Basophils Play a Pivotal Role in Immunoglobulin-G-Mediated but Not Immunoglobulin-E-Mediated Systemic Anaphylaxis
Ovalbumin
Macrophages
Immunology
Receptors, IgG
Mice, Transgenic
Allergens
Immunoglobulin E
Mice, Mutant Strains
Basophils
3. Good health
Mice, Inbred C57BL
Mice
03 medical and health sciences
KEYWORD
Infectious Diseases
0302 clinical medicine
Immunoglobulin G
Immunology and Allergy
Animals
Mast Cells
Platelet Activating Factor
Anaphylaxis
Signal Transduction
DOI:
10.1016/j.immuni.2008.02.008
Publication Date:
2008-04-11T19:38:36Z
AUTHORS (10)
ABSTRACT
Anaphylaxis is an acute, severe, and potentially fatal systemic allergic reaction. Immunoglobulin E (IgE), mast cells, and histamine have long been associated with anaphylaxis, but an alternative pathway mediated by IgG has been suggested to be more important in the elicitation of anaphylaxis. Here, we showed that basophils, the least common blood cells, were dispensable for IgE-mediated anaphylaxis but played a critical role in IgG-mediated, passive and active systemic anaphylaxis in mice. In vivo depletion of basophils but not macrophages, neutrophils, or NK cells ameliorated IgG-mediated passive anaphylaxis and rescued mice from death in active anaphylaxis. Upon capture of IgG-allergen complexes, basophils released platelet-activating factor (PAF), leading to increased vascular permeability. These results highlight a pivotal role for basophils in vivo and contrast two major, distinct pathways leading to allergen-induced systemic anaphylaxis: one mediated by basophils, IgG, and PAF and the other "classical" pathway mediated by mast cells, IgE, and histamine.
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