TABLE 12.
Vaccine type | Candidate | Current stage | Developer(s) |
---|---|---|---|
Attenuated | CVD 1208S based on S. flexneri 2a | Phase 1 | CVD |
WRSS1 based on S. sonnei | Phase 2b | WRAIR | |
ShigETEC LPS-free cell | Phase 1 | EveliQure | |
Vectored | Ty21a typhoid vaccine expressing O antigens of S. sonnei or a combination of S. sonnei, S. flexneri 2a and 3a, and S. dysenteriae O antigen | Preclinical | Protein Potential |
Inactivated | Sf2aWC, a formalin-killed S. flexneri 2a whole-cell vaccine | Phase 1 | WRAIR and PATH |
Shigella truncated mutant (350) | Preclinical | IVI and PATH | |
Conjugate | Chemical glycoconjugates of S. sonnei and S. flexneri 2a | Phase 3 | NIH Institute for Child Health and Human Development |
Recombinant bioconjugate | Phase 2b | LimmaTech Biologics and GSK | |
Synthetic glycoconjugate | Phase 2 | Institut Pasteur | |
Serotype-dependent mixture | InvaplexAR-DETOX, a chemically defined product consisting of invasion plasmid antigens and O antigens | Phase 1 | WRAIR |
GMMA consisting of Shigella outer membrane vesicles from an overproducing strain | Phase 2 | GSK | |
Outer membrane vesicles: naturally secreted outer membrane vesicles of Shigella | Preclinical | University of Navarra, Spain | |
Serotype-independent proteins | IpaD/IpaB (DB) fusion | Preclinical | PATH |
PSSP-1 (Pan-Shigella surface protein 1) | Preclinical | IVI | |
34-kDa OMP, an outer membrane protein conserved across multiple Shigella species | Preclinical | National Institute of Cholera and Enteric Diseases, India |
CVD, Center for Vaccine Development, University of Maryland; ETEC, enterotoxigenic Escherichia coli; GMMA, Generalized Modules for Membrane Antigens; GSK, GlaxoSmithKline; IVI, International Vaccine Institute, South Korea; LPS, lipopolysaccharide; NIH, U.S. National Institutes of Health; WRAIR, Walter Reed Army Institute of Research. Adapted from references 334 and 337.