Marked and persistent eosinophilia in the absence of clinical manifestations
Background Although most patients with hypereosinophilic syndromes (HES) present with clinical signs and symptoms attributable to eosinophilic tissue infiltration, some untreated patients remain asymptomatic or have signs and symptoms, such as allergic rhinitis, for which the relationship to periphe...
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creator | Chen, Yun-Yun K., BS Khoury, Paneez, MD Ware, JeanAnne M., MSN, CRNP Holland-Thomas, Nicole C., MSN Stoddard, Jennifer L., BS Gurprasad, Shakuntala, BS Waldner, Amy J., BA Klion, Amy D., MD |
description | Background Although most patients with hypereosinophilic syndromes (HES) present with clinical signs and symptoms attributable to eosinophilic tissue infiltration, some untreated patients remain asymptomatic or have signs and symptoms, such as allergic rhinitis, for which the relationship to peripheral eosinophilia is unclear (hypereosinophilia of unknown significance [HEUS ]). Objective To identify and characterize subjects with HEUS of 5 years duration or more as compared to untreated patients with symptomatic HES and healthy normal volunteers. Methods All subjects with eosinophilia underwent yearly evaluation, including a standardized clinical evaluation, whole blood flow cytometry to assess lymphocyte subsets and eosinophil activation, and serum collection. Peripheral blood mononuclear cells were cultured overnight with and without phorbol 12-myristate 13-acetate/ionomycin. Cytokines and chemokines were measured in serum and cell supernatants, and mRNA expression was assessed by using quantitative real-time PCR. Results Eight of the 210 subjects referred for the evaluation of eosinophilia (absolute eosinophil count [AEC] > 1500/μL) met the criteria for HEUS of 5 years duration or more (range, 7-29 years). Peak eosinophil count and surface expression of eosinophil activation markers were similar in subjects with HEUS and in untreated subjects with platelet-derived growth factor alpha–negative HES (n = 28). Aberrant or clonal T-cell populations were identified in 50% of the subjects with HEUS as compared to 29% of the subjects with HES ( P = .12). Increased levels of IL-5, GM-CSF, IL-9, and IL-17A were also comparable in subjects with HEUS and HES. Serum levels of IgE and IL-13 were significantly increased only in subjects with HES. Conclusions A small number of patients with persistent peripheral eosinophilia (AEC > 1500/μL) appear to have clinically benign disease. |
doi_str_mv | 10.1016/j.jaci.2013.06.037 |
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Objective To identify and characterize subjects with HEUS of 5 years duration or more as compared to untreated patients with symptomatic HES and healthy normal volunteers. Methods All subjects with eosinophilia underwent yearly evaluation, including a standardized clinical evaluation, whole blood flow cytometry to assess lymphocyte subsets and eosinophil activation, and serum collection. Peripheral blood mononuclear cells were cultured overnight with and without phorbol 12-myristate 13-acetate/ionomycin. Cytokines and chemokines were measured in serum and cell supernatants, and mRNA expression was assessed by using quantitative real-time PCR. Results Eight of the 210 subjects referred for the evaluation of eosinophilia (absolute eosinophil count [AEC] > 1500/μL) met the criteria for HEUS of 5 years duration or more (range, 7-29 years). Peak eosinophil count and surface expression of eosinophil activation markers were similar in subjects with HEUS and in untreated subjects with platelet-derived growth factor alpha–negative HES (n = 28). Aberrant or clonal T-cell populations were identified in 50% of the subjects with HEUS as compared to 29% of the subjects with HES ( P = .12). Increased levels of IL-5, GM-CSF, IL-9, and IL-17A were also comparable in subjects with HEUS and HES. Serum levels of IgE and IL-13 were significantly increased only in subjects with HES. Conclusions A small number of patients with persistent peripheral eosinophilia (AEC > 1500/μL) appear to have clinically benign disease.</description><identifier>ISSN: 0091-6749</identifier><identifier>EISSN: 1097-6825</identifier><identifier>DOI: 10.1016/j.jaci.2013.06.037</identifier><identifier>PMID: 23987798</identifier><identifier>CODEN: JACIBY</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Abdomen ; Adolescent ; Adult ; Aged ; Aged, 80 and over ; Allergy and Immunology ; Biological and medical sciences ; Blood banks ; Bone marrow ; Chemokine CCL17 - blood ; Chemokine CCL17 - genetics ; Chemokines ; Child ; cytokine ; Cytokines ; Cytokines - blood ; Cytokines - genetics ; Diarrhea ; Eosinophil ; Eosinophilia - blood ; Eosinophilia - diagnosis ; Eosinophilia - genetics ; Eosinophils - immunology ; Eosinophils - metabolism ; Female ; Fever ; Flow cytometry ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Gene expression ; Hematologic and hematopoietic diseases ; Hepatitis ; Humans ; hypereosinophilic syndrome ; Hypereosinophilic Syndrome - blood ; Hypereosinophilic Syndrome - diagnosis ; Hypereosinophilic Syndrome - genetics ; Immunopathology ; Laboratories ; Leukocyte Count ; Male ; Medical sciences ; Medical treatment ; Middle Aged ; Mortality ; Other diseases. Hematologic involvement in other diseases ; Pain ; pathogenesis ; Phenotype ; Review boards ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Studies ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Young Adult</subject><ispartof>Journal of allergy and clinical immunology, 2014-04, Vol.133 (4), p.1195-1202.e2</ispartof><rights>2013</rights><rights>2015 INIST-CNRS</rights><rights>Published by Mosby, Inc.</rights><rights>Copyright Elsevier Limited Apr 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c601t-f10478fe7bf5fc26e7e807be1c08cd92ffe230675f9845a2fde405c621b208cf3</citedby><cites>FETCH-LOGICAL-c601t-f10478fe7bf5fc26e7e807be1c08cd92ffe230675f9845a2fde405c621b208cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0091674913010543$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28447058$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23987798$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Yun-Yun K., BS</creatorcontrib><creatorcontrib>Khoury, Paneez, MD</creatorcontrib><creatorcontrib>Ware, JeanAnne M., MSN, CRNP</creatorcontrib><creatorcontrib>Holland-Thomas, Nicole C., MSN</creatorcontrib><creatorcontrib>Stoddard, Jennifer L., BS</creatorcontrib><creatorcontrib>Gurprasad, Shakuntala, BS</creatorcontrib><creatorcontrib>Waldner, Amy J., BA</creatorcontrib><creatorcontrib>Klion, Amy D., MD</creatorcontrib><title>Marked and persistent eosinophilia in the absence of clinical manifestations</title><title>Journal of allergy and clinical immunology</title><addtitle>J Allergy Clin Immunol</addtitle><description>Background Although most patients with hypereosinophilic syndromes (HES) present with clinical signs and symptoms attributable to eosinophilic tissue infiltration, some untreated patients remain asymptomatic or have signs and symptoms, such as allergic rhinitis, for which the relationship to peripheral eosinophilia is unclear (hypereosinophilia of unknown significance [HEUS ]). Objective To identify and characterize subjects with HEUS of 5 years duration or more as compared to untreated patients with symptomatic HES and healthy normal volunteers. Methods All subjects with eosinophilia underwent yearly evaluation, including a standardized clinical evaluation, whole blood flow cytometry to assess lymphocyte subsets and eosinophil activation, and serum collection. Peripheral blood mononuclear cells were cultured overnight with and without phorbol 12-myristate 13-acetate/ionomycin. Cytokines and chemokines were measured in serum and cell supernatants, and mRNA expression was assessed by using quantitative real-time PCR. Results Eight of the 210 subjects referred for the evaluation of eosinophilia (absolute eosinophil count [AEC] > 1500/μL) met the criteria for HEUS of 5 years duration or more (range, 7-29 years). Peak eosinophil count and surface expression of eosinophil activation markers were similar in subjects with HEUS and in untreated subjects with platelet-derived growth factor alpha–negative HES (n = 28). Aberrant or clonal T-cell populations were identified in 50% of the subjects with HEUS as compared to 29% of the subjects with HES ( P = .12). Increased levels of IL-5, GM-CSF, IL-9, and IL-17A were also comparable in subjects with HEUS and HES. Serum levels of IgE and IL-13 were significantly increased only in subjects with HES. Conclusions A small number of patients with persistent peripheral eosinophilia (AEC > 1500/μL) appear to have clinically benign disease.</description><subject>Abdomen</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Allergy and Immunology</subject><subject>Biological and medical sciences</subject><subject>Blood banks</subject><subject>Bone marrow</subject><subject>Chemokine CCL17 - blood</subject><subject>Chemokine CCL17 - genetics</subject><subject>Chemokines</subject><subject>Child</subject><subject>cytokine</subject><subject>Cytokines</subject><subject>Cytokines - blood</subject><subject>Cytokines - genetics</subject><subject>Diarrhea</subject><subject>Eosinophil</subject><subject>Eosinophilia - blood</subject><subject>Eosinophilia - diagnosis</subject><subject>Eosinophilia - genetics</subject><subject>Eosinophils - immunology</subject><subject>Eosinophils - metabolism</subject><subject>Female</subject><subject>Fever</subject><subject>Flow cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Gene expression</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hepatitis</subject><subject>Humans</subject><subject>hypereosinophilic syndrome</subject><subject>Hypereosinophilic Syndrome - blood</subject><subject>Hypereosinophilic Syndrome - diagnosis</subject><subject>Hypereosinophilic Syndrome - genetics</subject><subject>Immunopathology</subject><subject>Laboratories</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Other diseases. Hematologic involvement in other diseases</subject><subject>Pain</subject><subject>pathogenesis</subject><subject>Phenotype</subject><subject>Review boards</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Studies</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Young Adult</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl1rFDEUhgdR7Lb6B7yQARF6s-tJMpMPkIIUv2DFC_U6ZDInbqazyZrMFvrvzbDbVnshXoWQ55y8yXOq6gWBFQHC3wyrwVi_okDYCvgKmHhULQgoseSSto-rBYAiSy4adVKd5jxA2TOpnlYnlCkphJKLav3FpCvsaxP6eocp-zxhmGqM2Ye42_jRm9qHetpgbbqMwWIdXW1HH7w1Y701wTvMk5l8DPlZ9cSZMePz43pW_fjw_vvlp-X668fPl-_WS8uBTEtHoBHSoehc6yzlKFCC6JBYkLZX1DmkDLhonZJNa6jrsYHWcko6WgjHzqqLQ9_dvttib0viZEa9S35r0o2Oxuu_T4Lf6J_xWjPFWiV5aXB-bJDir33Jr7c-WxxHEzDusyYt55IpIuV_oIRIShWhBX31AB3iPoXyE5rwphFCcMUKRQ-UTTHnhO4uNwE9e9WDnr3q2asGrovXUvTyzxffldyKLMDrI2ByEeOSCdbne06W-6GdubcHDoufa49JZ-tnrb1PaCfdR__vHBcPym9H4QpvMN-_V2eqQX-bJ3AeQMKAQNsw9htvt9Y9</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Chen, Yun-Yun K., BS</creator><creator>Khoury, Paneez, MD</creator><creator>Ware, JeanAnne M., MSN, CRNP</creator><creator>Holland-Thomas, Nicole C., MSN</creator><creator>Stoddard, Jennifer L., BS</creator><creator>Gurprasad, Shakuntala, BS</creator><creator>Waldner, Amy J., BA</creator><creator>Klion, Amy D., MD</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140401</creationdate><title>Marked and persistent eosinophilia in the absence of clinical manifestations</title><author>Chen, Yun-Yun K., BS ; Khoury, Paneez, MD ; Ware, JeanAnne M., MSN, CRNP ; Holland-Thomas, Nicole C., MSN ; Stoddard, Jennifer L., BS ; Gurprasad, Shakuntala, BS ; Waldner, Amy J., BA ; Klion, Amy D., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c601t-f10478fe7bf5fc26e7e807be1c08cd92ffe230675f9845a2fde405c621b208cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Abdomen</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Allergy and Immunology</topic><topic>Biological and medical sciences</topic><topic>Blood banks</topic><topic>Bone marrow</topic><topic>Chemokine CCL17 - blood</topic><topic>Chemokine CCL17 - genetics</topic><topic>Chemokines</topic><topic>Child</topic><topic>cytokine</topic><topic>Cytokines</topic><topic>Cytokines - blood</topic><topic>Cytokines - genetics</topic><topic>Diarrhea</topic><topic>Eosinophil</topic><topic>Eosinophilia - blood</topic><topic>Eosinophilia - diagnosis</topic><topic>Eosinophilia - genetics</topic><topic>Eosinophils - immunology</topic><topic>Eosinophils - metabolism</topic><topic>Female</topic><topic>Fever</topic><topic>Flow cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Gene expression</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hepatitis</topic><topic>Humans</topic><topic>hypereosinophilic syndrome</topic><topic>Hypereosinophilic Syndrome - blood</topic><topic>Hypereosinophilic Syndrome - diagnosis</topic><topic>Hypereosinophilic Syndrome - genetics</topic><topic>Immunopathology</topic><topic>Laboratories</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Other diseases. Hematologic involvement in other diseases</topic><topic>Pain</topic><topic>pathogenesis</topic><topic>Phenotype</topic><topic>Review boards</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Studies</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Yun-Yun K., BS</creatorcontrib><creatorcontrib>Khoury, Paneez, MD</creatorcontrib><creatorcontrib>Ware, JeanAnne M., MSN, CRNP</creatorcontrib><creatorcontrib>Holland-Thomas, Nicole C., MSN</creatorcontrib><creatorcontrib>Stoddard, Jennifer L., BS</creatorcontrib><creatorcontrib>Gurprasad, Shakuntala, BS</creatorcontrib><creatorcontrib>Waldner, Amy J., BA</creatorcontrib><creatorcontrib>Klion, Amy D., MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Yun-Yun K., BS</au><au>Khoury, Paneez, MD</au><au>Ware, JeanAnne M., MSN, CRNP</au><au>Holland-Thomas, Nicole C., MSN</au><au>Stoddard, Jennifer L., BS</au><au>Gurprasad, Shakuntala, BS</au><au>Waldner, Amy J., BA</au><au>Klion, Amy D., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Marked and persistent eosinophilia in the absence of clinical manifestations</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>2014-04-01</date><risdate>2014</risdate><volume>133</volume><issue>4</issue><spage>1195</spage><epage>1202.e2</epage><pages>1195-1202.e2</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Background Although most patients with hypereosinophilic syndromes (HES) present with clinical signs and symptoms attributable to eosinophilic tissue infiltration, some untreated patients remain asymptomatic or have signs and symptoms, such as allergic rhinitis, for which the relationship to peripheral eosinophilia is unclear (hypereosinophilia of unknown significance [HEUS ]). Objective To identify and characterize subjects with HEUS of 5 years duration or more as compared to untreated patients with symptomatic HES and healthy normal volunteers. Methods All subjects with eosinophilia underwent yearly evaluation, including a standardized clinical evaluation, whole blood flow cytometry to assess lymphocyte subsets and eosinophil activation, and serum collection. Peripheral blood mononuclear cells were cultured overnight with and without phorbol 12-myristate 13-acetate/ionomycin. Cytokines and chemokines were measured in serum and cell supernatants, and mRNA expression was assessed by using quantitative real-time PCR. Results Eight of the 210 subjects referred for the evaluation of eosinophilia (absolute eosinophil count [AEC] > 1500/μL) met the criteria for HEUS of 5 years duration or more (range, 7-29 years). Peak eosinophil count and surface expression of eosinophil activation markers were similar in subjects with HEUS and in untreated subjects with platelet-derived growth factor alpha–negative HES (n = 28). Aberrant or clonal T-cell populations were identified in 50% of the subjects with HEUS as compared to 29% of the subjects with HES ( P = .12). Increased levels of IL-5, GM-CSF, IL-9, and IL-17A were also comparable in subjects with HEUS and HES. Serum levels of IgE and IL-13 were significantly increased only in subjects with HES. Conclusions A small number of patients with persistent peripheral eosinophilia (AEC > 1500/μL) appear to have clinically benign disease.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>23987798</pmid><doi>10.1016/j.jaci.2013.06.037</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Adolescent Adult Aged Aged, 80 and over Allergy and Immunology Biological and medical sciences Blood banks Bone marrow Chemokine CCL17 - blood Chemokine CCL17 - genetics Chemokines Child cytokine Cytokines Cytokines - blood Cytokines - genetics Diarrhea Eosinophil Eosinophilia - blood Eosinophilia - diagnosis Eosinophilia - genetics Eosinophils - immunology Eosinophils - metabolism Female Fever Flow cytometry Fundamental and applied biological sciences. Psychology Fundamental immunology Gene expression Hematologic and hematopoietic diseases Hepatitis Humans hypereosinophilic syndrome Hypereosinophilic Syndrome - blood Hypereosinophilic Syndrome - diagnosis Hypereosinophilic Syndrome - genetics Immunopathology Laboratories Leukocyte Count Male Medical sciences Medical treatment Middle Aged Mortality Other diseases. Hematologic involvement in other diseases Pain pathogenesis Phenotype Review boards Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Studies T-Lymphocytes - immunology T-Lymphocytes - metabolism Young Adult |
title | Marked and persistent eosinophilia in the absence of clinical manifestations |
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