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TLR Agonist Therapy of Metastatic Breast Cancer in Mice

Toll-like receptor (TLR) 7/8 and 9 agonists stimulate an innate immune response that supports the development of tumor-specific immunity. Previous studies showed that either agonist individually could cure mice of small tumors and that when used in combination, they could prevent the progression of...

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Autores principales: Klinman, Dennis M., Goguet, Emilie, Tross, Debra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168108/
https://www.ncbi.nlm.nih.gov/pubmed/37103328
http://dx.doi.org/10.1097/CJI.0000000000000467
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author Klinman, Dennis M.
Goguet, Emilie
Tross, Debra
author_facet Klinman, Dennis M.
Goguet, Emilie
Tross, Debra
author_sort Klinman, Dennis M.
collection PubMed
description Toll-like receptor (TLR) 7/8 and 9 agonists stimulate an innate immune response that supports the development of tumor-specific immunity. Previous studies showed that either agonist individually could cure mice of small tumors and that when used in combination, they could prevent the progression of larger tumors (>300 mm(3)). To examine whether these agents combined could control metastatic disease, syngeneic mice were challenged with the highly aggressive 66cl4 triple-negative breast tumor cell line. Treatment was not initiated until pulmonary metastases were established, as verified by bioluminescent imaging of luciferase-tagged tumor cells. Results show that combined therapy with TLR7/8 and TLR9 agonists delivered to both primary and metastatic tumor sites significantly reduced tumor burden and extended survival. The inclusion of cyclophosphamide and anti-PD-L1 resulted in optimal tumor control, characterized by a 5-fold increase in the average duration of survival.
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spelling pubmed-101681082023-05-10 TLR Agonist Therapy of Metastatic Breast Cancer in Mice Klinman, Dennis M. Goguet, Emilie Tross, Debra J Immunother Basic Studies Toll-like receptor (TLR) 7/8 and 9 agonists stimulate an innate immune response that supports the development of tumor-specific immunity. Previous studies showed that either agonist individually could cure mice of small tumors and that when used in combination, they could prevent the progression of larger tumors (>300 mm(3)). To examine whether these agents combined could control metastatic disease, syngeneic mice were challenged with the highly aggressive 66cl4 triple-negative breast tumor cell line. Treatment was not initiated until pulmonary metastases were established, as verified by bioluminescent imaging of luciferase-tagged tumor cells. Results show that combined therapy with TLR7/8 and TLR9 agonists delivered to both primary and metastatic tumor sites significantly reduced tumor burden and extended survival. The inclusion of cyclophosphamide and anti-PD-L1 resulted in optimal tumor control, characterized by a 5-fold increase in the average duration of survival. Lippincott Williams & Wilkins 2023-06 2023-04-28 /pmc/articles/PMC10168108/ /pubmed/37103328 http://dx.doi.org/10.1097/CJI.0000000000000467 Text en Written work prepared by employees of the Federal Government as part of their official duties is, under the U.S. Copyright Act, a “work of the United States Government” for which copyright protection under Title 17 of the United States Code is not available. As such, copyright does not extend to the contributions of employees of the Federal Government.
spellingShingle Basic Studies
Klinman, Dennis M.
Goguet, Emilie
Tross, Debra
TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title_full TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title_fullStr TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title_full_unstemmed TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title_short TLR Agonist Therapy of Metastatic Breast Cancer in Mice
title_sort tlr agonist therapy of metastatic breast cancer in mice
topic Basic Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168108/
https://www.ncbi.nlm.nih.gov/pubmed/37103328
http://dx.doi.org/10.1097/CJI.0000000000000467
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