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Characterization of lymphocyte responses to peanuts in normal children, peanut-allergic children, and allergic children who acquired tolerance to peanuts
Victor Turcanu, … , Soheila J. Maleki, Gideon Lack
Victor Turcanu, … , Soheila J. Maleki, Gideon Lack
Published April 1, 2003
Citation Information: J Clin Invest. 2003;111(7):1065-1072. https://doi.org/10.1172/JCI16142.
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Characterization of lymphocyte responses to peanuts in normal children, peanut-allergic children, and allergic children who acquired tolerance to peanuts

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Abstract

Comparing lymphocyte responses to allergenic and nonallergenic foods could reveal the differences between pathogenic and normal immune responses to foods. Defining the cytokine-producing phenotypes of peanut-specific lymphocytes from peanut-allergic children, children who outgrew peanut allergy, and children who have always tolerated peanuts may be useful for understanding the mechanisms of food tolerance. Investigating immune responses against foods is hindered, however, by the fact that circulating food antigen–specific lymphocytes are very rare. In a novel approach we used carboxyfluorescein succinimidyl ester to detect peanut-specific lymphocytes by flow cytometry. We confirmed that these cells are indeed peanut specific by cloning. Peanut-allergic donors show Th2 polarization of cytokine production by peanut-specific cells (IFN-γ low, TNF-α low, IL-4 high, IL-5 high, IL-13 high). Conversely, nonallergic children and children who have outgrown their allergy show Th1 skewing to peanut antigens (IFN-γhigh, TNF-α high, IL-4 low, IL-5 low, IL-13low), similarly to nonallergenic food antigens (β-lactoglobulin, OVA). This finding suggests that peanut antigens do not intrinsically induce Th2 skewing, but that the type of response depends upon the donor’s allergic status. In conclusion, food allergic status is characterized by a Th2 response whereas Th1-skewed responses underlie oral tolerance.

Authors

Victor Turcanu, Soheila J. Maleki, Gideon Lack

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Figure 5

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Th subset polarization of antigen-specific T lymphocytes from NA donors ...
Th subset polarization of antigen-specific T lymphocytes from NA donors (n = 9). PBMCs were isolated, CFSE labeled, and cultured in the presence of antigens for 7 days, then the cytokine-producing phenotype of antigen-specific (CFSElow) cells was assessed by flow cytometry. Th subset skewing was determined as ratios of CFSElow cell percentages that produce Th1-type (IFN-γ) or Th2-type (IL-4) cytokines (and also TNF-α and IL-13). Points represent data from different individuals, while bars show median values. Significance was determined using the paired t test for log-transformed data (*P < 0.05; **P < 0.020).

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