The suppressive tumor microenvironment: a challenge in cancer immunotherapy.

The suppressive tumor microenvironment: a challenge in cancer immunotherapy.
复制标题

DOI:
10.1021/mp1004228
复制
发表时间:
2011-06-06
影响因子:
4.9
通讯作者:
Huang L
Huang L
中科院分区:
医学2区
文献类型:
--
作者:
Vasievich EA;Huang L

文献摘要

参考文献

被引文献

相似文献

在这篇综述中,我们介绍了公众对疫苗和免疫疗法在癌症治疗中的看法。我们讨论了不同的免疫抑制细胞在肿瘤微环境中发挥的作用。深入讨论了肿瘤相关巨噬细胞(TAM)和M1和M2巨噬细胞表型。此外,髓源性抑制细胞(MDSC)和调节性T细胞(T细胞)在肿瘤微环境中发挥的作用也得到了解决。突出显示的是针对每种抑制性细胞类型使用的疗法的例子,这些疗法从假设到无效;从无效到成功。已经尝试了各种治疗方法来解决这个基本问题,实际上是允许癌性突变细胞存活,繁殖和超越身体的原因。有效的方法来禁用每一个特定的抑制类型的细胞已被介绍,这篇评论总结了讨论与一个表,以指导未来的发展。我们认为基因治疗是最具创新性和灵活性的方法,可以引导电荷专门改变肿瘤微环境。
In this review, we introduce the changing public perception of vaccines and immunotherapy in cancer treatments. We discuss the roles that different immunosuppressive cells play in the tumor microenvironment. Tumor associated macrophages (TAMs) and M1 and M2 macrophage phenotypes are discussed in depth. Additionally, the role that myeloid derived suppressor cells (MDSC) and T regulatory cells (Tregs) play in the tumor microenvironment is addressed. Highlighted are examples of therapies used against each suppressive cell type, which vary from the hypothetical to the ineffective; the inefficient to the successful. A variety of treatments have been tried to combat this fundamental problem, indeed the cause that allows cancerous mutated cells to survive, multiply and overtake the body. Efficient methods to disable each particular suppressive type of cell have been introduced; this review summarizes the discussion with a table to guide future development. We see gene therapy as the most innovative and flexible method to lead the charge to specifically modifying the tumor microenvironment.
DOI: 10.1016/j.bbrc.2007.10.182
发表时间: 2008-01-11
影响因子: 3.1
作者:
Koga, Mitsuhisa;Kai, Hisashi;Imaizumi, Tsutomu
通讯作者: Imaizumi, Tsutomu
DOI: 10.1136/gut.2010.211722
发表时间: 2011-03-01
期刊: GUT
影响因子: 24.5
作者:
Gonzalez-Aparicio, Manuela;Alzuguren, Pilar;Hernandez-Alcoceba, Ruben
通讯作者: Hernandez-Alcoceba, Ruben
DOI: 10.1038/sj.cgt.7700908
发表时间: 2006-04-01
影响因子: 6.4
作者:
Kagaya, T;Nakamoto, Y;Kaneko, S
通讯作者: Kaneko, S
DOI: 10.1056/nejmoa1001294
发表时间: 2010-07-29
影响因子: 158.5
作者:
Kantoff, Philip W.;Higano, Celestia S.;Young, J.
通讯作者: Young, J.
ISCOM 疫苗与 TLR9 激动剂相结合,打破了胰腺癌原位模型中调节性 T 细胞介导的免疫逃避
DOI: 10.1002/ijc.25399
发表时间: 2011-02-15
影响因子: 6.4
作者:
Jacobs, Collin;Duewell, Peter;Schnurr, Max
通讯作者: Schnurr, Max