دورية أكاديمية

Inhibition of Indoleamine-2,3-dioxygenase (IDO) in Glioblastoma Cells by Oncolytic Herpes Simplex Virus

التفاصيل البيبلوغرافية
العنوان: Inhibition of Indoleamine-2,3-dioxygenase (IDO) in Glioblastoma Cells by Oncolytic Herpes Simplex Virus
المؤلفون: Bonnie Reinhart, Lucia Mazzacurati, Adriana Forero, Chang-Sook Hong, Junichi Eguchi, Hideho Okada, Wendy Fellows, Ajay Niranjan, Justus B. Cohen, Joseph C. Glorioso, Paola Grandi
المصدر: Advances in Virology, Vol 2012 (2012)
بيانات النشر: Hindawi Limited, 2012.
سنة النشر: 2012
المجموعة: LCC:Microbiology
مصطلحات موضوعية: Microbiology, QR1-502
الوصف: Successful oncolytic virus treatment of malignant glioblastoma multiforme depends on widespread tumor-specific lytic virus replication and escape from mitigating innate immune responses to infection. Here we characterize a new HSV vector, JD0G, that is deleted for ICP0 and the joint sequences separating the unique long and short elements of the viral genome. We observed that JD0G replication was enhanced in certain glioblastoma cell lines compared to HEL cells, suggesting that a vector backbone deleted for ICP0 may be useful for treatment of glioblastoma. The innate immune response to virus infection can potentially impede oncolytic vector replication in human tumors. Indoleamine-2,3-dioxygenase (IDO) is expressed in response to interferon γ (IFNγ) and has been linked to both antiviral functions and to the immune escape of tumor cells. We observed that IFNγ treatment of human glioblastoma cells induced the expression of IDO and that this expression was quelled by infection with both wild-type and JD0G viruses. The role of IDO in inhibiting virus replication and the connection of this protein to the escape of tumor cells from immune surveillance suggest that IDO downregulation by HSV infection may enhance the oncolytic activity of vectors such as JD0G.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1687-8639
1687-8647
العلاقة: https://doaj.org/toc/1687-8639Test; https://doaj.org/toc/1687-8647Test
DOI: 10.1155/2012/815465
الوصول الحر: https://doaj.org/article/45761b7156644ee18c3de87d57e7388eTest
رقم الانضمام: edsdoj.45761b7156644ee18c3de87d57e7388e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16878639
16878647
DOI:10.1155/2012/815465