2012
DOI: 10.1016/j.dci.2011.07.010
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Immune responses elicited in rainbow trout through the administration of infectious pancreatic necrosis virus-like particles

Abstract: Virus like particles (VLPs) against viral pathogens not only constitute a novel approach for the development of antiviral vaccines for an specific virus, but also for the creation of multivalent vaccines in which antigens from other pathogens may be expressed on the surface of these VLPs. Despite positive results on protection for many of these VLPs in both fish and mammals, not many studies have focused on the immune response triggered by these particles; studies that may provide hints for the identification … Show more

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Cited by 22 publications
(13 citation statements)
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“…This is in agreement with past reports showing upregulation of CD4-1 transcripts in lymphoid organs of salmon and trout in response to immunogenic stimuli (16,(48)(49)(50)(51)(52)(53)(54), usually interpreted as an indicator of CD4 + T cell proliferation. Proliferation also has been reported for CD4-1 + cells isolated from ginbuna carp during allogeneic MLR as well as after Ag-specific stimulation (18).…”
Section: Discussionsupporting
confidence: 82%
“…This is in agreement with past reports showing upregulation of CD4-1 transcripts in lymphoid organs of salmon and trout in response to immunogenic stimuli (16,(48)(49)(50)(51)(52)(53)(54), usually interpreted as an indicator of CD4 + T cell proliferation. Proliferation also has been reported for CD4-1 + cells isolated from ginbuna carp during allogeneic MLR as well as after Ag-specific stimulation (18).…”
Section: Discussionsupporting
confidence: 82%
“…Rainbow trout infected with IPNV by bath challenge showed a decrease in serum IgM levels, while no changes were detected in IgT titers (60). Interestingly, intracoelomic injections of rainbow trout with IPNV viral-like particles induced a strong mobilization of IgM + and IgT + cells to the celomic cavity (61). Intracoelomic vaccination of rainbow trout against the bacteria Yersinia ruckeri induced IgM upregulation, but failed to affect IgT expression (62).…”
Section: Discussionmentioning
confidence: 99%
“…For each mRNA, gene expression was normalized by the elongation factor 1a (EF-1a) expression in each sample and expressed as 2 2DCt , where DCt is determined by subtracting the EF-1a Ct value from the target Ct as previously described [23]. All the primers used had already been optimized in previous studies [23][24][25]. Amplifications were performed in duplicate and negative controls with no template were always included in the reactions.…”
Section: Evaluation Of Immune Gene Expression By Real Time Pcrmentioning
confidence: 99%
“…Reaction mixtures containing 5 ml of 26 SYBR Green supermix, 1 ml of each primer (1 mM each) and 2 ml of cDNA template were incubated for 10 min at 95uC, followed by 40 amplification cycles (30 s at 95uC and 1 min at 60uC) and a dissociation cycle (30 s at 95uC, 1 min 60uC and 30 s at 95uC). For each mRNA, gene expression was normalized by the elongation factor 1a (EF-1a) expression in each sample and expressed as 2 2DCt , where DCt is determined by subtracting the EF-1a Ct value from the target Ct as previously described [23]. All the primers used had already been optimized in previous studies [23][24][25].…”
Section: Evaluation Of Immune Gene Expression By Real Time Pcrmentioning
confidence: 99%