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. 2018 Jan;40(1):e12506.
doi: 10.1111/pim.12506. Epub 2017 Dec 15.

Schistosoma mansoni-specific immune responses and allergy in Uganda

Collaborators, Affiliations

Schistosoma mansoni-specific immune responses and allergy in Uganda

G Nkurunungi et al. Parasite Immunol. 2018 Jan.

Abstract

Low allergy-related disease (ARD) prevalence in low-income countries may be partly attributed to helminth infections. In the Schistosoma mansoni (Sm)-endemic Lake Victoria islands (Uganda), we recently observed positive helminth-allergy associations, despite low ARD prevalence. To understand how Sm-induced cytokine and antibody profiles might influence allergic response profiles in this population, we assessed Schistosoma worm (SWA)- and egg antigen (SEA)-specific Th1 (IFN-γ), Th2 (IL-5, IL-13) and regulatory (IL-10) cytokine profiles (n = 407), and total (n = 471), SWA-, SEA- and allergen (house dust mite [HDM] and cockroach)-specific (as)IgE and IgG4 profiles (n = 2117) by ELISA. Wheeze was inversely associated with SWA-specific IFN-γ (P < .001) and IL-10 (P = .058), and SEA-specific IL-5 (P = .004). Conversely, having a detectable asIgE response was positively associated with SWA-specific IL-5 (P = .006) and IL-10 (P < .001). Total, SWA-, SEA- and allergen-specific IgE and IgG4 responses were higher among Sm Kato-Katz positive (SmKK+) and skin prick test (SPT)+ individuals compared to SmKK- and SPT- individuals. However, total and asIgG4/IgE ratios were lower among SPT+ and wheezing individuals. We conclude that, in this population, helminth-induced antibody and cytokine responses may underlie individual positive helminth-atopy associations, while the overall IgG4-IgE balance may contribute to the low overall prevalence of clinical allergies in such settings.

Keywords: ELISA; Schistosoma spp; allergy; cytokine; immunoglobulin.

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Figures

Figure 1
Figure 1
We hypothesize that the Th2 cytokine‐induced Sm‐specific IgE promotes potent, Sm‐specific, atopic effector responses and Sm elimination from the host, and also cross‐reactive responses to some allergens, resulting in positive Sm‐allergy associations. By contrast, Sm‐specific IL‐10, IgG4 and/or nonspecific polyclonally stimulated IgE inhibit these allergy‐related outcomes. White and shaded arrows denote promotion and inhibition, respectively

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