Loading…
Complement activation plays a key role in the side‐effects of rituximab treatment
Treatment with rituximab, a chimaeric anti‐CD20 monoclonal antibody, can be associated with moderate to severe first‐dose side‐effects, notably in patients with high numbers of circulating tumour cells. The aim of this study was to elucidate the mechanism of these side‐effects. At multiple early tim...
Saved in:
Published in: | British journal of haematology 2001-12, Vol.115 (4), p.807-811 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3 |
---|---|
cites | cdi_FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3 |
container_end_page | 811 |
container_issue | 4 |
container_start_page | 807 |
container_title | British journal of haematology |
container_volume | 115 |
creator | Van Der Kolk, L. E. Grillo‐López, A. J. Baars, J. W. Hack, C. E. Van Oers, M. H. J. |
description | Treatment with rituximab, a chimaeric anti‐CD20 monoclonal antibody, can be associated with moderate to severe first‐dose side‐effects, notably in patients with high numbers of circulating tumour cells. The aim of this study was to elucidate the mechanism of these side‐effects. At multiple early time points during the first infusion of rituximab, complement activation products (C3b/c and C4b/c) and cytokines [tumour necrosis factor alpha (TNF‐α), interleukin 6 (IL‐6) and IL‐8] were measured in five relapsed low‐grade non‐Hodgkin's lymphoma (NHL) patients. Infusion of rituximab induced rapid complement activation, preceding the release of TNF‐α, IL‐6 and IL‐8. Although the study group was small, the level of complement activation appeared to be correlated both with the number of circulating B cells prior to the infusion (r = 0·85; P = 0·07) and with the severity of the side‐effects. We conclude that complement plays a pivotal role in the pathogenesis of side‐effects of rituximab treatment. As complement activation can not be prevented by corticosteroids, it might be relevant to study the possible role of complement inhibitors during the first administration of rituximab. |
doi_str_mv | 10.1046/j.1365-2141.2001.03166.x |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72439606</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>99147627</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3</originalsourceid><addsrcrecordid>eNqNkMuO1DAQRS0EYpqBX0AWEuwSXPEjzoIF0wIGNBILYG05Tlm4yaOxHeje8Ql8I19CQrcYiRWrslTnXpUPIRRYCUyo57sSuJJFBQLKijEoGQelysMdsvm7uEs2jLG6WAL6gjxIabeAnEm4Ty4AtOAa-IZ82E7DvscBx0yty-GbzWEa6b63x0Qt_YJHGqceaRhp_ow0hQ5__fiJ3qPLiU6expDnQxhsS3NEm9eih-Set33CR-d5ST69fvVxe13cvH_zdvvypnCSa1VIL3XXMVtJBi1vW16B5CBq66tGNrblrNKt5y0I6WrXeYkddo3UvqsrXwvHL8mzU-8-Tl9nTNkMITnsezviNCdTV4I3iqkFfPIPuJvmOC63GWi0VEIovUD6BLk4pRTRm31c_hWPBphZrZudWeWaVa5ZrZs_1s1hiT4-98_tgN1t8Kx5AZ6eAZuc7X20owvpluNC8BrEwr04cd9Dj8f_PsBcvbteX_w3bsedyg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>198564468</pqid></control><display><type>article</type><title>Complement activation plays a key role in the side‐effects of rituximab treatment</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Van Der Kolk, L. E. ; Grillo‐López, A. J. ; Baars, J. W. ; Hack, C. E. ; Van Oers, M. H. J.</creator><creatorcontrib>Van Der Kolk, L. E. ; Grillo‐López, A. J. ; Baars, J. W. ; Hack, C. E. ; Van Oers, M. H. J.</creatorcontrib><description>Treatment with rituximab, a chimaeric anti‐CD20 monoclonal antibody, can be associated with moderate to severe first‐dose side‐effects, notably in patients with high numbers of circulating tumour cells. The aim of this study was to elucidate the mechanism of these side‐effects. At multiple early time points during the first infusion of rituximab, complement activation products (C3b/c and C4b/c) and cytokines [tumour necrosis factor alpha (TNF‐α), interleukin 6 (IL‐6) and IL‐8] were measured in five relapsed low‐grade non‐Hodgkin's lymphoma (NHL) patients. Infusion of rituximab induced rapid complement activation, preceding the release of TNF‐α, IL‐6 and IL‐8. Although the study group was small, the level of complement activation appeared to be correlated both with the number of circulating B cells prior to the infusion (r = 0·85; P = 0·07) and with the severity of the side‐effects. We conclude that complement plays a pivotal role in the pathogenesis of side‐effects of rituximab treatment. As complement activation can not be prevented by corticosteroids, it might be relevant to study the possible role of complement inhibitors during the first administration of rituximab.</description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1046/j.1365-2141.2001.03166.x</identifier><identifier>PMID: 11843813</identifier><identifier>CODEN: BJHEAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Murine-Derived ; Antineoplastic agents ; Antineoplastic Agents - adverse effects ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Complement Activation ; Complement C3b - analysis ; Complement C3c - analysis ; Complement C4 - analysis ; Complement C4b - analysis ; cytokines ; Cytokines - blood ; Female ; Hematology ; Humans ; Immunotherapy ; Interleukin-6 - blood ; Interleukin-8 - blood ; Lymphocyte Count ; Lymphoma, Non-Hodgkin - drug therapy ; Lymphoma, Non-Hodgkin - immunology ; Male ; Medical sciences ; Middle Aged ; non‐Hodgkin's lymphoma ; Peptide Fragments ; Pharmacology. Drug treatments ; Rituximab ; side‐effects ; Stimulation, Chemical ; Tumor Necrosis Factor-alpha - analysis</subject><ispartof>British journal of haematology, 2001-12, Vol.115 (4), p.807-811</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Dec 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3</citedby><cites>FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13443714$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11843813$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Van Der Kolk, L. E.</creatorcontrib><creatorcontrib>Grillo‐López, A. J.</creatorcontrib><creatorcontrib>Baars, J. W.</creatorcontrib><creatorcontrib>Hack, C. E.</creatorcontrib><creatorcontrib>Van Oers, M. H. J.</creatorcontrib><title>Complement activation plays a key role in the side‐effects of rituximab treatment</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description>Treatment with rituximab, a chimaeric anti‐CD20 monoclonal antibody, can be associated with moderate to severe first‐dose side‐effects, notably in patients with high numbers of circulating tumour cells. The aim of this study was to elucidate the mechanism of these side‐effects. At multiple early time points during the first infusion of rituximab, complement activation products (C3b/c and C4b/c) and cytokines [tumour necrosis factor alpha (TNF‐α), interleukin 6 (IL‐6) and IL‐8] were measured in five relapsed low‐grade non‐Hodgkin's lymphoma (NHL) patients. Infusion of rituximab induced rapid complement activation, preceding the release of TNF‐α, IL‐6 and IL‐8. Although the study group was small, the level of complement activation appeared to be correlated both with the number of circulating B cells prior to the infusion (r = 0·85; P = 0·07) and with the severity of the side‐effects. We conclude that complement plays a pivotal role in the pathogenesis of side‐effects of rituximab treatment. As complement activation can not be prevented by corticosteroids, it might be relevant to study the possible role of complement inhibitors during the first administration of rituximab.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Monoclonal, Murine-Derived</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Complement Activation</subject><subject>Complement C3b - analysis</subject><subject>Complement C3c - analysis</subject><subject>Complement C4 - analysis</subject><subject>Complement C4b - analysis</subject><subject>cytokines</subject><subject>Cytokines - blood</subject><subject>Female</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-8 - blood</subject><subject>Lymphocyte Count</subject><subject>Lymphoma, Non-Hodgkin - drug therapy</subject><subject>Lymphoma, Non-Hodgkin - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>non‐Hodgkin's lymphoma</subject><subject>Peptide Fragments</subject><subject>Pharmacology. Drug treatments</subject><subject>Rituximab</subject><subject>side‐effects</subject><subject>Stimulation, Chemical</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqNkMuO1DAQRS0EYpqBX0AWEuwSXPEjzoIF0wIGNBILYG05Tlm4yaOxHeje8Ql8I19CQrcYiRWrslTnXpUPIRRYCUyo57sSuJJFBQLKijEoGQelysMdsvm7uEs2jLG6WAL6gjxIabeAnEm4Ty4AtOAa-IZ82E7DvscBx0yty-GbzWEa6b63x0Qt_YJHGqceaRhp_ow0hQ5__fiJ3qPLiU6expDnQxhsS3NEm9eih-Set33CR-d5ST69fvVxe13cvH_zdvvypnCSa1VIL3XXMVtJBi1vW16B5CBq66tGNrblrNKt5y0I6WrXeYkddo3UvqsrXwvHL8mzU-8-Tl9nTNkMITnsezviNCdTV4I3iqkFfPIPuJvmOC63GWi0VEIovUD6BLk4pRTRm31c_hWPBphZrZudWeWaVa5ZrZs_1s1hiT4-98_tgN1t8Kx5AZ6eAZuc7X20owvpluNC8BrEwr04cd9Dj8f_PsBcvbteX_w3bsedyg</recordid><startdate>200112</startdate><enddate>200112</enddate><creator>Van Der Kolk, L. E.</creator><creator>Grillo‐López, A. J.</creator><creator>Baars, J. W.</creator><creator>Hack, C. E.</creator><creator>Van Oers, M. H. J.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Blackwell Publishing Ltd</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200112</creationdate><title>Complement activation plays a key role in the side‐effects of rituximab treatment</title><author>Van Der Kolk, L. E. ; Grillo‐López, A. J. ; Baars, J. W. ; Hack, C. E. ; Van Oers, M. H. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Monoclonal, Murine-Derived</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Complement Activation</topic><topic>Complement C3b - analysis</topic><topic>Complement C3c - analysis</topic><topic>Complement C4 - analysis</topic><topic>Complement C4b - analysis</topic><topic>cytokines</topic><topic>Cytokines - blood</topic><topic>Female</topic><topic>Hematology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-8 - blood</topic><topic>Lymphocyte Count</topic><topic>Lymphoma, Non-Hodgkin - drug therapy</topic><topic>Lymphoma, Non-Hodgkin - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>non‐Hodgkin's lymphoma</topic><topic>Peptide Fragments</topic><topic>Pharmacology. Drug treatments</topic><topic>Rituximab</topic><topic>side‐effects</topic><topic>Stimulation, Chemical</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van Der Kolk, L. E.</creatorcontrib><creatorcontrib>Grillo‐López, A. J.</creatorcontrib><creatorcontrib>Baars, J. W.</creatorcontrib><creatorcontrib>Hack, C. E.</creatorcontrib><creatorcontrib>Van Oers, M. H. J.</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van Der Kolk, L. E.</au><au>Grillo‐López, A. J.</au><au>Baars, J. W.</au><au>Hack, C. E.</au><au>Van Oers, M. H. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complement activation plays a key role in the side‐effects of rituximab treatment</atitle><jtitle>British journal of haematology</jtitle><addtitle>Br J Haematol</addtitle><date>2001-12</date><risdate>2001</risdate><volume>115</volume><issue>4</issue><spage>807</spage><epage>811</epage><pages>807-811</pages><issn>0007-1048</issn><eissn>1365-2141</eissn><coden>BJHEAL</coden><abstract>Treatment with rituximab, a chimaeric anti‐CD20 monoclonal antibody, can be associated with moderate to severe first‐dose side‐effects, notably in patients with high numbers of circulating tumour cells. The aim of this study was to elucidate the mechanism of these side‐effects. At multiple early time points during the first infusion of rituximab, complement activation products (C3b/c and C4b/c) and cytokines [tumour necrosis factor alpha (TNF‐α), interleukin 6 (IL‐6) and IL‐8] were measured in five relapsed low‐grade non‐Hodgkin's lymphoma (NHL) patients. Infusion of rituximab induced rapid complement activation, preceding the release of TNF‐α, IL‐6 and IL‐8. Although the study group was small, the level of complement activation appeared to be correlated both with the number of circulating B cells prior to the infusion (r = 0·85; P = 0·07) and with the severity of the side‐effects. We conclude that complement plays a pivotal role in the pathogenesis of side‐effects of rituximab treatment. As complement activation can not be prevented by corticosteroids, it might be relevant to study the possible role of complement inhibitors during the first administration of rituximab.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11843813</pmid><doi>10.1046/j.1365-2141.2001.03166.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0007-1048 |
ispartof | British journal of haematology, 2001-12, Vol.115 (4), p.807-811 |
issn | 0007-1048 1365-2141 |
language | eng |
recordid | cdi_proquest_miscellaneous_72439606 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Adult Aged Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Murine-Derived Antineoplastic agents Antineoplastic Agents - adverse effects Antineoplastic Agents - therapeutic use Biological and medical sciences Complement Activation Complement C3b - analysis Complement C3c - analysis Complement C4 - analysis Complement C4b - analysis cytokines Cytokines - blood Female Hematology Humans Immunotherapy Interleukin-6 - blood Interleukin-8 - blood Lymphocyte Count Lymphoma, Non-Hodgkin - drug therapy Lymphoma, Non-Hodgkin - immunology Male Medical sciences Middle Aged non‐Hodgkin's lymphoma Peptide Fragments Pharmacology. Drug treatments Rituximab side‐effects Stimulation, Chemical Tumor Necrosis Factor-alpha - analysis |
title | Complement activation plays a key role in the side‐effects of rituximab treatment |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T11%3A02%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Complement%20activation%20plays%20a%20key%20role%20in%20the%20side%E2%80%90effects%20of%20rituximab%20treatment&rft.jtitle=British%20journal%20of%20haematology&rft.au=Van%20Der%20Kolk,%20L.%20E.&rft.date=2001-12&rft.volume=115&rft.issue=4&rft.spage=807&rft.epage=811&rft.pages=807-811&rft.issn=0007-1048&rft.eissn=1365-2141&rft.coden=BJHEAL&rft_id=info:doi/10.1046/j.1365-2141.2001.03166.x&rft_dat=%3Cproquest_cross%3E99147627%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=198564468&rft_id=info:pmid/11843813&rfr_iscdi=true |