
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions β written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Salmonellosis future or investigational therapies
Introduction
Overview
Overview
Future studies are required to better understand the association between the different manifestations of the disease, and the respective bacterial genotypes. Additionally it is necessary to create humanized mouse models that will allow us understand the pathophysiology of the disease, and to test new drugs and vaccines. Current drugs undergoing investigation include: new antibiotics, electrolyte absorption enhancers; blockers of inflammatory and secretory toxins; and promoters of the intestinal repair.[1][2]
Future or Investigational Therapies
Future or Investigational Therapies
The different genotypes of salmonella have been associated with different manifestations of the disease, yet, this connection is not fully understood. Future studies are required to explain the potential genetic basis for the development of invasive non-typhoidal salmonella, and why certain non-typhoidal salmonella strains cause more severe disease than others.[1]
Research to create a new generation of humanized mouse models is also required. These models will allow to understand more of the pathogenesis of salmonella in human tissues, as well as to test the efficacy of new treatments and vaccines.[1]
Current therapeutic drugs being studied include:[2]
- New antibiotics
- Inflammatory and secretory toxin blockers
- Electrolyte absorption enhancers
- Promoters of intestinal repair
References
References
- β 1.0 1.1 1.2 Gal-Mor O, Boyle EC, Grassl GA (2014). “Same species, different diseases: how and why typhoidal and non-typhoidal Salmonella enterica serovars differ”. Front Microbiol. 5: 391. doi:10.3389/fmicb.2014.00391. PMIDΒ 25136336.
- β 2.0 2.1 Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV; et al. (2001). “Practice guidelines for the management of infectious diarrhea”. Clin Infect Dis. 32 (3): 331β51. doi:10.1086/318514. PMIDΒ 11170940.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: JoΓ£o AndrΓ© Alves Silva, M.D. [2] Jolanta Marszalek, M.D. [3]
