2006
DOI: 10.1111/j.1365-2222.2005.02415.x
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Evaluation of allergenicity of genetically modified soybean protein extract in a murine model of oral allergen‐specific sensitization

Abstract: obtained by specific IgE ELISA inhibition and by antigen-specific T cell proliferation demonstrated that wt-SE and gm-SE shared B and T epitopes. The present murine model of soybean sensitization established by the oral route should provide valuable information about risk assessment for food allergy from new proteins of genetically modified foods.

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Cited by 66 publications
(44 citation statements)
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“…In the present study, the serum IgG levels were significantly increased in 35-d-old piglets sensitised by glycinin. This indicated that glycinin peptides were absorbed into the blood and produced large quantities of IgG antibody in the serum, and they played an important role in the systemic immune response, which had been verified in previous studies (Helm et al 2002;Gizzarelli et al 2006).…”
Section: Discussionsupporting
confidence: 72%
“…In the present study, the serum IgG levels were significantly increased in 35-d-old piglets sensitised by glycinin. This indicated that glycinin peptides were absorbed into the blood and produced large quantities of IgG antibody in the serum, and they played an important role in the systemic immune response, which had been verified in previous studies (Helm et al 2002;Gizzarelli et al 2006).…”
Section: Discussionsupporting
confidence: 72%
“…Thus assessment of the immunoglobulin levels after antigen administration allows determination of allergenic potential. Gizzarelli et al (2006) showed that sensitization with both GE and wild-type soybean extracts induced high levels of antigen-specific IgE, IgG1 and low levels of specific IgG2a in Balb/c mice. Singh et al (2006) observed comparable immune response (IgE and IgG1) for transgenic and wild-type mustard in Balb/c mice.…”
Section: Discussionmentioning
confidence: 98%
“…The levels of β-conglycinin-specific IgE were measured by indirect ELISA following the procedures described by Gizzarelli et al [34] with slight modifications. Immulon II 96-well microplates (Dynatech Laboratories, Chantilly, VA) were coated with 20 μg/mL purified β-conglycinin in coating buffer (Sigma, St Louis, MO) and incubated for 3 h at 37°C.…”
Section: Measurement Of Serum β-Conglycinin-specific Igementioning
confidence: 99%