Aberrant IgA responses to the gut microbiota during infancy precede asthma and allergy development


Por: Dzidic M, Abrahamsson TR, Artacho A, Björkstén B, Collado MC, Mira A and Jenmalm MC

Publicada: 1 mar 2017 Ahead of Print: 13 ago 2016
Resumen:
Background: Although a reduced gut microbiota diversity and low mucosal total IgA levels in infancy have been associated with allergy development, IgA responses to the gut microbiota have not yet been studied. Objective: We sought to determine the proportions of IgA coating together with the characterization of the dominant bacteria, bound to IgA or not, in infant stool samples in relation to allergy development. Methods: A combination of flow cytometric cell sorting and deep sequencing of the 16S rDNA gene was used to characterize the bacterial recognition patterns by IgA in stool samples collected at 1 and 12 months of age from children staying healthy or having allergic symptoms up to 7 years of age. Results: The children with allergic manifestations, particularly asthma, during childhood had a lower proportion of IgA bound to fecal bacteria at 12months of age compared with healthy children. These alterations cannot be attributed to differences in IgA levels or bacterial load between the 2 groups. Moreover, the bacterial targets of early IgA responses (including coating of the Bacteroides genus), as well as IgA recognition patterns, differed between healthy children and children with allergic manifestations. Altered IgA recognition patterns in children with allergy were observed already at 1 month of age, when the IgA antibodies are predominantly maternally derived in breast-fed children. Conclusion: An aberrant IgAresponsiveness to the gutmicrobiota during infancy precedes asthma and allergy development, possibly indicating an impaired mucosal barrier function in allergic children.

Filiaciones:
:
 Department of Clinical and Experimental Medicine, Unit of Autoimmunity and Immune Regulation, Linköping University, Linköping, Sweden

 Department of Health and Genomics, FISABIO Foundation, Center for Advanced Research in Public Health, Valencia, Spain

 Institute of Agrochemistry and Food Technology, Spanish National Research Council (IATA-CSIC), Department of Biotechnology, Unit of Lactic Acid Bacteria and Probiotics, Valencia, Spain

Abrahamsson TR:
 Department of Clinical and Experimental Medicine, Division of Paediatrics, Linköping University, Linköping, Sweden

Björkstén B:
 Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

Collado MC:
 Institute of Agrochemistry and Food Technology, Spanish National Research Council (IATA-CSIC), Department of Biotechnology, Unit of Lactic Acid Bacteria and Probiotics, Valencia, Spain

:
 Department of Health and Genomics, FISABIO Foundation, Center for Advanced Research in Public Health, Valencia, Spain.

Jenmalm MC:
 Department of Clinical and Experimental Medicine, Unit of Autoimmunity and Immune Regulation, Linköping University, Linköping, Sweden.
ISSN: 00916749





JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Editorial
MOSBY-ELSEVIER, 360 PARK AVENUE SOUTH, NEW YORK, NY 10010-1710 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 139 Número: 3
Páginas: 1017-102514
WOS Id: 000397295800033
ID de PubMed: 27531072
imagen Green Submitted, Bronze

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