2018
DOI: 10.1016/j.fshw.2018.10.002
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Application of in vitro and in vivo models in the study of food allergy

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Cited by 42 publications
(32 citation statements)
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“…To identify the possible immune mechanisms associated with allergic reactions observed in zebrafish in response to tick saliva and red meat consumption, selected immune response and food allergy markers involved in T H 1 and T H 2 cellmediated responses (Lu et al, 2008;Huang et al, 2018) were characterized in the kidney and intestine involved in both innate and adaptive fish immunity (Liu et al, 2015;Brugman, 2016;Martins et al, 2019). The CD4 + T cells or T helper cells develop into T H 1 and T H 2 cells ( Figure 10A).…”
Section: Discussionmentioning
confidence: 99%
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“…To identify the possible immune mechanisms associated with allergic reactions observed in zebrafish in response to tick saliva and red meat consumption, selected immune response and food allergy markers involved in T H 1 and T H 2 cellmediated responses (Lu et al, 2008;Huang et al, 2018) were characterized in the kidney and intestine involved in both innate and adaptive fish immunity (Liu et al, 2015;Brugman, 2016;Martins et al, 2019). The CD4 + T cells or T helper cells develop into T H 1 and T H 2 cells ( Figure 10A).…”
Section: Discussionmentioning
confidence: 99%
“…Total RNA was extracted from zebrafish intestine and kidney samples using the AllPrep DNA/RNA/Protein (Qiagen, Hilden, Germany). The expression of selected zebrafish immune response and food allergy markers (Lu et al, 2008;Huang et al, 2018) akirin 2 (akr2), complement component c3a (c3a), interleukin 1-beta (il1b), interleukin 4 (il4), nuclear factor interleukin 3 regulated (nfil3), Toll-like receptor 4b (tlr4b), interferon-induced GTP-binding protein MxA (mxa), interferon (ifn), and MYD88 innate immune signal transduction adaptor (myd88) was analyzed by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) with gene-specific primers ( Supplementary Table 1) using the KAPA SYBR FAST one-step universal kit (Sigma-Aldrich) in the Rotor-Gene Q (Qiagen) thermocycler following manufacturer's recommendations. A dissociation curve was run at the end of the reactions to ensure that only one amplicon was formed and that the amplicon denatured consistently in the same temperature range for every sample (Ririe et al, 1997).…”
Section: Expression Of Selected Immune Response Markers By Quantitatimentioning
confidence: 99%
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“…The animal models are adequate as long as they have a GI system similar to the one of humans, produce IgE antibodies and manifest similar allergic reactions in response to food allergens. Among rodent models, Brown Norway and Wistar rats meet these conditions [ 15 ]. Although Brown Norway rats have been traditionally claimed as the most suitable model to study FA, Wistar rats have recently been demonstrated to increase IgE levels after oral immunization with OVA and to develop the key clinical manifestations of FA to peanut allergens [ 16 , 17 , 18 ].…”
Section: Introductionmentioning
confidence: 99%
“…Often, biopsies from allergic patients or animal's lung or gut are used (4); however, obtaining these specimens can be limiting the research opportunities. In vitro allergy models often consist of single-cell models, such as mast cells (MCs) or basophils (5). MCs or basophils represent cells of the allergic effector phase because their activation results in the acute allergic symptoms, meaning that in these models, allergy treatment can be studied in vitro rather than allergy prevention.…”
Section: Introductionmentioning
confidence: 99%