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It may soon be possible to identify patients who will develop tuberculosis, as scientists have identified changes in the blood specific to the disease. These findings are from an international study published in the Aug. 19 issue of Nature and conducted by doctors and researchers at Nationwide Childrens Hospital using blood profiling techniques to understand infections.
Tuberculosis (TB) is caused by the bacterium Mycobacterium tuberculosis, which usually attacks the lungs and can be fatal if not treated properly. Although TB is no longer a leading cause of death in the United States, it remains an epidemic in much of the world. One third of the worlds total population is infected with the microbes that cause TB; however, most people infected with M. tuberculosis remain asymptomatic with latent TB. People with latent TB have a 10 percent lifetime risk of developing active TB, but current tests can not identify which individuals will develop the disease.
"Tools to diagnose infections like TB, bronchiolitis and pneumonia have been developed and are actively used to classify patients as being infected with specific pathogens, but we are still unable to predict how each person is going to react to the infection," said one of the studys authors Octavio Ramilo, MD, chief of infectious diseases at Nationwide Childrens Hospital. "Its difficult to predict patient outcomes, and this is a real problem."
To combat this problem, Ramilo and Asuncion Mejias, MD, investigators at the Center for Vaccines and Immunity in The Research Institute at Nationwide Childrens Hospital, are using microarray technology to develop blood profiles in patients specific to infectious diseases.
"Each infectious agent, be it a virus or a bacterium, interacts with human immune cells in unique ways by triggering proteins on white blood cells," said Mejias. "We can identify patterns among the white blood cells activated proteins and identify a unique signature for each infectious agent."
Ramilo and Mejias' research has shown that gene expression microarray technology can be used to help develop blood transcriptional signatures.
"This technology allows us to see the whole picture of infection using a single blood sample, which is a really powerful tool for the clinic," said Mejias.
Its this gene expression microarray technology that allowed an international group of investigators, of which Drs. Ramilo and Mejias are part of, to provide the first complete description of the blood transcriptional signature of TB.
The study examined and compared blood drawn from patients in London, England and Cape Town, South Africa who had active TB, latent TB or who did not have TB. The team developed genome-wide transcriptional profiles for each of the patients and discovered a distinct characteristic, or "signature," of the blood from patients with active TB. X-rays of patients with this signature were consistent with signs of active TB.
"The study shows for the first time that the transcriptional signature in blood correlates with extent of disease in active TB patients," said Ramilo. "It validates the idea that this transcriptional signature is an accurate marker of TB infection."
The team also found that a subset of latent TB patients had signatures similar to those in active TB patients.
"The signature of active TB, which was observed in 10 to 20 percent of latent TB patients, may identify those individuals who will develop disease, but longitudinal studies are needed to assess this," said Ramilo.
The transcriptional signature was diminished in active TB patients after two months and completely extinguished by 12 months after treatment.
"These findings suggest that the blood transcriptional signature of active TB patients could be used to monitor how well a patients treatment is working," said Ramilo.
Mejias says that this study highlights the power that gene expression microarray technology could bring to the diagnosis and treatment of infectious diseases, as the blood transcriptional signatures are not limited to TB. Currently, the infectious disease investigators at Nationwide Childrens Hospital are developing transcriptional signatures using blood samples obtained from children with broncholitis and pneumonia and plan to correlate findings with clinical outcomes, similar to the recent TB study.
"It seems that we are developing a tool that can not only diagnose infectious diseases, but also indicate severity and eventually predict which patients are at risk for developing advanced symptoms. These capabilities are desperately needed in order to improve how patients recover from infections," said Ramilo.