Original Article

The dynamic changes and application value of MUC2 and sIgA in intestinal mucus layer of infants with food allergy

  • Nini DAI ,
  • Yajuan GAO ,
  • Jinbo SUN ,
  • Juan ZHANG ,
  • Zailing LI
Expand
  • Department of Pediatrics, Peking University Third Hospital, Beijing 100191, China

Received date: 2023-09-05

  Online published: 2024-04-09

Abstract

Objective To dynamically monitor and analyze the changes of fecal mucin 2 (MUC2) and secretory immunoglobulin A (sIgA) levels during the clinical treatment process of infants with food allergy, and to investigate the usefulness of food allergy’s interaction with sIgA and MUC2. Methods Fifty-two infants diagnosed with food allergy who received outpatient treatment from July 2022 to June 2023 were selected as the food allergy group. Simultaneously, 52 non-allergic diseases infants were chosen as the control group. The levels of fecal MUC2 and sIgA were compared between the two groups. Results There were 23 boys and 29 girls in the food allergy group and 26 boys and 26 girls in the control group. There were no statistically significant differences in age, delivery mode, feeding method, introduction of complementary foods and family history of allergic diseases between the two groups (P>0.05). The levels of fecal MUC2 and sIgA in the food allergy group were higher than those in the control group [(37.81±14.91) μg/mL vs. (25.33±14.29) μg/mL; 182.4(150.2-202.7) μg/mL vs. 147.7(131.4-157.9) μg/mL], and the differences were statistically significant (P<0.001). At the 2nd and 4th week of follow-up, fecal MUC2 level of children with food allergy group gradually decreased, but there was no statistical significance between groups (P>0.05). The level of fecal sIgA increased gradually, and the difference between groups was statistically significant (P<0.05). Binary logistic regression and ROC curve analysis showed that fecal MUC2 and sIgA both had area under the ROC curves above 0.7 (P<0.001), and the combination of the two could increase the diagnosis specificity. Conclusions There were differences in fecal MUC2 and sIgA levels between the two groups. With the improvement of clinical symptoms of children with food allergy, fecal MUC2 levels showed a downward trend and sIgA levels gradually increased, which may serve as potential biomarkers for the diagnosis of food allergy. The two groups' fecal MUC2 and sIgA levels varied from one another. With the improvement of clinical symptoms of children with food allergy, fecal MUC2 level had a downward trend and sIgA level gradually increased, suggesting that these markers could be useful for food allergy diagnosis.

Cite this article

Nini DAI , Yajuan GAO , Jinbo SUN , Juan ZHANG , Zailing LI . The dynamic changes and application value of MUC2 and sIgA in intestinal mucus layer of infants with food allergy[J]. Journal of Clinical Pediatrics, 2024 , 42(4) : 297 -304 . DOI: 10.12372/jcp.2024.23e0852

References

[1] Prescott SL, Pawankar R, Allen KJ, et al. A global survey of changing patterns of food allergy burden in children[J]. World Allergy Organ J, 2013, 6(1): 21.
[2] Sicherer SH, Sampson HA. Food allergy: epidemiology, pathogenesis, diagnosis, and treatment[J]. J Allergy Clin Immunol, 2014, 133(2): 291-307.
[3] Lopes JP, Sicherer S. Food allergy: epidemiology, pathogenesis, diagnosis, prevention, and treatment[J]. Curr Opin Immunol, 2020, 66: 57-64.
[4] Wang J, Zhou Y, Zhang H, et al. Pathogenesis of allergic diseases and implications for therapeutic interventions[J]. Signal Transduct Target Ther, 2023, 8(1): 138.
[5] Carroccio A, Scalici C, Maresi E, et al. Chronic constipation and food intolerance: a model of proctitis causing constipation[J]. Scand J Gastroenterol, 2005, 40(1): 33-42.
[6] Johansson ME, Hansson GC. Immunological aspects of intestinal mucus and mucins[J]. Nat Rev Immunol, 2016, 16(10): 639-649.
[7] Martens EC, Neumann M, Desai MS. Interactions of commensal and pathogenic microorganisms with the intestinal mucosal barrier[J]. Nat Rev Microbiol, 2018, 16(8): 457-470.
[8] Tadesse S, Corner G, Dhima E, et al. MUC2 mucin deficiency alters inflammatory and metabolic pathways in the mouse intestinal mucosa[J]. Oncotarget, 2017, 8(42): 71456-71470.
[9] Velcich A, Yang W, Heyer J, et al. Colorectal cancer in mice genetically deficient in the mucin muc2[J]. Science, 2002, 295(5560): 1726-1729.
[10] Paone P, Cani PD. Mucus barrier, mucins and gut microbiota: the expected slimy partners?[J]. Gut, 2020, 69(12): 2232-2243.
[11] 韩渤, 刘玥宏, 仇志强, 等. sIgA表达功能及其在肠道疾病的作用[J]. 世界华人消化杂志, 2017, 25(19): 1757-1763.
[12] Pietrzak B, Tomela K, Olejnik-Schmidt A, et al. Secretory IgA in intestinal mucosal secretions as an adaptive barrier against microbial cells[J]. Int J Mol Sci, 2020, 21(23): 9254.
[13] 中华医学会儿科学分会消化学组. 食物过敏相关消化道疾病诊断与管理专家共识[J]. 中华儿科杂志, 2017, 55(7): 487-492.
[14] 周薇, 赵京, 车会莲, 等. 中国儿童食物过敏循证指南[J]. 中华实用儿科临床杂志, 2022, 37(8): 572-583.
[15] Severity scoring of atopic dermatitis: the SCORAD index. Consensus report of the European task force on atopic dermatitis[J]. Dermatology, 1993, 186(1): 23-31.
[16] Loktionov A, Chhaya V, Bandaletova T, et al. Assessment of cytology and mucin 2 in colorectal mucus collected from patients with inflammatory bowel disease: results of a pilot trial[J]. J Gastroenterol Hepatol, 2016, 31(2): 326-333.
[17] Parrish A, Boudaud M, Kuehn A, et al. Intestinal mucus barrier: a missing piece of the puzzle in food allergy[J]. Trends Mol Med, 2022, 28(1): 36-50.
[18] Leon-Coria A, Kumar M, Workentine M, et al. Muc2 mucin and nonmucin microbiota confer distinct innate host defense in disease susceptibility and colonic injury[J]. Cell Mol Gastroenterol Hepatol, 2021, 11(1): 77-98.
[19] Van der Sluis M, De Koning BA, De Bruijn AC, et al. Muc2-deficient mice spontaneously develop colitis, indicating that MUC2 is critical for colonic protection[J]. Gastroenterology, 2006, 131(1): 117-129.
[20] Wenzel UA, Magnusson MK, Rydstr?m A, et al. Spontaneous colitis in Muc2-deficient mice reflects clinical and cellular features of active ulcerative colitis[J]. PLoS One, 2014, 9(6): e100217.
[21] Bollrath J, Powrie FM. Controlling the frontier: regulatory T-cells and intestinal homeostasis[J]. Semin Immunol, 2013, 25(5): 352-357.
[22] Shan M, Gentile M, Yeiser JR, et al. Mucus enhances gut homeostasis and oral tolerance by delivering immunoregulatory signals[J]. Science, 2013, 342(6157): 447-453.
[23] Virta LJ, Ashorn M, Kolho KL. Cow's milk allergy, asthma, and pediatric IBD[J]. J Pediatr Gastroenterol Nutr, 2013, 56(6): 649-651.
[24] Wasielewska Z, Dolińska A, Wilczyńska D, et al. Prevalence of allergic diseases in children with inflammatory bowel disease[J]. Postepy Dermatol Alergol, 2019, 36(3): 282-290.
[25] Larsson JM, Karlsson H, Crespo JG, et al. Altered O-glycosylation profile of MUC2 mucin occurs in active ulcerative colitis and is associated with increased inflammation[J]. Inflamm Bowel Dis, 2011, 17(11): 2299-2307.
[26] Grondin JA, Kwon YH, Far PM, et al. Mucins in Intestinal mucosal defense and inflammation: learning from clinical and experimental studies[J]. Front Immunol, 2020, 11: 2054.
[27] 李斐, 黎海芪. 卵清蛋白致敏小鼠肠道黏膜sIgA抗体反应的实验研究[J]. 中华儿科杂志, 2006, 44(4): 294-298.
[28] Sicherer SH, Sampson HA. Food allergy: a review and update on epidemiology, pathogenesis, diagnosis, prevention, and management[J]. J Allergy Clin Immunol, 2018, 141(1): 41-58.
[29] Roth-Walter F, Berin MC, Arnaboldi P, et al. Pasteurization of milk proteins promotes allergic sensitization by enhancing uptake through Peyer's patches[J]. Allergy, 2008, 63(7): 882-890.
[30] Frossard CP, Hauser C, Eigenmann PA. Antigen-specific secretory IgA antibodies in the gut are decreased in a mouse model of food allergy[J]. J Allergy Clin Immunol, 2004, 114(2): 377-382.
[31] Han B, Ma Y, Liu Y. Fucoxanthin Prevents the ovalbumin-Induced food allergic response by enhancing the intestinal epithelial barrier and regulating the intestinal flora[J]. J Agric Food Chem, 2022, 70(33): 10229-10238.
[32] Mestecky J, Russell MW, Elson CO. Intestinal IgA: novel views on its function in the defence of the largest mucosal surface[J]. Gut, 1999, 44(1): 2-5.
[33] Kukkonen K, Kuitunen M, Haahtela T, et al. High intestinal IgA associates with reduced risk of IgE-associated allergic diseases[J]. Pediatr Allergy Immunol, 2010, 21(1 Pt 1): 67-73.
[34] Konstantinou GN, Bencharitiwong R, Grishin A, et al. The role of casein-specific IgA and TGF-β in children with food protein-induced enterocolitis syndrome to milk[J]. Pediatr Allergy Immunol, 2014, 25(7): 651-656.
Outlines

/