Title:
Design of immunoactive biomaterials for therapeutic applications

dc.contributor.advisor Roy, Krishnendu
dc.contributor.advisor Luo, Ying
dc.contributor.author Su, Ni
dc.contributor.committeeMember Zhu, Huaiqiu
dc.contributor.committeeMember Chen, Haifeng
dc.contributor.committeeMember Gao, Weiping
dc.contributor.committeeMember Xiong, Jingwei
dc.contributor.committeeMember Zhou, Jin
dc.contributor.department Biomedical Engineering (Joint GT/Emory Department)
dc.date.accessioned 2019-08-21T13:48:49Z
dc.date.available 2019-08-21T13:48:49Z
dc.date.created 2018-08
dc.date.issued 2018-07-25
dc.date.submitted August 2018
dc.date.updated 2019-08-21T13:48:49Z
dc.description.abstract Immune system is a highly organized network, consisting of innate and adaptive immune responses. The immune system has a critical role in the health of organisms and can be either a cure or cause of disease. In recent years, with the expanded knowledge of immunology that both innate and adaptive immune cells are the key mediators in cancer immunotherapy and tissue repair/regeneration, immunomodulatory biomaterial design provides a new direction for related therapeutics. Therefore, the overall goal of this dissertation is to design biomaterials to modulate or qualitatively shape the immune response, which could be ultimately used for biomedical applications of cancer immunotherapy and regenerative medicine. On the side of cancer immunotherapy, we first designed a cancer vaccine based on tumor-derived exosome, and demonstrated both cellular and humoral anti-tumor immunity could be induced by immunization of the vaccine. The designed vaccine showed a long-term protection against pre-established lethal challenges of B-cell lymphoma in mice. On the side of regenerative medicine, mesenchymal stromal cells (MSCs) are known as the sensor and switch of inflammation. Their widely achieved therapeutic effects for degenerative diseases are mainly contributed by their secretion behavior. We then designed fibrous scaffolds with the aim to potentiate the paracrine function of MSCs for tissue regeneration. It’s proved that MSCs showed enhanced secretion of anti-inflammatory and elevated capacities to induce pro-regenerative macrophage phenotype, when potentiated by scaffolds. The conditioned medium from MSCs-scaffolds are demonstrated to promote skin wound healing of mice. Based on the knowledge and experience from the previous two studies, we designed a MSC exosomes loaded fibrous scaffolds material to directly interact with the immune system for regenerative immunomodulation. The results proved our hypothesis that the scaffolds could recruit immune cells to the transplant site and the loaded exosomes provide them with regenerative immunomodulatory signals, together generating pro-regenerative innate and adaptive immune responses locally and systemically. This dissertation brings new insights and inspirations for the design of therapeutic immunomodulatory biomaterial.
dc.description.degree Ph.D.
dc.format.mimetype application/pdf
dc.identifier.uri http://hdl.handle.net/1853/61626
dc.language.iso en_US
dc.publisher Georgia Institute of Technology
dc.subject Immune modulation
dc.subject Biomaterial design
dc.subject Cancer immunotherapy
dc.subject Regenerative medicine
dc.subject Mesenchymal stromal cell
dc.title Design of immunoactive biomaterials for therapeutic applications
dc.type Text
dc.type.genre Dissertation
dspace.entity.type Publication
local.contributor.advisor Roy, Krishnendu
local.contributor.corporatename Wallace H. Coulter Department of Biomedical Engineering
local.contributor.corporatename College of Engineering
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relation.isOrgUnitOfPublication da59be3c-3d0a-41da-91b9-ebe2ecc83b66
relation.isOrgUnitOfPublication 7c022d60-21d5-497c-b552-95e489a06569
thesis.degree.level Doctoral
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