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Published in: Cancer Immunology, Immunotherapy 2/2018

Open Access 01-02-2018 | Original Article

NY-ESO-1- and survivin-specific T-cell responses in the peripheral blood from patients with glioma

Authors: Zhenjiang Liu, Thomas Poiret, Oscar Persson, Qingda Meng, Lalit Rane, Jiri Bartek Jr., Julia Karbach, Hans-Michael Altmannsberger, Christopher Illies, Xiaohua Luo, Inti Harvey-Peredo, Elke Jäger, Ernest Dodoo, Markus Maeurer

Published in: Cancer Immunology, Immunotherapy | Issue 2/2018

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Abstract

The prognosis for patients with glioblastoma is grim. Ex vivo expanded tumor-associated antigen (TAA)-reactive T-cells from patients with glioma may represent a viable source for anticancer-directed cellular therapies. Immunohistochemistry was used to test the survivin (n = 40 samples) and NY-ESO-1 (n = 38 samples) protein expression in tumor specimens. T-cells from peripheral blood were stimulated with TAAs (synthetic peptides) in IL-2 and IL-7, or using a combination of IL-2, IL-15 and IL-21. CD4+ and CD8+ T-cells were tested for antigen-specific proliferation by flow cytometry, and IFN-γ production was tested by ELISA. Twenty-eight out of 38 cancer specimens exhibited NY-ESO-1 protein expression, 2/38 showed a strong universal (4+) NY-ESO-1 staining, and 9/40 cancer lesions exhibited a strong (4+) staining for survivin. We could detect antigen-specific IFN-γ responses in 25% blood samples for NY-ESO-1 and 30% for survivin. NY-ESO-1-expanded T-cells recognized naturally processed and presented epitopes. NY-ESO-1 or survivin expression in glioma represents viable targets for anticancer-directed T-cells for the biological therapy of patients with glioma.
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Metadata
Title
NY-ESO-1- and survivin-specific T-cell responses in the peripheral blood from patients with glioma
Authors
Zhenjiang Liu
Thomas Poiret
Oscar Persson
Qingda Meng
Lalit Rane
Jiri Bartek Jr.
Julia Karbach
Hans-Michael Altmannsberger
Christopher Illies
Xiaohua Luo
Inti Harvey-Peredo
Elke Jäger
Ernest Dodoo
Markus Maeurer
Publication date
01-02-2018
Publisher
Springer Berlin Heidelberg
Published in
Cancer Immunology, Immunotherapy / Issue 2/2018
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-017-2066-z

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