Global ETD Search

1	Enhancing monocyte effector functions in antibody therapy against cancer Fatehchand, Kavin, Fatehchand 18 September 2018 (has links) No description available. Biomedical Research Cellular Biology Cancer immunotherapy cancer antibody therapy FcgR signaling innate immunity monocytes
2	Role of Innate Immunity Activators in the Treatment of Acute Myeloid Leukemia Buteyn, Nathaniel J. January 2019 (has links) No description available. Molecular Biology AML immunotherapy ATRA retinoic acid CD38 daratumumab antibody therapy NOD2 MTP MTP-PE inflammation leukemia inflammasome IFN-gamma IFNg interferon NK cells natural killer cells acute myeloid leukemia innate immunity
3	Therapeutic Antibody Against Neisseria gonorrhoeae Lipooligosaccharide, a Phase-variable Virulence Factor Chakraborti, Srinjoy 25 May 2017 (has links) Neisseria gonorrhoeae (Ng) which causes gonorrhea has become multidrug-resistant, necessitating the development of novel therapeutics and vaccines. mAb 2C7 which targets an epitope within an important virulence factor, the lipooligosaccharide (LOS), is a candidate therapeutic mAb. Ninety-four percent of clinical isolates express the 2C7-epitope which is also a vaccine target. Ng expresses multiple LOS(s) due to phase-variation (pv) of LOS glycosyltransferase (lgt) genes. mAb 2C7 reactivity requires a lactose extension from the LOS core Heptose (Hep) II (i.e. lgtG ‘ON’ [G+]). Pv results in HepI with: two (2-), three (3-), four (4-), or five (5-) hexoses (Hex). How HepI glycans impact Ng infectivity and mAb 2C7 function are unknown and form the bases of this dissertation. Using isogenic mutants, I demonstrate that HepI LOS glycans modulate mAb 2C7 binding. mAb 2C7 causes complement (C’)-dependent bacteriolysis of three (2-Hex/G+, 4-Hex/G+, and 5-Hex/G+) of the HepI mutants in vitro. The 3-Hex/G+ mutant (resistant to C’-dependent bacteriolysis) is killed by neutrophils in the presence of mAb and C’. In mice, 2- and 3-Hex/G+ infections are significantly shorter than 4- and 5-Hex/G+ infections. A chimeric mAb 2C7 that hyperactivates C’, attenuates only 4- and 5-Hex/G+ infections. This study enhances understanding of the role of HepI LOS pv in gonococcal infections and shows that longer HepI glycans are necessary for prolonged infections in vivo. This is the first study that predicts in vitro efficacy of mAb 2C7 against all four targetable HepI glycans thereby strengthening the rationale for development of 2C7-epitope based vaccines and therapeutics. monoclonal antibody therapy mAb mAb 2C7 chimeric antibody therapeutic antibody complement complement activation classical complement pathway phagocytosis neutrophil opsonophagocytosis vaccine engineered antibody antibody engineering C1q C3 gonorrhea Neisseria gonorrhoeae vaccines for gonorrhea treatments for gonorrhea hexamerizing antibody hexamerizing IgG antibody hexamers IgG hexamers complement activating antibody complement activating IgG Amino Acids, Peptides, and Proteins Bacteriology Immunology of Infectious Disease Immunoprophylaxis and Therapy Pathogenic Microbiology

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