TY - JOUR
T1 - Repurposing isoxazoline veterinary drugs for control of vector-borne human diseases.
AU - Miglianico, Marie
AU - Eldering, Maarten
AU - Slater, Hannah
AU - Ferguson, Neil
AU - Ambrose, Pauline
AU - Lees, Rosemary
AU - Koolen, Karin M.J.
AU - Pruzinova, Katerina
AU - Jancarova, Magdalena
AU - Volf, Petr
AU - Koenraadt, Constantianus J.M.
AU - Duerr, Hans Peter
AU - Trevitt, Graham
AU - Yang, Baiyuan
AU - Chatterjee, Arnab K.
AU - Wisler, John
AU - Sturm, Angelika
AU - Bousema, Teun
AU - Sauerwein, Robert W.
AU - Schultz, Peter G.
AU - Tremblay, Matthew S.
AU - Dechering, Koen J.
PY - 2018/7/17
Y1 - 2018/7/17
N2 - Isoxazolines are oral insecticidal drugs currently licensed for ectoparasite control in companion animals. Here we propose their use in humans for the reduction of vector-borne disease incidence. Fluralaner and afoxolaner rapidly killed , , and mosquitoes and sand flies after feeding on a drug-supplemented blood meal, with IC values ranging from 33 to 575 nM, and were fully active against strains with preexisting resistance to common insecticides. Based on allometric scaling of preclinical pharmacokinetics data, we predict that a single human median dose of 260 mg (IQR, 177-407 mg) for afoxolaner, or 410 mg (IQR, 278-648 mg) for fluralaner, could provide an insecticidal effect lasting 50-90 days against mosquitoes and sand flies. Computational modeling showed that seasonal mass drug administration of such a single dose to a fraction of a regional population would dramatically reduce clinical cases of Zika and malaria in endemic settings. Isoxazolines therefore represent a promising new component of drug-based vector control.
AB - Isoxazolines are oral insecticidal drugs currently licensed for ectoparasite control in companion animals. Here we propose their use in humans for the reduction of vector-borne disease incidence. Fluralaner and afoxolaner rapidly killed , , and mosquitoes and sand flies after feeding on a drug-supplemented blood meal, with IC values ranging from 33 to 575 nM, and were fully active against strains with preexisting resistance to common insecticides. Based on allometric scaling of preclinical pharmacokinetics data, we predict that a single human median dose of 260 mg (IQR, 177-407 mg) for afoxolaner, or 410 mg (IQR, 278-648 mg) for fluralaner, could provide an insecticidal effect lasting 50-90 days against mosquitoes and sand flies. Computational modeling showed that seasonal mass drug administration of such a single dose to a fraction of a regional population would dramatically reduce clinical cases of Zika and malaria in endemic settings. Isoxazolines therefore represent a promising new component of drug-based vector control.
KW - Insecticide
KW - Isoxazoline
KW - Malaria
KW - Vector control
KW - Zika fever
U2 - 10.1073/pnas.1801338115
DO - 10.1073/pnas.1801338115
M3 - Article
SN - 0027-8424
VL - 115
SP - e6920-e6926
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 29
ER -