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Natalizumab in Multiple Sclerosis Treatment: From Biological Effects to Immune Monitoring
by
Khoy, Kathy
, Le Mauff, Brigitte
, Petit, Gautier
, Defer, Gilles
, Toutirais, Olivier
, Mariotte, Delphine
in
Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antigens
/ Autoimmune diseases
/ biotherapy
/ CD49d antigen
/ Cell migration
/ Central nervous system
/ Demyelinating diseases
/ Demyelination
/ Disease Susceptibility
/ drug modifying therapy
/ Drug Monitoring
/ Humans
/ Immunoglobulins
/ Immunology
/ Integrin
/ Integrin alpha4 - antagonists & inhibitors
/ Leukocytes
/ Leukocytes (mononuclear)
/ Leukoencephalitis
/ Leukoencephalopathy, Progressive Multifocal - complications
/ Ligands
/ Lymphocytes
/ Mab therapy monitoring
/ Molecular Targeted Therapy
/ Monoclonal antibodies
/ Multiple sclerosis
/ Multiple Sclerosis - diagnosis
/ Multiple Sclerosis - drug therapy
/ Multiple Sclerosis - etiology
/ Multiple Sclerosis - metabolism
/ natalizumab
/ Natalizumab - pharmacology
/ Natalizumab - therapeutic use
/ Patients
/ T-Lymphocyte Subsets - drug effects
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Treatment Outcome
/ VLA-4 antigen
2020
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Natalizumab in Multiple Sclerosis Treatment: From Biological Effects to Immune Monitoring
by
Khoy, Kathy
, Le Mauff, Brigitte
, Petit, Gautier
, Defer, Gilles
, Toutirais, Olivier
, Mariotte, Delphine
in
Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antigens
/ Autoimmune diseases
/ biotherapy
/ CD49d antigen
/ Cell migration
/ Central nervous system
/ Demyelinating diseases
/ Demyelination
/ Disease Susceptibility
/ drug modifying therapy
/ Drug Monitoring
/ Humans
/ Immunoglobulins
/ Immunology
/ Integrin
/ Integrin alpha4 - antagonists & inhibitors
/ Leukocytes
/ Leukocytes (mononuclear)
/ Leukoencephalitis
/ Leukoencephalopathy, Progressive Multifocal - complications
/ Ligands
/ Lymphocytes
/ Mab therapy monitoring
/ Molecular Targeted Therapy
/ Monoclonal antibodies
/ Multiple sclerosis
/ Multiple Sclerosis - diagnosis
/ Multiple Sclerosis - drug therapy
/ Multiple Sclerosis - etiology
/ Multiple Sclerosis - metabolism
/ natalizumab
/ Natalizumab - pharmacology
/ Natalizumab - therapeutic use
/ Patients
/ T-Lymphocyte Subsets - drug effects
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Treatment Outcome
/ VLA-4 antigen
2020
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Natalizumab in Multiple Sclerosis Treatment: From Biological Effects to Immune Monitoring
by
Khoy, Kathy
, Le Mauff, Brigitte
, Petit, Gautier
, Defer, Gilles
, Toutirais, Olivier
, Mariotte, Delphine
in
Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antigens
/ Autoimmune diseases
/ biotherapy
/ CD49d antigen
/ Cell migration
/ Central nervous system
/ Demyelinating diseases
/ Demyelination
/ Disease Susceptibility
/ drug modifying therapy
/ Drug Monitoring
/ Humans
/ Immunoglobulins
/ Immunology
/ Integrin
/ Integrin alpha4 - antagonists & inhibitors
/ Leukocytes
/ Leukocytes (mononuclear)
/ Leukoencephalitis
/ Leukoencephalopathy, Progressive Multifocal - complications
/ Ligands
/ Lymphocytes
/ Mab therapy monitoring
/ Molecular Targeted Therapy
/ Monoclonal antibodies
/ Multiple sclerosis
/ Multiple Sclerosis - diagnosis
/ Multiple Sclerosis - drug therapy
/ Multiple Sclerosis - etiology
/ Multiple Sclerosis - metabolism
/ natalizumab
/ Natalizumab - pharmacology
/ Natalizumab - therapeutic use
/ Patients
/ T-Lymphocyte Subsets - drug effects
/ T-Lymphocyte Subsets - immunology
/ T-Lymphocyte Subsets - metabolism
/ Treatment Outcome
/ VLA-4 antigen
2020
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Natalizumab in Multiple Sclerosis Treatment: From Biological Effects to Immune Monitoring
Journal Article
Natalizumab in Multiple Sclerosis Treatment: From Biological Effects to Immune Monitoring
2020
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Overview
Multiple sclerosis is a chronic demyelinating disease of the central nervous system (CNS) with an autoimmune component. Among the recent disease-modifying treatments available, Natalizumab, a monoclonal antibody directed against the alpha chain of the VLA-4 integrin (CD49d), is a potent inhibitor of cell migration toward the tissues including CNS. It potently reduces relapses and active brain lesions in the relapsing remitting form of the disease. However, it has also been associated with a severe infectious complication, the progressive multifocal leukoencephalitis (PML). Using the standard protocol with an injection every 4 weeks it has been shown by a close monitoring of the drug that trough levels soon reach a plateau with an almost saturation of the target cell receptor as well as a down modulation of this receptor. In this review, mechanisms of action involved in therapeutic efficacy as well as in PML risk will be discussed. Furthermore the interest of a biological monitoring that may be helpful to rapidly adapt treatment is presented. Indeed, development of anti-NAT antibodies, although sometimes unapparent, can be detected indirectly by normalization of CD49d expression on circulating mononuclear cells and might require to switch to another drug. On the other hand a stable modulation of CD49d expression might be useful to follow the circulating NAT levels and apply an extended interval dose scheme that could contribute to limiting the risk of PML.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
Antibodies, Monoclonal - pharmacology
/ Antibodies, Monoclonal - therapeutic use
/ Antigens
/ Humans
/ Integrin
/ Integrin alpha4 - antagonists & inhibitors
/ Leukoencephalopathy, Progressive Multifocal - complications
/ Ligands
/ Multiple Sclerosis - diagnosis
/ Multiple Sclerosis - drug therapy
/ Multiple Sclerosis - etiology
/ Multiple Sclerosis - metabolism
/ Natalizumab - therapeutic use
/ Patients
/ T-Lymphocyte Subsets - drug effects
/ T-Lymphocyte Subsets - immunology
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