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Known Allergen Structures Predict Schistosoma mansoni IgE-Binding Antigens in Human Infection

Farnell, Edward J., Tyagi, Nidhi, Ryan, Stephanie, Chalmers, Iain W., Pinot de Moira, Angela, Jones, Frances M., Wawrzyniak, Jakub, Fitzsimmons, Colin M., Tukahebwa, Edridah M., Furnham, Nicholas, Maizels, Rick M., Dunne, David W.·2015·Frontiers in Immunology

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Figure 1 SDS-PAGE of recombinant antigens following expression and purification. Proteins were run on a 4–12% gradient Bis-Tris gel and stained with Coomassie Blue.
Figure 1 SDS-PAGE of recombinant antigens following expression and purification. Proteins were run on a 4–12% gradient Bis-Tris gel and stained with Coomassie Blue.CC BY · PubMed Central
Figure 2 Prevalence of IgE (A), IgG4 (B), and IgG1 (C) responses (with 95% binomial CIs), both pre- and post-treatment with PZQ to recombinant antigens within the population (n = 222). Prevalences/proportions of responders were calculated following the application of assay sensitivity cut-offs (mean + 3σ) determined using sera from 26 normal European controls. Proteins were grouped into predicted IgE-binding antigens (I), antigens without known allergenic domains (II), and confirmed IgE-binding antigens (III).
Figure 2 Prevalence of IgE (A), IgG4 (B), and IgG1 (C) responses (with 95% binomial CIs), both pre- and post-treatment with PZQ to recombinant antigens within the population (n = 222). Prevalences/proportions of responders were calculated following the application of assay sensitivity cut-offs (mean + 3σ) determined using sera from 26 normal European controls. Proteins were grouped into predicted IgE-binding antigens (I), antigens without known allergenic domains (II), and confirmed IgE-binding antigens (III).CC BY · PubMed Central
Figure 3 Proportions of individuals responding with IgE alone, IgG4 alone, or IgG4 and IgE together post-treatment with PZQ. Prevalences/proportions of responders were calculated following the application of assay sensitivity cut-offs (mean + 3σ) determined using sera from 26 normal European controls. Two-sample test of proportions was used to compare the prevalence of individuals responding with IgE alone vs. those responding with IgE and IgG4 together (*p < 0.05, **p < 0.01, ***p < 0.001). Proteins were grouped into predicted IgE-binding antigens (I), antigens without known allergenic domains (II), and confirmed IgE-binding antigens (III).
Figure 3 Proportions of individuals responding with IgE alone, IgG4 alone, or IgG4 and IgE together post-treatment with PZQ. Prevalences/proportions of responders were calculated following the application of assay sensitivity cut-offs (mean + 3σ) determined using sera from 26 normal European controls. Two-sample test of proportions was used to compare the prevalence of individuals responding with IgE alone vs. those responding with IgE and IgG4 together (*p < 0.05, **p < 0.01, ***p < 0.001). Proteins were grouped into predicted IgE-binding antigens (I), antigens without known allergenic domains (II), and confirmed IgE-binding antigens (III).CC BY · PubMed Central
Figure 4 Comparison of the structures of SmLipocalin, SmThioredoxin, SmSOD with their respective IgE-binding counterparts identified from Allergome. Parasite allergen-like molecules were used to identify similar allergens by BLAST search of the Allergome database. Identities of the matched allergens with the corresponding E-values are shown below each matched pair. Structures were superimposed using LSQMAN and the quality of the alignment assessed by root mean squared deviation (RMSD). (A) Alignment of SmLipocalin (1VYF, cyan) and Der f 13 (2A0A, green). (B) Alignment of SmSOD (1TO4, cyan) and Tomato SOD (3HOG, green). (C) Alignment of SmThioredoxin (2XBI, cyan) and White Shrimp Thioredoxin (3ZZX, green).
Figure 4 Comparison of the structures of SmLipocalin, SmThioredoxin, SmSOD with their respective IgE-binding counterparts identified from Allergome. Parasite allergen-like molecules were used to identify similar allergens by BLAST search of the Allergome database. Identities of the matched allergens with the corresponding E-values are shown below each matched pair. Structures were superimposed using LSQMAN and the quality of the alignment assessed by root mean squared deviation (RMSD). (A) Alignment of SmLipocalin (1VYF, cyan) and Der f 13 (2A0A, green). (B) Alignment of SmSOD (1TO4, cyan) and Tomato SOD (3HOG, green). (C) Alignment of SmThioredoxin (2XBI, cyan) and White Shrimp Thioredoxin (3ZZX, green).CC BY · PubMed Central
Figure 5 Differential transcription of antigens in S. mansoni adult worms (A) and eggs (B) as determined by previously published microarray studies (35). Levels of antigen transcription were expressed as relative fluorescent units (RFU).
Figure 5 Differential transcription of antigens in S. mansoni adult worms (A) and eggs (B) as determined by previously published microarray studies (35). Levels of antigen transcription were expressed as relative fluorescent units (RFU).CC BY · PubMed Central
Figure 6 Relationships between antigen-specific natural log normalized geometric mean (GM) IgE levels and transcription of antigen in egg (A)*, natural log normalized GM IgG4 levels (B), GM age (C), or GM infection intensity (D) in individuals that respond to either IgG4 or IgE both pre- (open circles, short dashes) and post-treatment (filled circles, long dashes) with PZQ to a given antigen (β, SE, and p value calculated by linear regression). *SmHSP20 was excluded from this plot as it exerted undue influence on the linear regression model (Cook’s distance > 1).
Figure 6 Relationships between antigen-specific natural log normalized geometric mean (GM) IgE levels and transcription of antigen in egg (A)*, natural log normalized GM IgG4 levels (B), GM age (C), or GM infection intensity (D) in individuals that respond to either IgG4 or IgE both pre- (open circles, short dashes) and post-treatment (filled circles, long dashes) with PZQ to a given antigen (β, SE, and p value calculated by linear regression). *SmHSP20 was excluded from this plot as it exerted undue influence on the linear regression model (Cook’s distance > 1).CC BY · PubMed Central

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Authors
Farnell, E. J., Tyagi, N., Ryan, S., Chalmers, I. W., Pinot de Moira, A., Jones, F. M., Wawrzyniak, J., Fitzsimmons, C. M., Tukahebwa, E. M., Furnham, N., Maizels, R. M., & Dunne, D. W.
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Frontiers in Immunology
Published
2015-02-03
Volume
6
ISSN
1664-3224
Cited by
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CoChat. (2026). Citation check: Known Allergen Structures Predict Schistosoma mansoni IgE-Binding Antigens in Human Infection. https://app.cochat.ai/papers/10.3389/fimmu.2015.00026
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Farnell, E. J., Tyagi, N., Ryan, S., Chalmers, I. W., Pinot de Moira, A., Jones, F. M., Wawrzyniak, J., Fitzsimmons, C. M., Tukahebwa, E. M., Furnham, N., Maizels, R. M., & Dunne, D. W. (2015). Known Allergen Structures Predict Schistosoma mansoni IgE-Binding Antigens in Human Infection. Frontiers in Immunology. https://doi.org/10.3389/fimmu.2015.00026