Alinity m MPXV: The newest diagnostic test for emergency use against Mpox
Content Editor: Dr Tanya
October 25, 2024 at 1:00:00 PM
MPox, Emergency Use License, Diagnostics

Limited testing capacity and delays in confirming mpox cases continue to hinder efforts in Africa, allowing the virus to spread further.
In 2024, over 30,000 suspected cases were reported across the continent, with the highest numbers in the Democratic Republic of the Congo, Burundi, and Nigeria.
Notably, only 37% of suspected cases in the Democratic Republic of the Congo have been tested this year.
The presence of the monkeypox virus is confirmed through nucleic acid amplification testing (NAAT), including real-time or conventional polymerase chain reaction (PCR), as outlined in the WHO's Interim Guidance on diagnostic testing for mpox.
The lesion material is the recommended specimen type for confirming monkeypox virus (MPXV) infection through NAAT.
The Alinity m MPXV assay is a real-time PCR test that detects monkeypox virus (clade I/II) DNA in human skin lesion swabs.
By detecting DNA from pustular or vesicular rash samples, laboratory and health workers can confirm suspected mpox cases efficiently and effectively.
This first mpox diagnostic test listed under the Emergency Use Listing procedure represents a significant milestone in expanding testing availability in affected countries.
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