TY - JOUR
T1 - AI-driven discovery of antiretroviral drug bictegravir and etravirine as inhibitors against monkeypox and related poxviruses
AU - Wang, Yining
AU - Ünlü, Atabey
AU - Wang, Xin
AU - Çevrim, Elif
AU - Offermans, Dewy Mae
AU - Flesseman, Myrthe P.
AU - Zaeck, Luca M.
AU - Wu, Liping
AU - Bijvelds, Marcel J.C.
AU - Sam-Agudu, Nadia A.
AU - de Vries, Rory D.
AU - Raymond, Karine
AU - Li, Pengfei
AU - Olğaç, Abdurrahman
AU - Wang, Wenshi
AU - Doğan, Tunca
AU - Pan, Qiuwei
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12/2
Y1 - 2025/12/2
N2 - Monkeypox virus (MPXV) caused the 2022–2023 global mpox and the concurrent outbreaks in Africa, disproportionately affecting immunocompromised individuals such as people living with HIV. With no approved treatment available, we developed a robust artificial intelligence (AI) pipeline for discovering broad-spectrum poxvirus inhibitors that target the viral DNA polymerases. Among the identified leading candidates, we found that the clinically used antiretroviral drugs bictegravir and etravirine potently inhibit MPXV clade Ia, Ib and IIb infections in human intestinal and skin organoids. The broad anti-poxvirus activities of bictegravir and etravirine were further demonstrated against infections of other Orthopoxviruses such as vaccinia virus and cowpox virus. These findings support the repurposing of bictegravir and etravirine for treating mpox, especially for patients co-infected with HIV, warranting follow-up clinical investigation. The established AI pipeline and our antiviral drug discovery strategies bear major implications for responding to the ongoing mpox emergency and preparing for future poxvirus epidemics.
AB - Monkeypox virus (MPXV) caused the 2022–2023 global mpox and the concurrent outbreaks in Africa, disproportionately affecting immunocompromised individuals such as people living with HIV. With no approved treatment available, we developed a robust artificial intelligence (AI) pipeline for discovering broad-spectrum poxvirus inhibitors that target the viral DNA polymerases. Among the identified leading candidates, we found that the clinically used antiretroviral drugs bictegravir and etravirine potently inhibit MPXV clade Ia, Ib and IIb infections in human intestinal and skin organoids. The broad anti-poxvirus activities of bictegravir and etravirine were further demonstrated against infections of other Orthopoxviruses such as vaccinia virus and cowpox virus. These findings support the repurposing of bictegravir and etravirine for treating mpox, especially for patients co-infected with HIV, warranting follow-up clinical investigation. The established AI pipeline and our antiviral drug discovery strategies bear major implications for responding to the ongoing mpox emergency and preparing for future poxvirus epidemics.
UR - https://www.scopus.com/pages/publications/105023593259
U2 - 10.1038/s42003-025-09129-x
DO - 10.1038/s42003-025-09129-x
M3 - Article
C2 - 41331517
AN - SCOPUS:105023593259
SN - 2399-3642
VL - 8
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 1734
ER -