However, drug-resistant M. leprae strains have developed, prompting scientists to search for new treatment options. As a first step, researchers have started to decipher the exact way the bacterium interacts with the immune system, According to the ACS Central Science, researchers at Leiden University in the Netherlands

The cell walls of mycobacteria like M. leprae have a thick lipid layer containing glycolipids -; a combination of sugar and fat molecules -; that the human immune system can recognize and act against.

So, Jeroen D. C. Codée, Sho Yamasaki and colleagues wanted to better understand which glycolipids are responsible for leprosy’s symptoms, and how they interact with the immune system. The team extracted and synthesized the complex glycolipids from M. leprae, then exposed them to reporter cells expressing immune receptors.

The component that activated the most cells was PGL-III, a precursor to the bacterium’s most common glycolipid, PGL-I.

The team also discovered that this glycolipid used only its terminal sugar to bind an immune receptor called Mincle -; a unique interaction not previously reported.

Additionally, when mice without the Mincle receptor were exposed to M. leprae, they experienced worse infections than those with the receptor, suggesting that it plays an important role in the natural immune response against leprosy infection.

As a result, targeting this receptor or the PGL-III glycolipid could offer an alternative to the current, antibiotic-heavy treatment for leprosy.

Even more, the researchers say that the special structure-activity relationship between Mincle and PGL-III could be replicated to create other immunostimulatory drugs in the future.

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