Slow-Release Formulation of Cowpea Mosaic Virus for In Situ Vaccine Delivery to Treat Ovarian Cancer-Reference-Cited by-同舟云学术

Slow-Release Formulation of Cowpea Mosaic Virus for In Situ Vaccine Delivery to Treat Ovarian Cancer

Published:2018-02-21 Issue:5 Volume:5 Page:1700991
ISSN:2198-3844
Container-title:Advanced Science
language:en
Short-container-title:Adv. Sci.

Author:

Czapar Anna E.¹,Tiu Brylee David B.²,Veliz Frank A.²,Pokorski Jonathan K.³,Steinmetz Nicole F.²³⁴⁵⁶^ORCID

Affiliation:

1. Departments of Pathology; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

2. Department of Biomedical Engineering; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

3. Departments of Macromolecular Science and Engineering; Division of General Medical Sciences-Oncology; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

4. Departments of Materials Science and Engineering; Division of General Medical Sciences-Oncology; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

5. Departments of Radiology; Division of General Medical Sciences-Oncology; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

6. Departments of Case Comprehensive Cancer Center; Division of General Medical Sciences-Oncology; Case Western Reserve University; 2109 Adelbert Road Cleveland OH 44106 USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

Reference42 articles.

1. Ovarian cancer

2. CTLA-4 and PD-1 Pathway Blockade: Combinations in the Clinic

3. Direct Activation of STING in the Tumor Microenvironment Leads to Potent and Systemic Tumor Regression and Immunity

4. Induction of T-cell Immunity Overcomes Complete Resistance to PD-1 and CTLA-4 Blockade and Improves Survival in Pancreatic Carcinoma

5. The blockade of immune checkpoints in cancer immunotherapy

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