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A TLR and CLR Agonist Combination Induces Anti-Tumor Immunity against Peritoneal Carcinomatosis

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title
A TLR and CLR Agonist Combination Induces Anti-Tumor Immunity against Peritoneal Carcinomatosis
author
Dyevoich, Allison
abstract
Peritoneal carcinomatosis (PC) is a condition where primary tumors metastasize into the peritoneal cavity and induce malignant ascites. One strategy currently being explored to treat malignancies involves leukocyte activation through pattern recognition receptors (PRRs), including Toll-Like Receptors (TLRs) and C-type Lectin Receptors (CLRs). Our data shows that mice treated with a TLR and CLR agonist combination are afforded significant protection when challenged with an aggressive ascites-forming mammary tumor cell line (TA3-Ha). However, when mice lack B-1a cells, the protection is lost. Activated, antibody-secreting cells (ASCs) are found in the spleen, peritoneal cavity and visceral adipose tissue (VAT). Consistent with ASC differentiation, the treatment induces a significant increase in IgM and complement (C’) bound to tumor cells, both of which are critical components in the antitumor effect.
subject
Innate Immunity
Natural Antibody
Pattern Recognition Receptors
Type I Interferon
contributor
Haas, Karen M (committee chair)
Alexander-Miller, Martha (committee member)
Debinski, Waldemar (committee member)
Lyles, Douglas (committee member)
date
2020-01-08T09:35:21Z (accessioned)
2024-12-30T09:30:09Z (available)
2019 (issued)
degree
Microbiology & Immunology (discipline)
embargo
2024-12-30 (terms)
identifier
http://hdl.handle.net/10339/95947 (uri)
language
en (iso)
publisher
Wake Forest University
type
Dissertation

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