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Near-infrared Photoimmunotherapy Targeting Pancreatic Cancer With Tissue Factor Antibody

https://repo.qst.go.jp/records/72996
https://repo.qst.go.jp/records/72996
527784ba-32a1-40fc-bbf8-334b020a52bf
アイテムタイプ 会議発表用資料 / Presentation(1)
公開日 2018-11-08
タイトル
タイトル Near-infrared Photoimmunotherapy Targeting Pancreatic Cancer With Tissue Factor Antibody
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference output
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 U, Winn Aung

× U, Winn Aung

WEKO 719326

U, Winn Aung

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Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 719327

Tsuji, Atsushi

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Sugyo, Aya

× Sugyo, Aya

WEKO 719328

Sugyo, Aya

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Sudo, Hitomi

× Sudo, Hitomi

WEKO 719329

Sudo, Hitomi

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Takashima, Hiroki

× Takashima, Hiroki

WEKO 719330

Takashima, Hiroki

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Yasunaga, Masahiro

× Yasunaga, Masahiro

WEKO 719331

Yasunaga, Masahiro

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Matsumura, Yasuhiro

× Matsumura, Yasuhiro

WEKO 719332

Matsumura, Yasuhiro

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Higashi, Tatsuya

× Higashi, Tatsuya

WEKO 719333

Higashi, Tatsuya

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U Winn Aung

× U Winn Aung

WEKO 719334

en U Winn Aung

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辻 厚至

× 辻 厚至

WEKO 719335

en 辻 厚至

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須尭 綾

× 須尭 綾

WEKO 719336

en 須尭 綾

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須藤 仁美

× 須藤 仁美

WEKO 719337

en 須藤 仁美

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東 達也

× 東 達也

WEKO 719338

en 東 達也

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抄録
内容記述タイプ Abstract
内容記述 Purpose: Tissue Factor (TF) is a transmembrane protein and its overexpression is associated with increased tumor growth, tumor angiogenesis and metastatic potential in many malignancies, including pancreatic cancer. Near infrared photoimmunotherapy (NIR-PIT) is a new target-cell-specific cancer treatment that enables highly selective cell death after systemic administration of a photosensitizer-antibody conjugate followed by subsequent NIR light exposure. In this study, we describe the photoimmunotherapeutic effect induced by a rat IgG2b anti-TF monoclonal antibody (anti-TF mAb), conjugated to the photosensitizer, Indocyanine green (ICG), in a TF-expressing BxPC-3 pancreatic cancer model. Materials and methods: Specific binding of the anti-TF-ICG antibody to the TF-expressing BxPC-3 pancreatic cancer cell line was examined by fluorescence microscopy. NIR-PIT-induced cell death was determined by using cell viability imaging assay after exposure of the cells to NIR light. Anti-TF-ICG antibody accumulation in xenograft tumor was acquired in in vivo longitudinal fluorescence imaging. To conduct NIR-PIT, tumor-bearing mice were separated into 5 groups: (1) 100 μg of anti- TF-ICG i.v. administration followed by NIR light exposure (50 J/cm2) for two consecutive days (Day 1 and 2); (2) NIR light exposure (50 J/cm2) only for two consecutive days (Day 1 and 2); (3) 100 μg of anti-TF-ICG i.v. administration; (4) 100 μg of unlabeled anti-TF i.v. administration; (5) the untreated control. Biweekly tumor volume measurements, histopathological and immunohistochemical (IHC) analyses of tumors at 3 days post-administration of anti-TF-ICG antibody were performed to monitor the effect of treatments. Results: Dead cells were obviously seen with cell viability imaging assay. Tumor growth was significantly inhibited by NIR-PIT compared with the other control groups (P < 0.01) for 27 days. Tumors received NIR-PIT showed the evidence of necrotic cell death associated features on H&E staining and decreased cell proliferation marker Ki-67-positive cells on IHC examination. Conclusion: The anti-TF-ICG antibody is suitable as a photosensitizer-antibody conjugate for NIR-PIT. Furthermore, NIR-PIT with the anti-TF-ICG antibody conjugate promises to open a new avenue for treatment of TF-expressing pancreatic cancer and that could be ultimately applicable in clinical use.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 Annual Congress of the European Association of Nuclear Medicine 2018
発表年月日
日付 2018-10-13
日付タイプ Issued
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