EVALUATING THE CORRELATION BETWEEN IGG ANA IGE RESPONSES IN A RURAL IRAQI POPULATION INFECTED WITH ENTEROBIUS VERMICULARIS
Keywords:
Enterobius vermicularis, enterobiasis, total IgE, specific IgG, ELISA, Th2 immune response, humoral immunity, helminth infectionAbstract
Background: Helminths induce an immune response that is typically characterized as a Th2 response with elevated levels of specific antibodies. The interrelationship of total IgE and enterobiasis-specific IgG has been studied poorly to date. A global survey of research indicates that E. vermicularis infection continues to be among the most common helminthic parasites infecting humans globally, but it is especially prevalent in children. Objectives: The purpose of this research was to assess total serum IgE and specific (anti- Enterobius) IgG in infected subjects and to analyze whether there is an association between those antibody responses and Th2-mediated humoral immune response. Methods: This study used a cross-sectional approach in Mosul, Iraq, which involved 32 confirmed E. vermicularis infected subjects, and 36 control subjects who had no E. vermicularis infection. Total serum IgE and specific anti-E. vermicularis IgG concentrations were assessed by quantitative ELISA. Statistical analyses were conducted with t-tests for two means, ANOVA to compare three or more means, Pearson's correlation, and linear regression. Results: In comparison to healthy control subjects, individuals who had been infected showed significantly greater amounts of total IgE (422.0±41.3ng/ml), as well as a significantly greater amount of specific IgG (2,840±320ng/ml) (p<.001). The level of IgE was found to be at least nine times that of the level found in healthy control subjects; likewise, IgG levels were shown to be at least three times those of healthy controls. In addition to demonstrating this difference, a statistically significant positive relationship was also demonstrated for the levels of IgE and IgG among the infected subjects (r=0.68,p<.001); specifically, IgG explained 46% of the variation in IgE levels (R²=.46). Conclusions: Total IgE and specific anti- Enterobius IgG levels increase simultaneously with E. vermicularis infections, which indicates an activation of the Th2 mediated humoral immune response; therefore, this study contributes to our knowledge regarding host-parasite immunodynamics and may help us understand better how antibodies are regulated during enterobiasis.
References
Pinto HA, Geiger SM, de Melo AL, Mati VLT. Enterobiasis as a neglected worldwide disease: An appeal for action. Rev Soc Bras Med Trop. 2024;57:e01102-2024. doi:10.1590/0037-8682-0290-2024.
Aldamigh MA. Genetics of helminth infections: Immune system response, host-parasite interaction, and drug resistance. J Adv Vet Anim Res. 2025;12(1):123–131. doi:10.5455/javar.2025.l879.
World Health Organisation. Soil-transmitted helminth infections [Internet]. 2023 Mar 2 [cited 2026 Feb 19]. Available from: https://www.who.int/news-room/fact-sheets/detail/soil-transmitted-helminth-infections.
Hsiao YC, Wang JH, Chu CH, Chiu HY, Chiang CP, Lin CB. Is pinworm infection still a public health concern among children in resource-rich regions? BMC Public Health. 2022;22(1):2200. doi:10.1186/s12889-022-14641-4.
Lee SE, Lee YJ, Kim BH, Lee JH, Kim HS. The role of IgE in host defence against Enterobius vermicularis: A systematic review and meta-analysis. J Infect Public Health. 2024;17(2):245–253. doi:10.1016/j.jiph.2023.12.009.
Gazzinelli-Guimarães PH, Nutman TB. Helminth parasites and immune regulation. F1000Res. 2018;7:F1000 Faculty Rev-1685. doi:10.12688/f1000research.15596.1.
Mukai K, Tsai M, Starkl P, Marichal T, Galli SJ. IgE and mast cells in host defence against parasites and venoms. Semin Immunopathol. 2016;38(5):581–603. doi:10.1007/s00281-016-0565-1.
Wendt S, Trawinski H, Schubert S, Rodloff AC, Mössner J, Lübbert C. The diagnosis and treatment of pinworm infection. Dtsch Ärztebl Int. 2019;116(13):213–219. doi:10.3238/arztebl.2019.0213.
Jourdan PM, Lamberton PHL, Fenwick A, Addiss DG. Soil-transmitted helminth infections. Lancet. 2018;391(10117):252–265. doi:10.1016/S0140-6736(17)31930-X.
Harris NL, Loke P. Recent advances in type-2-cell-mediated immunity: Insights from helminth infection. Immunity. 2017;47(6):1024–1036. doi:10.1016/j.immuni.2017.11.015.
Maizels RM, McSorley HJ. Regulation of the host immune system by helminth parasites. J Allergy Clin Immunol. 2016;138(3):666–675. doi:10.1016/j.jaci.2016.07.007.
Fitzsimmons CM, Dunne DW. Survival of the fittest: allergology or parasitology? Trends Parasitol. 2009;25(10):447–451. doi:10.1016/j.pt.2009.07.004.
Stoyanova K, Pavlov S, Cvetkova T, Paunov T. Prevalence and age distribution of enterobiasis in North-Eastern Bulgaria. Helminthologia. 2020;57(2):100–108. doi:10.2478/helm-2020-0019.
Klein SL, Flanagan KL. Sex differences in immune responses. Nat Rev Immunol. 2016;16(10):626–638. doi:10.1038/nri.2016.90.
Allen JE, Maizels RM. Diversity and dialogue in immunity to helminths. Nat Rev Immunol. 2011;11(6):375–388. doi:10.1038/nri2992.
Turner JD, Jackson JA, Faulkner H, Behnke J, Else KJ, Kamgno J, et al. Intestinal infection intensity and IgE/IgG responses in helminth infections. Parasite Immunol. 2008;30(5):293–301. doi:10.1111/j.1365-3024.2008.01020.x.
Nutman TB. The immune response to helminth infection. Clin Immunol. 2021;225:108679. doi:10.1016/j.clim.2021.108679.
Cooper PJ, Chico ME, Sandoval C, Espinel I, Guevara A, Kennedy MW, et al. Human infection with Ascaris lumbricoides is associated with polarised cytokine responses and increased production of IgE and IgG. J Infect Dis. 2000;182(4):1207–1213. doi:10.1086/315847.
Ashiri A, Rafiei A, Nooruddin R, Anwar NS, Teymouri A, Ansari Moghaddam B, et al. Prevalence and diagnostic efficacy of IgG4 in Strongyloides stercoralis infection. Parasitology and Vector-Borne Diseases. 2025;18:291. doi:10.1186/s13071-025-06910-z.
Jasim SM. Prevalence of Enterobius vermicularis and its effect on IgE levels among children in Tikrit city. Microbes Infect Dis. 2025. doi:10.21608/mid.2025.416909.3143.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Kyzylorda Scholarly Review

This work is licensed under a Creative Commons Attribution 4.0 International License.
CC BY
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. CC BY includes the following elements:
BY: credit must be given to the creator.