Tumor-Specific T Cell Activation in Malignant Brain Tumors

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Tumor-Specific T Cell Activation in Malignant Brain Tumors. / Mohme, Malte; Neidert, Marian Christoph.

In: FRONT IMMUNOL, Vol. 11, 2020, p. 205.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

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@article{9471e957f5334cef86951de2e4fbad46,
title = "Tumor-Specific T Cell Activation in Malignant Brain Tumors",
abstract = "Due to their delicate locations as well as aggressive and infiltrative behavior, malignant brain tumors remain a therapeutic challenge. Harnessing the efficacy and specificity of the T-cell response to counteract malignant brain tumor progression and recurrence, represents an attractive treatment option. With the tremendous advances in the current era of immunotherapy, ongoing studies aim to determine the best treatment strategies for mounting a tumor-specific immune response against malignant brain tumors. However, immunosuppression in the local tumor environment, molecular and cellular heterogeneity as well as a lack of suitable targets for tumor-specific vaccination impede the successful implementation of immunotherapeutic treatment strategies in neuro-oncology. In this review, we therefore discuss the role of T cell exhaustion, the genetic and antigenic landscape, potential pitfalls and ongoing efforts to overcome the individual challenges in order to elicit a tumor-specific T cell response.",
author = "Malte Mohme and Neidert, {Marian Christoph}",
note = "Copyright {\textcopyright} 2020 Mohme and Neidert.",
year = "2020",
doi = "10.3389/fimmu.2020.00205",
language = "English",
volume = "11",
pages = "205",
journal = "FRONT IMMUNOL",
issn = "1664-3224",
publisher = "Lausanne : Frontiers Research Foundation",

}

RIS

TY - JOUR

T1 - Tumor-Specific T Cell Activation in Malignant Brain Tumors

AU - Mohme, Malte

AU - Neidert, Marian Christoph

N1 - Copyright © 2020 Mohme and Neidert.

PY - 2020

Y1 - 2020

N2 - Due to their delicate locations as well as aggressive and infiltrative behavior, malignant brain tumors remain a therapeutic challenge. Harnessing the efficacy and specificity of the T-cell response to counteract malignant brain tumor progression and recurrence, represents an attractive treatment option. With the tremendous advances in the current era of immunotherapy, ongoing studies aim to determine the best treatment strategies for mounting a tumor-specific immune response against malignant brain tumors. However, immunosuppression in the local tumor environment, molecular and cellular heterogeneity as well as a lack of suitable targets for tumor-specific vaccination impede the successful implementation of immunotherapeutic treatment strategies in neuro-oncology. In this review, we therefore discuss the role of T cell exhaustion, the genetic and antigenic landscape, potential pitfalls and ongoing efforts to overcome the individual challenges in order to elicit a tumor-specific T cell response.

AB - Due to their delicate locations as well as aggressive and infiltrative behavior, malignant brain tumors remain a therapeutic challenge. Harnessing the efficacy and specificity of the T-cell response to counteract malignant brain tumor progression and recurrence, represents an attractive treatment option. With the tremendous advances in the current era of immunotherapy, ongoing studies aim to determine the best treatment strategies for mounting a tumor-specific immune response against malignant brain tumors. However, immunosuppression in the local tumor environment, molecular and cellular heterogeneity as well as a lack of suitable targets for tumor-specific vaccination impede the successful implementation of immunotherapeutic treatment strategies in neuro-oncology. In this review, we therefore discuss the role of T cell exhaustion, the genetic and antigenic landscape, potential pitfalls and ongoing efforts to overcome the individual challenges in order to elicit a tumor-specific T cell response.

U2 - 10.3389/fimmu.2020.00205

DO - 10.3389/fimmu.2020.00205

M3 - SCORING: Review article

C2 - 32117316

VL - 11

SP - 205

JO - FRONT IMMUNOL

JF - FRONT IMMUNOL

SN - 1664-3224

ER -