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NLGN4X TCR transgenic T cells to treat gliomas.
Krämer, Christoper; Kilian, Michael; Chih, Yu-Chan; Kourtesakis, Alexandros; Hoffmann, Dirk C; Boschert, Tamara; Koopmann, Philipp; Sanghvi, Khwab; De Roia, Alice; Jung, Stefanie; Jähne, Kristine; Day, Bryan; Shultz, Lenny D; Ratliff, Miriam; Harbottle, Richard; Green, Edward W; Will, Rainer; Wick, Wolfgang; Platten, Michael; Bunse, Lukas.
Affiliation
  • Krämer C; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Kilian M; Department of Neurology, MCTN, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Chih YC; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Kourtesakis A; Department of Neurology, MCTN, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Hoffmann DC; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Boschert T; Faculty of Bioscience, Heidelberg University, Heidelberg, Germany.
  • Koopmann P; Faculty of Bioscience, Heidelberg University, Heidelberg, Germany.
  • Sanghvi K; Neurology Clinic, Heidelberg University Hospital, University of Heidelberg, Heidelberg, Germany.
  • De Roia A; DKTK CCU Neurooncology, DKFZ, Heidelberg, Germany.
  • Jung S; Faculty of Bioscience, Heidelberg University, Heidelberg, Germany.
  • Jähne K; Neurology Clinic, Heidelberg University Hospital, University of Heidelberg, Heidelberg, Germany.
  • Day B; DKTK CCU Neurooncology, DKFZ, Heidelberg, Germany.
  • Shultz LD; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Ratliff M; Faculty of Bioscience, Heidelberg University, Heidelberg, Germany.
  • Harbottle R; Helmholtz Institute of Translational Oncology (HI-TRON), Mainz, Germany.
  • Green EW; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Will R; Department of Neurology, MCTN, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Wick W; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Platten M; Faculty of Bioscience, Heidelberg University, Heidelberg, Germany.
  • Bunse L; German Cancer Consortium (DKTK) Clinical Cooperation Unit (CCU) Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Neuro Oncol ; 26(2): 266-278, 2024 02 02.
Article in En | MEDLINE | ID: mdl-37715782
ABSTRACT

BACKGROUND:

Neuroligin 4 X-linked (NLGN4X) harbors a human leukocyte antigen (HLA)-A*02-restricted tumor-associated antigen, overexpressed in human gliomas, that was found to induce specific cytotoxic T cell responses following multi-peptide vaccination in patients with newly diagnosed glioblastoma.

METHODS:

T cell receptor (TCR) discovery was performed using droplet-based single-cell TCR sequencing of NLGN4X-tetramer-sorted T cells postvaccination. The identified TCR was delivered to Jurkat T cells and primary human T cells (NLGN4X-TCR-T). Functional profiling of NLGN4X-TCR-T was performed by flow cytometry and cytotoxicity assays. Therapeutic efficacy of intracerebroventricular NLGN4X-TCR-T was assessed in NOD scid gamma (NSG) major histocompatibility complex (MHC) I/II knockout (KO) (NSG MHC I/II KO) mice bearing NLGN4X-expressing experimental gliomas.

RESULTS:

An HLA-A*02-restricted vaccine-induced T cell receptor specifically binding NLGN4X131-139 was applied for preclinical therapeutic use. Reactivity, cytotoxicity, and polyfunctionality of this NLGN4X-specific TCR are demonstrated in various cellular models. Intracerebroventricular administration of NLGN4X-TCR-T prolongs survival and leads to an objective response rate of 44.4% in experimental glioma-bearing NSG MHC I/II KO mice compared to 0.0% in control groups.

CONCLUSION:

NLGN4X-TCR-T demonstrate efficacy in a preclinical glioblastoma model. On a global scale, we provide the first evidence for the therapeutic retrieval of vaccine-induced human TCRs for the off-the-shelf treatment of glioblastoma patients.Keywords cell therapy | glioblastoma | T cell receptor | tumor antigen.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glioblastoma / Cancer Vaccines Limits: Animals / Humans Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2024 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glioblastoma / Cancer Vaccines Limits: Animals / Humans Language: En Journal: Neuro Oncol Journal subject: NEOPLASIAS / NEUROLOGIA Year: 2024 Type: Article Affiliation country: Germany