A research team led by Hiroshima University Professor Satoshi Okada has determined that enhanced bone resorption activity due to a faulty immune response may underpin multifocal osteomyelitis painful, chronic bone infections in children with MSMD, a rare genetic condition resulting from a range of immune system mutations.
About a quarter of the world's population is infected with tuberculosis bacteria, according to the World Health Organization, but only about 5 to 10 percent of those infected will develop symptoms. These pathogens are mycobacteria, which are everywhere, including in chlorine-treated tap water. Most people who encounter mycobacteria will never even know, but, for a few immunocompromised groups, the ubiquitous organisms can cause painful, difficult-to-treat conditions.
One such group has Mendelian susceptibility to mycobacterial disease (MSMD), a rare genetic condition discovered in 1996 that results from a range of mutations involved in the body's immune response. Only about 400 people mostly children in the world have been diagnosed, likely due to the clouded understanding of the disorder and the infections that can result from mycobacterial susceptibility.
Satoshi Okada, professor in the Department of Pediatrics, Hiroshima University's Graduate School of Biomedical and Health Sciences said, multifocal osteomyelitis bone infection at multiple points is among the representative manifestations of MSMD. However, it is unclear why patients with MSMD frequently develop multifocal osteomyelitis, chronic inflammatory bone diseases.
Now, a team led by Okada has revealed a molecular underpinning of chronic bone infection in patients with MSMD. According to Okada, this finding could lead to a better understanding of the full immune response and reactions that lead to multifocal osteomyelitis in patients with MSMD. They published their results on June 24 in The Journal of Allergy and Clinical Immunology.
First author Miyuki Tsumura, a research fellow in the Department of Pediatrics, Hiroshima University's Graduate School of Biomedical and Health Sciences said, the frequency of multifocal osteomyelitis is especially high in patients with MSMD due to an impaired response to a cell signal called interferon-gamma (IFN-γ). We initiated this study to investigate the possibility that IFN-γ signaling may play a role in the pathogenesis of multifocal osteomyelitis.
Analysis of lesions of osteomyelitis suggests enhanced numbers of osteoclasts, the cells responsible for resorbing old bone cells during growth and repair. IFN-γ can prevent osteoclast production, so the researchers said the enhanced numbers of osteoclasts may suggest an impaired response to IFN-γ. With osteoclast precursors derived from bone marrow cells cultivated from three patients with MSMD, caused by mutations that result in a defective response for IFN-γ, and healthy volunteers, the researchers examined osteoclast formation in the presence or absence of IFN-γ. When IFN-γ was added to healthy cells, osteoclast formation stopped, as expected. When it was added to the cells from patients with MSMD, the response has impaired the cells resisted the call to stop formation.
Okada said, these results suggest that impairment of IFN-γ-induced inhibition of osteoclast differentiation and bone resorption in the context of signaling molecule deficiencies, leading to excessive osteoclast proliferation and increased bone resorption at infection points, may underlie multifocal osteomyelitis.
The researchers plan to completely characterize the molecular mechanisms underlying multifocal osteomyelitis by further studying the overproduction of osteoclasts and investigating the role of osteoblasts cells that make new bone.
Journal Information: Miyuki Tsumura et al, Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ, Journal of Allergy and Clinical Immunology (2021). DOI: 10.1016/j.jaci.2021.05.018