TB research is underfunded but new medicines are on their way
Part two of a three part series on a neglected disease that kills over a hundred thousand South Africans every year

In this second article in a three-part series on TB, we look at what research is being done on new medicines and tests.
âTB has been neglected to a large degree,â said Dr Helen Cox, an epidemiologist at UCTâs Institute of Infectious Disease and Molecular Medicine.
âWhen you think of HIV and how many drugs and tests come through and how much work has moved in that area â itâs got to do with funding,â said Cox. The funding that has been allocated in the past to TB is âpitiful in comparison to HIVâ.
The US based Treatment Action Group estimates that in 2005 $358 million dollars was spent on TB research and development worldwide. Uncorrected for inflation this rose to 726 million dollars by 2016, but with some blips along the way (funding dropped between 2014 and 2015). Taking inflation into account however shows that spending has stagnated the past few years.
TB research and development funding is stagnant in real terms. Graph taken from The Ascent Begins: Tuberculosis Research Funding Trends, 2005â2016 by the Treatment Action Group.
This is not a lot of money for the size of the problem. By comparison a single US research institution, the National Institutes of Health, spends over a billion dollars annually on diabetes, and nearly three times that on HIV.
Current research is looking at new drugs that have fewer side-effects, shorter durations of treatment and different combinations of drugs. The hope is that by giving patients a drug regimen that is shorter and easier to take, they will be able to complete their treatment.
There are different types of drug-resistant TB. Multi-Drug Resistant (MDR) TB is when the standard drugs used to treat TB donât work for a patient. Extensively Drug Resistant (XDR) TB is even worse: It is MDR-TB plus resistance to two of the most effective drugs for treating MDR-TB. Before the introduction of new TB drugs, three quarters of people with XDR TB died within five years.
Despite this grim picture, there is progress.
TB Alliance, a non-profit organisation developing new TB drugs, has had good preliminary results with their Nix-TB trial. The trial is testing a combination of three drugs for XDR TB â bedaquiline, linezolid and pretomanid.
The aim of the trial is to cure XDR TB patients within six to nine months â versus the standard treatment for XDR TB, which can take up to two years.
Pretomanid hasnât yet been approved in South Africa for use outside of clinical trials, but bedaquiline and linezolid are increasingly being used to treat drug-resistant TB.
Dr Sean Wasserman, an infectious diseases physician at UCT, said the results from Nix-TB are âvery excitingâ but there is still concern over how many people will relapse (get sick again from TB) and the toxicity of linezolid.
Another trial called STREAM-2 is comparing a regimen with bedaquiline against one of the common ways of treating MDR-TB. Its results are expected in 2021.
TB Alliance have also begun a new trial called ZeNix which tests a lower dose and shorter duration of the drug linezolid, which has a very high toxicity.
Another trial that is bringing renewed hope is the endTB trial that also has sites in South Africa, and is testing a number of different drug regimens for patients with drug resistant TB. Besides bedaquiline it also uses a newish drug called delamanid.
Bedaquiline has been approved for use in South Africa but delamanid is only available under strict conditions at very few sites around the country.
âIt is imperative that the Medicines Control Council take urgent action to help expand access to delamanid,â MedĂŠcins Sans Frontières Dr Anja Reuter, said last year. âWhen products are registered, access improves.â
What about a vaccine for TB?
The current vaccine for TB, the BCG vaccine, doesnât work very well.
Cox explains, âWe know that people who have had TB and are cured are still at very high risk of getting TB again, so if a previous disease doesnât even prevent you from getting TB again itâs really hard to find a vaccine that will.â
So while the vaccine is useful in preventing severe TB in children, it doesnât work well in adults.
âVaccines are such a complex area and we certainly need to be encouraging much more money into research because clearly if we could find a vaccine that would be the holy grail of TB,â said Cox.
Are the tests good enough?
Testing for TB isnât always straightforward, particularly if you are HIV-positive. But a machine called the GeneXpert that allows for rapid testing of both TB and whether you could have drug resistant TB, has improved the way we find TB cases. South Africa is now also rolling out an even better version â the GeneXpert Ultra. But the tests are still far from perfect and donât work well in all settings or for all patients.
The use of x-rays could also be making a comeback with both Cox and Wasserman mentioning their importance in testing for TB.
âWe are not doing enough systematic x-ray screening,â said Wasserman. He explained that this was how TB was tested for in Europe after the second world war. âThey went out with these mobile chest x-rays and found people with TB and put them on treatment. We are just not doing that enough,â said Wasserman.
Cox said that while x-rays are labour intensive, there are new programmes for digitally aided x-ray reading so that you donât need a qualified radiologist to read every x-ray.
Another useful test detects TB in the urine of people sick with HIV (i.e. people with low CD4 counts). Itâs called the TB-LAM test and itâs cheap.
But to really make a dent in TB, Cox said that we need âmuch better toolsâ and âmuch more funding needs to go into research and developmentâ.
âWe need to do what we know works [and do this] much better and we need to focus on research for new tools and new ways of doing things,â said Cox.
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