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Deletion of immune evasion genes provides an effective vaccine design for tumor-associated herpesviruses.

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第一作者： Gurpreet,Brar

第一单位： Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA, 90095, USA.

作者： Gurpreet,Brar ^[1] ; Nisar A,Farhat ^[1] ; Alisa,Sukhina ^[1] ; Alex K,Lam ^[1] ; Yong Hoon,Kim ^[1] ; Tiffany,Hsu ^[1] ; Leming,Tong ^[1] ; Wai Wai,Lin ^[2] ; Carl F,Ware ^[2] ; Marcia A,Blackman ^[3] ; Ren,Sun ^[1] ; Ting-Ting,Wu ^[4]

作者单位： Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA, 90095, USA. ^[1] Laboratory of Molecular Immunology, Infectious and Inflammatory Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, 10901 North Torrey Pines Road, La Jolla, CA, 92037, USA. ^[2] Trudeau Institute, Saranac Lake, New York, NY, 12983, USA. ^[3] Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA, 90095, USA. twu@mednet.ucla.edu. ^[4]

DOI 10.1038/s41541-020-00251-x

PMID 33298958

发布时间 2024-04-30

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2020年5卷1期

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Deletion of immune evasion genes provides an effective vaccine design for tumor-associated herpesviruses.

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Deletion of immune evasion genes provides an effective vaccine design for tumor-associated herpesviruses.

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