Anti-Wolbachia drugs for filariasis
The mutualistic association between Wolbachia endosymbionts and their filarial nematode hosts has been exploited as a validated drug target delivering macrofilaricidal outcomes. Limitations of existing antibiotics to scale-up have driven the search for new drugs, which are effective in shorter regim...
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Published in | Trends in parasitology Vol. 37; no. 12; pp. 1068 - 1081 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.12.2021
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Subjects | |
Online Access | Get full text |
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Summary: | The mutualistic association between Wolbachia endosymbionts and their filarial nematode hosts has been exploited as a validated drug target delivering macrofilaricidal outcomes. Limitations of existing antibiotics to scale-up have driven the search for new drugs, which are effective in shorter regimens of 7 days or less. Here, we review the last 14 years of anti-Wolbachia drug discovery by the anti-Wolbachia (A·WOL) consortium, which has screened more than two million compounds, delivering thousands of hit compounds. Refined screening models integrated with robust pharmacokinetic/pharmacodynamic (PK/PD) driven optimisation and selection strategies have delivered the first two drug candidates specifically designed to target Wolbachia. AWZ1066S and ABBV-4083 are currently progressing through clinical trials with the aim of delivering safe and effective macrofilaricides to support the elimination of onchocerciasis and lymphatic filariasis.
Wolbachia bacterial endosymbionts are a validated drug target for onchocerciasis and lymphatic filariasis delivering macrofilaricidal outcomes.The need for a macrofilaricide is recognised as a critical requirement for onchocerciasis elimination by the World Health Organization (WHO) neglected tropical disease (NTD) roadmap 2021–2030.The anti-Wolbachia (A·WOL) consortium has screened >two million compounds delivering 20 000+ hits and dozens of new chemical series.Two A·WOL clinical candidates – AWZ1066S and ABBV-4083 – are currently progressing through Phase I and Phase II clinical trials. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 1471-4922 1471-5007 1471-5007 |
DOI: | 10.1016/j.pt.2021.06.004 |