The new antibody is in a test tube, with the image of the lungs from the mice in the background. Photo courtesy of NTU Singapore.
Scientists from Nanyang Technological University (NTU) Singapore have developed an antibody which boosts the survival chances for patients suffering from influenza and pneumonia. Proven effective in lab tests, the antibody is now being made suitable for use in humans. The scientists are also using the new antibody to develop a diagnostic kit which can help doctors accurately track the recovery progress of flu and pneumonia patients.
The patent-pending antibody has generated much interest globally. Two biotech multi-national corporations, Abcam based in the United Kingdom and Adipogen International based in the United States, have won the rights to license the antibody. The two multinational companies will produce the antibody for sale to global organisations doing research in vaccine and drug development.
The breakthrough finding was published in the latest issue of the journal Cell Reports.
Influenza epidemics, such as the deadly 1918 Spanish Flu which killed more than 50 million people or the severe acute respiratory syndrome (SARS) outbreak in 2002, are of big concern to governments and the general populace worldwide. The World Health Organization estimated that influenza results in about 3 million to 5 million cases of severe illness worldwide each year, with about 250,000 to 500,000 deaths annually.
Pneumonia is the leading cause of death in children worldwide accounting for 15 percent of all deaths for children under 5 years old, and is among the top 10 leading causes of death in the United States.
This new antibody was developed by NTU Singapore's associate professor Andrew Tan, who led an interdisciplinary team of scientists from Singapore.
"While it will take up to eight years to develop the antibody into a useable treatment for human patients, we are currently developing a diagnostic kit which should be commercialized in about three years," says Tan.
"The kit will help doctors diagnose the severity of pneumonia and the efficacy of the prescribed treatment. This is done by detecting the concentration of a particular protein called ANGPTL4, which is present in samples taken from patients suffering from upper respiratory tract infections."
The new antibody works by blocking ANGPTL4 which was found to be in high concentration in the tissue samples taken from patients suffering from pneumonia.
"When the antibody we developed was given to mice suffering from pneumonia and influenza which had high levels of ANGPTL4, these mice recovered much faster than the other mice which didn't receive the antibodies," Tan says.
"We know that ANGPTL4 usually helps to regulate blood vessel leakiness. But this is the first time we have shown that by blocking this protein, we are able to control the natural response of inflammation, which in turn reduces the damage that inflammation does to the lungs."
"The concentration of ANGPTL4 correlates to the amount of inflammation the patient is having," Tan explains. "With our diagnostic kit, doctors will be able to see if a particular treatment is working for a patient. This is done by observing whether the concentration of ANGPTL4 is decreasing or not."
Associate professor Vincent Chow from NUS Yong Loo Lin School of Medicine, a co-author of the paper, says, "This study reveals the potential diagnostic and therapeutic value of targeting ANGPTL4 in pneumonia, and warrants further detailed clinical investigation in pneumonia patients."
When a patient is suffering from a lung infection such as influenza and SARS, the inflammation process is started as part of the body's natural defence. Inflammation is beneficial during this stage, as it has been shown to help get rid of the pathogens (harmful bacteria, virus or parasite) causing the infection.
However in many cases, inflammation continues after the harmful pathogen is flushed out of the body. The continued inflammation causes a build-up of fluids in the lungs and also internal bleeding, and the patient will take longer to recover. In severe avian flu and SARS infections, excess inflammation was shown to cause more deaths than the infection.
First author of the paper and NTU researcher Li Liang said they proved that ANGPTL4 caused blood vessels in the lungs to be leakier, which allowed more white blood cells and other antibodies to enter the lungs to combat the infection. By blocking ANGPTL4, the 'leakiness' of the blood vessels is lessened, thus reducing the inflammation process.
This antibody project took the research team two years to complete, and was jointly funded by NTU Singapore, the National Medical Research Council Singapore and the Ministry of Education, Singapore.
Source: Nanyang Technological University