Format

Send to

Choose Destination
Cancer Immunol Immunother. 2018 Oct;67(10):1545-1558. doi: 10.1007/s00262-018-2214-0. Epub 2018 Jul 27.

High-grade glioma associated immunosuppression does not prevent immune responses induced by therapeutic vaccines in combination with Treg depletion.

Author information

1
Department of Neurosurgery, University Medical Center Würzburg, Würzburg, Germany.
2
Department of Pediatric Oncology, University Children's Hospital Würzburg, Josef-Schneider-Strasse 2, 97080, Würzburg, Germany.
3
Department of Pediatric Neurosurgery, University Medical Center, Würzburg, Germany.
4
Department of Neuropathology, Institute of Pathology, University of Würzburg, Würzburg, Germany.
5
Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
6
Department of Epidemiology and Biostatistics, University Medical Center, Würzburg, Germany.
7
Department of Pediatric Oncology, University Children's Hospital Würzburg, Josef-Schneider-Strasse 2, 97080, Würzburg, Germany. eyrich_m@ukw.de.

Abstract

High-grade gliomas (HGG) exert systemic immunosuppression, which is of particular importance as immunotherapeutic strategies such as therapeutic vaccines are increasingly used to treat HGGs. In a first cohort of 61 HGG patients we evaluated a panel of 30 hematological and 34 plasma biomarkers. Then, we investigated in a second cohort of 11 relapsed HGG patients receiving immunomodulation with metronomic cyclophosphamide upfront to a DC-based vaccine whether immune abnormalities persisted and whether they hampered induction of IFNγ+ T-cell responses. HGG patients from the first cohort showed increased numbers of leukocytes, neutrophils and MDSCs and in parallel reduced numbers of CD4+/CD8+ T-cells, plasmacytoid and conventional DC2s. MDSCs and T-cell alterations were more profound in WHO IV° glioma patients. Moreover, levels of MDSCs and epidermal growth factor were negatively associated with survival. Serum levels of IL-2, IL-4, IL-5 and IL-10 were altered in HGG patients, however, without any impact on clinical outcome. In the immunotherapy cohort, 6-month overall survival was 100%. Metronomic cyclophosphamide led to > 40% reduction of regulatory T cells (Treg). In parallel to Treg-depletion, MDSCs and DC subsets became indistinguishable from healthy controls, whereas T-lymphopenia persisted. Despite low T-cells, IFNγ-responses could be induced in 9/10 analyzed cases. Importantly, frequency of CD8+VLA-4+ T-cells with CNS-homing properties, but not of CD4+ VLA-4+ T-cells, increased during vaccination. Our study identifies several features of systemic immunosuppression in HGGs. Metronomic cyclophosphamide in combination with an active immunization alleviates the latter and the combined treatment allows induction of a high rate of anti-glioma immune responses.

KEYWORDS:

CNS homing; DC vaccines; High-grade glioma; Immunosuppression; MDSCs; Treg depletion

PMID:
30054667
PMCID:
PMC6182405
DOI:
10.1007/s00262-018-2214-0
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Springer Icon for PubMed Central
Loading ...
Support Center