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Titlebook: Immunotherapy of Cancer; Mary L. Disis Book 2006 Humana Press 2006 Antigen.T cell.cell.cell therapy.clinical trial.cytokine.cytokines.imag

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樓主: Menthol
41#
發(fā)表于 2025-3-28 17:48:26 | 只看該作者
Autologous Tumor-Derived Heat Shock Protein Vaccine as a New Paradigm for Individualized Cancer The induced in response to the accumulation of misfolded proteins in the cell. They are essential in chaperoning proteins and maintaining the correct conformation of protein substrates. Recently, these molecules have been implicated in bridging innate and adaptive immunity, owing to their ability to ch
42#
發(fā)表于 2025-3-28 20:36:00 | 只看該作者
43#
發(fā)表于 2025-3-29 02:26:39 | 只看該作者
44#
發(fā)表于 2025-3-29 06:14:42 | 只看該作者
45#
發(fā)表于 2025-3-29 07:26:03 | 只看該作者
46#
發(fā)表于 2025-3-29 14:34:09 | 只看該作者
Tumor-Induced Immune Suppression and Immune Escape,ression in patients with malignant disease. These findings have provided the rationale for the development of active specific immunotherapy for the treatment of malignant disease. The enthusiastic application of active specific immunotherapy in a large number of patients has conclusively shown that:
47#
發(fā)表于 2025-3-29 16:55:06 | 只看該作者
The Tumor Microenvironment,ingly clear. Survival and expansion of tumor cells cannot be achieved in the absence of a favorable microenvironment, the main components of which are leukocytes, vascular cells, and fibroblasts. This tumor microenvironment critically provides growth factors and survival signals for tumor cell proli
48#
發(fā)表于 2025-3-29 21:06:41 | 只看該作者
49#
發(fā)表于 2025-3-30 01:42:40 | 只看該作者
Fast-Lane Evolution in the Tumor Microenvironment,une system to those related to the genetic instability of cancer cells. We have discussed elsewhere the relevance of immune polymorphism and immune adaptation to the study of tumor host interactions in the tumor microenvironment. In this chapter, we describe changes occurring during the natural hist
50#
發(fā)表于 2025-3-30 07:03:34 | 只看該作者
Manipulating Immunological Checkpoints to Maximize Antitumor Immunity,nto clinically meaningful tumor regressions, particularly in advanced disease. It is increasingly clear that tumor-specific immune tolerance represents a layered system of controls that keep the immune system turned off. Immunoregulatory checkpoints map locoregionally to the tumor microenvironment a
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