Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria

Oncolytic bacteria are a classification of bacteria with a natural ability to specifically target solid tumors and, in the process, stimulate a potent immune response. Currently, these include species of <i>Klebsiella</i>, <i>Listeria</i>, <i>Mycobacteria</i>, <...

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Published in:Pharmaceutics
Main Authors: Jason M. Roe, Kevin Seely, Caleb J. Bussard, Emily Eischen Martin, Elizabeth G. Mouw, Kenneth W. Bayles, Michael A. Hollingsworth, Amanda E. Brooks, Kaitlin M. Dailey
Format: Article
Language:English
Published: MDPI AG 2023-07-01
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Online Access:https://www.mdpi.com/1999-4923/15/7/2004
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author Jason M. Roe
Kevin Seely
Caleb J. Bussard
Emily Eischen Martin
Elizabeth G. Mouw
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Kaitlin M. Dailey
author_facet Jason M. Roe
Kevin Seely
Caleb J. Bussard
Emily Eischen Martin
Elizabeth G. Mouw
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Kaitlin M. Dailey
author_sort Jason M. Roe
collection DOAJ
container_title Pharmaceutics
description Oncolytic bacteria are a classification of bacteria with a natural ability to specifically target solid tumors and, in the process, stimulate a potent immune response. Currently, these include species of <i>Klebsiella</i>, <i>Listeria</i>, <i>Mycobacteria</i>, <i>Streptococcus</i>/<i>Serratia</i> (Coley’s Toxin), <i>Proteus</i>, <i>Salmonella</i>, and <i>Clostridium</i>. Advancements in techniques and methodology, including genetic engineering, create opportunities to “hijack” typical host–pathogen interactions and subsequently harness oncolytic capacities. Engineering, sometimes termed “domestication”, of oncolytic bacterial species is especially beneficial when solid tumors are inaccessible or metastasize early in development. This review examines reported oncolytic bacteria–host immune interactions and details the known mechanisms of these interactions to the protein level. A synopsis of the presented membrane surface molecules that elicit particularly promising oncolytic capacities is paired with the stimulated localized and systemic immunogenic effects. In addition, oncolytic bacterial progression toward clinical translation through engineering efforts are discussed, with thorough attention given to strains that have accomplished Phase III clinical trial initiation. In addition to therapeutic mitigation after the tumor has formed, some bacterial species, referred to as “prophylactic”, may even be able to prevent or “derail” tumor formation through anti-inflammatory capabilities. These promising species and their particularly favorable characteristics are summarized as well. A complete understanding of the bacteria–host interaction will likely be necessary to assess anti-cancer capacities and unlock the full cancer therapeutic potential of oncolytic bacteria.
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spelling doaj-art-cbabaab1fee549e4bb6e1a4925d48eec2025-08-19T22:48:33ZengMDPI AGPharmaceutics1999-49232023-07-01157200410.3390/pharmaceutics15072004Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic BacteriaJason M. Roe0Kevin Seely1Caleb J. Bussard2Emily Eischen Martin3Elizabeth G. Mouw4Kenneth W. Bayles5Michael A. Hollingsworth6Amanda E. Brooks7Kaitlin M. Dailey8College of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USACollege of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USACollege of Osteopathic Medicine, Rocky Vista University, Parker, CO 80130, USACollege of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USACollege of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USADepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198, USAEppley Institute for Cancer Research, University of Nebraska Medical Center, Omaha, NE 68198, USACollege of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USAEppley Institute for Cancer Research, University of Nebraska Medical Center, Omaha, NE 68198, USAOncolytic bacteria are a classification of bacteria with a natural ability to specifically target solid tumors and, in the process, stimulate a potent immune response. Currently, these include species of <i>Klebsiella</i>, <i>Listeria</i>, <i>Mycobacteria</i>, <i>Streptococcus</i>/<i>Serratia</i> (Coley’s Toxin), <i>Proteus</i>, <i>Salmonella</i>, and <i>Clostridium</i>. Advancements in techniques and methodology, including genetic engineering, create opportunities to “hijack” typical host–pathogen interactions and subsequently harness oncolytic capacities. Engineering, sometimes termed “domestication”, of oncolytic bacterial species is especially beneficial when solid tumors are inaccessible or metastasize early in development. This review examines reported oncolytic bacteria–host immune interactions and details the known mechanisms of these interactions to the protein level. A synopsis of the presented membrane surface molecules that elicit particularly promising oncolytic capacities is paired with the stimulated localized and systemic immunogenic effects. In addition, oncolytic bacterial progression toward clinical translation through engineering efforts are discussed, with thorough attention given to strains that have accomplished Phase III clinical trial initiation. In addition to therapeutic mitigation after the tumor has formed, some bacterial species, referred to as “prophylactic”, may even be able to prevent or “derail” tumor formation through anti-inflammatory capabilities. These promising species and their particularly favorable characteristics are summarized as well. A complete understanding of the bacteria–host interaction will likely be necessary to assess anti-cancer capacities and unlock the full cancer therapeutic potential of oncolytic bacteria.https://www.mdpi.com/1999-4923/15/7/2004oncolytic bacteriabacterial-mediated cancer therapeuticshost–pathogen interactionimmune responsesynthetic biologyprogrammable medicine
spellingShingle Jason M. Roe
Kevin Seely
Caleb J. Bussard
Emily Eischen Martin
Elizabeth G. Mouw
Kenneth W. Bayles
Michael A. Hollingsworth
Amanda E. Brooks
Kaitlin M. Dailey
Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
oncolytic bacteria
bacterial-mediated cancer therapeutics
host–pathogen interaction
immune response
synthetic biology
programmable medicine
title Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
title_full Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
title_fullStr Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
title_full_unstemmed Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
title_short Hacking the Immune Response to Solid Tumors: Harnessing the Anti-Cancer Capacities of Oncolytic Bacteria
title_sort hacking the immune response to solid tumors harnessing the anti cancer capacities of oncolytic bacteria
topic oncolytic bacteria
bacterial-mediated cancer therapeutics
host–pathogen interaction
immune response
synthetic biology
programmable medicine
url https://www.mdpi.com/1999-4923/15/7/2004
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