This photomicrograph
reveals Mycobacterium tuberculosis bacteria using acid-fast Ziehl-Neelsen
stain; Magnified 1000 X. The acid-fast stains depend on the ability of
mycobacteria to retain dye when treated with mineral acid or an …more
A team of scientists led
by Oxford University have made a discovery that could improve our chances of
developing an effective vaccine against Tuberculosis.
The researchers have
identified new biomarkers for Tuberculosis (TB) which have shown for the first
time why immunity from the widely used Bacillus Calmette-Guérin (BCG) vaccine
is so variable. The biomarkers will also provide valuable clues to assess
whether potential new vaccines could be effective.
TB remains one of the
world's major killer diseases, causing TB disease in 9.6 million people and 1.5
million deaths in 2014. The only available vaccine, Bacillus Calmette-Guérin
(BCG), works well (estimated 50% effective) to prevent severe disease in
children but is very variable (0% to 80% effective) in how well it protects
against lung disease, particularly in countries where TB is most common.
While BCG is one of the
safest and most widely used vaccines worldwide, there is one key issue: It is
currently very difficult to determine whether it will work or not. This also
makes it really hard to determine if any new vaccines might work.
For many vaccines,
medics and scientists can use what are called immune correlates or biomarkers,
typically in the blood, which can be measured to determine whether a vaccine
has successfully induced immunity. Not only are these correlates useful in
measuring the success of existing vaccination programmes, they are also invaluable
in assessing whether potential new vaccines could be effective.
With a pressing need for
a TB vaccine that is more effective than BCG, a research team drawn from a
number of groups at Oxford University, working with colleagues from the South
African Tuberculosis Vaccine Initiative at the University of Cape Town and the
London School of Hygiene & Tropical Medicine, set out to identify immune
correlates that could facilitate TB vaccine development. The team, funded by
the Wellcome Trust and Aeras, and led by Professor Helen McShane and Dr Helen
Fletcher, studied immune responses in infants in South Africa who were taking
part in a TB vaccine trial.
Professor McShane said:
'We looked at a number of factors that could be used as immune correlates, to
try and find biomarkers that will help us develop a better vaccine.'
The team carried out
tests for twenty-two possible factors. One - levels of activated HLA-DR+CD4+
T-cells - was linked to higher TB disease risk. Meanwhile, BCG-specific
Interferon-gamma secreting T-cells indicated lower TB risk, with higher levels
of these cells directly linked to greater reduction of the risk of TB.
Antibodies to a TB
protein, Ag85A, were also identified as a possible correlate. Higher levels of
Ag85A antibody were associated with lower TB risk. However, the team cautions
that other environmental and disease factors could also cause Ag85A antibody
levels to rise and so there may not be a direct link between the antibody and
TB risk.
Professor McShane said:
'These are useful results which ideally would now be confirmed in further
trials. They show that antigen-specific T cells are important in protection
against TB, but that activated T cells increase the risk".
Dr Helen Fletcher from
the London School of Hygiene & Tropical Medicine, said: "For the first
time we have some evidence of how BCG might work, and also what could block it
from working. Although there is still much work to do, these findings may bring
us a step closer to developing a more effective vaccine for TB."
Dr Tom Scriba from the
South African Tuberculosis Vaccine Initiative said: 'TB is still a major
international killer, and rates of TB disease in some areas of South Africa are
among the highest in the world. These findings provide important clues about
the type of immunity TB vaccines should elicit, and bring us closer to our
vision, a world without TB.'
The team is continuing
its work to develop a TB vaccine,
aiming to protect more people from the disease.

More information: T cell activation is an Immune Correlate
of Risk in BCG vaccine infants, Nature Communications, April 12,
2016, DOI:
10.1038/NCOMMS11290
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