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>, <...
| Published in: | Pharmaceutics |
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| Main Authors: | , , , , , , , , |
| Format: | Article |
| Language: | English |
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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. |
| format | Article |
| id | doaj-art-cbabaab1fee549e4bb6e1a4925d48eec |
| institution | Directory of Open Access Journals |
| issn | 1999-4923 |
| language | English |
| publishDate | 2023-07-01 |
| publisher | MDPI AG |
| record_format | Article |
| 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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