Cited by 28Mast cells and histamineFood Allergy and Anaphylaxis ResearchDrug-Induced Adverse Reactions

Omalizumab effectively prevents recurrent refractory anaphylaxis in a patient with monoclonal mast cell activation syndrome

Jagdis, Amanda, Vadas, Peter·2014·Annals of Allergy, Asthma & Immunology

Integrity signals

Registry

Crossref · 10.1016/j.anai.2014.05.001

Cites

10 of 10 references verified0 citation errors · 0 not checkable

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  • Response to additional drugs, including multitargeted tyrosine kinase inhibitors (in patients with SM, such as midostaurin) and anti-IgE therapy (omalizumab), may be considered an indirect sign of MCA or MCAS.

    “Response to additional drugs, including multitargeted tyrosine kinase inhibitors (in patients with SM, such as midostaurin) and anti-IgE therapy (ie, omalizumab) may be considered an indirect sign of MCA or MCAS.”

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Authors
Jagdis, A., & Vadas, P.
Affiliations
St. Michael's Hospital (CA)
Corresponding author
Jagdis, Amanda
Venue
Annals of Allergy, Asthma & Immunology
Publisher
Elsevier BV
Published
2014-07
Volume
113
Issue
1
Pages
115-116
ISSN
1081-1206 (ISSN-L)
OpenAlex
W2120848364
Cited by
28
References
10
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2021: 1 · 2020: 4 · 2019: 4 · 2018: 6 · 2017: 2 · 2016: 2 · 2015: 3
FWCI
0.99
Type
journal article
Language
en
Open access
closed
Locations
  • Annals of Allergy Asthma & Immunology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
  • Health Sciences › Medicine › Immunology and Allergy › Food Allergy and Anaphylaxis Research
  • Health Sciences › Medicine › Pharmacology › Drug-Induced Adverse Reactions
Keywords
omalizumab, anaphylaxis, refractory anaphylaxis, mast cell degranulation, mastocytosis, anti-IgE therapy, hypotension
MeSH terms
Omalizumab, Adult, Anaphylaxis, Antibodies, Anti-Idiotypic, Clone Cells, Female, Humans, Mast Cells, Recurrence, Syndrome, Cell Degranulation, Treatment Outcome, Anti-Allergic Agents, Antibodies, Monoclonal, Humanized

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