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The Journal of Allergy and Clinical Immunology
Volume 123, Issue 1
, Pages
53-58
, January 2009
Targeting IL-4/IL-13 signaling to alleviate oral allergen–induced diarrhea
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Ablated intestinal anaphylaxis in the absence of IL-4 and IL-13. A, Protocol timeline. B, Occurrence of diarrhea was assessed in OVA/alum-primed wild type, IL-13−/−, IL-4/13−/−, and IL-4−/− mice (n =
Ablated intestinal anaphylaxis in the absence of IL-4 and IL-13. A, Protocol timeline. B, Occurrence of diarrhea was assessed in OVA/alum-primed wild type, IL-13−/−, IL-4/13−/−, and IL-4−/− mice (n = 9-14 mice per group) up to 60 minutes after each intragastric inoculation with 50 mg of OVA. D, Jejunum mast cell numbers were assessed by means of morphometric analysis of chloroacetate esterase–stained cells. C and E, IgE (Fig 1, C) and MMCP1 (Fig 1, E) levels were measured by means of ELISA in blood drawn 60 to 90 minutes after the last saline or OVA inoculation. Serum IgE and MMCP1 levels were 490 ± 204 ng/mL and 9.7 ± 7.8 pg/mL, respectively, in naive wild-type mice, which had 35 ± 25 mast cells/mm3 of jejunum. i.p., Intraperitoneal; WT, wild-type; Sal, saline; n.s., not significant. ∗∗P < .01, ∗∗∗P < .001.
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IL-13 contributes to IgE and mast cell allergic responses. A, Diarrhea occurrences in OVA/alum–primed wild-type and IL-13Rα1−/− mice after 1 to 6 intragastric inoculations with 10 mg of OVA. B-D, SeruIL-13 contributes to IgE and mast cell allergic responses. A, Diarrhea occurrences in OVA/alum–primed wild-type and IL-13Rα1−/− mice after 1 to 6 intragastric inoculations with 10 mg of OVA. B-D, Serum IgE levels (Fig 2, B), jejunum mast cell numbers (Fig 2, C), and serum MMCP1 levels (Fig 2, D) were compared in wild-type and IL-13Rα1–deficient mice (7-18 per group). WT, Wild-type; KO, knockout. ∗∗P < .01.
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Prophylactic effects of anti-IL-4Rα mAb. OVA/alum-primed BALB/c mice (5 per group) were injected intraperitoneally with either 2 mg of 4-3 anti-IL-4Rα mAb or a control IgG1 mAb 1 day before the firstProphylactic effects of anti-IL-4Rα mAb. OVA/alum-primed BALB/c mice (5 per group) were injected intraperitoneally with either 2 mg of 4-3 anti-IL-4Rα mAb or a control IgG1 mAb 1 day before the first intragastric inoculation with OVA. A, Development of diarrhea was assessed during the 60 minutes after each intragastric OVA inoculation. B, Representative jejunum section of antibody-treated mice stained with chloroacetate esterase. C, Intestinal mast cell numbers were assessed by means of morphometric analysis. D and E, Blood MMCP1 (Fig 3, D) and total IgE (Fig 3, E) levels were assessed 1 to 2 hours after the last allergen exposure. i.g., Intragastric; Ab, antibody; Ctl, control. ∗∗P < .01.
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IL-4 and IL-13 are not required during the effector phase of allergic diarrhea. A, Once diarrhea had developed (after 4 intragastric challenges with OVA), BALB/c mice (6 per group) were injected withIL-4 and IL-13 are not required during the effector phase of allergic diarrhea. A, Once diarrhea had developed (after 4 intragastric challenges with OVA), BALB/c mice (6 per group) were injected with 2 mg of 4-3 or control IgG1 mAb before the fifth, sixth, and seventh OVA inoculations (n = 6 mice per group). B, One week and 3 OVA inoculations later, mice were killed, and plasma IgE levels were determined. C and D, Jejunum mast cell numbers (Fig 4, C) and MMCP1 blood levels (Fig 4, D) were assessed 1 to 2 hours after the last OVA inoculation. Ab, Antibody; Ctl, control; i.v., intravenous; i.p., intraperitoneal; i.g., intragastric. ∗P < .05, ∗∗P < .01.
Supported in part by National Institutes of Health grant AI45898-05, the Campaign Urging Research for Eosinophilic Diseases (CURED), the Food Allergy Project, and the US Department of Veterans Affairs.
Disclosure of potential conflict of interest: F. D. Finkelman has served as a consultant for Amgen and Abbott. M. E. Rothenberg has served as a speaker and consultant for Merck and as a consultant for Ception Therapeutics, Novartis, and Nycomed and has received research support from the National Institutes of Health, the Food Allergy and Anaphylaxis Network, and the Dana Foundation. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(08)01742-9
doi: 10.1016/j.jaci.2008.10.001
© 2009 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
« Previous
Next »
The Journal of Allergy and Clinical Immunology
Volume 123, Issue 1
, Pages
53-58
, January 2009
