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Secretory immunoglobulin A (s-IgA) reactivity to acute psychosocial stress in children and adolescents: The influence of pubertal development and history of maltreatment

Laia Marqués-Feixa, Águeda Castro-Quintas, Helena Palma‐Gudiel, Soledad Romero, Ástrid Morer, Marta Rapado‐Castro, María Martín, Iñaki Zorrilla, Hilario Blasco-Fontecilla, Maite Ramírez, María Mayoral, Iria Méndez, Nerea San Martín-González, María Rodrigo-Yanguas, José Luis Monteserín-García, Lourdes Fañanás, María José Muñoz, Eulalia Anglada, Ariadna Mas, María José Lobato, Pilar Santamarina, Silvia Gadea, Maddi Laborde, Carmen Moreno, Lydia Gayubo, María Marín Vila

2022Brain Behavior and Immunity14 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Mucosal secretory immunoglobulin A (s-IgA) is an antibody protein-complex that plays a crucial role in immune first defense against infection. Although different immune biomarkers have been associated with stress-related psychopathology, s-IgA remains poorly studied, especially in youth. OBJECTIVES: The present study investigated how s-IgA behaves in front of acute psychosocial stress in children and adolescents, including possible variability associated with developmental stage and history of childhood maltreatment (CM). METHODS: 94 children and adolescents from 7 to 17 years (54 with a current psychiatric diagnostic and 40 healthy controls) drawn from a larger Spanish study were explored (EPI-Young Stress Project). To assess biological reactivity, participants provided five saliva samples during an acute laboratory-based psychosocial stressor, the Trier Social Stress Test for Children (TSST-C). Samples were assayed for s-IgA, as well as for cortisol. Pubertal development was ascertained by Tanner stage and CM following TASSCV criteria. RESULTS: We observed s-IgA fluctuations throughout the stressor, indicating the validity of TSST-C to stimulate s-IgA secretion (F(4,199) = 6.200, p <.001). Although s-IgA trajectories followed a reactivity and recovery pattern in adolescents, children exhibited no s-IgA response when faced with stress (F(4,197) = 3.406, p =.010). An interaction was found between s-IgA and CM (F(4,203) = 2.643, p =.035). Interestingly, an interaction between developmental stage, CM history and s-IgA reactivity was identified (F(12,343) = 2.036, p =.017); while children non-exposed to maltreatment exhibited no s-IgA changes to acute stress, children with a history of CM showed a similar response to adolescents, increasing their s-IgA levels after the psychosocial stressor. CONCLUSION: Acute psychosocial stress stimulates s-IgA secretion, but only after puberty. However, children with a history of maltreatment exhibited a response resembling that of adolescents, suggesting an early maturation of the immune system. Further studies are needed to clarify the validity of s-IgA as an acute stress biomarker, including additional measures during stress exposure.

Topics & Concepts

Trier social stress testStressorPsychosocialPsychopathologySalivaImmunoglobulin APsychologyAntibodyReactivity (psychology)Immune systemSecretory IgAErikson's stages of psychosocial developmentImmunologyClinical psychologyMedicineDevelopmental psychologyInternal medicinePsychiatryImmunoglobulin GFight-or-flight responseBiologyAlternative medicineBiochemistryGenePathologyStress Responses and CortisolTryptophan and brain disordersChild and Adolescent Psychosocial and Emotional Development
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