Evaluation of Significance of Lymphocyte Subpopulations and Non-specific Serologic Markers in B-cell Non-Hodgkin’s Lymphoma Patients
The use of rituximab brought attention to the hosts’ immune system and to the microenvironment in non-Hodgkin’s lymphoma cases. Our aim was to identify prognostic factors that can be measured easily to indicate the current state of the patient’s immune status and possible reaction against malignant...
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creator | Pósfai, Éva Irsai, Gábor Illés, Árpád Méhes, Gábor Marton, Imelda Molnár, Csaba Csípő, István Baráth, Sándor Gergely, Lajos |
description | The use of rituximab brought attention to the hosts’ immune system and to the microenvironment in non-Hodgkin’s lymphoma cases. Our aim was to identify prognostic factors that can be measured easily to indicate the current state of the patient’s immune status and possible reaction against malignant cells. In the retrospective analysis (2000–2008), 66 patients diagnosed with B-cell non-Hodgkin’s lymphomas were enrolled (40 women, 26 men; mean age: 51 years). White blood cells, lymphocytes, CD3 +; CD4 +; CD8 + T-cells, immunoglobulin types A; G; M, anti-cardiolipin antibody isotypes A; G; M; and levels of beta-2-microglobulin were measured before the initiation of the first cycle of chemotherapy, during and after 4-weeks treatment. As for CD 3+ T-lymphocytes, the absolute CD 3+ T –lymphocyte numbers were higher before (0.78 × 10
9
/L) versus during (0.27 × 10
9
/L) treatment, and increased percentages were detected in pre- (66.57 %) and post-treatment (75.32 %). Absolute numbers of CD 8+ T-lymphocyte levels showed reduction before (0.26 × 10
9
/L) versus during (0.10 × 10
9
/L) therapy, but were elevated after (0.28 × 10
9
/L) treatment, while increased percentage before (21.99 %) versus after (29.85 %), and during (24.56 %) versus after (29.85 %) therapy were seen. Average white blood cell numbers were increased before (9.71 × 10
9
/L) versus during (12.07 × 10
9
/L) treatment, while decreased numbers could be observed, after (5.47 × 10
9
/L) treatment. IgA levels were decreased before (2.51 g/L) versus after (1.63 g/L) therapy. IgG levels were higher before (12.25 g/L) vs. after (8.64 g/L) treatment. IgM levels were decreased before (1.76 g/L) and after (0.83 g/L) as well as before (1.76 g/L) versus during (0.73 g/L) treatment. Anti-cardiolipin antibody type A level were decreased before (2.76 U/ml) versus after (2.49 U/ml) treatment. Decreased level of beta-2-microglobulin could be observed before (2.91 mg/L) versus post (2.28 mg/L) chemotherapy. Findings may provide better insight into the effects of immuno-chemotherapy on the hosts’ immune system. |
doi_str_mv | 10.1007/s12253-014-9744-3 |
format | Article |
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9
/L) versus during (0.27 × 10
9
/L) treatment, and increased percentages were detected in pre- (66.57 %) and post-treatment (75.32 %). Absolute numbers of CD 8+ T-lymphocyte levels showed reduction before (0.26 × 10
9
/L) versus during (0.10 × 10
9
/L) therapy, but were elevated after (0.28 × 10
9
/L) treatment, while increased percentage before (21.99 %) versus after (29.85 %), and during (24.56 %) versus after (29.85 %) therapy were seen. Average white blood cell numbers were increased before (9.71 × 10
9
/L) versus during (12.07 × 10
9
/L) treatment, while decreased numbers could be observed, after (5.47 × 10
9
/L) treatment. IgA levels were decreased before (2.51 g/L) versus after (1.63 g/L) therapy. IgG levels were higher before (12.25 g/L) vs. after (8.64 g/L) treatment. IgM levels were decreased before (1.76 g/L) and after (0.83 g/L) as well as before (1.76 g/L) versus during (0.73 g/L) treatment. Anti-cardiolipin antibody type A level were decreased before (2.76 U/ml) versus after (2.49 U/ml) treatment. Decreased level of beta-2-microglobulin could be observed before (2.91 mg/L) versus post (2.28 mg/L) chemotherapy. Findings may provide better insight into the effects of immuno-chemotherapy on the hosts’ immune system.</description><identifier>ISSN: 1219-4956</identifier><identifier>EISSN: 1532-2807</identifier><identifier>DOI: 10.1007/s12253-014-9744-3</identifier><identifier>PMID: 24488335</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biomarkers - blood ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Female ; Follow-Up Studies ; Humans ; Immunology ; Lymphocyte Subsets - immunology ; Lymphocyte Subsets - metabolism ; Lymphoma, B-Cell - blood ; Lymphoma, B-Cell - immunology ; Lymphoma, B-Cell - pathology ; Male ; Middle Aged ; Neoplasm Staging ; Oncology ; Pathology ; Prognosis ; Retrospective Studies ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Young Adult</subject><ispartof>Pathology oncology research, 2014-07, Vol.20 (3), p.649-654</ispartof><rights>Arányi Lajos Foundation 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-5a7a78633acc497da17c0a73a15b80cd15f71be6287181fdc664209be8bfaeb73</citedby><cites>FETCH-LOGICAL-c518t-5a7a78633acc497da17c0a73a15b80cd15f71be6287181fdc664209be8bfaeb73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12253-014-9744-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12253-014-9744-3$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24488335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pósfai, Éva</creatorcontrib><creatorcontrib>Irsai, Gábor</creatorcontrib><creatorcontrib>Illés, Árpád</creatorcontrib><creatorcontrib>Méhes, Gábor</creatorcontrib><creatorcontrib>Marton, Imelda</creatorcontrib><creatorcontrib>Molnár, Csaba</creatorcontrib><creatorcontrib>Csípő, István</creatorcontrib><creatorcontrib>Baráth, Sándor</creatorcontrib><creatorcontrib>Gergely, Lajos</creatorcontrib><title>Evaluation of Significance of Lymphocyte Subpopulations and Non-specific Serologic Markers in B-cell Non-Hodgkin’s Lymphoma Patients</title><title>Pathology oncology research</title><addtitle>Pathol. Oncol. Res</addtitle><addtitle>Pathol Oncol Res</addtitle><description>The use of rituximab brought attention to the hosts’ immune system and to the microenvironment in non-Hodgkin’s lymphoma cases. Our aim was to identify prognostic factors that can be measured easily to indicate the current state of the patient’s immune status and possible reaction against malignant cells. In the retrospective analysis (2000–2008), 66 patients diagnosed with B-cell non-Hodgkin’s lymphomas were enrolled (40 women, 26 men; mean age: 51 years). White blood cells, lymphocytes, CD3 +; CD4 +; CD8 + T-cells, immunoglobulin types A; G; M, anti-cardiolipin antibody isotypes A; G; M; and levels of beta-2-microglobulin were measured before the initiation of the first cycle of chemotherapy, during and after 4-weeks treatment. As for CD 3+ T-lymphocytes, the absolute CD 3+ T –lymphocyte numbers were higher before (0.78 × 10
9
/L) versus during (0.27 × 10
9
/L) treatment, and increased percentages were detected in pre- (66.57 %) and post-treatment (75.32 %). Absolute numbers of CD 8+ T-lymphocyte levels showed reduction before (0.26 × 10
9
/L) versus during (0.10 × 10
9
/L) therapy, but were elevated after (0.28 × 10
9
/L) treatment, while increased percentage before (21.99 %) versus after (29.85 %), and during (24.56 %) versus after (29.85 %) therapy were seen. Average white blood cell numbers were increased before (9.71 × 10
9
/L) versus during (12.07 × 10
9
/L) treatment, while decreased numbers could be observed, after (5.47 × 10
9
/L) treatment. IgA levels were decreased before (2.51 g/L) versus after (1.63 g/L) therapy. IgG levels were higher before (12.25 g/L) vs. after (8.64 g/L) treatment. IgM levels were decreased before (1.76 g/L) and after (0.83 g/L) as well as before (1.76 g/L) versus during (0.73 g/L) treatment. Anti-cardiolipin antibody type A level were decreased before (2.76 U/ml) versus after (2.49 U/ml) treatment. Decreased level of beta-2-microglobulin could be observed before (2.91 mg/L) versus post (2.28 mg/L) chemotherapy. Findings may provide better insight into the effects of immuno-chemotherapy on the hosts’ immune system.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biomarkers - blood</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunology</subject><subject>Lymphocyte Subsets - immunology</subject><subject>Lymphocyte Subsets - metabolism</subject><subject>Lymphoma, B-Cell - blood</subject><subject>Lymphoma, B-Cell - immunology</subject><subject>Lymphoma, B-Cell - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Young Adult</subject><issn>1219-4956</issn><issn>1532-2807</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkctu1DAYRq0K1Bs8ABtkiQ0bg-92lqUqLdJwkQbWluM4Q9rETu0EaXas-g59PZ4EpzMghITEyr_l8x3b-gB4RvArgrF6nQmlgiFMOKoU54gdgGMiGEVUY_WozJRUiFdCHoGTnK9xychKHoIjyrnWjIljcHfxzfaznboYYGzhutuEru2cDc4v-9V2GL9Gt508XM_1GMe5f2AztKGBH2JAefRuScC1T7GPmzK9t-nGpwy7AN8g5_v-AbyKzeamCz--3-e9drDwU7H5MOUn4HFr--yf7tdT8OXtxefzK7T6ePnu_GyFnCB6QsIqq7RkzDrHK9VYohy2ilkiao1dQ0SrSO0l1Ypo0jZOSk5xVXtdt9bXip2ClzvvmOLt7PNkhi4vT7TBxzkbIqTUQgkm_wNlFZcVZaygL_5Cr-OcQvnIQikiSgW0UGRHuRRzTr41Y-oGm7aGYLP0aXZ9mtKnWfo0i_n53jzXg29-J34VWAC6A3I5Chuf_rj6n9afeyassw</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Pósfai, Éva</creator><creator>Irsai, Gábor</creator><creator>Illés, Árpád</creator><creator>Méhes, Gábor</creator><creator>Marton, Imelda</creator><creator>Molnár, Csaba</creator><creator>Csípő, István</creator><creator>Baráth, Sándor</creator><creator>Gergely, Lajos</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20140701</creationdate><title>Evaluation of Significance of Lymphocyte Subpopulations and Non-specific Serologic Markers in B-cell Non-Hodgkin’s Lymphoma Patients</title><author>Pósfai, Éva ; Irsai, Gábor ; Illés, Árpád ; Méhes, Gábor ; Marton, Imelda ; Molnár, Csaba ; Csípő, István ; Baráth, Sándor ; Gergely, Lajos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-5a7a78633acc497da17c0a73a15b80cd15f71be6287181fdc664209be8bfaeb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers - blood</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunology</topic><topic>Lymphocyte Subsets - immunology</topic><topic>Lymphocyte Subsets - metabolism</topic><topic>Lymphoma, B-Cell - blood</topic><topic>Lymphoma, B-Cell - immunology</topic><topic>Lymphoma, B-Cell - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Pathology</topic><topic>Prognosis</topic><topic>Retrospective 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>Pósfai, Éva</creatorcontrib><creatorcontrib>Irsai, Gábor</creatorcontrib><creatorcontrib>Illés, Árpád</creatorcontrib><creatorcontrib>Méhes, Gábor</creatorcontrib><creatorcontrib>Marton, Imelda</creatorcontrib><creatorcontrib>Molnár, Csaba</creatorcontrib><creatorcontrib>Csípő, István</creatorcontrib><creatorcontrib>Baráth, Sándor</creatorcontrib><creatorcontrib>Gergely, Lajos</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology oncology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pósfai, Éva</au><au>Irsai, Gábor</au><au>Illés, Árpád</au><au>Méhes, Gábor</au><au>Marton, Imelda</au><au>Molnár, Csaba</au><au>Csípő, István</au><au>Baráth, Sándor</au><au>Gergely, Lajos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of Significance of Lymphocyte Subpopulations and Non-specific Serologic Markers in B-cell Non-Hodgkin’s Lymphoma Patients</atitle><jtitle>Pathology oncology research</jtitle><stitle>Pathol. Oncol. Res</stitle><addtitle>Pathol Oncol Res</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>20</volume><issue>3</issue><spage>649</spage><epage>654</epage><pages>649-654</pages><issn>1219-4956</issn><eissn>1532-2807</eissn><abstract>The use of rituximab brought attention to the hosts’ immune system and to the microenvironment in non-Hodgkin’s lymphoma cases. Our aim was to identify prognostic factors that can be measured easily to indicate the current state of the patient’s immune status and possible reaction against malignant cells. In the retrospective analysis (2000–2008), 66 patients diagnosed with B-cell non-Hodgkin’s lymphomas were enrolled (40 women, 26 men; mean age: 51 years). White blood cells, lymphocytes, CD3 +; CD4 +; CD8 + T-cells, immunoglobulin types A; G; M, anti-cardiolipin antibody isotypes A; G; M; and levels of beta-2-microglobulin were measured before the initiation of the first cycle of chemotherapy, during and after 4-weeks treatment. As for CD 3+ T-lymphocytes, the absolute CD 3+ T –lymphocyte numbers were higher before (0.78 × 10
9
/L) versus during (0.27 × 10
9
/L) treatment, and increased percentages were detected in pre- (66.57 %) and post-treatment (75.32 %). Absolute numbers of CD 8+ T-lymphocyte levels showed reduction before (0.26 × 10
9
/L) versus during (0.10 × 10
9
/L) therapy, but were elevated after (0.28 × 10
9
/L) treatment, while increased percentage before (21.99 %) versus after (29.85 %), and during (24.56 %) versus after (29.85 %) therapy were seen. Average white blood cell numbers were increased before (9.71 × 10
9
/L) versus during (12.07 × 10
9
/L) treatment, while decreased numbers could be observed, after (5.47 × 10
9
/L) treatment. IgA levels were decreased before (2.51 g/L) versus after (1.63 g/L) therapy. IgG levels were higher before (12.25 g/L) vs. after (8.64 g/L) treatment. IgM levels were decreased before (1.76 g/L) and after (0.83 g/L) as well as before (1.76 g/L) versus during (0.73 g/L) treatment. Anti-cardiolipin antibody type A level were decreased before (2.76 U/ml) versus after (2.49 U/ml) treatment. Decreased level of beta-2-microglobulin could be observed before (2.91 mg/L) versus post (2.28 mg/L) chemotherapy. Findings may provide better insight into the effects of immuno-chemotherapy on the hosts’ immune system.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>24488335</pmid><doi>10.1007/s12253-014-9744-3</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Biomarkers - blood Biomedical and Life Sciences Biomedicine Cancer Research Female Follow-Up Studies Humans Immunology Lymphocyte Subsets - immunology Lymphocyte Subsets - metabolism Lymphoma, B-Cell - blood Lymphoma, B-Cell - immunology Lymphoma, B-Cell - pathology Male Middle Aged Neoplasm Staging Oncology Pathology Prognosis Retrospective Studies T-Lymphocytes - immunology T-Lymphocytes - metabolism Young Adult |
title | Evaluation of Significance of Lymphocyte Subpopulations and Non-specific Serologic Markers in B-cell Non-Hodgkin’s Lymphoma Patients |
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