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July 09, 2013; 81 (2) Article

T-cell response against varicella-zoster virus in fingolimod-treated MS patients

Meret E. Ricklin, Johannes Lorscheider, Anne Waschbisch, Cecile Paroz, Satish K. Mehta, Duane L. Pierson, Jens Kuhle, Bettina Fischer-Barnicol, Till Sprenger, Raija L.P. Lindberg, Ludwig Kappos, Tobias Derfuss
First published May 22, 2013, DOI: https://doi.org/10.1212/WNL.0b013e31829a3311
Meret E. Ricklin
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Johannes Lorscheider
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Anne Waschbisch
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Cecile Paroz
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Satish K. Mehta
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Duane L. Pierson
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Jens Kuhle
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Bettina Fischer-Barnicol
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Till Sprenger
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Raija L.P. Lindberg
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Ludwig Kappos
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Tobias Derfuss
From Clinical Neuroimmunology, Department of Biomedicine (M.E.R., J.L., C.P., J.K., R.L.P.L., L.K., T.D.), and Divisions of Diagnostic and Interventional Neuroradiology, Department of Radiology and Nuclear Medicine (T.S.), University of Basel; Department of Neurology (J.L., J.K., B.F.-B., T.S., L.K., T.D.), University Hospital Basel, Switzerland; Department of Neurology (A.W.), University Hospital Erlangen, Germany; and Microbiology Lab (S.K.M.), Johnson Space Center–NASA, Houston, TX.
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Full PDF
Citation
T-cell response against varicella-zoster virus in fingolimod-treated MS patients
Meret E. Ricklin, Johannes Lorscheider, Anne Waschbisch, Cecile Paroz, Satish K. Mehta, Duane L. Pierson, Jens Kuhle, Bettina Fischer-Barnicol, Till Sprenger, Raija L.P. Lindberg, Ludwig Kappos, Tobias Derfuss
Neurology Jul 2013, 81 (2) 174-181; DOI: 10.1212/WNL.0b013e31829a3311

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Abstract

Objective: To study the immune response against varicella-zoster virus (VZV) in patients with multiple sclerosis before and during fingolimod therapy.

Methods: The VZV-specific immune response was studied using interferon (IFN)-γ enzyme-linked immunosorbent spot assay, proliferation assays, and upregulation of T-cell activation markers in patients before (n = 38) and after 3 months of fingolimod therapy (n = 34), in untreated (n = 33) and IFN-β–treated (n = 25) patients with multiple sclerosis, and in healthy controls (n = 22). Viral replication was analyzed by using real-time PCR in 76 peripheral blood mononuclear cell samples and 146 saliva samples.

Results: Treatment with fingolimod led to a marked reduction of CD3+ T cells with a relative decrease of naive and central memory T cells and an increase of effector memory T cells. Expression of the activation markers CD137 and CD69 upon VZV stimulation was unaltered by fingolimod. However, the absolute number of cells proliferating upon VZV stimulation was reduced in the blood of patients treated with fingolimod. Also, VZV-specific and Epstein-Barr virus (EBV)-specific IFN-γ–producing cells were reduced after fingolimod therapy. Seven of the 35 patients treated with fingolimod showed signs of VZV or EBV reactivation in saliva compared with 3 of the 111 controls. None of the 76 tested samples showed signs of viral reactivation in the peripheral blood mononuclear cells.

Conclusion: Patients treated with fingolimod show a slightly reduced antiviral T-cell response. This reduced response is accompanied by a subclinical reactivation of VZV or EBV in the saliva of 20% of patients treated with fingolimod.

GLOSSARY

CFSE=
carboxyfluorescein diacetate succinimidyl ester;
EBV=
Epstein-Barr virus;
ELISpot=
enzyme-linked immunosorbent spot;
FITC=
fluorescein isothiocyanate;
FTY=
fingolimod;
IFN=
interferon;
IgG=
immunoglobulin G;
MS=
multiple sclerosis;
PBMC=
peripheral blood mononuclear cell;
PE=
phycoerythrin;
pFTY=
before treatment with fingolimod;
TCM=
central memory T cells;
TEM=
effector memory T cells;
VZV=
varicella-zoster

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at www.neurology.org

  • Received August 9, 2012.
  • Accepted in final form March 19, 2013.
  • © 2013 American Academy of Neurology
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