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Inflammatory markers, oxidative stress, and antioxidant capacity in healthy allo-HSCT donors during hematopoietic stem cell mobilization
The aim of this study is to investigate the impact of mobilization with granulocyte colony stimulating factor (G‐CSF) and apheresis procedure on inflammatory and oxidative stress markers, and antioxidant capacity in healthy allo‐HSCT donors. The study was conducted in the Stem Cell Transplantation U...
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Published in: | Journal of clinical apheresis 2015-08, Vol.30 (4), p.197-203 |
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container_title | Journal of clinical apheresis |
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creator | İlhan, Çiğdem Suyanı, Elif Sucak, Gülsan Türköz Paşaoğlu, Özge Tuğçe Akı, Şahika Zeynep Paşaoğlu, Hatice |
description | The aim of this study is to investigate the impact of mobilization with granulocyte colony stimulating factor (G‐CSF) and apheresis procedure on inflammatory and oxidative stress markers, and antioxidant capacity in healthy allo‐HSCT donors. The study was conducted in the Stem Cell Transplantation Unit of Gazi University Hospital between October 2010 and March 2011, and 25 consecutive allo‐HSCT donors were included. The alteration in the serum levels of iron, iron binding capacity, albumin, ferritin, IL‐6, hs‐CRP, TAC, MDA, and AOPP were determined at five different time points. (1) Prior to the first dose of G‐CSF (T0), (2) preapheresis (on the fourth day of G‐CSF before the apeheresis procedure) (T1), (3) immediately postapheresis (T2), (4) 24 h postapheresis (T3), and (5) a week after apheresis (T4). Serum ferritin levels increased steadily after administration of G‐CSF and remained high up toT4. Both serum IL‐6 and hs‐CRP levels began to increase in the T1 sampling and reached to a maximum level at T3 and decreased even below the basal levels at T4. Serum AOPP levels decreased at preapheresis and postapheresis time points, while they increased at T3 and T4 samples. Serum MDA levels decreased at T1, T2, T3, and T4 samples. Serum TAC increased significantly and steadily at all time points post G‐CSF. In conclusion; mobilization with G‐CSF and apheresis caused a transient inflammatory reaction and a protein limited oxidative stress in healthy allo‐HCT donors. J. Clin. Apheresis 30:197–203, 2015. © 2014 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/jca.21361 |
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The study was conducted in the Stem Cell Transplantation Unit of Gazi University Hospital between October 2010 and March 2011, and 25 consecutive allo‐HSCT donors were included. The alteration in the serum levels of iron, iron binding capacity, albumin, ferritin, IL‐6, hs‐CRP, TAC, MDA, and AOPP were determined at five different time points. (1) Prior to the first dose of G‐CSF (T0), (2) preapheresis (on the fourth day of G‐CSF before the apeheresis procedure) (T1), (3) immediately postapheresis (T2), (4) 24 h postapheresis (T3), and (5) a week after apheresis (T4). Serum ferritin levels increased steadily after administration of G‐CSF and remained high up toT4. Both serum IL‐6 and hs‐CRP levels began to increase in the T1 sampling and reached to a maximum level at T3 and decreased even below the basal levels at T4. Serum AOPP levels decreased at preapheresis and postapheresis time points, while they increased at T3 and T4 samples. Serum MDA levels decreased at T1, T2, T3, and T4 samples. Serum TAC increased significantly and steadily at all time points post G‐CSF. In conclusion; mobilization with G‐CSF and apheresis caused a transient inflammatory reaction and a protein limited oxidative stress in healthy allo‐HCT donors. J. Clin. Apheresis 30:197–203, 2015. © 2014 Wiley Periodicals, Inc.</description><identifier>ISSN: 0733-2459</identifier><identifier>EISSN: 1098-1101</identifier><identifier>DOI: 10.1002/jca.21361</identifier><identifier>PMID: 25270291</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adult ; Advanced Oxidation Protein Products - blood ; Aged ; Albumins - metabolism ; Antigens, CD34 - metabolism ; antioxidant capacity ; Antioxidants - metabolism ; Blood Component Removal ; C-Reactive Protein - metabolism ; donor ; Female ; Ferritins - blood ; Granulocyte Colony-Stimulating Factor - pharmacology ; Hematopoietic Stem Cell Mobilization ; Hematopoietic Stem Cell Transplantation ; Humans ; Inflammation - blood ; Interleukin-6 - blood ; Iron - blood ; Male ; Malondialdehyde - blood ; Middle Aged ; mobilization ; Oxidative Stress ; Oxygen - metabolism ; Prospective Studies ; Serum Albumin - metabolism ; Transplantation, Homologous ; Young Adult</subject><ispartof>Journal of clinical apheresis, 2015-08, Vol.30 (4), p.197-203</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4611-ff7c883f2f243dea2f6bdb9909f33ba6d8d74b164bc4597e360aea37d273ebc03</citedby><cites>FETCH-LOGICAL-c4611-ff7c883f2f243dea2f6bdb9909f33ba6d8d74b164bc4597e360aea37d273ebc03</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/25270291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>İlhan, Çiğdem</creatorcontrib><creatorcontrib>Suyanı, Elif</creatorcontrib><creatorcontrib>Sucak, Gülsan Türköz</creatorcontrib><creatorcontrib>Paşaoğlu, Özge Tuğçe</creatorcontrib><creatorcontrib>Akı, Şahika Zeynep</creatorcontrib><creatorcontrib>Paşaoğlu, Hatice</creatorcontrib><title>Inflammatory markers, oxidative stress, and antioxidant capacity in healthy allo-HSCT donors during hematopoietic stem cell mobilization</title><title>Journal of clinical apheresis</title><addtitle>J. Clin. Apheresis</addtitle><description>The aim of this study is to investigate the impact of mobilization with granulocyte colony stimulating factor (G‐CSF) and apheresis procedure on inflammatory and oxidative stress markers, and antioxidant capacity in healthy allo‐HSCT donors. The study was conducted in the Stem Cell Transplantation Unit of Gazi University Hospital between October 2010 and March 2011, and 25 consecutive allo‐HSCT donors were included. The alteration in the serum levels of iron, iron binding capacity, albumin, ferritin, IL‐6, hs‐CRP, TAC, MDA, and AOPP were determined at five different time points. (1) Prior to the first dose of G‐CSF (T0), (2) preapheresis (on the fourth day of G‐CSF before the apeheresis procedure) (T1), (3) immediately postapheresis (T2), (4) 24 h postapheresis (T3), and (5) a week after apheresis (T4). Serum ferritin levels increased steadily after administration of G‐CSF and remained high up toT4. Both serum IL‐6 and hs‐CRP levels began to increase in the T1 sampling and reached to a maximum level at T3 and decreased even below the basal levels at T4. Serum AOPP levels decreased at preapheresis and postapheresis time points, while they increased at T3 and T4 samples. Serum MDA levels decreased at T1, T2, T3, and T4 samples. Serum TAC increased significantly and steadily at all time points post G‐CSF. In conclusion; mobilization with G‐CSF and apheresis caused a transient inflammatory reaction and a protein limited oxidative stress in healthy allo‐HCT donors. J. Clin. Apheresis 30:197–203, 2015. © 2014 Wiley Periodicals, Inc.</description><subject>Adult</subject><subject>Advanced Oxidation Protein Products - blood</subject><subject>Aged</subject><subject>Albumins - metabolism</subject><subject>Antigens, CD34 - metabolism</subject><subject>antioxidant capacity</subject><subject>Antioxidants - metabolism</subject><subject>Blood Component Removal</subject><subject>C-Reactive Protein - metabolism</subject><subject>donor</subject><subject>Female</subject><subject>Ferritins - blood</subject><subject>Granulocyte Colony-Stimulating Factor - pharmacology</subject><subject>Hematopoietic Stem Cell Mobilization</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Humans</subject><subject>Inflammation - blood</subject><subject>Interleukin-6 - blood</subject><subject>Iron - blood</subject><subject>Male</subject><subject>Malondialdehyde - blood</subject><subject>Middle Aged</subject><subject>mobilization</subject><subject>Oxidative Stress</subject><subject>Oxygen - metabolism</subject><subject>Prospective Studies</subject><subject>Serum Albumin - metabolism</subject><subject>Transplantation, Homologous</subject><subject>Young Adult</subject><issn>0733-2459</issn><issn>1098-1101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kctu1DAUhi0EokNhwQsgS2xaibS-JPFkWY3otFW5iA50aTm-UA-JPdgONH2CPnadTtsFEgvLks_nz8fnB-AtRgcYIXK4luKAYFrjZ2CGUTMvMEb4OZghRmlByqrZAa9iXCOEmoZWL8EOqQhDpMEzcHvqTCf6XiQfRtiL8EuH-AH6a6tEsn80jCnomE-EU3kle19xCUqxEdKmEVoHr7To0tUIRdf54uRisYLKOx8iVEOw7meuT_6NtzpZmY26h1J3Hex9azt7kx_y7jV4YUQX9ZuHfRd8P_64WpwU51-Wp4uj80KWNcaFMUzO59QQQ0qqtCCmblXbNKgxlLaiVnPFyhbXZSvzv5mmNRJaUKYIo7qViO6Cva13E_zvQcfEexunboTTfogcM1TSiiBaZfT9P-jaD8Hl7iaKNhQjNlH7W0oGH2PQhm-CzYMcOUZ8iofnePh9PJl992Ac2l6rJ_IxjwwcboG_ttPj_038bHH0qCy2N2ye6_XTjRwkrxllFb_8vOQ_Pn39drm8WPGS3gHaRKrq</recordid><startdate>201508</startdate><enddate>201508</enddate><creator>İlhan, Çiğdem</creator><creator>Suyanı, Elif</creator><creator>Sucak, Gülsan Türköz</creator><creator>Paşaoğlu, Özge Tuğçe</creator><creator>Akı, Şahika Zeynep</creator><creator>Paşaoğlu, Hatice</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>K9.</scope><scope>7X8</scope></search><sort><creationdate>201508</creationdate><title>Inflammatory markers, oxidative stress, and antioxidant capacity in healthy allo-HSCT donors during hematopoietic stem cell mobilization</title><author>İlhan, Çiğdem ; Suyanı, Elif ; Sucak, Gülsan Türköz ; Paşaoğlu, Özge Tuğçe ; Akı, Şahika Zeynep ; Paşaoğlu, Hatice</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4611-ff7c883f2f243dea2f6bdb9909f33ba6d8d74b164bc4597e360aea37d273ebc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Advanced Oxidation Protein Products - blood</topic><topic>Aged</topic><topic>Albumins - metabolism</topic><topic>Antigens, CD34 - metabolism</topic><topic>antioxidant capacity</topic><topic>Antioxidants - metabolism</topic><topic>Blood Component Removal</topic><topic>C-Reactive Protein - metabolism</topic><topic>donor</topic><topic>Female</topic><topic>Ferritins - blood</topic><topic>Granulocyte Colony-Stimulating Factor - pharmacology</topic><topic>Hematopoietic Stem Cell Mobilization</topic><topic>Hematopoietic Stem Cell Transplantation</topic><topic>Humans</topic><topic>Inflammation - blood</topic><topic>Interleukin-6 - blood</topic><topic>Iron - blood</topic><topic>Male</topic><topic>Malondialdehyde - blood</topic><topic>Middle Aged</topic><topic>mobilization</topic><topic>Oxidative Stress</topic><topic>Oxygen - metabolism</topic><topic>Prospective Studies</topic><topic>Serum Albumin - metabolism</topic><topic>Transplantation, Homologous</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>İlhan, Çiğdem</creatorcontrib><creatorcontrib>Suyanı, Elif</creatorcontrib><creatorcontrib>Sucak, Gülsan Türköz</creatorcontrib><creatorcontrib>Paşaoğlu, Özge Tuğçe</creatorcontrib><creatorcontrib>Akı, Şahika Zeynep</creatorcontrib><creatorcontrib>Paşaoğlu, Hatice</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical apheresis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>İlhan, Çiğdem</au><au>Suyanı, Elif</au><au>Sucak, Gülsan Türköz</au><au>Paşaoğlu, Özge Tuğçe</au><au>Akı, Şahika Zeynep</au><au>Paşaoğlu, Hatice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammatory markers, oxidative stress, and antioxidant capacity in healthy allo-HSCT donors during hematopoietic stem cell mobilization</atitle><jtitle>Journal of clinical apheresis</jtitle><addtitle>J. Clin. Apheresis</addtitle><date>2015-08</date><risdate>2015</risdate><volume>30</volume><issue>4</issue><spage>197</spage><epage>203</epage><pages>197-203</pages><issn>0733-2459</issn><eissn>1098-1101</eissn><abstract>The aim of this study is to investigate the impact of mobilization with granulocyte colony stimulating factor (G‐CSF) and apheresis procedure on inflammatory and oxidative stress markers, and antioxidant capacity in healthy allo‐HSCT donors. The study was conducted in the Stem Cell Transplantation Unit of Gazi University Hospital between October 2010 and March 2011, and 25 consecutive allo‐HSCT donors were included. The alteration in the serum levels of iron, iron binding capacity, albumin, ferritin, IL‐6, hs‐CRP, TAC, MDA, and AOPP were determined at five different time points. (1) Prior to the first dose of G‐CSF (T0), (2) preapheresis (on the fourth day of G‐CSF before the apeheresis procedure) (T1), (3) immediately postapheresis (T2), (4) 24 h postapheresis (T3), and (5) a week after apheresis (T4). Serum ferritin levels increased steadily after administration of G‐CSF and remained high up toT4. Both serum IL‐6 and hs‐CRP levels began to increase in the T1 sampling and reached to a maximum level at T3 and decreased even below the basal levels at T4. Serum AOPP levels decreased at preapheresis and postapheresis time points, while they increased at T3 and T4 samples. Serum MDA levels decreased at T1, T2, T3, and T4 samples. Serum TAC increased significantly and steadily at all time points post G‐CSF. In conclusion; mobilization with G‐CSF and apheresis caused a transient inflammatory reaction and a protein limited oxidative stress in healthy allo‐HCT donors. J. Clin. Apheresis 30:197–203, 2015. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25270291</pmid><doi>10.1002/jca.21361</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Advanced Oxidation Protein Products - blood Aged Albumins - metabolism Antigens, CD34 - metabolism antioxidant capacity Antioxidants - metabolism Blood Component Removal C-Reactive Protein - metabolism donor Female Ferritins - blood Granulocyte Colony-Stimulating Factor - pharmacology Hematopoietic Stem Cell Mobilization Hematopoietic Stem Cell Transplantation Humans Inflammation - blood Interleukin-6 - blood Iron - blood Male Malondialdehyde - blood Middle Aged mobilization Oxidative Stress Oxygen - metabolism Prospective Studies Serum Albumin - metabolism Transplantation, Homologous Young Adult |
title | Inflammatory markers, oxidative stress, and antioxidant capacity in healthy allo-HSCT donors during hematopoietic stem cell mobilization |
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