RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Injectable hydrogels for personalized cancer immunotherapies.
Injectable hydrogels for personalized cancer immunotherapies.
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癌症免疫治疗领域已显示出显著增长,研究人员目前正专注于增强和延长局部免疫调节的有效策略。可注射水凝胶(IHs)已成为封装和控制小分子及细胞释放的多功能平台,因其在增强抗肿瘤免疫反应的同时抑制转移和复发的潜力而备受关注。IHs递送自然杀伤(NK)细胞、T细胞和抗原呈递细胞(APCs)为治疗癌症提供了一种可行的方法。事实上,它可以绕过细胞外基质,逐渐将小分子或细胞释放到肿瘤微环境中,从而增强针对癌细胞的免疫反应。本综述概述了利用IHs递送NK细胞、T细胞、APCs、化学免疫治疗、放射免疫治疗和光热免疫治疗的癌症免疫治疗最新进展。首先,我们介绍IHs作为递送基质,然后总结其用于局部递送小分子和免疫细胞以引发强效抗癌免疫反应的应用。
此外,我们讨论了用于局部联合治疗的IHs系统的最新进展,包括化学免疫治疗、放射免疫治疗、光热免疫治疗、光动力免疫治疗和基因免疫治疗。通过全面审视IHs在癌症免疫治疗中的应用,本综述旨在突出IHs作为免疫治疗递送有效载体的潜力,促进癌症治疗创新策略的发展。
此外,我们证明使用基于水凝胶的平台靶向递送免疫细胞,如NK细胞、T细胞和树突状细胞(DCs),在癌症治疗中具有显著潜力。这些创新方法已实现肿瘤生长的实质性减少,展示了水凝胶增强免疫治疗疗效的能力。意义声明:随着癌症免疫治疗的不断扩展,治疗药物的递送方式变得越来越关键。本综述聚焦于IHS的前瞻性进展,强调其革新局部免疫治疗递送的潜力。通过高效封装和控制T细胞、NK细胞、APC及各种治疗药物等关键免疫组分的释放,IHS提供了一条开创性途径来放大免疫反应、减缓转移并减少复发。其在化疗免疫治疗、放射免疫治疗和光热免疫治疗等新兴联合治疗中的作用进一步凸显了其适应性。理解IHS在癌症治疗中的重要性至关重要,这暗示了癌症治疗动态的转变,并预示着一个聚焦、持久且强大的治疗策略新时代的到来。
The field of cancer immunotherapy has shown significant growth, and researchers are now focusing on effective strategies to enhance and prolong local immunomodulation. Injectable hydrogels (IHs) have emerged as versatile platforms for encapsulating and controlling the release of small molecules and cells, drawing significant attention for their potential to enhance antitumor immune responses while inhibiting metastasis and recurrence. IHs delivering natural killer (NK) cells, T cells, and antigen-presenting cells (APCs) offer a viable method for treating cancer.
Indeed, it can bypass the extracellular matrix and gradually release small molecules or cells into the tumor microenvironment, thereby boosting immune responses against cancer cells. This review provides an overview of the recent advancements in cancer immunotherapy using IHs for delivering NK cells, T cells, APCs, chemoimmunotherapy, radio-immunotherapy, and photothermal-immunotherapy.
First, we introduce IHs as a delivery matrix, then summarize their applications for the local delivery of small molecules and immune cells to elicit robust anticancer immune responses.
Additionally, we discuss recent progress in IHs systems used for local combination therapy, including chemoimmunotherapy, radio-immunotherapy, photothermal-immunotherapy, photodynamic-immunotherapy, and gene-immunotherapy. By comprehensively examining the utilization of IHs in cancer immunotherapy, this review aims to highlight the potential of IHs as effective carriers for immunotherapy delivery, facilitating the development of innovative strategies for cancer treatment.
In addition, we demonstrate that using hydrogel-based platforms for the targeted delivery of immune cells, such as NK cells, T cells, and dendritic cells (DCs), has remarkable potential in cancer therapy. These innovative approaches have yielded substantial reductions in tumor growth, showcasing the ability of hydrogels to enhance the efficacy of immune-based treatments. STATEMENT OF SIGNIFICANCE: As cancer immunotherapy continues to expand, the mode of therapeutic agent delivery becomes increasingly critical. This review spotlights the forward-looking progress of IHs, emphasizing their potential to revolutionize localized immunotherapy delivery.
By efficiently encapsulating and controlling the release of essential immune components such as T cells, NK cells, APCs, and various therapeutic agents, IHs offer a pioneering pathway to amplify immune reactions, moderate metastasis, and reduce recurrence.
Their adaptability further shines when considering their role in emerging combination therapies, including chemoimmunotherapy, radio-immunotherapy, and photothermal-immunotherapy. Understanding IHs' significance in cancer therapy is essential, suggesting a shift in cancer treatment dynamics and heralding a novel period of focused, enduring, and powerful therapeutic strategies.
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