Predicting immunological responses from clinical and molecular data to better inform cancer immunotherapy
Name
1129251768-MIT.pdf
Size
2.49 MB
Format
Adobe PDF
Checksum (MD5)
f7236fefbd6011685f1794e4d4463c6d
Author(s)
Liu, Jacqueline,M. Eng.Massachusetts Institute of Technology.
Advisor(s)
Ernest Fraenkel.
Date Issued
2019
Publisher
Massachusetts Institute of Technology
Abstract
Cancer immunotherapies have shown remarkable success in treating previously fatal forms of cancer, but their response rates remain low, and they are associated with potentially life-threatening side effects. We used machine-learning approaches to explore two aspects of cancer immunotherapy. First, we developed methods for determining the strength of a patient's immune system prior to therapy. Examining flu vaccination responses, we identified genes and biological features that predict a healthy individual's ability to mount a response to an immunological challenge. Second, we examined the sensitivity of cancer cell lines to natural killer cells, as an initial step toward a new type of immunotherapy. Here, we predicted the sensitivity of several hundred cancer cell lines using a range of molecular data. These preliminary studies form a basis for ongoing research into the molecular and cellular aspects of immune therapeutics.
Description
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Thesis: M. Eng., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, 2019
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 63-64).
Subjects
Electrical Engineering and Computer Science.
MIT Department
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Terms of Use
MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.
Persistent DSpace Link