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'An amazing ride': Study offers dengue treatment hope

  • Published at 07:54 am October 7th, 2021
mosquito dengue

The treatment appears to be effect whether taken before infection and also after the virus is contracted

Dengue affects tens of millions each year, producing brutal symptoms that have earned it the moniker "breakbone fever," but new research may have found the first-ever treatment for the virus.

Tests in cell cultures and mice found that a newly identified compound can effectively disarm dengue, stopping it from replicating and preventing disease, according to a study published Wednesday in the journal Nature.

And it appears to be effective whether taken protectively before infection or as a treatment after the virus is contracted.

It is an "exciting" development in the battle against dengue, according to Scott Biering and Eva Harris of the University of California, Berkeley's School of Public Health.

It "represents a major advance in the field of dengue therapeutics," the pair, who were not involved in the research, wrote in a review in Nature.

There is no doubt about the threat posed by the mosquito-borne dengue virus, which is estimated to infect at least 98 million people a year and is endemic in 128 countries worldwide.

It can cause intense flu-like symptoms and sometimes develops into severe dengue which can be fatal.

And because there are four different strains, infection with one does not protect against another, and catching dengue a second time is often more serious.

No treatment exists so far, with efforts focusing instead on reducing transmission -- including a programme that infects mosquitoes with disease-resistant bacteria.

A vaccine called Dengvaxia is approved for use only in some countries and is effective against a single strain.


Enter the unassumingly named JNJ-A07, a compound found by screening thousands of potential candidates, in a process researcher Johan Neyts described as "looking for a needle in a haystack".

It turned out to be worth the wait.

Its effect "in infected animals is unprecedented", Neyts, who helped lead the research, told AFP.

"Even if treatment is started at the time of peak viral replication there is important antiviral activity," added Neyts, a professor of virology at the University of Leuven, Belgium.

JNJ-A07 works by targeting the interaction between two proteins in the dengue virus that are key to its replication, and it worked effectively against all four strains.

Also Read - Dengue: Record hospitalizations in September

Dengue can evolve quickly, but the team found JNJ-A07 was unlikely to face significant challenges from drug resistance.

"It took us in the lab, in infected cells, almost half a year before we could obtain important resistance (to the treatment)," said Neyts.

"Given that the barrier to resistance is so high, it is very unlikely that this will clinically be a problem."

Intriguingly, the mutations that caused resistance also appeared to make the virus incapable of replicating in mosquito cells.

That could suggest that even if the virus develops resistance to JNJ-A07, it would no longer be transmissible via mosquitoes, effectively reaching a dead-end in its host.

Clinical trials in progress 

Promisingly, the compound was effective whether administered to mice before infection or afterwards.

The version of the compound reported in Nature has now been "further slightly optimised" and is in clinical development by Johnson & Johnson, Neyts said.

In a statement, Johnson & Johnson chief scientific officer Paul Stoffels said the work had "tremendous potential to transform the world's fight against this significant and growing public threat".

There are still questions to answer, however, including whether the compound could increase vulnerability to reinfection.

When people contract dengue, the presence of the virus in their blood -- known as viraemia -- generally stimulates a potent immune response that protects them from future infection.

But in some people, the immune response is weaker and that leaves them vulnerable to reinfection with different strains, which can produce more serious symptoms.

Given that JNJ-A07 works to reduce viraemia, Biering and Harris said the research was needed into whether this might leave people more susceptible to reinfection.

Despite the unknowns, Neyts said the study offered exciting possibilities.

"Seeing the compound work so potently in animals was breathtaking," he said, describing the research as "an amazing ride".

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