Detection of serum and salivary IgE and IgG.sub.1 immunoglobulins specific for diagnosis of food allergy

• Published in: PloS one 2019-04, Vol.14 (4), p.e0214745
• Main Authors: Nunes, Marília Porto Oliveira, van Tilburg, Maurício Fraga, Tramontina Florean, Eridan Orlando Pereira, Guedes, Maria Izabel Florindo
• Format: Article
• Language: English
• Subjects: Allergy; Care and treatment; Children; Clinical trials; Corn; Diagnosis; Enzyme-linked immunosorbent assay; Food hypersensitivity; Health; Immunoglobulin E; Immunoglobulins; Milk; Milk allergy; Milk proteins; Nuts (Food); Peanuts; Risk factors; Saliva; Wheat
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0214745

Given the growing incidence and prevalence of life-threatening food allergies, health concerns have raised new perspectives for in vivo and in vitro diagnostic methodologies, pointing to saliva as a promising material, already used to diagnose other pathologies. Based on the above considerations, this study aimed to verify the possible use of saliva for the detection of IgE and IgG.sub.1 in the diagnosis of food allergy. This was a randomized, cross-sectional clinical study with a quantitative approach, developed at a hospital referral center in allergy in the state of Ceará, from January to July 2015. The sample consisted of 36 children of both sexes, aged between 1 and 60 months, with a diagnosis of cow's milk protein allergy (CMPA) by the RAST test. Children hospitalized or under immunosuppressive drugs were excluded from the study. Serum and saliva samples of the participants were collected and subsequently subjected to the indirect immunoenzymatic assay (ELISA) for the detection of specific serum and salivary immunoglobulins for food: corn, papaya, cow's milk, egg white, wheat, soybeans, peanuts, nuts, kiwi, cacao, fish, shrimp, bananas and tomatoes. For comparison of serum and saliva results, the T-test of independent samples and Mann-Whitney were adopted, for samples with normal and non-normal distribution respectively. A confidence interval of 95% was adopted for significant results. It was observed that 100% (n = 36) of the participants presented cow's milk allergy through the indirect ELISA, detecting IgE or IgG.sub.1 in serum and saliva. When serum IgE and IgG.sub.1 concentrations were compared, there was no statistical difference (p > 0.05) in 12 of the 14 foods evaluated. The same amount (n = 12) of non-significant differences (p > 0.05) was observed in the comparison of the 14 foods under IgE and IgG.sub.1 contractions in saliva. In the verification of the average values of IgE present in the serum and saliva of the foods, only cow's milk, fish and papaya showed statistically significant differences (p < 0.05). Of the total food evaluated, only the average levels of IgG.sub.1 present in serum and saliva showed a significant value (p < 0.05) in banana and tomato. These findings indicate that the detection of IgE and IgG.sub.1 in saliva proves to be as efficient as in the serum. The use of the salivary technique for use in the diagnosis of food allergy is suggested.