Structure-based engineering of immunomodulatory agents for the treatment of cancer

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Abstract/Contents

Abstract
Immune-based therapies for cancer are powerful, lasting, and generally less toxic than most other cancer treatment paradigms. Consequently, the development of new immunotherapeutic agents and the study of the interplay between tumors and the immune system have emerged as central lines of research for this nascent field of medicine. Here, I describe my efforts to improve an existing cancer immunotherapy (Interleukin-2), to study an experimental immunotherapeutic agent (Interleukin-15), and to generate novel protein therapeutics against an emerging target of cancer immune evasion (CD47). These studies highlight a structure- and mechanism-based approach to protein engineering in the development of next-generation cancer immunotherapies.

Description

Type of resource text
Form electronic; electronic resource; remote
Extent 1 online resource.
Publication date 2016
Issuance monographic
Language English

Creators/Contributors

Associated with Ring, Aaron Michael
Associated with Stanford University, Department of Structural Biology.
Primary advisor Garcia, K. Christopher
Thesis advisor Garcia, K. Christopher
Thesis advisor Kobilka, Brian K
Thesis advisor Majeti, Ravindra, 1972-
Thesis advisor Weissman, Irving L
Advisor Kobilka, Brian K
Advisor Majeti, Ravindra, 1972-
Advisor Weissman, Irving L

Subjects

Genre Theses

Bibliographic information

Statement of responsibility Aaron Michael Ring.
Note Submitted to the Department of Structural Biology.
Thesis Thesis (Ph.D.)--Stanford University, 2016.
Location electronic resource

Access conditions

Copyright
© 2016 by Aaron Michael Ring
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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