Use of bioengineered human commensal gut bacteria-derived microvesicles for mucosal plague vaccine delivery and immunization. (15th April 2019)

• Record Type: Journal Article
• Authors: Carvalho, A L; Miquel-Clopés, A; Wegmann, U; Jones, E; Stentz, R; Telatin, A; Walker, N J; Butcher, W A; Brown, P J; Holmes, S; Dennis, M J; Williamson, E D; Funnell, S G P; Stock, M; Carding, S R
• Is Part Of: Clinical and experimental immunology. Volume 196:Number 3(2019)
• Page Start: 287
• Page End: 304
• Publication Date: 2019-04-15
• Subjects: antibodies -- gut bacteria -- humoral immunity -- mucosal vaccine -- non-human primates -- outer membrane vesicles -- plague; Immunopathology -- Periodicals; 616.079
• DOI: 10.1111/cei.13301
• Languages: English
• ISSNs: 0009-9104

Abstract

Abstract: Plague caused by the Gram-negative bacterium, Yersinia pestis, is still endemic in parts of the world today. Protection against pneumonic plague is essential to prevent the development and spread of epidemics. Despite this, there are currently no licensed plague vaccines in the western world. Here we describe the means of delivering biologically active plague vaccine antigens directly to mucosal sites of plague infection using highly stable microvesicles (outer membrane vesicles; OMVs) that are naturally produced by the abundant and harmless human commensal gut bacterium Bacteroides thetaiotaomicron (Bt). Bt was engineered to express major plague protective antigens in its OMVs, specifically Fraction 1 (F1) in the outer membrane and LcrV (V antigen) in the lumen, for targeted delivery to the gastrointestinal (GI) and respiratory tracts in a non-human primate (NHP) host. Our key findings were that Bt OMVs stably expresses F1 and V plague antigens, particularly the V antigen, in the correct, immunogenic form. When delivered intranasally V-OMVs elicited substantive and specific immune and antibody responses, both in the serum [immunoglobulin (Ig)G] and in the upper and lower respiratory tract (IgA); this included the generation of serum antibodies able to kill plague bacteria. Our results also showed that Bt OMV-based vaccines had many desirable characteristics, including: biosafety and an absence of any adverse effects, pathology or gross alteration of resident microbial communities (microbiotas); high stability and thermo-tolerance; needle-free delivery; intrinsic adjuvanticity; the ability to stimulate both humoral and cell-mediated immune responses; and targeting of primary sites of plague infection. Graphical Abstract: