2018
DOI: 10.1017/s0031182018001889
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The resistance againstTrichinella spiralisinfection induced by primary infection with respiratory syncytial virus

Abstract: Human infections withTrichinella spiralisand respiratory syncytial virus (RSV) are common, asT. spiralisinfections are re-emerging in various parts of the world and RSV infections remain a threat for infants. Yet, studies investigating the relationship pertaining to the two are severely lacking. In particular, immune response inductionviaRSV andT. spiralisremain largely elusive. Here, we investigated the resistance againstT. spiralisinfection induced upon primary infection with RSV. RSV, notorious for causing … Show more

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Cited by 3 publications
(2 citation statements)
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“…Moreover, T. spiralis downregulated pro-inflammatory cytokines e.g., nuclear factor-κB (NF-κB) and the inflammatory cellular infiltration in the lung as well as increased the antioxidant enzyme expression e.g.,NAD( P )H:quinone oxidoreductase (NQO1) which decreased the RSV oxidative stress in coinfected mice with subsequent improvement of lung inflammation ( Chu et al, 2020 ). Vice versa, Chu et al (2019) indicated that immune responses induced by RSV infection contribute to resistance against subsequent T. spiralis infection.…”
Section: Trichinella -Derived Molecules: a Panacea For Moder...mentioning
confidence: 99%
“…Moreover, T. spiralis downregulated pro-inflammatory cytokines e.g., nuclear factor-κB (NF-κB) and the inflammatory cellular infiltration in the lung as well as increased the antioxidant enzyme expression e.g.,NAD( P )H:quinone oxidoreductase (NQO1) which decreased the RSV oxidative stress in coinfected mice with subsequent improvement of lung inflammation ( Chu et al, 2020 ). Vice versa, Chu et al (2019) indicated that immune responses induced by RSV infection contribute to resistance against subsequent T. spiralis infection.…”
Section: Trichinella -Derived Molecules: a Panacea For Moder...mentioning
confidence: 99%
“…CD4 + and CD8 + T cells populations from splenocytes of mice at 1-month post-challenge infection were analyzed by flow cytometry. Splenocytes (1×10 6 cell/ml) in staining buffer (2% bovine serum albumin and 0.1% sodium azide in 0.1 M PBS) were incubated for 15 min at 4°C with Fc Block (clone 2.4G2; BD Biosciences) [19]. For surface staining, cells were incubated with surface antibodies (CD3e-PE-Cy5, CD4-FITC, CD8a-PE, BD Biosciences) at 4°C for 30 min.…”
Section: Methodsmentioning
confidence: 99%