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 inTrends in parasitology Vol. 37; no. 12; pp. 1068 - 1081
Main Authors Johnston, Kelly L., Hong, W. David, Turner, Joseph D., O’Neill, Paul M., Ward, Stephen A., Taylor, Mark J.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.12.2021
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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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ISSN:1471-4922
1471-5007
1471-5007
DOI:10.1016/j.pt.2021.06.004