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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...

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Published in:British journal of haematology 2001-12, Vol.115 (4), p.807-811
Main Authors: Van Der Kolk, L. E., Grillo‐López, A. J., Baars, J. W., Hack, C. E., Van Oers, M. H. J.
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cited_by cdi_FETCH-LOGICAL-c5386-5f58dd0a2501b3bb32153147af2959ab3028bf3b145c7cdf5eded958fd72f74c3
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container_title British journal of haematology
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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
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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. 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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
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