“UNITAID has announced major investment for cutting-edge
point-of-care diagnostic tools essential for better treatment, better detection
of resistance, better quality of care in people living with HIV and better
diagnosis of HIV for children,” said Dr Denis Broun, Executive Director of
UNITAID at the 19th International AIDS Conference (AIDS
2012) in Washington DC.
The investment, expected to be over US$140 million, is being
committed to projects implemented by the Clinton Health Access Initiative
(CHAI), UNICEF and Médecins Sans Frontières (MSF) to increase access to
affordable point-of-care HIV diagnostics adapted for use in resource-poor
settings.
“The existing tools we have today are heavy and expensive,
requiring sophisticated laboratory abilities, and as a result most people
cannot access them,” said Dr Broun. “It is estimated that 30% have access to
early infant diagnosis, 30% have access to CD4 and only 10% have access to
viral load.”
The sort of diagnostic tests UNITAID wants to move forward
(by committing funds to help new manufacturers with
tests in late-stage development to get over the obstacles to putting their
products on the market) should be much less complex and expensive to run. For
instance, viral load tests and the equipment used to perform them are
expensive, running from US $100,000 to 200,000 per machine, with each test costing about $100.
“The machines we’re looking at will cost around $5000 with
tests that will cost less than $10 per test,” said Dr Broun.
UNITAID has published reports on its website describing the
current HIV diagnostics market landscape, and aidsmap will publish further
reports on the issue over the coming days.
In addition to UNITAID’s unique approach to helping the
manufacturers, Dr Broun also stressed that a major part of their approach is to
“bring tests to people who need them, through partners such as CHAI,
UNICEF and MSF who would be the ones rolling tests out in Sub-Saharan Africa.”
One of UNITAID’s arrangements is with CHAI and UNICEF
(focusing mostly on CD4 cell tests and early infant diagnosis), the other with
MSF, which is looking at all three. (MSF has launched a major campaign to bring
access to viral load testing to people living with HIV in resource-limited settings;
see a new report available at www.aids2012.msf.org.)
“It is time to end the double standard in HIV care between
developed and developing countries,” said MSF’s Dr Eric Goemare, wearing a
T-shirt saying “VIRAL LOAD UNDETECTABLE.”
Clinical, and immunological monitoring for treatment failure,
simply doesn’t work well, according to Dr Goemare, who described how changes in
CD4 cell counts or clinical criteria were poorly reflective of whether
treatment had actually ceased working. However, since there are only two real
regimens in sub-Saharan Africa, clinicians are reluctant to switch treatments.
Consequently, they tend to switch late, leading to resistance and, quite
possibly, more HIV transmission.
“But also, it is
psychologically important for patient to have viral load [information], achieving
undetectable as a target,” he said. “When a person knows their viral load is
undetectable, it provides motivation to stick to their treatment for the long
haul.”
“If we use the B+ regimen (ART for life for pregnant women
living with HIV) for prevention of vertical transmission to children, we
absolutely need to know those women’s viral load are undetectable,” said Dr
Goemare.
Dr Chewe Luo of UNICEF agreed.
“The buzzword at this conference is the beginning of the end
of HIV and for us at UNICEF it is the beginning of the end of HIV in children,”
she said.
Yet: “Only 28% of children living with HIV are accessing
ARVs… there are critical reasons for that… but essentially, we have very little
access to testing for children living with HIV in resource limited settings."
The standard test for early infant diagnosis, HIV DNA PCR,
remains inaccessible for many children, she said.
“A few years ago we thought that dried blood spots (DBS) for
early infant diagnosis (EID) would be a game changer, but its delivery is
awfully complicated,” she said. Dried blood spots have been used to capture
samples that can be sent to a central laboratory for HIV DNA PCR testing.
“We did a five-country evaluation of the performance of DBS
for EID. It is actually disappointing to see how much investment has been
poured in, to achieve so little in return. We didn’t know whether up to 75% of
children who were identified by early infant diagnosis were alive at year one.
Maybe 50% of the 75% were lost in linking to care because of the complexity of
collecting the sample, or getting the result back to the mother when they come
back to the clinic. So point of care is really where we want to go. If we don’t
treat as many of the children as possible within the first few months of life,
50% will have died.”
“And when it comes to PMTCT, where are mothers actually
accessing antenatal care? Not in the big
hospitals… They are actually accessing
antenatal care in very poorly resourced clinics in rural settings, and the idea
that we can do CD4 before initiating treatment for life in these women in a lot
of places is a dream that cannot be achieved.”
“I visited a clinic in Zambia recently, and asked a nurse
what they would do if a woman tested positive, and she said, ‘Well, we ask them
to try to get a CD4,’ and I said, 'Well where do they get a CD4?' So the default
is that these women end up with a suboptimal therapy and they are more likely
to get resistance,” said Dr Luo.
Dr David Ripin of CHAI agreed: “Many people start treatment
later than they should and have worse access than they should, maybe babies
don’t get diagnosed and without treatment die before the age of two. And many
adults languish on failed first-line ARV regimens.”
Point-of-care diagnostics will bring these tests out of the
centralised laboratory and get them to the patient so they can get their results
immediately. It is hoped that point-of-care diagnostics will dramatically
improve HIV care by increasing uptake of treatment, reducing losses to
follow-up and eliminating waste of performing tests with results that are never
received by patients and never acted upon.
“About half of these tests are never received, representing
lost opportunities to treat when it needs to start, and potentially more HIV
transmission,” he said.
aidsmap will report more on these initiatives over the next
days.