Published online in the Journal of Infectious Diseases, the study investigated the proteins that are released by a break down of the lung structure in TB patients. Lung damage causes both transmission of infection and mortality.
They found that fragments released by break down of the lung’s key proteins (collagen and elastin), are increased in the sputum of patients with TB. They also discovered that one particular collagen fragment, PIIINP, was elevated in blood samples from patients with TB.
Dr Paul Elkington, from the University of Southampton who led the study, believes that these new markers could be used to screen individuals and halt transmission between population groups.
He says: “Tuberculosis continues to kill almost one and a half million people worldwide and is becoming increasingly resistant to drugs used to treat it. First-line TB tests and treatments in the developing world have not changed for over 30 years.
“These lung breakdown products have never been identified in TB before, and have the potential to be used as new markers to identify patients with TB and monitor the effect of new treatments on lung damage. This may permit population screening to find and treat highly infectious individuals to break the cycle of transmission, especially in developing world countries where TB is most prominent.”
The research was carried out in collaboration with Imperial College London and in South Africa at the University of Cape Town and the KwaZulu-Natal Research Institute for Tuberculosis and HIV (K-RITH) in Durban. It was primarily funded by the Wellcome Trust and K-RITH.
The team are now investigating all fragments released by lung destruction to develop new test kits that can be done at the patient’s bedside.
Bill Bishai, Director of the K-RITH, comments: “This study is a major step forward towards finding improved tests for diagnosing TB and for determining whether the TB is improving with therapy or worsening with therapy as such would be seen when patients have resistant TB. Improved diagnostic tests are desperately needed, not only to improve patient care in resource-poor countries, but also to accelerate clinical trials with new therapies.”
University of Southampton