法 Download PDFInfo
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Description
(1) 少なくとも1種の免疫チェックポイント受容体、
(2) CD8、並びに
(3) CD44及びCD45ROからなる群より選択される少なくとも1種の細胞表面分子
の、T細胞上での発現を調べることを含み、前記(1)の免疫チェックポイント分子が陽性であり、CD8陽性であり、かつ、CD44高発現及び/又はCD45RO高発現であるT細胞集団の誘導が、前記患者において前記抗がん剤が治療効果を現していることを示す、方法を提供する。
(1) 少なくとも1種の免疫チェックポイント受容体
(2) CD8
(3) CD44及びCD45ROからなる群より選択される少なくとも1種の細胞表面分子
(a) 患者由来試料のフローサイトメトリー解析
(b) 抗CD8抗体を固定化した支持体を用いて患者由来試料中のCD8+ 細胞を捕捉、洗浄の後、測定対象の細胞表面分子に対する複数の抗体にそれぞれ異なるシグナルを発する標識物質を結合させた複数の標識抗体と同時に反応させ、シグナルを区別して同時に測定・解析を行なう。
(c) 患者由来試料をプロテアーゼ等の適当な酵素で前処理して細胞表面分子をステム部分から切断し、遊離した細胞表面分子群をマルチプルELISAにて測定する。
(d) 細胞表面分子のmRNAをRT-PCRにてマルチプレックス測定する。
(i) 高い細胞傷害活性を有する抗CD4抗体
(ii) 細胞毒成分が結合された、抗CD4抗体又はその抗原結合性断片
WO 2010/074266に記載された方法により、ADCC活性が増強された抗ヒトCD4ヒト化抗体IT1208(可変領域としてWO 2010/074266に記載のHV2及びLV0を含む、サブタイプはIgG1)を作製した。Biacore T100を用いて測定された抗体結合活性はKD(nM)<0.009であり、高い結合活性を有していた。
C57BL/6系統マウス(雌、7週齢)の右側腹部にマウスメラノーマ細胞株B16F10(5x105 cells/mouse)を皮下移植した後、下記の通りに抗体投与を行なった(Day0=がん細胞移植日)。
その後 Prolong Gold reagent (Life Technologies)で包埋し、SP5 共焦点顕微鏡 (Leica Microsystems)で免疫染色像を観察した。
C57BL/6系統マウス(雌、7週齢)の右側腹部にマウスメラノーマ細胞株B16F10(5x105 cells/mouse)を皮下移植した後、下記の通りに抗体投与を行なった(Day0=がん細胞移植日)。
TNF-α(Tnf)、IFN-γ(Ifng)、Cxcl10、Cd274、Fasl、Prf1、グランザイム(Gzmb)
Claims (13)
- 抗CD4抗体を有効成分とする抗がん剤、抑制性の免疫チェックポイント分子に対するアンタゴニストを有効成分とする抗がん剤、及び共刺激性の免疫チェックポイント分子に対するアゴニストを有効成分とする抗がん剤から選択される少なくとも1種の抗がん剤によるがん療法の治療効果を試験する方法であって、前記少なくとも1種の抗がん剤が投与された患者由来の試料を用いて、
(1) 少なくとも1種の免疫チェックポイント受容体、
(2) CD8、並びに
(3) CD44及びCD45ROからなる群より選択される少なくとも1種の細胞表面分子
の、T細胞上での発現を調べることを含み、前記(1)の免疫チェックポイント分子が陽性であり、CD8陽性であり、かつ、CD44高発現及び/又はCD45RO高発現であるT細胞集団の誘導が、前記患者において前記抗がん剤が治療効果を現していることを示す、方法。 - 前記(1)が、PD-1、CD137及びTIM-3からなる群より選択される少なくとも1種である、請求項1記載の方法。
- CD45RAのT細胞上での発現を調べることをさらに含み、前記T細胞集団はCD45RA陰性である、請求項1又は2記載の方法。
- CD62LのT細胞上での発現を調べることをさらに含み、前記T細胞集団はCD62L低発現である、請求項1ないし3のいずれか1項に記載の方法。
- CCR7のT細胞上での発現を調べることをさらに含み、前記T細胞集団はCCR7陰性である、請求項1ないし4のいずれか1項に記載の方法。
- 前記試料が血液試料である、請求項1ないし5のいずれか1項に記載の方法。
- フローサイトメトリー解析により前記発現解析が行われる、請求項1ないし6のいずれか1項に記載の方法。
- 抗CD4抗体を有効成分とする抗がん剤は、高い細胞傷害活性を有する抗CD4抗体、又は細胞毒成分を結合させた抗CD4抗体若しくはその抗原結合性断片を有効成分として含有する抗がん剤である、請求項1ないし7のいずれか1項に記載の方法。
- 抑制性の免疫チェックポイント分子は、PD-1、CTLA-4、LAG-3、TIM-3、BTLA、PD-L1、PD-L2、CD80、CD86、GAL9、及びHVEMからなる群より選択される少なくとも1種であり、共刺激性の免疫チェックポイント分子は、CD137、OX40、GITR、CD137L、OX40L、及びTNFSF18からなる群より選択される少なくとも1種である、請求項1ないし8のいずれか1項に記載の方法。
- 前記アンタゴニスト及び前記アゴニストが免疫チェックポイント分子に対する抗体である、請求項1ないし9のいずれか1項に記載の方法。
- 免疫チェックポイント分子に対する抗体は、アンタゴニスト性抗PD-1抗体、抗PD-L1抗体、抗PD-L2抗体、アゴニスト性抗CD137抗体、アゴニスト性抗OX40抗体、及びアンタゴニスト性抗CTLA-4抗体からなる群より選択される少なくとも1種である、請求項10記載の方法。
- 抗CD4抗体を有効成分とする抗がん剤によるがん療法の治療効果を試験する方法である、請求項1ないし8のいずれか1項に記載の方法。
- 抗CD4抗体を有効成分とする抗がん剤と、免疫チェックポイント分子に対する抗体を有効成分とする抗がん剤の少なくとも1種との併用によるがん療法の治療効果を試験する方法である、請求項1ないし11のいずれか1項に記載の方法。
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WO2015190538A1 (ja) | 2014-06-11 | 2015-12-17 | Idacセラノスティクス株式会社 | 免疫チェックポイント制御剤の副作用低減方法 |
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EP3229025A4 (en) | 2018-04-25 |
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EP3229025B1 (en) | 2019-07-17 |
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