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Updated: Jan 19, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
Graphene oxide arms oncolytic measles virus for improved effectiveness of cancer therapy
Mao Xia1, Dongjun Luo2, Jie Dong3
1Department of Laboratory Medicine, The Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, 210008, China.
Background:
Replication-competent oncolytic viruses (OVs) have been proven to be a potent anticancer weapon for clinical therapy. The preexisting neutralizing antibody in patients is a big challenge for oncolytic efficacy of OVs. Graphene oxide sheets (GOS) possess excellent biological compatibility and are easy to decorate for targeted delivery.
Methods:
We generated PEI-GOS-PEG-FA (Polyethyleneimine-Graphene oxide sheets-Polyethylene glycol-Folic acid). After intravenous injection, the distribution of PEI-GOS-PEG-FA in tumor-bearing mice was visualized by the IVIS Lumina XR system. Then, the oncolytic measles virus (MV-Edm) was coated with PEI-GOS-PEG-FA to form a viral-GOS complex (GOS/MV-Edm). The oncolytic effects of GOS/MV-Edm were investigated both in vitro and in vivo.
Results:
GOS/MV-Edm exhibited higher infectivity and enhanced oncolysis. In tumor-bearing mice, GOS/MV-Edm had significantly elevated viral replication within the tumor mass, and achieved an improved antitumor effect. Then, we confirmed that GOS/MV-Edm entered cancer cells via the folate receptor instead of CD46, a natural cognate receptor of MV-Edm. GOS/MV-Edm remained the infectivity in murine cells that lack CD46. Finally, we found that GOS/MV-Edm was effectively protected from neutralization in the presence of antiserum both in vitro and in vivo. In passively antiserum immunized tumor-bearing mice, the survival was remarkably improved with intravenous injection of GOS/MV-Edm.
Conclusion:
Our findings demonstrate that GOS/MV-Edm displays significantly elevated viral replication within the tumor mass, leading to an improved antitumor effect in solid tumor mouse model. Our study provided a novel strategy to arm OVs for more efficient cancer therapy. That may become a promising therapeutic strategy for cancer patients.
Insights
Graphene oxide sheets (GOS) protected oncolytic viruses (OVs) from neutralizing antibodies, enhancing tumor targeting and improving cancer therapy outcomes in mice.
Area of Science:
- Nanomedicine
- Virology
- Oncology
Background:
- Replication-competent oncolytic viruses (OVs) are effective anticancer agents.
- Preexisting neutralizing antibodies pose a challenge to OV efficacy.
- Graphene oxide sheets (GOS) offer biocompatibility and targeted delivery potential.
Purpose of the Study:
- To develop a strategy to overcome antibody neutralization of OVs.
- To enhance the oncolytic efficacy of measles virus (MV-Edm) using GOS.
- To evaluate the targeted delivery and antitumor effects of the modified OV.
Main Methods:
- PEI-GOS-PEG-FA nanoparticles were synthesized.
- PEI-GOS-PEG-FA was used to coat MV-Edm, forming GOS/MV-Edm.
- In vitro and in vivo studies assessed infectivity, tumor targeting, viral replication, and antitumor effects.
Main Results:
- GOS/MV-Edm demonstrated enhanced infectivity and oncolysis.
- Elevated viral replication and improved antitumor effects were observed in tumor-bearing mice.
- GOS/MV-Edm utilized folate receptors for cancer cell entry and was protected from antibody neutralization.
Conclusions:
- GOS/MV-Edm significantly enhances viral replication and antitumor effects in solid tumors.
- This GOS-based strategy offers a promising approach for improving OV cancer therapy.
- The findings suggest a novel therapeutic strategy for cancer patients.
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