4.2 Article

Toll like receptors in self-recovering hepatitis E patients with or without pregnancy

期刊

HUMAN IMMUNOLOGY
卷 75, 期 12, 页码 1147-1154

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.humimm.2014.10.011

关键词

Hepatitis E; Pregnancy; Toll like receptors; MyD-dependent pathway; TRIF mediated pathway

资金

  1. Indian Council of Medical Research (ICMR), Ministry of health and family welfare, Government of India
  2. University Grant Commission (UGC), India

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Hepatitis E virus (HEV) causes high mortality among pregnant women. Pathogenesis of HEV, especially during pregnancy, is poorly understood. Our aim was to assess the role of Toll-like-receptors (TLRs) in hepatitis E patients with pregnancy (Antenatal care, ANC) or without pregnancy (non-ANC). The patient categories included acute-phase, non-ANC (n = 46) and ANC patients (2nd/3rd trimesters, n = 13) and non-ANC patients (n = 31) during convalescence. Controls included apparently healthy non-ANC (n = 30) and ANC subjects in the first (n = 10) and later (2nd/3rd, n = 20) trimesters. TLR2/TLR3/TLR4/TLR7/TLR8 levels were determined by flow-cytometry. Cytokine responses induced by TLR-specific-ligands-stimulated-PBMCs from ANC/non-ANC-patients and TLR-signaling-molecules (non-ANC-patients) were measured. PBMCs were used to assess gene expression levels by TaqMan-Low-Density-Array. Compared to the temporal activation of TLR4/TLR7/TLR8 at protein and mRNA levels, the ANC-patients and controls exhibited reduced TLRs indicative of impaired TLR response. Stimulation of PBMCs with TLR-specific ligands led to the induction of type-I interferons, IFN beta by the non-ANC group and IFN alpha, by the ANC category. Involvement of MyD88-independent (TLR3/TLR4) and MyD88-dependent (TLR4/TLR7/TLR8) pathways and association of TLR4/TLR7/TLR8 with recovery was documented in the non-ANC-patients. Except for robust type-I-interferon response, HEV infection could not modulate pregnancy-related diminished immune response. The results have implications in the understanding of HEV pathogenesis. (C) 2014 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.

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