Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk

The advancement of cancer immunotherapy faces barriers which limit its efficacy. These include weak immunogenicity of the tumor, as well as immunosuppressive mechanisms which prevent effective antitumor immune responses. Recent studies suggest that aberrant expression of cancer testis antigens (CTAs...

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Main Authors: Kyle K. Payne, Amir A. Toor, Xiang-Yang Wang, Masoud H. Manjili
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Clinical and Developmental Immunology
Online Access:http://dx.doi.org/10.1155/2012/760965
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spelling doaj-634837ec7edd474ba5cfe3d50a6de7da2020-11-24T22:22:17ZengHindawi LimitedClinical and Developmental Immunology1740-25221740-25302012-01-01201210.1155/2012/760965760965Immunotherapy of Cancer: Reprogramming Tumor-Immune CrosstalkKyle K. Payne0Amir A. Toor1Xiang-Yang Wang2Masoud H. Manjili3Department of Microbiology & Immunology, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USADepartment of Internal Medicine, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USADepartment of Human and Molecular Genetics, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USADepartment of Microbiology & Immunology, Massey Cancer Center, Virginia Commonwealth University, Richmond, VA 23298, USAThe advancement of cancer immunotherapy faces barriers which limit its efficacy. These include weak immunogenicity of the tumor, as well as immunosuppressive mechanisms which prevent effective antitumor immune responses. Recent studies suggest that aberrant expression of cancer testis antigens (CTAs) can generate robust antitumor immune responses, which implicates CTAs as potential targets for immunotherapy. However, the heterogeneity of tumor cells in the presence and quantity of CTA expression results in tumor escape from CTA-specific immune responses. Thus, the ability to modulate the tumor cell epigenome to homogenously induce expression of such antigens will likely render the tumor more immunogenic. Additionally, emerging studies suggest that suppression of antitumor immune responses may be overcome by reprogramming innate and adaptive immune cells. Therefore, this paper discusses recent studies which address barriers to successful cancer immunotherapy and proposes a strategy of modulation of tumor-immune cell crosstalk to improve responses in carcinoma patients.http://dx.doi.org/10.1155/2012/760965
collection DOAJ
language English
format Article
sources DOAJ
author Kyle K. Payne
Amir A. Toor
Xiang-Yang Wang
Masoud H. Manjili
spellingShingle Kyle K. Payne
Amir A. Toor
Xiang-Yang Wang
Masoud H. Manjili
Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
Clinical and Developmental Immunology
author_facet Kyle K. Payne
Amir A. Toor
Xiang-Yang Wang
Masoud H. Manjili
author_sort Kyle K. Payne
title Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
title_short Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
title_full Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
title_fullStr Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
title_full_unstemmed Immunotherapy of Cancer: Reprogramming Tumor-Immune Crosstalk
title_sort immunotherapy of cancer: reprogramming tumor-immune crosstalk
publisher Hindawi Limited
series Clinical and Developmental Immunology
issn 1740-2522
1740-2530
publishDate 2012-01-01
description The advancement of cancer immunotherapy faces barriers which limit its efficacy. These include weak immunogenicity of the tumor, as well as immunosuppressive mechanisms which prevent effective antitumor immune responses. Recent studies suggest that aberrant expression of cancer testis antigens (CTAs) can generate robust antitumor immune responses, which implicates CTAs as potential targets for immunotherapy. However, the heterogeneity of tumor cells in the presence and quantity of CTA expression results in tumor escape from CTA-specific immune responses. Thus, the ability to modulate the tumor cell epigenome to homogenously induce expression of such antigens will likely render the tumor more immunogenic. Additionally, emerging studies suggest that suppression of antitumor immune responses may be overcome by reprogramming innate and adaptive immune cells. Therefore, this paper discusses recent studies which address barriers to successful cancer immunotherapy and proposes a strategy of modulation of tumor-immune cell crosstalk to improve responses in carcinoma patients.
url http://dx.doi.org/10.1155/2012/760965
work_keys_str_mv AT kylekpayne immunotherapyofcancerreprogrammingtumorimmunecrosstalk
AT amiratoor immunotherapyofcancerreprogrammingtumorimmunecrosstalk
AT xiangyangwang immunotherapyofcancerreprogrammingtumorimmunecrosstalk
AT masoudhmanjili immunotherapyofcancerreprogrammingtumorimmunecrosstalk
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