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Stem Cell Factor Neutralization Protects From Severe Anaphylaxis in a Murine Model of Food Allergy

dc.contributor.authorPtaschinski, C
dc.contributor.authorRasky, AJ
dc.contributor.authorFonseca, W
dc.contributor.authorLukacs, NW
dc.coverage.spatialSwitzerland
dc.date.accessioned2023-12-05T21:31:08Z
dc.date.available2023-12-05T21:31:08Z
dc.date.issued2021-03-09
dc.identifier.issn1664-3224
dc.identifier.issn1664-3224
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/33786039
dc.identifier.urihttps://hdl.handle.net/2027.42/191691en
dc.description.abstractFood allergy is a growing public health problem with ~15 million people affected in the United States. In allergic food disease, IgE on mast cells bind to ingested antigens leading to the activation and degranulation of mast cells. Stem cell factor (SCF) is mast cell growth and activation factor that is required for peripheral tissue mast cells. We targeted a specific isoform of SCF, the larger 248 amino acid form, that drives peripheral tissue mast cell differentiation using a specific monoclonal antibody in a model of food allergy. Ovalbumin sensitized and intragastrically challenged mice were monitored for symptoms of anaphylaxis including respiratory distress, diarrhea, and a reduction in body temperature. During the second week of challenges, allergic mice were injected with an antibody to block SCF248 or given IgG control. Mice treated with α-SCF248 had a decreased incidence of diarrhea and no reduction in body temperature suggesting a reduction in anaphylaxis compared to IgG control treated animals. Re-stimulated mesenteric lymph nodes indicated that α-SCF248 treated mice had decreased OVA-specific Th2 cytokine production compared to IgG control treated allergic animals. The reduction of food induced anaphylaxis was accompanied by a significant reduction in gut leak. The mesenteric lymph node cells were analyzed by flow cytometry and showed a decrease in the number of type 2 innate lymphoid cells in mice injected with α-SCF248. Morphometric enumeration of esterase+ mast cells demonstrated a significant reduction throughout the small intestine. Using a more chronic model of persistent food-induced anaphylaxis, short term therapeutic treatment with α-SCF248 during established disease effectively blocked food induced anaphylaxis. Together, these data suggest that therapeutically blocking SCF248 in food allergic animals can reduce the severity of food allergy by reducing mast cell mediated disease activation.
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherFrontiers
dc.relation.haspartARTN 604192
dc.rightsLicence for published version: Creative Commons Attribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectanaphylaxis
dc.subjectfood allergy
dc.subjectinnate lymphoid cell
dc.subjectmast cell
dc.subjectstem cell factor
dc.subjectAllergens
dc.subjectAnaphylaxis
dc.subjectAnimals
dc.subjectAntibodies, Monoclonal
dc.subjectAntibodies, Neutralizing
dc.subjectBiomarkers
dc.subjectBiopsy
dc.subjectChemokine CCL2
dc.subjectDisease Models, Animal
dc.subjectFemale
dc.subjectFood Hypersensitivity
dc.subjectImmunoglobulin E
dc.subjectImmunophenotyping
dc.subjectIntestinal Mucosa
dc.subjectMast Cells
dc.subjectMice
dc.subjectStem Cell Factor
dc.subjectTh2 Cells
dc.titleStem Cell Factor Neutralization Protects From Severe Anaphylaxis in a Murine Model of Food Allergy
dc.typeArticle
dc.identifier.pmid33786039
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/191691/2/Stem Cell Factor Neutralization Protects From Severe Anaphylaxis in a Murine Model of Food Allergy.pdf
dc.identifier.doi10.3389/fimmu.2021.604192
dc.identifier.doihttps://dx.doi.org/10.7302/21871
dc.identifier.sourceFrontiers in Immunology
dc.description.versionPublished version
dc.date.updated2023-12-05T21:31:04Z
dc.identifier.orcid0000-0002-8982-4633
dc.identifier.orcid0000-0003-2403-6481
dc.identifier.volume12
dc.identifier.startpage604192
dc.identifier.name-orcidPtaschinski, C
dc.identifier.name-orcidRasky, AJ
dc.identifier.name-orcidFonseca, W; 0000-0002-8982-4633
dc.identifier.name-orcidLukacs, NW; 0000-0003-2403-6481
dc.working.doi10.7302/21871en
dc.owningcollnamePathology, Department of


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Licence for published version: Creative Commons Attribution 4.0 International
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