4.5 Article

Serum IL-10 as a marker of severe dengue infection

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BMC INFECTIOUS DISEASES
卷 13, 期 -, 页码 -

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BIOMED CENTRAL LTD
DOI: 10.1186/1471-2334-13-341

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  1. International Society of Infectious Diseases, National Science Foundation Sri Lanka [RG/HS/01]
  2. Medical Research Council (UK)
  3. MRC [MC_UU_12010/5, G0701693, MC_U137881017] Funding Source: UKRI
  4. Medical Research Council [G1000800h, MC_UU_12010/5, G0701693, MC_U137881017] Funding Source: researchfish

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Background: Several studies have shown that serum IL-10, IFN gamma and MIF are elevated in patients in severe dengue (SD) and could be used as potential biomarkers. We proceeded to determine if these cytokines could be used as biomarkers in a large cohort of adult dengue patients with varying severity of dengue infection. Methods: Serum IL-10 levels were determined in 259 of whom 40 had severe dengue infection. Serum IFN gamma and IFN alpha levels were done in 78 and MIF levels were done in 65 patients with acute dengue infection. Clinical features and laboratory investigations were undertaken during the febrile and critical phase. Results: We found that serum IL-10 levels were significantly higher (p = 0.001) in patients with SD, when compared to those with non SD. Serum IL-10 levels significantly and inversely correlated with white cell counts (R = -0.23, p = 0.0002) and lymphocyte counts (R = -0.29, p < 0.0001) but significantly and positively correlated with aspartate tranaminase levels (R = 0.16, p = 0.01) and alanine transaminase levels (R = 0.22, p = 0.007). However, IL-10 levels did not have a good predictive value in discriminating those who were likely to develop SD (AUC = 0.66). Serum IFN gamma levels were also significantly higher (p = 0.04) in patients with SD when compared to non SD. There was no difference (p = 0.34) in serum IFN alpha levels and serum MIF levels (p = 0.15) in patients with SD and non SD. Conclusion: Although serum IL-10 was significantly elevated in patients with SD it had a poor discriminatory value in identifying those with SD and non SD and therefore, is unsuitable to be used as a robust biomarker in this cohort.

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