Cargando…
Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1
Oncolytic viruses provide a biologically multi-faceted treatment option for patients who cannot be cured with currently available treatment options. We constructed an oncolytic adenovirus, TILT-123, to support T-cell therapies and immune checkpoint inhibitors in solid tumors. Adenoviruses are immuno...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911972/ https://www.ncbi.nlm.nih.gov/pubmed/33513935 http://dx.doi.org/10.3390/cells10020246 |
_version_ | 1783656467528679424 |
---|---|
author | Havunen, Riikka Kalliokoski, Riikka Siurala, Mikko Sorsa, Suvi Santos, João M. Cervera-Carrascon, Victor Anttila, Marjukka Hemminki, Akseli |
author_facet | Havunen, Riikka Kalliokoski, Riikka Siurala, Mikko Sorsa, Suvi Santos, João M. Cervera-Carrascon, Victor Anttila, Marjukka Hemminki, Akseli |
author_sort | Havunen, Riikka |
collection | PubMed |
description | Oncolytic viruses provide a biologically multi-faceted treatment option for patients who cannot be cured with currently available treatment options. We constructed an oncolytic adenovirus, TILT-123, to support T-cell therapies and immune checkpoint inhibitors in solid tumors. Adenoviruses are immunogenic by nature, are easy to produce in large quantities, and can carry relatively large transgenes. They are the most commonly used gene therapy vectors and are well tolerated in patients. TILT-123 expresses two potent cytokines, tumor necrosis factor alpha and interleukin-2, to stimulate especially the T-cell compartment in the tumor microenvironment. Before entering clinical studies, the safety and biodistribution of TILT-123 was studied in Syrian hamsters and in mice. The results show that TILT-123 is safe in animals as monotherapy and in combination with an immune checkpoint inhibitor anti-PD-1. The virus treatment induces acute changes in circulating immune cell compartments, but the levels return to normal by the middle of the treatment period. The virus is rapidly cleared from healthy tissues, and it does not cause damage to vital organs. The results support the initiation of a phase 1 dose-escalation trial, where melanoma patients receiving a tumor-infiltrating lymphocyte therapy are treated with TILT-123 (NCT04217473). |
format | Online Article Text |
id | pubmed-7911972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79119722021-02-28 Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 Havunen, Riikka Kalliokoski, Riikka Siurala, Mikko Sorsa, Suvi Santos, João M. Cervera-Carrascon, Victor Anttila, Marjukka Hemminki, Akseli Cells Article Oncolytic viruses provide a biologically multi-faceted treatment option for patients who cannot be cured with currently available treatment options. We constructed an oncolytic adenovirus, TILT-123, to support T-cell therapies and immune checkpoint inhibitors in solid tumors. Adenoviruses are immunogenic by nature, are easy to produce in large quantities, and can carry relatively large transgenes. They are the most commonly used gene therapy vectors and are well tolerated in patients. TILT-123 expresses two potent cytokines, tumor necrosis factor alpha and interleukin-2, to stimulate especially the T-cell compartment in the tumor microenvironment. Before entering clinical studies, the safety and biodistribution of TILT-123 was studied in Syrian hamsters and in mice. The results show that TILT-123 is safe in animals as monotherapy and in combination with an immune checkpoint inhibitor anti-PD-1. The virus treatment induces acute changes in circulating immune cell compartments, but the levels return to normal by the middle of the treatment period. The virus is rapidly cleared from healthy tissues, and it does not cause damage to vital organs. The results support the initiation of a phase 1 dose-escalation trial, where melanoma patients receiving a tumor-infiltrating lymphocyte therapy are treated with TILT-123 (NCT04217473). MDPI 2021-01-27 /pmc/articles/PMC7911972/ /pubmed/33513935 http://dx.doi.org/10.3390/cells10020246 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Havunen, Riikka Kalliokoski, Riikka Siurala, Mikko Sorsa, Suvi Santos, João M. Cervera-Carrascon, Victor Anttila, Marjukka Hemminki, Akseli Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title | Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title_full | Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title_fullStr | Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title_full_unstemmed | Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title_short | Cytokine-Coding Oncolytic Adenovirus TILT-123 Is Safe, Selective, and Effective as a Single Agent and in Combination with Immune Checkpoint Inhibitor Anti-PD-1 |
title_sort | cytokine-coding oncolytic adenovirus tilt-123 is safe, selective, and effective as a single agent and in combination with immune checkpoint inhibitor anti-pd-1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911972/ https://www.ncbi.nlm.nih.gov/pubmed/33513935 http://dx.doi.org/10.3390/cells10020246 |
work_keys_str_mv | AT havunenriikka cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT kalliokoskiriikka cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT siuralamikko cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT sorsasuvi cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT santosjoaom cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT cerveracarrasconvictor cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT anttilamarjukka cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 AT hemminkiakseli cytokinecodingoncolyticadenovirustilt123issafeselectiveandeffectiveasasingleagentandincombinationwithimmunecheckpointinhibitorantipd1 |