Swine pseudorabies virus attenuated vaccine reprograms the kidney cancer tumor microenvironment and synergizes with PD‐1 blockade

The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer has become an escalating concern that necessitates vigilant surveillance. Nowadays, surgical intervention remains the optimal therapeutic approach for...

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Published inJournal of medical virology Vol. 96; no. 4; pp. e29568 - n/a
Main Authors Gui, Mengxuan, Wu, Chongxin, Qi, Ruoyao, Zeng, Yue, Huang, Pengfei, Cao, Jiali, Chen, Tian, Chen, Kaiyun, Lin, Lina, Han, Qiangyuan, He, Peiqing, Fu, Rao, Wu, Qian, Yuan, Quan, Zhang, Tianying, Xia, Ningshao, Wang, Guosong, Chen, Yixin
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Published United States Wiley Subscription Services, Inc 01.04.2024
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Abstract The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer has become an escalating concern that necessitates vigilant surveillance. Nowadays, surgical intervention remains the optimal therapeutic approach for kidney cancer, while the availability of efficacious treatments for advanced tumors remains limited. Oncolytic viruses, an emerging form of immunotherapy, have demonstrated encouraging anti‐neoplastic properties and are progressively garnering public acceptance. However, research on oncolytic viruses in kidney cancer is relatively limited. Furthermore, given the high complexity and heterogeneity of kidney cancer, it is crucial to identify an optimal oncolytic virus agent that is better suited for its treatment. The present study investigates the oncolytic activity of the Pseudorabies virus live attenuated vaccine (PRV‐LAV) against KC. The findings clearly demonstrate that PRV‐LAV exhibits robust oncolytic activity targeting KC cell lines. Furthermore, the therapeutic efficacy of PRV‐LAV was confirmed in both a subcutaneous tumor‐bearing nude mouse model and a syngeneic mouse model of KC. Combined RNA‐seq analysis and flow cytometry revealed that PRV‐LAV treatment substantially enhances the infiltration of a diverse range of lymphocytes, including T cells, B cells, macrophages, and NK cells. Additionally, PRV‐LAV treatment enhances T cell activation and exerts antitumor effects. Importantly, the combination of PRV‐LAV with anti‐PD‐1 antibodies, an approved drug for KC treatment, synergistically enhances the efficacy against KC. Overall, the discovery of PRV‐LAV as an effective oncolytic virus holds significant importance for improving the treatment efficacy and survival rates of KC patients.
AbstractList The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer has become an escalating concern that necessitates vigilant surveillance. Nowadays, surgical intervention remains the optimal therapeutic approach for kidney cancer, while the availability of efficacious treatments for advanced tumors remains limited. Oncolytic viruses, an emerging form of immunotherapy, have demonstrated encouraging anti‐neoplastic properties and are progressively garnering public acceptance. However, research on oncolytic viruses in kidney cancer is relatively limited. Furthermore, given the high complexity and heterogeneity of kidney cancer, it is crucial to identify an optimal oncolytic virus agent that is better suited for its treatment. The present study investigates the oncolytic activity of the Pseudorabies virus live attenuated vaccine (PRV‐LAV) against KC. The findings clearly demonstrate that PRV‐LAV exhibits robust oncolytic activity targeting KC cell lines. Furthermore, the therapeutic efficacy of PRV‐LAV was confirmed in both a subcutaneous tumor‐bearing nude mouse model and a syngeneic mouse model of KC. Combined RNA‐seq analysis and flow cytometry revealed that PRV‐LAV treatment substantially enhances the infiltration of a diverse range of lymphocytes, including T cells, B cells, macrophages, and NK cells. Additionally, PRV‐LAV treatment enhances T cell activation and exerts antitumor effects. Importantly, the combination of PRV‐LAV with anti‐PD‐1 antibodies, an approved drug for KC treatment, synergistically enhances the efficacy against KC. Overall, the discovery of PRV‐LAV as an effective oncolytic virus holds significant importance for improving the treatment efficacy and survival rates of KC patients.
Abstract The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer has become an escalating concern that necessitates vigilant surveillance. Nowadays, surgical intervention remains the optimal therapeutic approach for kidney cancer, while the availability of efficacious treatments for advanced tumors remains limited. Oncolytic viruses, an emerging form of immunotherapy, have demonstrated encouraging anti‐neoplastic properties and are progressively garnering public acceptance. However, research on oncolytic viruses in kidney cancer is relatively limited. Furthermore, given the high complexity and heterogeneity of kidney cancer, it is crucial to identify an optimal oncolytic virus agent that is better suited for its treatment. The present study investigates the oncolytic activity of the Pseudorabies virus live attenuated vaccine (PRV‐LAV) against KC. The findings clearly demonstrate that PRV‐LAV exhibits robust oncolytic activity targeting KC cell lines. Furthermore, the therapeutic efficacy of PRV‐LAV was confirmed in both a subcutaneous tumor‐bearing nude mouse model and a syngeneic mouse model of KC. Combined RNA‐seq analysis and flow cytometry revealed that PRV‐LAV treatment substantially enhances the infiltration of a diverse range of lymphocytes, including T cells, B cells, macrophages, and NK cells. Additionally, PRV‐LAV treatment enhances T cell activation and exerts antitumor effects. Importantly, the combination of PRV‐LAV with anti‐PD‐1 antibodies, an approved drug for KC treatment, synergistically enhances the efficacy against KC. Overall, the discovery of PRV‐LAV as an effective oncolytic virus holds significant importance for improving the treatment efficacy and survival rates of KC patients.
Author Gui, Mengxuan
Cao, Jiali
Zeng, Yue
Lin, Lina
Yuan, Quan
Chen, Kaiyun
Xia, Ningshao
He, Peiqing
Fu, Rao
Wu, Qian
Huang, Pengfei
Chen, Tian
Zhang, Tianying
Han, Qiangyuan
Wang, Guosong
Qi, Ruoyao
Wu, Chongxin
Chen, Yixin
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  surname: Xia
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Keywords cancer therapy
immune checkpoint inhibitors
tumor microenvironment
oncolytic virus
Language English
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Notes Mengxuan Gui, Chongxin Wu, Ruoyao Qi, and Yue Zeng contributed equally to this study.
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Snippet The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer has become...
Abstract The global incidence rate of kidney cancer (KC) has been steadily increasing over the past 30 years. With the aging global population, kidney cancer...
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pubmed
wiley
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StartPage e29568
SubjectTerms Animals
Antibodies
Anticancer properties
Antitumor activity
Cancer
cancer therapy
Cancer vaccines
Cell activation
Cell Line, Tumor
Effectiveness
Flow cytometry
Herpesvirus 1, Suid - genetics
Heterogeneity
Humans
immune checkpoint inhibitors
Immunotherapy
Kidney cancer
Kidney Neoplasms
Kidneys
Lymphocytes
Lymphocytes B
Lymphocytes T
Macrophages
Metastases
Mice
Oncolysis
oncolytic virus
Oncolytic Viruses - genetics
Programmed Cell Death 1 Receptor
Pseudorabies
Survival
Swine
Tumor Microenvironment
Tumors
Vaccines
Vaccines, Attenuated
Viruses
Title Swine pseudorabies virus attenuated vaccine reprograms the kidney cancer tumor microenvironment and synergizes with PD‐1 blockade
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.29568
https://www.ncbi.nlm.nih.gov/pubmed/38549430
https://www.proquest.com/docview/3048359790
https://search.proquest.com/docview/3022569027
Volume 96
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