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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Veröffentlicht in:Journal of allergy and clinical immunology 2014-04, Vol.133 (4), p.1195-1202.e2
Hauptverfasser: 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
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container_end_page 1202.e2
container_issue 4
container_start_page 1195
container_title Journal of allergy and clinical immunology
container_volume 133
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] &gt; 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 &gt; 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28447058$$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] &gt; 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 &gt; 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. 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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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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] &gt; 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 &gt; 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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