Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy

Malignant gliomas are the most common primary brain tumor in adults, with over 12,000 new cases diagnosed in the United States each year. Over the last decade, investigators have reliably identified human cytomegalovirus (HCMV) proteins, nucleic acids, and virions in most high-grade gliomas, includ...

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Main Authors: Daniel eLandi, Meenakshi eHegde, Nabil eAhmed
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-11-01
Series:Frontiers in Oncology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00338/full
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spelling doaj-236594e0458b4492831234847de747852020-11-24T23:19:38ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2014-11-01410.3389/fonc.2014.00338117359Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapyDaniel eLandi0Daniel eLandi1Meenakshi eHegde2Meenakshi eHegde3Nabil eAhmed4Nabil eAhmed5Nabil eAhmed6Baylor College of MedicineTexas Childrens HospitalBaylor College of MedicineTexas Childrens HospitalBaylor College of MedicineTexas Childrens HospitalHouston Methodist HospitalMalignant gliomas are the most common primary brain tumor in adults, with over 12,000 new cases diagnosed in the United States each year. Over the last decade, investigators have reliably identified human cytomegalovirus (HCMV) proteins, nucleic acids, and virions in most high-grade gliomas, including glioblastoma (GBM). This discovery is significant because human cytomegalovirus gene products can be targeted by immune-based therapies.In this review, we describe the current level of understanding regarding the presence and role in pathogenesis of HCMV in GBM. We describe our success detecting and expanding HCMV-specific cytotoxic T lymphocytes to kill GBM cells and explain how these cells can be used as a platform for enhanced cellular therapies. We discuss alternative approaches that capitalize on HCMV infection to treat patients with HCMV-positive tumors. Adoptive cellular therapy for HCMV-positive GBM has been tried in a small number of patients with some benefit, but we reason why, to date, these approaches generally fail to generate long-term remission or cure. We conjecture how cellular therapy for GBM can be improved and describe the barriers that must be overcome to cure these patients.http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00338/fullCytomegalovirusGlioblastomaImmunotherapycytotoxic T lymphocyte (CTL)adoptive cellular therapy
collection DOAJ
language English
format Article
sources DOAJ
author Daniel eLandi
Daniel eLandi
Meenakshi eHegde
Meenakshi eHegde
Nabil eAhmed
Nabil eAhmed
Nabil eAhmed
spellingShingle Daniel eLandi
Daniel eLandi
Meenakshi eHegde
Meenakshi eHegde
Nabil eAhmed
Nabil eAhmed
Nabil eAhmed
Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
Frontiers in Oncology
Cytomegalovirus
Glioblastoma
Immunotherapy
cytotoxic T lymphocyte (CTL)
adoptive cellular therapy
author_facet Daniel eLandi
Daniel eLandi
Meenakshi eHegde
Meenakshi eHegde
Nabil eAhmed
Nabil eAhmed
Nabil eAhmed
author_sort Daniel eLandi
title Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
title_short Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
title_full Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
title_fullStr Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
title_full_unstemmed Human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
title_sort human cytomegalovirus antigens in malignant gliomas as targets for adoptive cellular therapy
publisher Frontiers Media S.A.
series Frontiers in Oncology
issn 2234-943X
publishDate 2014-11-01
description Malignant gliomas are the most common primary brain tumor in adults, with over 12,000 new cases diagnosed in the United States each year. Over the last decade, investigators have reliably identified human cytomegalovirus (HCMV) proteins, nucleic acids, and virions in most high-grade gliomas, including glioblastoma (GBM). This discovery is significant because human cytomegalovirus gene products can be targeted by immune-based therapies.In this review, we describe the current level of understanding regarding the presence and role in pathogenesis of HCMV in GBM. We describe our success detecting and expanding HCMV-specific cytotoxic T lymphocytes to kill GBM cells and explain how these cells can be used as a platform for enhanced cellular therapies. We discuss alternative approaches that capitalize on HCMV infection to treat patients with HCMV-positive tumors. Adoptive cellular therapy for HCMV-positive GBM has been tried in a small number of patients with some benefit, but we reason why, to date, these approaches generally fail to generate long-term remission or cure. We conjecture how cellular therapy for GBM can be improved and describe the barriers that must be overcome to cure these patients.
topic Cytomegalovirus
Glioblastoma
Immunotherapy
cytotoxic T lymphocyte (CTL)
adoptive cellular therapy
url http://journal.frontiersin.org/Journal/10.3389/fonc.2014.00338/full
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