Immunological Study of Childhood Acute ITP at Onset

We attempted to search for any specific change in the immune system during the onset of childhood acute immune thrombocytopenic purpura (ITP) in order to clarify the pathophysiology of acute ITP by examining the lymphocyte subset, lymphocyte blastogenic response, serum complements, and immunoglob-ul...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pediatric hematology and oncology 1992, Vol.9 (1), p.11-19
Hauptverfasser: Koyanagi, Hideki, Kishida, Kunio, Shimomura, Kunihisa, Kurokawa, Michiko, Deguchi, Tomohiro, Shimoda, Yuuji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 19
container_issue 1
container_start_page 11
container_title Pediatric hematology and oncology
container_volume 9
creator Koyanagi, Hideki
Kishida, Kunio
Shimomura, Kunihisa
Kurokawa, Michiko
Deguchi, Tomohiro
Shimoda, Yuuji
description We attempted to search for any specific change in the immune system during the onset of childhood acute immune thrombocytopenic purpura (ITP) in order to clarify the pathophysiology of acute ITP by examining the lymphocyte subset, lymphocyte blastogenic response, serum complements, and immunoglob-ulins in 18 patients with childhood acute ITP and 18 controls (control values after normalization). At the onset of acute ITP the levels of serum complements and IgG and IgA were found to be within the normal ranges, but serum IgM levels were paier than 200 mg/dL in six cases among 18 patients. Lymphocyte blastogenic response to phytohemagglutinin (PHA) and concanavalin A (ConA) was depressed in patients relative to controls (PHA: p < 0.05, ConA: p < 0.01). Lymphocyte blastogenic response to pokewood mitogen (PWM) was lower than that of the control, but no statistical significance was observed. There was no difference in the proportion of CD3, CD4, CD8, SmIg, SmIgG, SmIgM, SmIgA, and SmIgD. The CD4/CD8 ratio was not different from that of controls. The proportion of CD38 was higher than that of control, but no significant difference from the control was observed Increase in the serum IgM level and proportion of CD38 and depressed lymphocyte blastogenic response may be the influence of preceding infection. It has been reported that the CD4/CD8 ratio is depressed due to an increase in the CD8 level in acute and convalescent phases of viral infection. However, the proportion of CD8 was not necessarily increased in our patient in whom preceding infection was obvious. The immunological status of the patients with acute ITP at onset differs from that afier infection
doi_str_mv 10.3109/08880019209006391
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_3109_08880019209006391</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72875498</sourcerecordid><originalsourceid>FETCH-LOGICAL-c430t-b4b12d8ba19395f793ebe8e5ce43ed1572204cb46e5b8b49208f935427fa50173</originalsourceid><addsrcrecordid>eNp9kF1LwzAUhoMoc05_gBdCL8S7aj6bBL0Zw4_BYILzuqRpajvSZiYtsn9vR6cigle5eJ_3nJwHgHMErwmC8gYKISBEEkMJYUIkOgBjxDCKYZLIQzDe5XEPiGNwEsIaQogJxyMwQowJzvEYkHldd42z7q3SykYvbZdvI1dEs7KyeelcHk1115povnqOVBstm2DaU3BUKBvM2f6dgNeH-9XsKV4sH-ez6SLWlMA2zmiGcC4yhSSRrOCSmMwIw7ShxOSIcYwh1RlNDMtERvsjRCEJo5gXikHEyQRcDXM33r13JrRpXQVtrFWNcV1IORacUSl6EA2g9i4Eb4p046ta-W2KYLoTlf4R1Xcu9sO7rDb5T2Mw0-eX-1yF3kzhVaOr8I0xxBPEdqvvBqxqCudr9eG8zdNWba3zXx3y3y9uf9VLo2xbauVNunadb3q9_9zwCftykp4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72875498</pqid></control><display><type>article</type><title>Immunological Study of Childhood Acute ITP at Onset</title><source>MEDLINE</source><source>Taylor &amp; Francis Medical Library - CRKN</source><source>Taylor &amp; Francis Journals Complete</source><creator>Koyanagi, Hideki ; Kishida, Kunio ; Shimomura, Kunihisa ; Kurokawa, Michiko ; Deguchi, Tomohiro ; Shimoda, Yuuji</creator><creatorcontrib>Koyanagi, Hideki ; Kishida, Kunio ; Shimomura, Kunihisa ; Kurokawa, Michiko ; Deguchi, Tomohiro ; Shimoda, Yuuji</creatorcontrib><description>We attempted to search for any specific change in the immune system during the onset of childhood acute immune thrombocytopenic purpura (ITP) in order to clarify the pathophysiology of acute ITP by examining the lymphocyte subset, lymphocyte blastogenic response, serum complements, and immunoglob-ulins in 18 patients with childhood acute ITP and 18 controls (control values after normalization). At the onset of acute ITP the levels of serum complements and IgG and IgA were found to be within the normal ranges, but serum IgM levels were paier than 200 mg/dL in six cases among 18 patients. Lymphocyte blastogenic response to phytohemagglutinin (PHA) and concanavalin A (ConA) was depressed in patients relative to controls (PHA: p &lt; 0.05, ConA: p &lt; 0.01). Lymphocyte blastogenic response to pokewood mitogen (PWM) was lower than that of the control, but no statistical significance was observed. There was no difference in the proportion of CD3, CD4, CD8, SmIg, SmIgG, SmIgM, SmIgA, and SmIgD. The CD4/CD8 ratio was not different from that of controls. The proportion of CD38 was higher than that of control, but no significant difference from the control was observed Increase in the serum IgM level and proportion of CD38 and depressed lymphocyte blastogenic response may be the influence of preceding infection. It has been reported that the CD4/CD8 ratio is depressed due to an increase in the CD8 level in acute and convalescent phases of viral infection. However, the proportion of CD8 was not necessarily increased in our patient in whom preceding infection was obvious. The immunological status of the patients with acute ITP at onset differs from that afier infection</description><identifier>ISSN: 0888-0018</identifier><identifier>EISSN: 1521-0669</identifier><identifier>DOI: 10.3109/08880019209006391</identifier><identifier>PMID: 1558772</identifier><identifier>CODEN: PHONEN</identifier><language>eng</language><publisher>Philadelphia, PA: Informa UK Ltd</publisher><subject>Acute Disease ; acute ITP lymphocyte bladogentc response ; ADP-ribosyl Cyclase ; ADP-ribosyl Cyclase 1 ; Antigens, CD ; Antigens, Differentiation - analysis ; Biological and medical sciences ; Child ; Child, Preschool ; Female ; Hematologic and hematopoietic diseases ; Humans ; Infant ; Lymphocyte Activation ; lymphocyte subset ; Lymphocyte Subsets - immunology ; Male ; Medical sciences ; Membrane Glycoproteins ; Platelet diseases and coagulopathies ; Purpura, Thrombocytopenic, Idiopathic - immunology</subject><ispartof>Pediatric hematology and oncology, 1992, Vol.9 (1), p.11-19</ispartof><rights>1992 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1992</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-b4b12d8ba19395f793ebe8e5ce43ed1572204cb46e5b8b49208f935427fa50173</citedby><cites>FETCH-LOGICAL-c430t-b4b12d8ba19395f793ebe8e5ce43ed1572204cb46e5b8b49208f935427fa50173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/08880019209006391$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/08880019209006391$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,776,780,4010,27900,27901,27902,59620,59726,60409,60515,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=5176158$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1558772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koyanagi, Hideki</creatorcontrib><creatorcontrib>Kishida, Kunio</creatorcontrib><creatorcontrib>Shimomura, Kunihisa</creatorcontrib><creatorcontrib>Kurokawa, Michiko</creatorcontrib><creatorcontrib>Deguchi, Tomohiro</creatorcontrib><creatorcontrib>Shimoda, Yuuji</creatorcontrib><title>Immunological Study of Childhood Acute ITP at Onset</title><title>Pediatric hematology and oncology</title><addtitle>Pediatr Hematol Oncol</addtitle><description>We attempted to search for any specific change in the immune system during the onset of childhood acute immune thrombocytopenic purpura (ITP) in order to clarify the pathophysiology of acute ITP by examining the lymphocyte subset, lymphocyte blastogenic response, serum complements, and immunoglob-ulins in 18 patients with childhood acute ITP and 18 controls (control values after normalization). At the onset of acute ITP the levels of serum complements and IgG and IgA were found to be within the normal ranges, but serum IgM levels were paier than 200 mg/dL in six cases among 18 patients. Lymphocyte blastogenic response to phytohemagglutinin (PHA) and concanavalin A (ConA) was depressed in patients relative to controls (PHA: p &lt; 0.05, ConA: p &lt; 0.01). Lymphocyte blastogenic response to pokewood mitogen (PWM) was lower than that of the control, but no statistical significance was observed. There was no difference in the proportion of CD3, CD4, CD8, SmIg, SmIgG, SmIgM, SmIgA, and SmIgD. The CD4/CD8 ratio was not different from that of controls. The proportion of CD38 was higher than that of control, but no significant difference from the control was observed Increase in the serum IgM level and proportion of CD38 and depressed lymphocyte blastogenic response may be the influence of preceding infection. It has been reported that the CD4/CD8 ratio is depressed due to an increase in the CD8 level in acute and convalescent phases of viral infection. However, the proportion of CD8 was not necessarily increased in our patient in whom preceding infection was obvious. The immunological status of the patients with acute ITP at onset differs from that afier infection</description><subject>Acute Disease</subject><subject>acute ITP lymphocyte bladogentc response</subject><subject>ADP-ribosyl Cyclase</subject><subject>ADP-ribosyl Cyclase 1</subject><subject>Antigens, CD</subject><subject>Antigens, Differentiation - analysis</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Lymphocyte Activation</subject><subject>lymphocyte subset</subject><subject>Lymphocyte Subsets - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins</subject><subject>Platelet diseases and coagulopathies</subject><subject>Purpura, Thrombocytopenic, Idiopathic - immunology</subject><issn>0888-0018</issn><issn>1521-0669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1LwzAUhoMoc05_gBdCL8S7aj6bBL0Zw4_BYILzuqRpajvSZiYtsn9vR6cigle5eJ_3nJwHgHMErwmC8gYKISBEEkMJYUIkOgBjxDCKYZLIQzDe5XEPiGNwEsIaQogJxyMwQowJzvEYkHldd42z7q3SykYvbZdvI1dEs7KyeelcHk1115povnqOVBstm2DaU3BUKBvM2f6dgNeH-9XsKV4sH-ez6SLWlMA2zmiGcC4yhSSRrOCSmMwIw7ShxOSIcYwh1RlNDMtERvsjRCEJo5gXikHEyQRcDXM33r13JrRpXQVtrFWNcV1IORacUSl6EA2g9i4Eb4p046ta-W2KYLoTlf4R1Xcu9sO7rDb5T2Mw0-eX-1yF3kzhVaOr8I0xxBPEdqvvBqxqCudr9eG8zdNWba3zXx3y3y9uf9VLo2xbauVNunadb3q9_9zwCftykp4</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Koyanagi, Hideki</creator><creator>Kishida, Kunio</creator><creator>Shimomura, Kunihisa</creator><creator>Kurokawa, Michiko</creator><creator>Deguchi, Tomohiro</creator><creator>Shimoda, Yuuji</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</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>7X8</scope></search><sort><creationdate>1992</creationdate><title>Immunological Study of Childhood Acute ITP at Onset</title><author>Koyanagi, Hideki ; Kishida, Kunio ; Shimomura, Kunihisa ; Kurokawa, Michiko ; Deguchi, Tomohiro ; Shimoda, Yuuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-b4b12d8ba19395f793ebe8e5ce43ed1572204cb46e5b8b49208f935427fa50173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Acute Disease</topic><topic>acute ITP lymphocyte bladogentc response</topic><topic>ADP-ribosyl Cyclase</topic><topic>ADP-ribosyl Cyclase 1</topic><topic>Antigens, CD</topic><topic>Antigens, Differentiation - analysis</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Lymphocyte Activation</topic><topic>lymphocyte subset</topic><topic>Lymphocyte Subsets - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins</topic><topic>Platelet diseases and coagulopathies</topic><topic>Purpura, Thrombocytopenic, Idiopathic - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koyanagi, Hideki</creatorcontrib><creatorcontrib>Kishida, Kunio</creatorcontrib><creatorcontrib>Shimomura, Kunihisa</creatorcontrib><creatorcontrib>Kurokawa, Michiko</creatorcontrib><creatorcontrib>Deguchi, Tomohiro</creatorcontrib><creatorcontrib>Shimoda, Yuuji</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>MEDLINE - Academic</collection><jtitle>Pediatric hematology and oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koyanagi, Hideki</au><au>Kishida, Kunio</au><au>Shimomura, Kunihisa</au><au>Kurokawa, Michiko</au><au>Deguchi, Tomohiro</au><au>Shimoda, Yuuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunological Study of Childhood Acute ITP at Onset</atitle><jtitle>Pediatric hematology and oncology</jtitle><addtitle>Pediatr Hematol Oncol</addtitle><date>1992</date><risdate>1992</risdate><volume>9</volume><issue>1</issue><spage>11</spage><epage>19</epage><pages>11-19</pages><issn>0888-0018</issn><eissn>1521-0669</eissn><coden>PHONEN</coden><abstract>We attempted to search for any specific change in the immune system during the onset of childhood acute immune thrombocytopenic purpura (ITP) in order to clarify the pathophysiology of acute ITP by examining the lymphocyte subset, lymphocyte blastogenic response, serum complements, and immunoglob-ulins in 18 patients with childhood acute ITP and 18 controls (control values after normalization). At the onset of acute ITP the levels of serum complements and IgG and IgA were found to be within the normal ranges, but serum IgM levels were paier than 200 mg/dL in six cases among 18 patients. Lymphocyte blastogenic response to phytohemagglutinin (PHA) and concanavalin A (ConA) was depressed in patients relative to controls (PHA: p &lt; 0.05, ConA: p &lt; 0.01). Lymphocyte blastogenic response to pokewood mitogen (PWM) was lower than that of the control, but no statistical significance was observed. There was no difference in the proportion of CD3, CD4, CD8, SmIg, SmIgG, SmIgM, SmIgA, and SmIgD. The CD4/CD8 ratio was not different from that of controls. The proportion of CD38 was higher than that of control, but no significant difference from the control was observed Increase in the serum IgM level and proportion of CD38 and depressed lymphocyte blastogenic response may be the influence of preceding infection. It has been reported that the CD4/CD8 ratio is depressed due to an increase in the CD8 level in acute and convalescent phases of viral infection. However, the proportion of CD8 was not necessarily increased in our patient in whom preceding infection was obvious. The immunological status of the patients with acute ITP at onset differs from that afier infection</abstract><cop>Philadelphia, PA</cop><pub>Informa UK Ltd</pub><pmid>1558772</pmid><doi>10.3109/08880019209006391</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0888-0018
ispartof Pediatric hematology and oncology, 1992, Vol.9 (1), p.11-19
issn 0888-0018
1521-0669
language eng
recordid cdi_crossref_primary_10_3109_08880019209006391
source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects Acute Disease
acute ITP lymphocyte bladogentc response
ADP-ribosyl Cyclase
ADP-ribosyl Cyclase 1
Antigens, CD
Antigens, Differentiation - analysis
Biological and medical sciences
Child
Child, Preschool
Female
Hematologic and hematopoietic diseases
Humans
Infant
Lymphocyte Activation
lymphocyte subset
Lymphocyte Subsets - immunology
Male
Medical sciences
Membrane Glycoproteins
Platelet diseases and coagulopathies
Purpura, Thrombocytopenic, Idiopathic - immunology
title Immunological Study of Childhood Acute ITP at Onset
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T16%3A05%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunological%20Study%20of%20Childhood%20Acute%20ITP%20at%20Onset&rft.jtitle=Pediatric%20hematology%20and%20oncology&rft.au=Koyanagi,%20Hideki&rft.date=1992&rft.volume=9&rft.issue=1&rft.spage=11&rft.epage=19&rft.pages=11-19&rft.issn=0888-0018&rft.eissn=1521-0669&rft.coden=PHONEN&rft_id=info:doi/10.3109/08880019209006391&rft_dat=%3Cproquest_cross%3E72875498%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=72875498&rft_id=info:pmid/1558772&rfr_iscdi=true