Lymphocytes in Peyer patches regulate clinical tolerance in a murine model of food allergy  Christophe P. Frossard, MS, Laurence Tropia, Conrad Hauser,

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Presentation transcript:

Lymphocytes in Peyer patches regulate clinical tolerance in a murine model of food allergy  Christophe P. Frossard, MS, Laurence Tropia, Conrad Hauser, MD, Philippe A. Eigenmann, MD  Journal of Allergy and Clinical Immunology  Volume 113, Issue 5, Pages 958-964 (May 2004) DOI: 10.1016/j.jaci.2003.12.017

Fig 1 β-Lactoglobulin–specific serum IgG1 (A), IgG2a (C), and IgE (E) antibody titers by ELISA. Numbers of BLG-specific IgG1 (B) and IgG2a (D) antibody-producing cells counted by ELISPOT in spleen or in Peyer patches. Results are pooled from at least 3 different experiences. ND, Not detectable. ∗∗P<.001, SENS (mice sensitized with β-lactoglobulin) vs CTX; ∗P<.05, TOL (mice tolerized with β-lactoglobulin) vs CTX; +P<.05, TOL vs SENS in SC; otherwise P=not significant. Journal of Allergy and Clinical Immunology 2004 113, 958-964DOI: (10.1016/j.jaci.2003.12.017)

Fig 2 Antigen-activated MNC (A) or PPC (B) proliferation. CD3+ cells were isolated from CTX mice and activated with BLG (CTXBLG) or OVO (CTXOVO), BLG or OVO-activated cells from TOL mice (mice tolerized with β-lactoglobulin) (TOLBLG and TOLOVO), or BLG or OVO-activated cells from SENS mice (mice sensitized with β-lactoglobulin) (SENSBLG and SENSOVO). Results shown are from pooled cells in one representative experiment. Journal of Allergy and Clinical Immunology 2004 113, 958-964DOI: (10.1016/j.jaci.2003.12.017)

Fig 3 Numbers of unstimulated and BLG-specific IFN-g (A and B), IL-4 (C and D), and IL-10 (E and F) producing cells counted by ELISPOT. Results are pooled from 3 different experiments. *P<.05, TOL (mice tolerized with β-lactoglobulin) vs SENS (mice sensitized with β-lactoglobulin); **P<.05, SENS vs CTX; +P<.05, TOL vs CTX; otherwise P=not significant. Journal of Allergy and Clinical Immunology 2004 113, 958-964DOI: (10.1016/j.jaci.2003.12.017)

Fig 4 Naive mice (nontol) or mice previously orally tolerized to BLG (pretol) were subsequently sensitized (ip) with BLG adsorbed to alumn. BLG-specific serum IgG1 (A), IgG2a (B), and IgE (C) antibody titers from pretol and nontol mice. Antigen-activated proliferation of cells from pooled SC (D) or MNC (E). ∗P<.05, nontol vs pretol. Journal of Allergy and Clinical Immunology 2004 113, 958-964DOI: (10.1016/j.jaci.2003.12.017)

Fig 5 β-Lactoglobulin–specific serum IgG1 antibody titers after adoptive transfer of MNC (A) or PPC (C). Numbers of IgG1 antibody-secreting cells counted by ELISPOT in SC or PP after adoptive transfer of MNC (B) or PPC (D). Results are pooled data from two different experiments. ∗P<.01, SENS (mice sensitized with β-lactoglobulin) vs TOL (mice tolerized with β-lactoglobulin); ∗∗P<.001, SENS vs TOL. Journal of Allergy and Clinical Immunology 2004 113, 958-964DOI: (10.1016/j.jaci.2003.12.017)