Impaired Inflammatory Response to LPS in Type 2 Diabetes Mellitus

Type 2 diabetes mellitus (T2DM) is a severe health problem worldwide, reaching epidemic levels. High susceptibility to infections of T2DM patients indicates dysregulated immune responses to pathogens. However, innate immune responses, including monocyte functions, in T2DM are poorly investigated. Th...

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Main Authors: Lusine Khondkaryan (Author), Sona Margaryan (Author), David Poghosyan (Author), Gayane Manukyan (Author)
Format: Book
Published: Hindawi Limited, 2018-01-01T00:00:00Z.
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100 1 0 |a Lusine Khondkaryan  |e author 
700 1 0 |a Sona Margaryan  |e author 
700 1 0 |a David Poghosyan  |e author 
700 1 0 |a Gayane Manukyan  |e author 
245 0 0 |a Impaired Inflammatory Response to LPS in Type 2 Diabetes Mellitus 
260 |b Hindawi Limited,   |c 2018-01-01T00:00:00Z. 
500 |a 2090-8040 
500 |a 2042-0099 
500 |a 10.1155/2018/2157434 
520 |a Type 2 diabetes mellitus (T2DM) is a severe health problem worldwide, reaching epidemic levels. High susceptibility to infections of T2DM patients indicates dysregulated immune responses to pathogens. However, innate immune responses, including monocyte functions, in T2DM are poorly investigated. Therefore, in this study we aimed to assess lipopolysaccharide- (LPS-) induced immune responses of circulating monocytes from T2DM patients. The results showed that monocytes from T2DM were hyporesponsive to LPS challenge as reflected by significantly suppressed secretion of TNFα (p<0.01) and expression of CD11b (p<0.001) and TLR4 (p<0.001) compared to those in monocytes from healthy subjects. Furthermore, LPS-induced IL-10 levels were similar in diabetic and healthy supernatants, while expression levels of CD163 were found to be downregulated on monocytes from T2DM (p<0.001) suggesting impaired ability of monocytes to switch their phenotype to anti-inflammatory. Taken together, our results suggest compromised function of monocytes in T2DM, which may explain, at least partly, high incidence of infection in these patients. 
546 |a EN 
690 |a Pathology 
690 |a RB1-214 
655 7 |a article  |2 local 
786 0 |n International Journal of Inflammation, Vol 2018 (2018) 
787 0 |n http://dx.doi.org/10.1155/2018/2157434 
787 0 |n https://doaj.org/toc/2090-8040 
787 0 |n https://doaj.org/toc/2042-0099 
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