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Palabras clave – provistas por la editorial

B cell maturation; CD4+ cells; T cell maturation; primary immune deficiency; autoimmunity; connective tissue diseases; atopic diseases; atopy; allergy; selective IgA deficiency; primary immunodeficiency; autoimmune diseases; Immunoglobulin E; Immunoglobulin deficiency; infections; malignancy; 22q11.2 deletion syndrome; activated phosphoinositide 3-kinase d syndrome; common variable immunodeficiency; complement deficiency; CTLA-4; Immune dysregulation; LRBA; severe combined immunodeficiency; X-linked agammaglobulinemia; anti-SARS-CoV-2 antibodies; COVID-19; SARS-CoV-2; PIMS-TS; Foxp3; IPEX; CVID; primary immunodeficiencies; epigenetics; DNA methylation; inborn errors of immunity; DiGeorge syndrome; 22q11.2 deletion; thymic output; dendritic cells; immunodeficiency; copy number variations; array-CGH; IKZF1; IKAROS; de novo mutation; R162Q; immune response; heterologous vaccine; humoral response; T-cell response; autoimmune lymphoproliferative syndrome; lymphoproliferation; gastrointestinal infections; Giardia; giardiasis; refractory; treatment; immunology; immunogenetic; eosinophilic gastrointestinal disorders; eosinophilic esophagitis; unclassified primary antibody deficiency; primary antibody deficiency; transient hypogammaglobulinemia of infancy; children; TNFRSF13B mutations; isolated IgM deficiency; n/a