| Literature DB >> 25612733 |
Joan Hui Juan Lim1, Sharada Ravikumar1, Yan-Ming Wang2, Thomas Paulraj Thamboo3, Lizhen Ong4, Jinmiao Chen5, Jessamine Geraldine Goh1, Sen Hee Tay6, Lufei Chengchen7, Mar Soe Win8, Winnie Leong1, Titus Lau9, Roger Foo10, Haris Mirza11, Kevin Shyong Wei Tan11, Sunil Sethi4, Ai Leng Khoo12, Wee Joo Chng13, Motomi Osato7, Mihai G Netea14, Yue Wang2, Louis Yi Ann Chai1.
Abstract
Vitamin D level is linked to susceptibility to infections, but its relevance in candidemia is unknown. We aimed to investigate the in vivo sequelae of vitamin D3 supplementation in systemic Candida infection. Implicating the role of vitamin D in Candida infections, we showed that candidemic patients had significantly lower 25-OHD concentrations. Candida-infected mice treated with low-dose 1,25(OH)2D3 had reduced fungal burden and better survival relative to untreated mice. Conversely, higher 1,25(OH)2D3 doses led to poor outcomes. Mechanistically, low-dose 1,25(OH)2D3 induced proinflammatory immune responses. This was mediated through suppression of SOCS3 and induction of vitamin D receptor binding with the vitamin D-response elements in the promoter of the gene encoding interferon γ. These beneficial effects were negated with higher vitamin D3 doses. While the antiinflammatory effects of vitamin D3 are well described, we found that, conversely, lower doses conferred proinflammatory benefits in Candida infection. Our study highlights caution against extreme deviations of vitamin D levels during infections.Entities:
Keywords: 1,25(OH)2D3; cytokine; interferon gamma; suppressor of cytokine signaling (SOCS)
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Year: 2015 PMID: 25612733 DOI: 10.1093/infdis/jiv033
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226