2021
Gamma-delta T cells in Glioblastoma patients
KOHLOVÁ, Barbora, Martin PISKÁČEK, Marie TOMANDLOVÁ, Veronika MOTÚZOVÁ, Vít ZMÁTLO et. al.Základní údaje
Originální název
Gamma-delta T cells in Glioblastoma patients
Autoři
KOHLOVÁ, Barbora, Martin PISKÁČEK, Marie TOMANDLOVÁ, Veronika MOTÚZOVÁ, Vít ZMÁTLO, Vilém JURÁŇ, Marek SOVA, Václav VYBÍHAL, Pavel FADRUS, Tomáš KAZDA a Andrea KNIGHT
Vydání
The 9th International γδ T Cell Conference, 2021
Další údaje
Jazyk
angličtina
Typ výsledku
Vyžádané přednášky
Obor
30204 Oncology
Stát vydavatele
Čína
Utajení
není předmětem státního či obchodního tajemství
Organizační jednotka
Lékařská fakulta
Klíčová slova anglicky
Gamma-delta T lymphocytes; Glioblastoma patients
Změněno: 21. 12. 2021 08:14, Mgr. Tereza Miškechová
Anotace
V originále
Gamma-delta (γδ) T cells are important effector lymphocytes of innate immunity with proven antitumour reactivity against aggressive glioblastoma brain tumour (GBM). Therapeutic approaches to GBM have had limited success particularly due to the protective brain barrier and the tumour immunosuppressive microenvironment. The GBM-infiltrating γδ T lymphocytes (TILs) have not been extensively investigated.In this study, we examined Vδ1 a Vδ2 γδ T cell populations in peripheral blood and paired tumour tissue samples from GBM patients (n=33) following the resection and throughtout the therapy follow-up. Tumour samples were processed using enzymatic kits and gentleMACSTM Dissociator (Miltenyi Biotec Inc.) and TIL γδ T cells were analyzed by flow cytometry.We found infiltration of both intratumoral CD3+ γδ T cell subsets in 73% tested tumour samples. We detected Vδ1 γδ T cell in the range 0-0.5% (median 0.26%). Majority of GBM patients presented the Vδ2 subset among TILs in the range 0- 12% (median 3.2%). Functional studies showed prominent cytotoxicity of magnetically sorted Vδ1 a Vδ2 γδ T cells against GBM cell lines and more importantly against primary tumours. Next, we identified the EphA2 receptor as one of the targets for tumour reactive Vδ1 γδ T cells. Specifically, we found that blocking of EphA2 expression resulted in significant inhibition of GBM tumour killing mediated by Vδ1 γδ T cells. Furthermore, multiplex analysis of soluble proteins by Luminex® 200™ in patients‘ plasma samples identified significantly elevated levels of MICA, check-point inhibitors B7-H3 (CD276), PD-L1 (B7-H1, CD274), Galectin-9 and Nectin-4. The patient’s clinical course, therapeutic protocols and RNAseq data will be discussed.
Návaznosti
NV19-05-00410, projekt VaV |
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