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 inJournal of neuroimmunology Vol. 180; no. 1; pp. 63 - 70
Main Authors Cross, Anne H., Stark, Jennifer L., Lauber, Joanne, Ramsbottom, Michael J., Lyons, Jeri-Anne
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.11.2006
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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.
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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Issue 1
Keywords Multiple sclerosis
Myelin basic protein antibodies
Treatment
Autoantibodies
B lymphocytes
Rituximab
Myelin oligodendrocyte glycoprotein antibodies
Language English
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Snippet 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...
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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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https://dx.doi.org/10.1016/j.jneuroim.2006.06.029
https://www.ncbi.nlm.nih.gov/pubmed/16904756
https://www.proquest.com/docview/19507084
https://www.proquest.com/docview/68137844
https://pubmed.ncbi.nlm.nih.gov/PMC1769354
Volume 180
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