Defects in T Cell Trafficking and Resistance to Cancer Immunotherapy

個数:1
紙書籍版価格
¥24,313
  • 電子書籍
  • ポイントキャンペーン

Defects in T Cell Trafficking and Resistance to Cancer Immunotherapy

  • 著者名:Donnadieu, Emmanuel (EDT)
  • 価格 ¥18,312 (本体¥16,648)
  • Springer(2016/08/30発売)
  • 2025→2026年!Kinoppy電子書籍・電子洋書全点ポイント30倍キャンペーン(~1/1)
  • ポイント 4,980pt (実際に付与されるポイントはご注文内容確認画面でご確認下さい)
  • 言語:ENG
  • ISBN:9783319422213
  • eISBN:9783319422237

ファイル: /

Description

This volume focuses on recent advances in understanding T cells as key players in antitumor immune responses, and as a result T cell-based immunotherapy is starting to transform the treatment of advanced cancers. However, despite recent successes, many patients with cancer fail to respond to these treatments. Defective migration of T cells into and within tumors is considered as an important resistance mechanism to cancer immunotherapy.

The volume includes three sections. The first section covers general knowledge about T cell trafficking during a normal immune response but also during tumor development. The second section provides an in-depth description of the different obstacles that prevent T cells from migrating and contacting tumor cells. The third section explores therapeutic strategies to improve trafficking of T cells into tumors and, thus, to enhance the effectiveness of cancer immunotherapy.

Table of Contents

Introduction.- Basic rules of T cell migration.- Regulation of anti-tumor T cell migration and function: contribution of real-time imaging.- 

Vascular normalization, T cell trafficking and anti-tumor immunity.- Disruption of anti-tumor T cell responses by cancer-associated fibroblasts.- Cancer-associated Tertiary Lymphoid Structures, from basic knowledge toward therapeutic target in clinic.- Homing Improvement: Boosting T Cell Trafficking for Cancer Immunotherapy.- Chemokines and T cell trafficking into tumors. Strategies to enhance recruitment of T cells into tumors.- Strategies to enhance migration and persistence of chimeric antigen receptor (CAR)-T cells into tumors.

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