Conference paper
Authors list: Darji, A; Mohamed, W; Domann, E; Chakraborty, T
Publication year: 2003
Pages: S102-S109
Journal: Vaccine
Volume number: 21
ISSN: 0264-410X
DOI Link: https://doi.org/10.1016/S0264-410X(03)00208-1
Conference: Euroconference/Workshop on Novel Strategies of Mucosal Immunisation through Exploitation of Mechanisms of Innate Immunity in Pathogen-Host Interaction (INNAMORA)
Publisher: Elsevier
Abstract:
We have generated isogenic Listeria monocytogenes mutant strains to study the induction of protective immunity in mice. These strains harbored either a specific deletion within the actin nucleator (actA) and/or have multiple deletions within the actA and phospholipase B (plcB) genes. In comparison to the wild type parental L. monocytogenes EGDe strains, the mutant strains were extremely low in virulence and were rapidly eliminated by the host during the first days of infection. Nevertheless, a single immunization with both mutant strains (EGDe DeltaactA2 and DeltaactADeltaplcB) efficiently induced and maintained effector memory (CD8(+)) T cells and has provided animals with a state of long-lasting protective immunity against wild type L. monocytogenes. These mutant strains can be used as live vaccines against the corresponding virulent pathogen and as carriers for introducing heterologous protective antigens into animals and humans. (C) 2003 Elsevier Science Ltd. All rights reserved.
Citation Styles
Harvard Citation style: Darji, A., Mohamed, W., Domann, E. and Chakraborty, T. (2003) Induction of immune responses by attenuated isogenic mutant strains of Listeria monocytogenes, Vaccine, 21, pp. S102-S109. https://doi.org/10.1016/S0264-410X(03)00208-1
APA Citation style: Darji, A., Mohamed, W., Domann, E., & Chakraborty, T. (2003). Induction of immune responses by attenuated isogenic mutant strains of Listeria monocytogenes. Vaccine. 21, S102-S109. https://doi.org/10.1016/S0264-410X(03)00208-1
Keywords
BACTERIAL-INFECTIONS; CELL-MEDIATED-IMMUNITY; ESTABLISHED TUMORS; isogenic L. monocytogenes mutants; LIVE VACCINE VEHICLE; PHOSPHOLIPASE-C