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Rigshospitalet - a part of Copenhagen University Hospital
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In vitro 4-1BB stimulation promotes expansion of CD8+ tumor-infiltrating lymphocytes from various sarcoma subtypes

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

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  2. Evaluation of complement proteins as screening markers for colorectal cancer

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  3. Successful treatment with Ipilimumab and Interleukin-2 in two patients with metastatic melanoma and systemic autoimmune disease

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  4. Efficient tumor cell lysis mediated by a Bcl-X(L) specific T cell clone isolated from a breast cancer patient

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  1. Preoperative Embolization of a Solitary Fibrous Tumor Originating from External Auditory Meatus: A Case Report with Literature Review

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  2. No detectable remodelling in adult human menisci: an analysis based on the C14 bomb pulse

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Tumor-specific tumor-infiltrating lymphocytes (TILs) can be in vitro expanded and have the ability to induce complete and durable tumor regression in some patients with melanoma following adoptive cell therapy (ACT). In this preclinical study, we investigated the feasibility of expanding TIL from sarcomas, as well as performing functional in vitro analyses on these. TILs were expanded in vitro by the use of IL2 stimulation with or without the addition of 4-1BB and CD3 antibodies. Phenotypical and functional analyses were mainly performed by flow cytometry. TILs were expanded from 25 of 28 (89%) tumor samples from patients with 9 different sarcoma subtypes. TILs were predominantly αβ T-cells of effector memory subtype with CD4+  dominance. In particular, CD8+ TIL highly expressed LAG3 and to a lesser degree PD-1 and BTLA. In total, 10 of 20 TIL cultures demonstrated in vitro recognition of autologous tumor. In some cases, the fraction of tumor-reactive T cells was more than 20%. 4-1BB stimulation augmented expansion kinetics and favored CD8+ occurrence. In conclusion, TIL expansion from sarcoma is feasible and expanded TILs highly express LAG3 and comprise multifunctional tumor-reactive T-cells.

Original languageEnglish
JournalCancer immunology, immunotherapy
Volume69
Issue number11
Pages (from-to)2179-2191
Number of pages13
ISSN0340-7004
DOIs
Publication statusPublished - Nov 2020

    Research areas

  • 4-1BB Ligand/pharmacology, Adult, Aged, Aged, 80 and over, CD8-Positive T-Lymphocytes/drug effects, Cell Culture Techniques/methods, Female, Humans, Lymphocytes, Tumor-Infiltrating/drug effects, Male, Middle Aged, Sarcoma/immunology, Tumor Cells, Cultured

ID: 61244280