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Multivariate analysis of T‐cell functional defects and circulating serum factors in hodgkin's disease
A comprehensive immunologic and serologic analysis was performed on 31 untreated patients with Hodgkin's disease. Immune evaluations stressed T‐cell functional activity and included traditional parameters (PHA responsiveness and delayed hypersensitivity skin reactivity), as well as newer functi...
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Published in: | Cancer 1981-08, Vol.48 (4), p.964-973 |
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creator | Schulof, Richard S. Bockman, Richard S. Garofalo, John A. Cirrincione, Constance Cunningham‐Rundles, Susanna Fernandes, Gabriel Day, Noorbibi K. Pinsky, Carl M. Incefy, Genevieve S. Thaler, Howard T. Good, Robert A. Gupta, Sudhir |
description | A comprehensive immunologic and serologic analysis was performed on 31 untreated patients with Hodgkin's disease. Immune evaluations stressed T‐cell functional activity and included traditional parameters (PHA responsiveness and delayed hypersensitivity skin reactivity), as well as newer functional assays (T‐cell colony formation, chemotaxis, spontaneous and antibody‐dependent cytotoxicity, and concanavalin A‐induced suppressor cell activity (CISA)). Serum factors included ferritin, prostaglandins, zinc, copper, immune complexes, and thymic hormone activity. Every patient exhibited at least one T‐cell or serum abnormality. The greatest percentage of patients exhibited T‐cell defects in chemotaxis (85%), colony formation (81%), and PHA reactivity (64%). Immune defects were more common with advanced disease but were not related to absolute T‐cell or monocyte count, skin test anergy, or abnormalities of Tμ/Tγ cell proportions. Linear relationships were identified among abnormalities in the three assays employing mononuclear cells (PHA, colony formation, CISA) which may have reflected the inhibitory influence of monocytes present in the mononuclear cell preparations. Low serum zinc correlated with marked impairment of T‐cell chemotaxis. Elevated prostaglandins were associated with high PHA reactivity and with depressed colony formation. Our results indicate that many complex factors, including intrinsic T‐cell defects, contribute to the impaired immunity associated with Hodgkin's disease. |
doi_str_mv | 10.1002/1097-0142(19810815)48:4<964::AID-CNCR2820480419>3.0.CO;2-B |
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Immune evaluations stressed T‐cell functional activity and included traditional parameters (PHA responsiveness and delayed hypersensitivity skin reactivity), as well as newer functional assays (T‐cell colony formation, chemotaxis, spontaneous and antibody‐dependent cytotoxicity, and concanavalin A‐induced suppressor cell activity (CISA)). Serum factors included ferritin, prostaglandins, zinc, copper, immune complexes, and thymic hormone activity. Every patient exhibited at least one T‐cell or serum abnormality. The greatest percentage of patients exhibited T‐cell defects in chemotaxis (85%), colony formation (81%), and PHA reactivity (64%). Immune defects were more common with advanced disease but were not related to absolute T‐cell or monocyte count, skin test anergy, or abnormalities of Tμ/Tγ cell proportions. Linear relationships were identified among abnormalities in the three assays employing mononuclear cells (PHA, colony formation, CISA) which may have reflected the inhibitory influence of monocytes present in the mononuclear cell preparations. Low serum zinc correlated with marked impairment of T‐cell chemotaxis. Elevated prostaglandins were associated with high PHA reactivity and with depressed colony formation. Our results indicate that many complex factors, including intrinsic T‐cell defects, contribute to the impaired immunity associated with Hodgkin's disease.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19810815)48:4<964::AID-CNCR2820480419>3.0.CO;2-B</identifier><identifier>PMID: 6456060</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adolescent ; Adult ; Aged ; Antibody-Dependent Cell Cytotoxicity ; Antigen-Antibody Complex - analysis ; Female ; Ferritins - blood ; Hodgkin Disease - immunology ; Hodgkin Disease - metabolism ; Humans ; Leukocyte Count ; Lymphocyte Activation ; Male ; Middle Aged ; Prostaglandins E - blood ; Skin Tests ; T-Lymphocytes - immunology ; T-Lymphocytes, Regulatory</subject><ispartof>Cancer, 1981-08, Vol.48 (4), p.964-973</ispartof><rights>Copyright © 1981 American Cancer Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4979-b5eed570b63d6e7cca46fc93c4b8dc1ee124719b2e7356880a9be316cca76fcb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6456060$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schulof, Richard S.</creatorcontrib><creatorcontrib>Bockman, Richard S.</creatorcontrib><creatorcontrib>Garofalo, John A.</creatorcontrib><creatorcontrib>Cirrincione, Constance</creatorcontrib><creatorcontrib>Cunningham‐Rundles, Susanna</creatorcontrib><creatorcontrib>Fernandes, Gabriel</creatorcontrib><creatorcontrib>Day, Noorbibi K.</creatorcontrib><creatorcontrib>Pinsky, Carl M.</creatorcontrib><creatorcontrib>Incefy, Genevieve S.</creatorcontrib><creatorcontrib>Thaler, Howard T.</creatorcontrib><creatorcontrib>Good, Robert A.</creatorcontrib><creatorcontrib>Gupta, Sudhir</creatorcontrib><title>Multivariate analysis of T‐cell functional defects and circulating serum factors in hodgkin's disease</title><title>Cancer</title><addtitle>Cancer</addtitle><description>A comprehensive immunologic and serologic analysis was performed on 31 untreated patients with Hodgkin's disease. Immune evaluations stressed T‐cell functional activity and included traditional parameters (PHA responsiveness and delayed hypersensitivity skin reactivity), as well as newer functional assays (T‐cell colony formation, chemotaxis, spontaneous and antibody‐dependent cytotoxicity, and concanavalin A‐induced suppressor cell activity (CISA)). Serum factors included ferritin, prostaglandins, zinc, copper, immune complexes, and thymic hormone activity. Every patient exhibited at least one T‐cell or serum abnormality. The greatest percentage of patients exhibited T‐cell defects in chemotaxis (85%), colony formation (81%), and PHA reactivity (64%). Immune defects were more common with advanced disease but were not related to absolute T‐cell or monocyte count, skin test anergy, or abnormalities of Tμ/Tγ cell proportions. Linear relationships were identified among abnormalities in the three assays employing mononuclear cells (PHA, colony formation, CISA) which may have reflected the inhibitory influence of monocytes present in the mononuclear cell preparations. Low serum zinc correlated with marked impairment of T‐cell chemotaxis. Elevated prostaglandins were associated with high PHA reactivity and with depressed colony formation. Our results indicate that many complex factors, including intrinsic T‐cell defects, contribute to the impaired immunity associated with Hodgkin's disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibody-Dependent Cell Cytotoxicity</subject><subject>Antigen-Antibody Complex - analysis</subject><subject>Female</subject><subject>Ferritins - blood</subject><subject>Hodgkin Disease - immunology</subject><subject>Hodgkin Disease - metabolism</subject><subject>Humans</subject><subject>Leukocyte Count</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prostaglandins E - blood</subject><subject>Skin Tests</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes, Regulatory</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNqVkd2K1DAUx4Mo67j6CEKu_LjomK8m6SjCTv1aWB2QFcSbQ5qejnE77dq0ytz5CD6jT2KGGRf0QvEqhP8v55ycHyFLzuacMfGIs8JkjCvxgBeWM8vzh8ou1JNCq8Xi5PRZVr4p3wormLJM8eKpnLN5uXossuU1Mrt6fJ3MGGM2y5V8f5PcivFTuhqRyyNypFWumWYzsn49tWP44obgRqSuc-02hkj7hp7_-PbdY9vSZur8GPoU0Rob9GNMXE19GPzUujF0axpxmDa0cX7sh0hDRz_29foidPcjrUNEF_E2udG4NuKdw3lM3r14fl6-ys5WL0_Lk7PMq8IUWZUj1rlhlZa1RuO9U7rxhfSqsrXniFwow4tKoJG5tpa5okLJdQJNAit5TO7t614O_ecJ4wibEHffcB32UwQjDdNK8X-CPJdS5dwk8MMe9EMf44ANXA5h44YtcAY7XbDbOOw2Dr90gbKgIOkCSLrgd10ggUG5AgHLVPzuYYqp2mB9VfrgJ-W4z7-GFrf_1fmvjf9I5E-Q1rTq</recordid><startdate>19810815</startdate><enddate>19810815</enddate><creator>Schulof, Richard S.</creator><creator>Bockman, Richard S.</creator><creator>Garofalo, John A.</creator><creator>Cirrincione, Constance</creator><creator>Cunningham‐Rundles, Susanna</creator><creator>Fernandes, Gabriel</creator><creator>Day, Noorbibi K.</creator><creator>Pinsky, Carl M.</creator><creator>Incefy, Genevieve S.</creator><creator>Thaler, Howard T.</creator><creator>Good, Robert A.</creator><creator>Gupta, Sudhir</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19810815</creationdate><title>Multivariate analysis of T‐cell functional defects and circulating serum factors in hodgkin's disease</title><author>Schulof, Richard S. ; Bockman, Richard S. ; Garofalo, John A. ; Cirrincione, Constance ; Cunningham‐Rundles, Susanna ; Fernandes, Gabriel ; Day, Noorbibi K. ; Pinsky, Carl M. ; Incefy, Genevieve S. ; Thaler, Howard T. ; Good, Robert A. ; Gupta, Sudhir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4979-b5eed570b63d6e7cca46fc93c4b8dc1ee124719b2e7356880a9be316cca76fcb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antibody-Dependent Cell Cytotoxicity</topic><topic>Antigen-Antibody Complex - analysis</topic><topic>Female</topic><topic>Ferritins - blood</topic><topic>Hodgkin Disease - immunology</topic><topic>Hodgkin Disease - metabolism</topic><topic>Humans</topic><topic>Leukocyte Count</topic><topic>Lymphocyte Activation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prostaglandins E - blood</topic><topic>Skin Tests</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes, Regulatory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schulof, Richard S.</creatorcontrib><creatorcontrib>Bockman, Richard S.</creatorcontrib><creatorcontrib>Garofalo, John A.</creatorcontrib><creatorcontrib>Cirrincione, Constance</creatorcontrib><creatorcontrib>Cunningham‐Rundles, Susanna</creatorcontrib><creatorcontrib>Fernandes, Gabriel</creatorcontrib><creatorcontrib>Day, Noorbibi K.</creatorcontrib><creatorcontrib>Pinsky, Carl M.</creatorcontrib><creatorcontrib>Incefy, Genevieve S.</creatorcontrib><creatorcontrib>Thaler, Howard T.</creatorcontrib><creatorcontrib>Good, Robert A.</creatorcontrib><creatorcontrib>Gupta, Sudhir</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schulof, Richard S.</au><au>Bockman, Richard S.</au><au>Garofalo, John A.</au><au>Cirrincione, Constance</au><au>Cunningham‐Rundles, Susanna</au><au>Fernandes, Gabriel</au><au>Day, Noorbibi K.</au><au>Pinsky, Carl M.</au><au>Incefy, Genevieve S.</au><au>Thaler, Howard T.</au><au>Good, Robert A.</au><au>Gupta, Sudhir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multivariate analysis of T‐cell functional defects and circulating serum factors in hodgkin's disease</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1981-08-15</date><risdate>1981</risdate><volume>48</volume><issue>4</issue><spage>964</spage><epage>973</epage><pages>964-973</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>A comprehensive immunologic and serologic analysis was performed on 31 untreated patients with Hodgkin's disease. Immune evaluations stressed T‐cell functional activity and included traditional parameters (PHA responsiveness and delayed hypersensitivity skin reactivity), as well as newer functional assays (T‐cell colony formation, chemotaxis, spontaneous and antibody‐dependent cytotoxicity, and concanavalin A‐induced suppressor cell activity (CISA)). Serum factors included ferritin, prostaglandins, zinc, copper, immune complexes, and thymic hormone activity. Every patient exhibited at least one T‐cell or serum abnormality. The greatest percentage of patients exhibited T‐cell defects in chemotaxis (85%), colony formation (81%), and PHA reactivity (64%). Immune defects were more common with advanced disease but were not related to absolute T‐cell or monocyte count, skin test anergy, or abnormalities of Tμ/Tγ cell proportions. Linear relationships were identified among abnormalities in the three assays employing mononuclear cells (PHA, colony formation, CISA) which may have reflected the inhibitory influence of monocytes present in the mononuclear cell preparations. Low serum zinc correlated with marked impairment of T‐cell chemotaxis. Elevated prostaglandins were associated with high PHA reactivity and with depressed colony formation. Our results indicate that many complex factors, including intrinsic T‐cell defects, contribute to the impaired immunity associated with Hodgkin's disease.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>6456060</pmid><doi>10.1002/1097-0142(19810815)48:4<964::AID-CNCR2820480419>3.0.CO;2-B</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antibody-Dependent Cell Cytotoxicity Antigen-Antibody Complex - analysis Female Ferritins - blood Hodgkin Disease - immunology Hodgkin Disease - metabolism Humans Leukocyte Count Lymphocyte Activation Male Middle Aged Prostaglandins E - blood Skin Tests T-Lymphocytes - immunology T-Lymphocytes, Regulatory |
title | Multivariate analysis of T‐cell functional defects and circulating serum factors in hodgkin's disease |
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