Recovery from desensitization of IgE‐dependent responses in human lung mast cells
Summary Background Clinical desensitization and oral food immunotherapy are therapeutic interventions that allow individuals who react adversely to an allergen (drug or food) to be made tolerant to the allergen. However, tolerance is brief, and allergen hypersensitivity can recur within days followi...
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Veröffentlicht in: | Clinical and experimental allergy 2017-08, Vol.47 (8), p.1022-1031 |
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creator | Lewis, A. MacGlashan, D. W. Suvarna, S. K. Peachell, P. T. |
description | Summary
Background
Clinical desensitization and oral food immunotherapy are therapeutic interventions that allow individuals who react adversely to an allergen (drug or food) to be made tolerant to the allergen. However, tolerance is brief, and allergen hypersensitivity can recur within days following allergen withdrawal.
Objective
We hypothesize that the reason these treatments are temporary reflects rapid recovery of mast cells from a desensitized state. We sought to test this.
Methods
Desensitization of IgE‐mediated histamine release from human lung mast cells was explored by methods that partially replicate the pattern of treatment during clinical desensitization. Specific and non‐specific desensitization and changes in surface IgE were examined following desensitization. Recovery from desensitization was also studied.
Results
Desensitization of mast cell responses was readily induced with concentrations of antigen or anti‐IgE that were suboptimal for secretion. There was little or no non‐specific desensitization when lung mast cells were exposed to antigens. There was no loss of cell surface IgE following desensitization. Removing the desensitizing stimulus from the media following desensitization allowed the cells to recover with half‐point of recovery of ~1.5 days and complete recovery after 5 days. Both the functional response and histamine content recovered within this time frame. The recovery appeared possible because both antigens and anti‐IgE dissociated rapidly from cells after washing to remove excess stimulus.
Conclusions and Clinical Relevance
Human lung mast cells readily recover from a desensitized state following removal of desensitizing antigen. This finding provides a potential explanation for the ephemeral nature of clinical desensitization. |
doi_str_mv | 10.1111/cea.12912 |
format | Article |
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Background
Clinical desensitization and oral food immunotherapy are therapeutic interventions that allow individuals who react adversely to an allergen (drug or food) to be made tolerant to the allergen. However, tolerance is brief, and allergen hypersensitivity can recur within days following allergen withdrawal.
Objective
We hypothesize that the reason these treatments are temporary reflects rapid recovery of mast cells from a desensitized state. We sought to test this.
Methods
Desensitization of IgE‐mediated histamine release from human lung mast cells was explored by methods that partially replicate the pattern of treatment during clinical desensitization. Specific and non‐specific desensitization and changes in surface IgE were examined following desensitization. Recovery from desensitization was also studied.
Results
Desensitization of mast cell responses was readily induced with concentrations of antigen or anti‐IgE that were suboptimal for secretion. There was little or no non‐specific desensitization when lung mast cells were exposed to antigens. There was no loss of cell surface IgE following desensitization. Removing the desensitizing stimulus from the media following desensitization allowed the cells to recover with half‐point of recovery of ~1.5 days and complete recovery after 5 days. Both the functional response and histamine content recovered within this time frame. The recovery appeared possible because both antigens and anti‐IgE dissociated rapidly from cells after washing to remove excess stimulus.
Conclusions and Clinical Relevance
Human lung mast cells readily recover from a desensitized state following removal of desensitizing antigen. This finding provides a potential explanation for the ephemeral nature of clinical desensitization.</description><identifier>ISSN: 0954-7894</identifier><identifier>EISSN: 1365-2222</identifier><identifier>DOI: 10.1111/cea.12912</identifier><identifier>PMID: 28236656</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Allergens ; antigen ; Antigens ; anti‐IgE ; Cell surface ; Desensitization ; Food allergies ; Histamine ; human lung mast cell ; Hypersensitivity ; IgE ; Immunoglobulin E ; Immunological tolerance ; Immunotherapy ; Lungs ; Mast cells ; Secretion ; Test procedures ; Therapeutic applications</subject><ispartof>Clinical and experimental allergy, 2017-08, Vol.47 (8), p.1022-1031</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4192-ec4e36f055dc362091e20ce8f9d37c3635140ffc3559584d412e4fc585b90c3a3</citedby><cites>FETCH-LOGICAL-c4192-ec4e36f055dc362091e20ce8f9d37c3635140ffc3559584d412e4fc585b90c3a3</cites><orcidid>0000-0001-7272-3011</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcea.12912$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcea.12912$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28236656$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lewis, A.</creatorcontrib><creatorcontrib>MacGlashan, D. W.</creatorcontrib><creatorcontrib>Suvarna, S. K.</creatorcontrib><creatorcontrib>Peachell, P. T.</creatorcontrib><title>Recovery from desensitization of IgE‐dependent responses in human lung mast cells</title><title>Clinical and experimental allergy</title><addtitle>Clin Exp Allergy</addtitle><description>Summary
Background
Clinical desensitization and oral food immunotherapy are therapeutic interventions that allow individuals who react adversely to an allergen (drug or food) to be made tolerant to the allergen. However, tolerance is brief, and allergen hypersensitivity can recur within days following allergen withdrawal.
Objective
We hypothesize that the reason these treatments are temporary reflects rapid recovery of mast cells from a desensitized state. We sought to test this.
Methods
Desensitization of IgE‐mediated histamine release from human lung mast cells was explored by methods that partially replicate the pattern of treatment during clinical desensitization. Specific and non‐specific desensitization and changes in surface IgE were examined following desensitization. Recovery from desensitization was also studied.
Results
Desensitization of mast cell responses was readily induced with concentrations of antigen or anti‐IgE that were suboptimal for secretion. There was little or no non‐specific desensitization when lung mast cells were exposed to antigens. There was no loss of cell surface IgE following desensitization. Removing the desensitizing stimulus from the media following desensitization allowed the cells to recover with half‐point of recovery of ~1.5 days and complete recovery after 5 days. Both the functional response and histamine content recovered within this time frame. The recovery appeared possible because both antigens and anti‐IgE dissociated rapidly from cells after washing to remove excess stimulus.
Conclusions and Clinical Relevance
Human lung mast cells readily recover from a desensitized state following removal of desensitizing antigen. This finding provides a potential explanation for the ephemeral nature of clinical desensitization.</description><subject>Allergens</subject><subject>antigen</subject><subject>Antigens</subject><subject>anti‐IgE</subject><subject>Cell surface</subject><subject>Desensitization</subject><subject>Food allergies</subject><subject>Histamine</subject><subject>human lung mast cell</subject><subject>Hypersensitivity</subject><subject>IgE</subject><subject>Immunoglobulin E</subject><subject>Immunological tolerance</subject><subject>Immunotherapy</subject><subject>Lungs</subject><subject>Mast cells</subject><subject>Secretion</subject><subject>Test procedures</subject><subject>Therapeutic applications</subject><issn>0954-7894</issn><issn>1365-2222</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKxDAUhoMoOl4WvoAE3OiimmvbLGUYLyAIXtahk55opU3GpFXGlY_gM_okRmd0IfhvDhw-fn4-hHYpOaIpxwaqI8oUZStoRHkuM5ayikZESZEVpRIbaDPGR0IIl6pcRxusZDzPZT5CN9dg_DOEObbBd7iGCC42ffNa9Y132Ft8cT_5eHuvYQauBtfjAHHmXYSIG4cfhq5yuB3cPe6q2GMDbRu30Zqt2gg7y7uF7k4nt-Pz7PLq7GJ8cpkZQRXLwAjguSVS1obnjCgKjBgorap5kT5cUkGsNVxKJUtRC8pAWCNLOVXE8IpvoYNF7yz4pwFir7smfi2oHPghaloWTBaiEHlC9_-gj34ILq3TaQpXZSEZS9ThgjLBxxjA6llouirMNSX6y7ROpvW36cTuLRuHaQf1L_mjNgHHC-ClaWH-f5MeT04WlZ_Pzodb</recordid><startdate>201708</startdate><enddate>201708</enddate><creator>Lewis, A.</creator><creator>MacGlashan, D. W.</creator><creator>Suvarna, S. K.</creator><creator>Peachell, P. T.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7272-3011</orcidid></search><sort><creationdate>201708</creationdate><title>Recovery from desensitization of IgE‐dependent responses in human lung mast cells</title><author>Lewis, A. ; MacGlashan, D. W. ; Suvarna, S. K. ; Peachell, P. T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4192-ec4e36f055dc362091e20ce8f9d37c3635140ffc3559584d412e4fc585b90c3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Allergens</topic><topic>antigen</topic><topic>Antigens</topic><topic>anti‐IgE</topic><topic>Cell surface</topic><topic>Desensitization</topic><topic>Food allergies</topic><topic>Histamine</topic><topic>human lung mast cell</topic><topic>Hypersensitivity</topic><topic>IgE</topic><topic>Immunoglobulin E</topic><topic>Immunological tolerance</topic><topic>Immunotherapy</topic><topic>Lungs</topic><topic>Mast cells</topic><topic>Secretion</topic><topic>Test procedures</topic><topic>Therapeutic applications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lewis, A.</creatorcontrib><creatorcontrib>MacGlashan, D. W.</creatorcontrib><creatorcontrib>Suvarna, S. K.</creatorcontrib><creatorcontrib>Peachell, P. T.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental allergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lewis, A.</au><au>MacGlashan, D. W.</au><au>Suvarna, S. K.</au><au>Peachell, P. T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recovery from desensitization of IgE‐dependent responses in human lung mast cells</atitle><jtitle>Clinical and experimental allergy</jtitle><addtitle>Clin Exp Allergy</addtitle><date>2017-08</date><risdate>2017</risdate><volume>47</volume><issue>8</issue><spage>1022</spage><epage>1031</epage><pages>1022-1031</pages><issn>0954-7894</issn><eissn>1365-2222</eissn><abstract>Summary
Background
Clinical desensitization and oral food immunotherapy are therapeutic interventions that allow individuals who react adversely to an allergen (drug or food) to be made tolerant to the allergen. However, tolerance is brief, and allergen hypersensitivity can recur within days following allergen withdrawal.
Objective
We hypothesize that the reason these treatments are temporary reflects rapid recovery of mast cells from a desensitized state. We sought to test this.
Methods
Desensitization of IgE‐mediated histamine release from human lung mast cells was explored by methods that partially replicate the pattern of treatment during clinical desensitization. Specific and non‐specific desensitization and changes in surface IgE were examined following desensitization. Recovery from desensitization was also studied.
Results
Desensitization of mast cell responses was readily induced with concentrations of antigen or anti‐IgE that were suboptimal for secretion. There was little or no non‐specific desensitization when lung mast cells were exposed to antigens. There was no loss of cell surface IgE following desensitization. Removing the desensitizing stimulus from the media following desensitization allowed the cells to recover with half‐point of recovery of ~1.5 days and complete recovery after 5 days. Both the functional response and histamine content recovered within this time frame. The recovery appeared possible because both antigens and anti‐IgE dissociated rapidly from cells after washing to remove excess stimulus.
Conclusions and Clinical Relevance
Human lung mast cells readily recover from a desensitized state following removal of desensitizing antigen. This finding provides a potential explanation for the ephemeral nature of clinical desensitization.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28236656</pmid><doi>10.1111/cea.12912</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-7272-3011</orcidid></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete |
subjects | Allergens antigen Antigens anti‐IgE Cell surface Desensitization Food allergies Histamine human lung mast cell Hypersensitivity IgE Immunoglobulin E Immunological tolerance Immunotherapy Lungs Mast cells Secretion Test procedures Therapeutic applications |
title | Recovery from desensitization of IgE‐dependent responses in human lung mast cells |
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