Salmonellosis future or investigational therapies: Difference between revisions
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==Overview== | ==Overview== | ||
Future studies are required to better understand the association between the different manifestations of the disease, and the respective bacterial [[genotype]]s. 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 [[toxin]]s; and promoters of the [[intestinal]] repair.<ref name="pmid25136336">{{cite journal| author=Gal-Mor O, Boyle EC, Grassl GA| title=Same species, different diseases: how and why typhoidal and non-typhoidal Salmonella enterica serovars differ. | journal=Front Microbiol | year= 2014 | volume= 5 | issue= | pages= 391 | pmid=25136336 | doi=10.3389/fmicb.2014.00391 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25136336 }} </ref><ref name="pmid11170940">{{cite journal| author=Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV et al.| title=Practice guidelines for the management of infectious diarrhea. | journal=Clin Infect Dis | year= 2001 | volume= 32 | issue= 3 | pages= 331-51 | pmid=11170940 | doi=10.1086/318514 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11170940 }} </ref> | Future studies are required to better understand the association between the different manifestations of the disease, and the respective bacterial [[genotype]]s. 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 [[toxin]]s; and promoters of the [[intestinal]] repair.<ref name="pmid25136336">{{cite journal| author=Gal-Mor O, Boyle EC, Grassl GA| title=Same species, different diseases: how and why typhoidal and non-typhoidal Salmonella enterica serovars differ. | journal=Front Microbiol | year= 2014 | volume= 5 | issue= | pages= 391 | pmid=25136336 | doi=10.3389/fmicb.2014.00391 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25136336 }} </ref><ref name="pmid11170940">{{cite journal| author=Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV et al.| title=Practice guidelines for the management of infectious diarrhea. | journal=Clin Infect Dis | year= 2001 | volume= 32 | issue= 3 | pages= 331-51 | pmid=11170940 | doi=10.1086/318514 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11170940 }} </ref> | ||
==Future or Investigational Therapies== | ==Future or Investigational Therapies== | ||
Revision as of 13:38, 21 August 2014
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2] Jolanta Marszalek, M.D. [3]
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
The different genotypes of salmonella have been associated with different manifestations of the disease, yet, the process 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 under study include:[2]
- New antibiotics
- Inflammatory and secretory toxin blockers
- Electrolyte absorption enhancers
- Promoters of intestinal repair
References
- ↑ 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. PMID 25136336.
- ↑ 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): 331–51. doi:10.1086/318514. PMID 11170940.