論文

査読有り
2017年

Plasmodium products persist in the bone marrow and promote chronic bone loss

Science Immunology
  • Michelle S.J. Lee
  • Kenta Maruyama
  • Yukiko Fujita
  • Aki Konishi
  • Patrick M. Lelliott
  • Sawako Itagaki
  • Toshihiro Horii
  • Jing wen Lin
  • Shahid M. Khan
  • Etsushi Kuroda
  • Shizuo Akira
  • Ken J. Ishii
  • Cevayir Coban
  • 全て表示

2
12
記述言語
掲載種別
研究論文(学術雑誌)
DOI
10.1126/sciimmunol.aam8093

2017 © The Authors. Although malaria is a life-threatening disease with severe complications, most people develop partial immunity and suffer from mild symptoms. However, incomplete recovery from infection causes chronic illness, and little is known of the potential outcomes of this chronicity. We found that malaria causes bone loss and growth retardation as a result of chronic bone inflammation induced by Plasmodium products. Acute malaria infection severely suppresses bone homeostasis, but sustained accumulation of Plasmodium products in the bone marrow niche induces MyD88-dependent inflammatory responses in osteoclast and osteoblast precursors, leading to increased RANKL expression and overstimulation of osteoclastogenesis, favoring bone resorption. Infection with a mutant parasite with impaired hemoglobin digestion that produces little hemozoin, a major Plasmodium by-product, did not cause bone loss. Supplementation of alfacalcidol, a vitamin D3 analog, could prevent the bone loss. These results highlight the risk of bone loss in malaria-infected patients and the potential benefits of coupling bone therapy with antimalarial treatment.

リンク情報
DOI
https://doi.org/10.1126/sciimmunol.aam8093
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28783657
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044461158&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85044461158&origin=inward
ID情報
  • DOI : 10.1126/sciimmunol.aam8093
  • eISSN : 2470-9468
  • PubMed ID : 28783657
  • SCOPUS ID : 85044461158

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