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Tissue-Specific Expression of the Low-Affinity IgG Receptor, FcγRIIb, on Human Mast Cells.
Burton, Oliver T; Epp, Alexandra; Fanny, Manoussa E; Miller, Samuel J; Stranks, Amanda J; Teague, Jessica E; Clark, Rachael A; van de Rijn, Matt; Oettgen, Hans C.
Afiliación
  • Burton OT; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Epp A; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Fanny ME; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Miller SJ; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Stranks AJ; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
  • Teague JE; Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • Clark RA; Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, United States.
  • van de Rijn M; Department of Pathology, Stanford University Medical Center, Palo Alto, CA, United States.
  • Oettgen HC; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Front Immunol ; 9: 1244, 2018.
Article en En | MEDLINE | ID: mdl-29928276
Immediate hypersensitivity reactions are induced by the interaction of allergens with specific IgE antibodies bound via FcεRI to mast cells and basophils. While these specific IgE antibodies are needed to trigger such reactions, not all individuals harboring IgE exhibit symptoms of allergy. The lack of responsiveness seen in some subjects correlates with the presence of IgG antibodies of the same specificity. In cell culture studies and in vivo animal models of food allergy and anaphylaxis such IgG antibodies have been shown to exert suppression via FcγRIIb. However, the reported absence of this inhibitory receptor on primary mast cells derived from human skin has raised questions about the role of IgG-mediated inhibition of immediate hypersensitivity in human subjects. Here, we tested the hypothesis that mast cell FcγRIIb expression might be tissue specific. Utilizing a combination of flow cytometry, quantitative PCR, and immunofluorescence staining of mast cells derived from the tissues of humanized mice, human skin, or in fixed paraffin-embedded sections of human tissues, we confirm that FcγRIIb is absent from dermal mast cells but is expressed by mast cells throughout the gastrointestinal tract. IgE-induced systemic anaphylaxis in humanized mice is strongly inhibited by antigen-specific IgG. These findings support the concept that IgG, signaling via FcγRIIb, plays a physiological role in suppressing hypersensitivity reactions.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Receptores de IgG / Mastocitos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Receptores de IgG / Mastocitos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza