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...
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Veröffentlicht in: | Pediatric hematology and oncology 1992, Vol.9 (1), p.11-19 |
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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 |
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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&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 < 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</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 & 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 < 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</abstract><cop>Philadelphia, PA</cop><pub>Informa UK Ltd</pub><pmid>1558772</pmid><doi>10.3109/08880019209006391</doi><tpages>9</tpages></addata></record> |
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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 |
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