Chikungunya future or investigational therapies: Difference between revisions

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| style="padding: 5px 5px; background: #DCDCDC;" | Assay type
| style="padding: 5px 5px; background: #DCDCDC;" | Assay type
| style="padding: 5px 5px; background: #F5F5F5;" |In vitro (vero cells)
| style="padding: 5px 5px; background: #F5F5F5;" |''In vitro'' (vero cells)
| style="padding: 5px 5px; background: #F5F5F5;" |Human
| style="padding: 5px 5px; background: #F5F5F5;" |Human
| style="padding: 5px 5px; background: #F5F5F5;" |In vitro (vero cells)
| style="padding: 5px 5px; background: #F5F5F5;" |''In vitro'' (vero cells)
| style="padding: 5px 5px; background: #F5F5F5;" |In vitro (vero and primary human fibroblast cells)
| style="padding: 5px 5px; background: #F5F5F5;" |''In vitro'' (vero and primary human fibroblast cells)
| style="padding: 5px 5px; background: #F5F5F5;" |In vitro (BHK21 cells)
| style="padding: 5px 5px; background: #F5F5F5;" |''In vitro'' (BHK21 cells)
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| style="padding: 5px 5px; background: #DCDCDC;" | Hypothesized target
| style="padding: 5px 5px; background: #DCDCDC;" | Hypothesized target
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| style="padding: 5px 5px; background: #DCDCDC;" | Advantages
| style="padding: 5px 5px; background: #DCDCDC;" | Advantages
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" | In vitro study proved that it blocks the production of proinflammatory cytokines and the proliferation of
| style="padding: 5px 5px; background: #F5F5F5;" |
monocytes, macrophages, and lymphocytes
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| style="padding: 5px 5px; background: #F5F5F5;" |Faster resolution of joint and soft tissue manifestations.
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" |Showed a significant inhibition of CHIKV at a low concentration.
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" |Well-tolerated with minimal side effects
| style="padding: 5px 5px; background: #F5F5F5;" |Minimal cytotoxicity
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| style="padding: 5px 5px; background: #DCDCDC;" | Disadvantages
| style="padding: 5px 5px; background: #DCDCDC;" | Disadvantages
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| style="padding: 5px 5px; background: #F5F5F5;" | In vivo study required.
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" |Involvement of a small number of patients and lack of planning as randomly distributed patients were not
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compared with a placebo group.
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" | The antiviral activity has been difficult to replicate in vivo.
| style="padding: 5px 5px; background: #F5F5F5;" |
| style="padding: 5px 5px; background: #F5F5F5;" | Not tested in in vivo system.
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| style="padding: 5px 5px; background: #F5F5F5;" | Not tested in in vivo system.
| style="padding: 5px 5px; background: #DCDCDC;" | References
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| style="padding: 5px 5px; background: #FFF;" colspan="6"| <SMALL>Table adapted from </SMALL>
| style="padding: 5px 5px; background: #FFF;" colspan="6"| <SMALL>Table adapted from </SMALL>

Revision as of 18:21, 18 June 2014

Chikungunya Microchapters

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Future Therapies

Chloroquine Ribavirin 6-Azauridine Arbidol Harringtonine
Assay type In vitro (vero cells) Human In vitro (vero cells) In vitro (vero and primary human fibroblast cells) In vitro (BHK21 cells)
Hypothesized target Disrupted endosome-mediated CHIKV internalization, possibly through the prevention of endosomal acidification. Can interact with the intracellular viral RNA production. Inhibition of orotidine monophosphate decarboxylase, an enzyme involved in the de novo biosynthesis of pyrimidine, cytidine, and thymidine. Inhibition of virus mediated fusion and blocking of the viral entry into the target cells through inhibition of glycoprotein conformational changes that are essential for the fusion process. Affects CHIKV RNA production inside the infected cell as well as viral protein expression such as the nsP3 and the E2 proteins.
Advantages In vitro study proved that it blocks the production of proinflammatory cytokines and the proliferation of

monocytes, macrophages, and lymphocytes

Faster resolution of joint and soft tissue manifestations. Showed a significant inhibition of CHIKV at a low concentration. Well-tolerated with minimal side effects Minimal cytotoxicity
Disadvantages In vivo study required. Involvement of a small number of patients and lack of planning as randomly distributed patients were not

compared with a placebo group.

The antiviral activity has been difficult to replicate in vivo. Not tested in in vivo system. Not tested in in vivo system.
Table adapted from

References

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