Identifying and Cloning Neoepitope Specific T-Cells from Newly Diagnosed Glioma Patients

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Presented by
Ed Green
Ed Green
German Cancer Research Center (DKFZ)

Covered in this Webinar
The principals of adoptive cell therapies
Discussion of the NOA16 peptide vaccination clinical trial
How combining scRNA- and T cell receptor (TCR)-sequencing was used to identify an IDH1.R132H reactive TCR
How we’re doing high throughput screening with TWIST libraries to identify better TCRs

Identifying and Cloning Neoepitope Specific, CD4+ T Cells from Newly Diagnosed Glioma Patients in a Phase I Vaccination Trial Targeting Mutant IDH1

Mutated isocitrate dehydrogenase 1 (IDH1) defines a molecularly distinct subtype of diffuse gliomas, and in previous work we showed that vaccinating mice with an IDH1.R132H-specific peptide induced tumor-specific therapeutic T helper cell responses and subsequent tumors control. In a multicenter, single-arm, open-label, first-in-man phase I trial involving vaccinating 33 patients with grade 3 and 4 IDH1.R132H+ve astrocytomas we were able to show vaccine-induced immune responses in 93.3 % of patients. By combining scRNA- and T cell receptor (TCR)-sequencing, we were able to identify and clone TCRs from patients, and have gone on to show that these are IDH1.R132H reactive. These results provide new hope for patients with IDH1.R132H mutated brain tumours, and point towards future applications of such TCRs in (personalised) adoptive cell therapies.

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