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Monocyte activation and disease activity in multiple sclerosis. A longitudinal analysis of serum MRP8/14 levels
In active multiple sclerosis (MS) lesions macrophages expressing myeloid related protein (MRP) 8/14 are present. The aim of this study was to determine whether serum levels of MRP8/14 complexes are related to disease activity in MS. In a longitudinal study of 16 relapsing remitting (RR) MS patients...
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Published in: | Journal of neuroimmunology 2004-03, Vol.148 (1), p.172-177 |
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container_title | Journal of neuroimmunology |
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creator | Floris, Sarah van der Goes, Annette Killestein, Joep Knol, Dirk L. Barkhof, Frederik Polman, Chris H. Dijkstra, Christine D. de Vries, Helga E. Meilof, Jan F. |
description | In active multiple sclerosis (MS) lesions macrophages expressing myeloid related protein (MRP) 8/14 are present. The aim of this study was to determine whether serum levels of MRP8/14 complexes are related to disease activity in MS. In a longitudinal study of 16 relapsing remitting (RR) MS patients that underwent monthly gadolinium diethylentriaminepenta acid (Gd-DTPA) magnetic resonance imaging (MRI), the relation between serum MRP8/14 levels and disease activity was investigated. Patients were participating in a monoclonal antibody study targeting a specific T cell population (Vβ5.2/5.3
+ T-cells). In time, within patients large variations in serum MRP8/14 levels were observed. Serum MRP8/14 levels were not related to changes in clinical disease activity or increase in Gd-DTPA lesion enhancement. Neither did comparison of active (>1 relapse in follow-up period) with inactive (0–1 relapse) MS patients reveal any differences in MRP8/14 levels. Therefore, we conclude that although MRP8/14 expression is a good histopathological marker for monocyte activation, serum levels of these proteins do not correlate with disease activity in RR MS. |
doi_str_mv | 10.1016/j.jneuroim.2003.11.005 |
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+ T-cells). In time, within patients large variations in serum MRP8/14 levels were observed. Serum MRP8/14 levels were not related to changes in clinical disease activity or increase in Gd-DTPA lesion enhancement. Neither did comparison of active (>1 relapse in follow-up period) with inactive (0–1 relapse) MS patients reveal any differences in MRP8/14 levels. Therefore, we conclude that although MRP8/14 expression is a good histopathological marker for monocyte activation, serum levels of these proteins do not correlate with disease activity in RR MS.</description><identifier>ISSN: 0165-5728</identifier><identifier>EISSN: 1872-8421</identifier><identifier>DOI: 10.1016/j.jneuroim.2003.11.005</identifier><identifier>PMID: 14975598</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Blood–brain barrier ; Calgranulin A - blood ; Calgranulin B - blood ; Enzyme-Linked Immunosorbent Assay - methods ; Female ; Follow-Up Studies ; Gadolinium DTPA - metabolism ; Humans ; Longitudinal ; Longitudinal Studies ; Macrophage ; Magnetic Resonance Imaging - methods ; Male ; Middle Aged ; Monocytes - metabolism ; Monocytes - pathology ; MRI ; MRP8/14 ; Multiple sclerosis ; Multiple Sclerosis, Relapsing-Remitting - blood ; Multiple Sclerosis, Relapsing-Remitting - pathology ; Receptors, Antigen, T-Cell, alpha-beta - immunology ; Receptors, Antigen, T-Cell, alpha-beta - metabolism ; Statistics, Nonparametric ; Time Factors</subject><ispartof>Journal of neuroimmunology, 2004-03, Vol.148 (1), p.172-177</ispartof><rights>2003 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-4c025323dd16cdbeda754f1daf4eb50d674925c27317037c6c540ca88a07e4a63</citedby><cites>FETCH-LOGICAL-c395t-4c025323dd16cdbeda754f1daf4eb50d674925c27317037c6c540ca88a07e4a63</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/14975598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Floris, Sarah</creatorcontrib><creatorcontrib>van der Goes, Annette</creatorcontrib><creatorcontrib>Killestein, Joep</creatorcontrib><creatorcontrib>Knol, Dirk L.</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>Polman, Chris H.</creatorcontrib><creatorcontrib>Dijkstra, Christine D.</creatorcontrib><creatorcontrib>de Vries, Helga E.</creatorcontrib><creatorcontrib>Meilof, Jan F.</creatorcontrib><title>Monocyte activation and disease activity in multiple sclerosis. A longitudinal analysis of serum MRP8/14 levels</title><title>Journal of neuroimmunology</title><addtitle>J Neuroimmunol</addtitle><description>In active multiple sclerosis (MS) lesions macrophages expressing myeloid related protein (MRP) 8/14 are present. The aim of this study was to determine whether serum levels of MRP8/14 complexes are related to disease activity in MS. In a longitudinal study of 16 relapsing remitting (RR) MS patients that underwent monthly gadolinium diethylentriaminepenta acid (Gd-DTPA) magnetic resonance imaging (MRI), the relation between serum MRP8/14 levels and disease activity was investigated. Patients were participating in a monoclonal antibody study targeting a specific T cell population (Vβ5.2/5.3
+ T-cells). In time, within patients large variations in serum MRP8/14 levels were observed. Serum MRP8/14 levels were not related to changes in clinical disease activity or increase in Gd-DTPA lesion enhancement. Neither did comparison of active (>1 relapse in follow-up period) with inactive (0–1 relapse) MS patients reveal any differences in MRP8/14 levels. Therefore, we conclude that although MRP8/14 expression is a good histopathological marker for monocyte activation, serum levels of these proteins do not correlate with disease activity in RR MS.</description><subject>Adult</subject><subject>Blood–brain barrier</subject><subject>Calgranulin A - blood</subject><subject>Calgranulin B - blood</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gadolinium DTPA - metabolism</subject><subject>Humans</subject><subject>Longitudinal</subject><subject>Longitudinal Studies</subject><subject>Macrophage</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monocytes - metabolism</subject><subject>Monocytes - pathology</subject><subject>MRI</subject><subject>MRP8/14</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis, Relapsing-Remitting - blood</subject><subject>Multiple Sclerosis, Relapsing-Remitting - pathology</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - immunology</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - metabolism</subject><subject>Statistics, Nonparametric</subject><subject>Time Factors</subject><issn>0165-5728</issn><issn>1872-8421</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkU1r3DAQhkVpaTZp_0LQqTc7Gkuy5FtD6EcgoaW0Z6GVxkWLbG0leWH_fb3slh5zEoyed4aZh5BbYC0w6O927W7GJacwtR1jvAVoGZOvyAa06hotOnhNNisoG6k6fUWuS9kxBpKL4S25AjEoKQe9Iek5zckdK1LrajjYGtJM7eypDwVtuZRDPdIw02mJNewj0uIi5lRCaek9jWn-Heriw2zjGrXxuH7QNNKCeZno84_v-g4EjXjAWN6RN6ONBd9f3hvy6_Onnw9fm6dvXx4f7p8axwdZG-FYJ3nHvYfe-S16q6QYwdtR4FYy3ysxdNJ1ioNiXLneScGc1doyhcL2_IZ8OPfd5_RnwVLNFIrDGO2MaSlGM1BcSvkiCEoJrdUJ7M-gWzcvGUezz2Gy-WiAmZMTszP_nJiTEwNgVidr8PYyYdlO6P_HLhJW4OMZWO-Dh4DZFBdwduhDRleNT-GlGX8BAD6iCg</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Floris, Sarah</creator><creator>van der Goes, Annette</creator><creator>Killestein, Joep</creator><creator>Knol, Dirk L.</creator><creator>Barkhof, Frederik</creator><creator>Polman, Chris H.</creator><creator>Dijkstra, Christine D.</creator><creator>de Vries, Helga E.</creator><creator>Meilof, Jan F.</creator><general>Elsevier 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>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20040301</creationdate><title>Monocyte activation and disease activity in multiple sclerosis. A longitudinal analysis of serum MRP8/14 levels</title><author>Floris, Sarah ; van der Goes, Annette ; Killestein, Joep ; Knol, Dirk L. ; Barkhof, Frederik ; Polman, Chris H. ; Dijkstra, Christine D. ; de Vries, Helga E. ; Meilof, Jan F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-4c025323dd16cdbeda754f1daf4eb50d674925c27317037c6c540ca88a07e4a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Blood–brain barrier</topic><topic>Calgranulin A - blood</topic><topic>Calgranulin B - blood</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gadolinium DTPA - metabolism</topic><topic>Humans</topic><topic>Longitudinal</topic><topic>Longitudinal Studies</topic><topic>Macrophage</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocytes - metabolism</topic><topic>Monocytes - pathology</topic><topic>MRI</topic><topic>MRP8/14</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis, Relapsing-Remitting - blood</topic><topic>Multiple Sclerosis, Relapsing-Remitting - pathology</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - immunology</topic><topic>Receptors, Antigen, T-Cell, alpha-beta - metabolism</topic><topic>Statistics, Nonparametric</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Floris, Sarah</creatorcontrib><creatorcontrib>van der Goes, Annette</creatorcontrib><creatorcontrib>Killestein, Joep</creatorcontrib><creatorcontrib>Knol, Dirk L.</creatorcontrib><creatorcontrib>Barkhof, Frederik</creatorcontrib><creatorcontrib>Polman, Chris H.</creatorcontrib><creatorcontrib>Dijkstra, Christine D.</creatorcontrib><creatorcontrib>de Vries, Helga E.</creatorcontrib><creatorcontrib>Meilof, Jan F.</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>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuroimmunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Floris, Sarah</au><au>van der Goes, Annette</au><au>Killestein, Joep</au><au>Knol, Dirk L.</au><au>Barkhof, Frederik</au><au>Polman, Chris H.</au><au>Dijkstra, Christine D.</au><au>de Vries, Helga E.</au><au>Meilof, Jan F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monocyte activation and disease activity in multiple sclerosis. A longitudinal analysis of serum MRP8/14 levels</atitle><jtitle>Journal of neuroimmunology</jtitle><addtitle>J Neuroimmunol</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>148</volume><issue>1</issue><spage>172</spage><epage>177</epage><pages>172-177</pages><issn>0165-5728</issn><eissn>1872-8421</eissn><abstract>In active multiple sclerosis (MS) lesions macrophages expressing myeloid related protein (MRP) 8/14 are present. The aim of this study was to determine whether serum levels of MRP8/14 complexes are related to disease activity in MS. In a longitudinal study of 16 relapsing remitting (RR) MS patients that underwent monthly gadolinium diethylentriaminepenta acid (Gd-DTPA) magnetic resonance imaging (MRI), the relation between serum MRP8/14 levels and disease activity was investigated. Patients were participating in a monoclonal antibody study targeting a specific T cell population (Vβ5.2/5.3
+ T-cells). In time, within patients large variations in serum MRP8/14 levels were observed. Serum MRP8/14 levels were not related to changes in clinical disease activity or increase in Gd-DTPA lesion enhancement. Neither did comparison of active (>1 relapse in follow-up period) with inactive (0–1 relapse) MS patients reveal any differences in MRP8/14 levels. Therefore, we conclude that although MRP8/14 expression is a good histopathological marker for monocyte activation, serum levels of these proteins do not correlate with disease activity in RR MS.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>14975598</pmid><doi>10.1016/j.jneuroim.2003.11.005</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Blood–brain barrier Calgranulin A - blood Calgranulin B - blood Enzyme-Linked Immunosorbent Assay - methods Female Follow-Up Studies Gadolinium DTPA - metabolism Humans Longitudinal Longitudinal Studies Macrophage Magnetic Resonance Imaging - methods Male Middle Aged Monocytes - metabolism Monocytes - pathology MRI MRP8/14 Multiple sclerosis Multiple Sclerosis, Relapsing-Remitting - blood Multiple Sclerosis, Relapsing-Remitting - pathology Receptors, Antigen, T-Cell, alpha-beta - immunology Receptors, Antigen, T-Cell, alpha-beta - metabolism Statistics, Nonparametric Time Factors |
title | Monocyte activation and disease activity in multiple sclerosis. A longitudinal analysis of serum MRP8/14 levels |
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