2011
DOI: 10.2478/v10039-011-0033-z
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Evaluation of CXCL10, CXCL11, CXCL12 and CXCL13 chemokines in serum and cerebrospinal fluid in patients with tick borne encephalitis (TBE)

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Cited by 67 publications
(61 citation statements)
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“…TBEV stimulates IFNb expression in murine and human cells and the response to more pathogenic virus strains is stronger [29,36]. Type I IFNs expression during TBEV infection in vivo has not been studied so far, but we have previously detected increased concentrations of interferon-induced chemokine IP-10 in serum and csf of TBE patients, pointing to IFN-mediated response [37]. Here we confirm the IFNb up-regulation during TBE, from the early neurologic phase to the convalescence period.…”
Section: Polymorphismsupporting
confidence: 80%
“…TBEV stimulates IFNb expression in murine and human cells and the response to more pathogenic virus strains is stronger [29,36]. Type I IFNs expression during TBEV infection in vivo has not been studied so far, but we have previously detected increased concentrations of interferon-induced chemokine IP-10 in serum and csf of TBE patients, pointing to IFN-mediated response [37]. Here we confirm the IFNb up-regulation during TBE, from the early neurologic phase to the convalescence period.…”
Section: Polymorphismsupporting
confidence: 80%
“…T cells has been observed in the brains of fatal human TBEV cases [95,99]. Human TBE patients have elevated CCL3, CXCL10, and CXCL13 levels in the serum; CCL2, CCL3, CCL5, and CXCL10-13 have been detected in CSF, perhaps implicating the role of a Th-1-mediated response and the trafficking of T lymphocytes into the CNS [100][101][102]. Moreover, CCL2 and CCL5 were found to be elevated in the CSF of TBE patients even after the acute symptoms subsided [103,104].…”
Section: Tick-borne Encephalitis Virusmentioning
confidence: 98%
“…In TBEV-infected patients presenting with neuroinvasive disease, two studies reported high levels of CXCL10 in the CSF (Lepej et al, 2007; Zajkowska et al, 2011); cytoanalysis of CSF samples revealed that the majority of CD4 + T-cells were positive for CXCR3. These data suggest that the CXCL10:CXCR3 axis may also be critical for T-cell migration into the CNS.…”
Section: The Role Of Chemokine Receptors In the Pathogenesis Of Arbovmentioning
confidence: 99%