Polymeric antigens as targeted probes of immunity
Name
1199083213-MIT.pdf
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18.09 MB
Format
Adobe PDF
Checksum (MD5)
8ccbf253316bbbfc23a4c77a0bd8666e
Author(s)
Jarvis, Cassie Marie.
Advisor(s)
Laura L. Kiessling.
Date Issued
2020
Publisher
Massachusetts Institute of Technology
Abstract
Multivalent carbohydrate interactions play a critical role in many immunological processes, including pathogen recognition and immune activation. Synthetic polymers can mimic multivalent glycans and probe different facets of immunity to ultimately inform the design of effective vaccines. In Chapter 1, I review how antigen physical properties and lectin signaling can direct dendritic cell (DC)-mediated immune responses. The DC lectin DC-SIGN is involved in both immune activation and evasion. In Chapter 2, I generated glycopolymers bearing a multivalent display of a DC-SIGN-targeting aryl mannoside ligand to investigate how antigen features influence DC-SIGN-mediated responses. Specifically, I found that antigen size alters trafficking through DCSIGN. Large polymer aggregates were trafficked to the same subcellular DC reservoirs that harbor HIV, whereas small soluble polymers were routed to endosomes.
In light of these findings, in Chapter 3 we designed a nanoparticle vaccine platform using the same aryl mannoside ligand to efficiently target antigen to DC-SIGN for endosomal routing and antigen presentation. Functionalized bacteriophage Q[beta] virus-like particles elicited DC-mediated proinflammatory Th1-type immune responses, which are effective against intracellular pathogens and tumors. As many vaccines function by generating neutralizing antibodies, we used polymeric antigens to interrogate B cell activation. In Chapter 4, I used ROMP polymers to target B cells and systematically evaluated key antigen features that promote B cell activation and antibody production. The most robust responses were induced by polymers with a high valency of B and T cell epitopes where the T cell epitope is readily liberated upon endosomal processing. Optimal polymer designs stimulated more robust B cell activation than a comparable protein conjugate.
Overall, my thesis work identified numerous antigen parameters that can be tuned to direct and optimize DC and B cell activation for the design of effective targeted synthetic vaccines.
Description
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2020
Cataloged from the PDF of thesis. "February 2020."
Includes bibliographical references.
Subjects
Chemistry.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
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MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.
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