A slight rise in temperature and inflammation - such as a fever - speeds up cellular 'clock' in which proteins switch genes on and off to respond to infection.
‘Body heat can speed up our key defense system to fight against tumors, wounds, and infections.
The researchers have demonstrated that small rises in temperature (such as during a fever) speed up the speed of a cellular 'clock' that controls the response to infections - and this new understanding could lead to more effective and fast-working drugs which target a key protein involved in this process.
Biologists found that inflammatory signals activate 'Nuclear Factor kappa B' (NF-κB) proteins to start a 'clock' ticking, in which NF-κB proteins move backward and forwards into and out of the cell nucleus, where they switch genes on and off.
This allows cells to respond to a tumor, wound or infection. When NF-κB is uncontrolled, it is associated with inflammatory diseases, such as Crohn's disease, psoriasis and rheumatoid arthritis.
At a body temperature of 34 degrees, the NF-κB clock slows down. At higher temperatures than the normal 37-degree body temperature (such as in fever, 40 degrees), the NF-κB clock speeds up.
Mathematicians at the University of Warwick's Systems Biology Centre calculated how temperature increases make the cycle speed up.
They predicted that a protein called A20 - which is essential to avoid inflammatory disease - might be critically involved in this process. The experimentalists then removed A20 from cells and found that the NF-kB clock lost its sensitivity to increases in temperature.
Lead mathematician Professor David Rand, Professor of Mathematics and a member of the University of Warwick's Zeeman Institute for Systems Biology and Infectious Disease Epidemiology (SBIDER), explained that in normal life the 24-hour body clock controls small (1.5 degrees) changes in body temperature.
He commented: "the lower body temperature during sleep might provide a fascinating explanation into how shift work, jet lag or sleep disorders cause increased inflammatory disease".
Mathematician Dan Woodcock from the University of Warwick said: "this is a good example of how mathematical modeling of cells can lead to useful new biological understanding."
While the activities of many NF-kB controlled genes were not affected by temperature, a key group of genes showed altered profiles at the different temperatures. These temperature sensitive genes included key inflammatory regulators and controllers of cell communication that can alter cell responses.
This study shows that temperature changes inflammation in cells and tissues in a biologically organized way and suggests that new drugs might more precisely change the inflammatory response by targeting the A20 protein.
Professor Mike White, the lead biologist from the University of Manchester, said the study provides a possible explanation of how both environmental and body temperature affects our health:
"We have known for some time that influenza and cold epidemics tend to be worse in the winter when temperatures are cooler. Also, mice living at higher temperatures suffer less from inflammation and cancer. These changes may now be explained by altered immune responses at different temperatures."