Literature DB >> 25949880

Discordant humoral and cellular immune responses to Cytomegalovirus (CMV) in glioblastoma patients whose tumors are positive for CMV.

Afsar Rahbar1, Inti Peredo2, Nina Wolmer Solberg1, Chato Taher1, Mensur Dzabic1, Xinling Xu1, Petra Skarman1, Olesja Fornara1, Charlotte Tammik1, Koon Yaiw1, Vanessa Wilhelmi1, Alice Assinger1, Giuseppe Stragliotto3, Cecilia Söderberg-Naucler1.   

Abstract

Background. Glioblastoma (GBM) is the most common malignant brain tumor in adults and is nearly always fatal. Emerging evidence suggests that human Cytomegalovirus (HCMV) is present in 90-100% of GBMs and that add-on antiviral treatment for HCMV show promise to improve survival. Methods. In a randomized, placebo-controlled trial of valganciclovir in 42 GBM patients, blood samples were collected for analyses of HCMV DNA, RNA, reactivity against HCMV peptides, IgG, and IgM at baseline and at 3, 12, and 24 weeks of treatment. Results. All 42 tumors were positive for HCMV protein. All patients examined had at least one blood sample positive for HCMV DNA, 63% were HCMV RNA positive, and 21% were IgM positive. However, 29% of GBM patients were IgG negative for HCMV. Five of these samples were positive in an enzyme-linked immunosorbent assay (ELISA) that used antigens derived from a clinical isolate. Blood T cells from 11 of 13 (85%) HCMV IgG-negative GBM patients reacted against HCMV peptides. Valganciclovir did not affect IgG titers, DNA, or RNA levels of the HCMV immediate early (HCMV IE) gene in blood. Conclusion. In GBM patients, HCMV activity is higher than in healthy controls and serology is a poor test to define previous or active HCMV infection in these patients.

Entities:  

Keywords:  ELISA, enzyme-linked immunosorbent assay; FACS, flow cytometry analyses; FITC, fluorescein isothiocyanate; GBM, glioblastoma; HCMV IE, human Cytomegalovirus-immediate early; HCMV, human Cytomegalovirus; HIV, human immunodeficiency virus; HSV, herpes simplex virus; PBMC, Peripheral blood mononuclear cells; PBS, Phosphate buffered saline; PCR, polymerase chain reaction; SEB, staphylococcal snterotoxin B; VIGAS study, Efficacy and Safety of Valcyte® as an Add-on Therapy in Patients with Malignant Glioblastoma and cytomegalovirus infection; Valcyte; cytomegalovirus; glioblastoma; peptides stimulation; serology; valganciclovir

Year:  2015        PMID: 25949880      PMCID: PMC4404865          DOI: 10.4161/2162402X.2014.982391

Source DB:  PubMed          Journal:  Oncoimmunology        ISSN: 2162-4011            Impact factor:   8.110


  47 in total

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Journal:  Transfusion       Date:  2001-10       Impact factor: 3.157

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4.  Survival in patients with glioblastoma receiving valganciclovir.

Authors:  Cecilia Söderberg-Nauclér; Afsar Rahbar; Giuseppe Stragliotto
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8.  Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial.

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9.  Identification of novel virus-specific antigens by CD4⁺ and CD8⁺ T cells from asymptomatic HSV-2 seropositive and seronegative donors.

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10.  HIV-specific cytotoxic T-cells in HIV-exposed but uninfected Gambian women.

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  11 in total

1.  Enhanced neutrophil activity is associated with shorter time to tumor progression in glioblastoma patients.

Authors:  Afsar Rahbar; Madeleine Cederarv; Nina Wolmer-Solberg; Charlotte Tammik; Giuseppe Stragliotto; Inti Peredo; Olesja Fornara; Xinling Xu; Mensur Dzabic; Chato Taher; Petra Skarman; Cecilia Söderberg-Nauclér
Journal:  Oncoimmunology       Date:  2015-08-24       Impact factor: 8.110

Review 2.  Anticancer effects of the microbiome and its products.

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Review 6.  Platelets in Viral Infections - Brave Soldiers or Trojan Horses.

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Journal:  Oncoimmunology       Date:  2017-06-05       Impact factor: 8.110

8.  Detection of human cytomegalovirus in glioblastoma among Taiwanese subjects.

Authors:  Ching-Fen Yang; Hsiang-Ling Ho; Shih-Chieh Lin; Chih-Yi Hsu; Donald Ming-Tak Ho
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9.  Epstein-Barr virus- and cytomegalovirus-specific immune response in patients with brain cancer.

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