Drug Targets, Known in the HIV World, Get Scrutinized for TB Potential
NEW YORK, NY, FEB 29,
2008 – The TB Alliance is exploring a group of drug targets that is unknown
in the world of TB drugs but well known to others. In the fight against
HIV/AIDS, the so-called protease inhibitors have become powerful components of
current antiretroviral therapies. But the potential of inhibitors against the
same family of enzymes from Mycobacterium tuberculosis (M.tb),
the causative agent of TB, remains unexplored. If inhibitors of M.tb
proteases can be discovered, their novelty would make them potentially powerful
drugs against multidrug-resistant and extremely drug-resistant TB (MDR-TB and
XDR-TB).
In partnership with Prof. Tanya Parish at the Infectious Disease Research
Institute (IDRI), a Seattle-based non-profit scientific research institute, the
TB Alliance will work out which of the many proteases in M.tb might
make the best targets for TB drugs. The first priority will be proteases that
are essential for M.tb's survival in animals. Parish has a promising
start on this part of the project, as several proteases seem to be important for
M.tb to stay alive in low oxygen or low nutrient conditions. Survival
in these circumstances is thought to be critical for the persistence of M.tb
in humans, so drugs that prevent this survival have a good chance of shortening
TB treatments.
The collaboration will then focus on generating M.tb strains that
produce more or less than normal of a particular protease. Potential drugs that
shut down a particular protease would be expected to struggle in M.tb
strains that have a lot of that target protease, but do especially well in
M.tb strains that have little of the protease. This approach allows the
team to focus on a single target, but to do so in the context of whole cells.
Drug candidates that work in whole cells are more likely to advance, as they
have already passed the test of penetrating and working within cells.
About the Global Alliance for TB Drug Development:
The TB Alliance is a not-for-profit, product development partnership accelerating the discovery and development of new TB drugs that will shorten treatment, be effective against susceptible and resistant strains, be compatible with antiretroviral therapies for those HIV-TB patients currently on such therapies, and improve treatment of latent infection.
Working with public and private partners worldwide, the TB Alliance is leading the development of the most comprehensive portfolio of TB drug candidates in history, and is committed to ensuring that approved new regimens are affordable, adopted and available to those who need them.
The TB Alliance operates with funding from the Bill & Melinda Gates Foundation, Irish Aid, the Netherlands Ministry of Foreign Affairs (DGIS), the United Kingdom Department for International Development (DFID), and the United States Agency for International Development (USAID) and in-kind support from the National Institute for Allergy and Infectious Diseases (NIAID). For more information on TB drug development and the TB Alliance, please visit www.tballiance.org.