Literature DB >> 19487650

Natalizumab treatment is associated with peripheral sequestration of proinflammatory T cells.

P Kivisäkk1, B C Healy, V Viglietta, F J Quintana, M A Hootstein, H L Weiner, S J Khoury.   

Abstract

BACKGROUND: Natalizumab is an antibody directed against integrin alpha4 that reduces disease activity in patients with multiple sclerosis (MS) by blocking migration of T and B cells into the CNS. The goal of this study was to characterize the effects of natalizumab treatment on cytokine production and expression of activation markers, costimulatory molecules, and trafficking determinants on CD4+ and CD8+ T cells.
METHODS: In a longitudinal study, we investigated the expression of surface makers and cytokine expression on peripheral blood lymphocytes from 28 patients with MS who started natalizumab treatment and were followed for 1 year. A mixed effects model was used to compare pretreatment to on-treatment measurements.
RESULTS: The frequency of CD4+ T cells producing interferon-gamma, tumor necrosis factor, and interleukin (IL)-17 upon anti-CD3 stimulation increased 6 months after initiation of natalizumab treatment and remained elevated throughout the follow-up. The frequency of CD4+ T cells expressing CD25, HLA-DR, and CCR6 ex vivo was increased at one or more time points during treatment. Among CD8+ T cells, the frequency of cells producing IL-2 and IL-17 after stimulation was increased during natalizumab treatment, as was the frequency of CD8+ T cells expressing CD58 and CCR5 ex vivo. The increase in the frequency of activated cells could not be replicated by in vitro exposure to natalizumab.
CONCLUSION: Natalizumab treatment increases the percentage of activated leukocytes producing proinflammatory cytokines in blood, presumably due to sequestration of activated cells in the peripheral circulation.

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Year:  2009        PMID: 19487650      PMCID: PMC2690969          DOI: 10.1212/WNL.0b013e3181a8266f

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  39 in total

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Journal:  Nature       Date:  1992-03-05       Impact factor: 49.962

2.  Discordant effects of anti-VLA-4 treatment before and after onset of relapsing experimental autoimmune encephalomyelitis.

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4.  Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis.

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Journal:  Nat Med       Date:  2002-05       Impact factor: 53.440

5.  Differential effects of treatment with a small-molecule VLA-4 antagonist before and after onset of relapsing EAE.

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7.  Randomized multicenter trial of natalizumab in acute MS relapses: clinical and MRI effects.

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9.  Surface expression of alpha 4 integrin by CD4 T cells is required for their entry into brain parenchyma.

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Journal:  J Exp Med       Date:  1993-01-01       Impact factor: 14.307

10.  A controlled trial of natalizumab for relapsing multiple sclerosis.

Authors:  David H Miller; Omar A Khan; William A Sheremata; Lance D Blumhardt; George P A Rice; Michele A Libonati; Allison J Willmer-Hulme; Catherine M Dalton; Katherine A Miszkiel; Paul W O'Connor
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  56 in total

1.  Anaphylaxis and mortality induced by treatment of mice with anti-VLA-4 antibody and pertussis toxin.

Authors:  Niannian Ji; Nagarjun Rao; Neal M Guentzel; Bernard P Arulanandam; Thomas G Forsthuber
Journal:  J Immunol       Date:  2011-01-26       Impact factor: 5.422

2.  Oestrogen-mediated protection of experimental autoimmune encephalomyelitis in the absence of Foxp3+ regulatory T cells implicates compensatory pathways including regulatory B cells.

Authors:  Sandhya Subramanian; Melissa Yates; Arthur A Vandenbark; Halina Offner
Journal:  Immunology       Date:  2010-11-23       Impact factor: 7.397

3.  Natalizumab and the development of extensive brain lesions in neuromyelitis optica.

Authors:  Maciej Juryńczyk; Krzysztof Zaleski; Krzysztof Selmaj
Journal:  J Neurol       Date:  2013-05-30       Impact factor: 4.849

4.  Multiple sclerosis symptom recrudescence at the end of the natalizumab dosing cycle.

Authors:  John N Ratchford; Regina Brock-Simmons; Amanda Augsburger; Sonya U Steele; Kristie Mohn; Mandi Rhone; Jinyan Bo; Kathleen Costello
Journal:  Int J MS Care       Date:  2014

5.  Immune reconstitution inflammatory syndrome in natalizumab-associated PML.

Authors:  I L Tan; J C McArthur; D B Clifford; E O Major; A Nath
Journal:  Neurology       Date:  2011-08-10       Impact factor: 9.910

Review 6.  The anatomical and cellular basis of immune surveillance in the central nervous system.

Authors:  Richard M Ransohoff; Britta Engelhardt
Journal:  Nat Rev Immunol       Date:  2012-08-20       Impact factor: 53.106

7.  Multiple sclerosis: Natalizumab to fingolimod--the washout whitewash.

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Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

8.  Long-term follow-up of peripheral lymphocyte subsets in a cohort of multiple sclerosis patients treated with natalizumab.

Authors:  T Koudriavtseva; E Sbardella; E Trento; V Bordignon; G D'Agosto; P Cordiali-Fei
Journal:  Clin Exp Immunol       Date:  2014-06       Impact factor: 4.330

9.  Galectin-9 protein is up-regulated in astrocytes by tumor necrosis factor and promotes encephalitogenic T-cell apoptosis.

Authors:  Andrew J Steelman; Roger Smith; C Jane Welsh; Jianrong Li
Journal:  J Biol Chem       Date:  2013-07-08       Impact factor: 5.157

10.  Hematopoietic mobilization: Potential biomarker of response to natalizumab in multiple sclerosis.

Authors:  Miriam Mattoscio; Richard Nicholas; Maria P Sormani; Omar Malik; Jean S Lee; Adam D Waldman; Francesco Dazzi; Paolo A Muraro
Journal:  Neurology       Date:  2015-03-11       Impact factor: 9.910

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