Elevated local TGF-β1 level predisposes a closed bone fracture to tuberculosis infection.

Med Hypotheses

Department of Orthopaedics, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, #88 Jiefang Road, Hangzhou 310009, PR China.

Published: September 2012

AI Article Synopsis

  • - Tuberculosis (TB) occurring after a closed bone fracture is rare, especially in patients with no prior TB history or infection signs at the time of fracture.
  • - Transforming growth factor-beta 1 (TGF-β1) is known to be important for various cell functions and is significantly elevated during bone healing, suggesting it might influence TB progression.
  • - The hypothesis states that increased TGF-β1 levels at bone fracture sites could make those areas more susceptible to TB infection, supported by findings that TGF-β1 can suppress immune responses involved in fighting infections.

Article Abstract

Tuberculosis (TB) occurring after a closed bone fracture in the patient with no history of TB and no evidence of TB infection at the time of initial fracture is a rare entity. Transforming growth factor-beta 1 (TGF-β1) is a ubiquitous growth factor that is implicated in the regulation of the proliferation, differentiation, migration, and survival of many different cell types. Recent studies have demonstrated that the local level of TGF-β1 in bone is significantly elevated during fracture healing and TGF-β1 plays an important role in TB progression. Given the above background, we hypothesize that elevated local TGF-β1 level predisposes a closed bone fracture to TB infection. This was supported by conclusions drawn from literature reviews: (1) the local level of TGF-β1 in bone is significantly elevated during fracture healing; (2) TGF-β1 inhibits T lymphocyte activation; (3) TGF-β1 is a potent macrophage-deactivating molecule; (4) TGF-β1 suppresses the production and activity of some proinflammatory cytokines.

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http://dx.doi.org/10.1016/j.mehy.2012.06.005DOI Listing

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