Rituximab reduces B cells and T cells in cerebrospinal fluid of multiple sclerosis patients
Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months...
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Published in | Journal of neuroimmunology Vol. 180; no. 1; pp. 63 - 70 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.11.2006
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Subjects | |
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Abstract | Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months post-treatment. ELISAs demonstrated modest reductions in serum antibodies to myelin oligodendrocyte glycoprotein and myelin basic protein in some subjects. Beta-interferon neutralizing antibodies were reduced in three subjects, but developed anew after treatment in three others, suggesting caution in considering rituximab as a means to eliminate NABs. In summary, rituximab depleted B cells from CSF at 24 weeks after initial treatment, and this B cell depletion was associated with a reduction in CSF T cells as well. |
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AbstractList | Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months post-treatment. ELISAs demonstrated modest reductions in serum antibodies to myelin oligodendrocyte glycoprotein and myelin basic protein in some subjects. Beta-interferon neutralizing antibodies were reduced in three subjects, but developed anew after treatment in three others, suggesting caution in considering rituximab as a means to eliminate NABs. In summary, rituximab depleted B cells from CSF at 24 weeks after initial treatment, and this B cell depletion was associated with a reduction in CSF T cells as well. Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months post-treatment. ELISAs demonstrated modest reductions in serum antibodies to myelin oligodendrocyte glycoprotein and myelin basic protein in some subjects. Beta-interferon neutralizing antibodies were reduced in three subjects, but developed anew after treatment in three others, suggesting caution in considering rituximab as a means to eliminate NABs. In summary, rituximab depleted B cells from CSF at 24 weeks after initial treatment, and this B cell depletion was associated with a reduction in CSF T cells as well.Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months post-treatment. ELISAs demonstrated modest reductions in serum antibodies to myelin oligodendrocyte glycoprotein and myelin basic protein in some subjects. Beta-interferon neutralizing antibodies were reduced in three subjects, but developed anew after treatment in three others, suggesting caution in considering rituximab as a means to eliminate NABs. In summary, rituximab depleted B cells from CSF at 24 weeks after initial treatment, and this B cell depletion was associated with a reduction in CSF T cells as well. Effects of B cell depletion by rituximab, a monoclonal antibody to CD20, were studied in patients with relapsing MS that had not responded optimally to standard immunomodulatory therapies. Flow cytometry demonstrated reduced cerebrospinal fluid (CSF) B cells and T cells in most patients at 6 months post-treatment. ELISAs demonstrated modest reductions in serum antibodies to myelin oligodendrocyte glycoprotein and myelin basic protein in some subjects. Beta-interferon neutralizing antibodies were reduced in three subjects, but developed anew after treatment in three others, suggesting caution in considering rituximab as a means to eliminate NABs. In summary, rituximab depleted B cells from CSF at 24 weeks after initial treatment, and this B cell depletion was associated with a reduction in CSF T cells as well. |
Author | Ramsbottom, Michael J. Cross, Anne H. Stark, Jennifer L. Lyons, Jeri-Anne Lauber, Joanne |
Author_xml | – sequence: 1 givenname: Anne H. surname: Cross fullname: Cross, Anne H. email: crossa@neuro.wustl.edu organization: Box 8111, Department of Neurology, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA – sequence: 2 givenname: Jennifer L. surname: Stark fullname: Stark, Jennifer L. organization: Box 8111, Department of Neurology, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA – sequence: 3 givenname: Joanne surname: Lauber fullname: Lauber, Joanne organization: Box 8111, Department of Neurology, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA – sequence: 4 givenname: Michael J. surname: Ramsbottom fullname: Ramsbottom, Michael J. organization: Box 8111, Department of Neurology, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA – sequence: 5 givenname: Jeri-Anne surname: Lyons fullname: Lyons, Jeri-Anne organization: Department of Health Sciences, University of Wisconsin-Milwaukee, Milwaukee, WI, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/16904756$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Adult Antibodies, Monoclonal - immunology Antibodies, Monoclonal - pharmacology Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Murine-Derived Antibody Formation - drug effects Antibody Formation - immunology Antigens, CD20 - immunology Autoantibodies Autoantibodies - analysis Autoantibodies - blood Autoantibodies - immunology B lymphocytes B-Lymphocytes - drug effects B-Lymphocytes - immunology Cerebrospinal Fluid - cytology Cerebrospinal Fluid - immunology Down-Regulation - drug effects Down-Regulation - immunology Female Flow Cytometry Glatiramer Acetate Humans Immunity, Cellular - drug effects Immunity, Cellular - immunology Immunologic Factors - immunology Immunologic Factors - pharmacology Immunologic Factors - therapeutic use Immunosuppression - methods Interferon beta-1a Interferon beta-1b Interferon-beta - therapeutic use Male Middle Aged Multiple sclerosis Multiple Sclerosis, Relapsing-Remitting - cerebrospinal fluid Multiple Sclerosis, Relapsing-Remitting - drug therapy Multiple Sclerosis, Relapsing-Remitting - immunology Myelin basic protein antibodies Myelin oligodendrocyte glycoprotein antibodies Myelin Proteins - immunology Peptides - therapeutic use Rituximab T-Lymphocytes - drug effects T-Lymphocytes - immunology Treatment Treatment Outcome |
Title | Rituximab reduces B cells and T cells in cerebrospinal fluid of multiple sclerosis patients |
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