Researchers have developed a "smart" drug that targets inflammation in a site-specific manner and could enhance the body's natural ability to fight infection and reduce side effects.
Researchers at Ben-Gurion University of the Negev (BGU) in Israel and University of Colorado said the novel anti-inflammatory molecule, when injected, is as a non-active drug.
However, a localised site with excessive inflammation will activate it. Most other anti-inflammatory agents effectively inhibit inflammatory processes, though in a non-specific manner and in areas that include sites of necessary normal inflammatory homeostasis.
"This development is important because inhibition of inflammation in a non-specific manner reduces the natural ability to fight infections and is a common side effect of anti-inflammatory biologic therapeutics," said Dr Peleg Rider of BGU's Department of Clinical Biochemistry and Pharmacology.
When a non-specific agent is used, any patient who suffers from local inflammation might then be exposed to opportunistic infections at distant sites, such as lungs, risking, for example, tuberculosis.
This risk is mainly of concern to immunosuppressed patients, as well as older patients and patients undergoing chemotherapy as part of an anti-cancer treatment course.
The protein molecule is actually a chimera comprised of two domains, both originating from the potent inflammatory cytokine family of IL-1.
The first part of the protein holds the functional part of the molecule inactive, as occurs in normal living cells, and is connected to a potent natural inhibitor of IL-1.
When it encounters inflammatory enzymes, the molecule is cleaved and the functional part becomes active.
Rider, along with BGU's Dr Eli Lewis and Professor Charles Dinarello of the University of Colorado, demonstrated their findings in a mouse model of local inflammation.
They showed that leukocytes, which infiltrate inflammatory sites, indeed activate the chimeric protein, which in turn reduces local inflammation. The activation of the protein correlated with the amount of inflammatory stimuli.
The study is published in the Journal of Immunology.
