Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis
IntroductionHerpes zoster, which can have a major impact on quality of life, results from reactivation of a latent varicella zoster virus (VZV) infection. We hypothesized that giant cell arteritis (GCA) patients are at increased risk of herpes zoster because of treatment with high-dose glucocorticoi...
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Frontiers Media S.A.
2017-10-01
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Online Access: | http://journal.frontiersin.org/article/10.3389/fimmu.2017.01377/full |
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author | Christien Rondaan Kornelis S. M. van der Geest Elisabeth Eelsing Annemieke M. H. Boots Nicolaas A. Bos Johanna Westra Elisabeth Brouwer |
author_facet | Christien Rondaan Kornelis S. M. van der Geest Elisabeth Eelsing Annemieke M. H. Boots Nicolaas A. Bos Johanna Westra Elisabeth Brouwer |
author_sort | Christien Rondaan |
collection | DOAJ |
description | IntroductionHerpes zoster, which can have a major impact on quality of life, results from reactivation of a latent varicella zoster virus (VZV) infection. We hypothesized that giant cell arteritis (GCA) patients are at increased risk of herpes zoster because of treatment with high-dose glucocorticoids and advanced age. Aim of the study, therefore, was to determine cell-mediated and humoral immunity to VZV in patients with GCA, patients with closely related disease polymyalgia rheumatica (PMR; treated with lower doses of glucocorticoids) and healthy controls (HCs).MethodsCell-mediated immunity to VZV was determined by performing interferon-γ (IFNγ) enzyme-linked immunospot and intracellular cytokine flow cytometry measurements in 11 GCA and 15 PMR patients and in 26 age/sex-matched HCs. Immunoglobulin G antibodies to VZV glycoprotein (VZV-IgG) were measured in serum samples of 35 GCA and 26 PMR patients at different times of follow-up and in 58 age and sex-matched HCs by an enzyme-linked immunosorbent assay.ResultsThe number of VZV-specific IFNγ spot-forming cells was significantly lower in GCA patients on treatment, than in age-matched HCs (p = 0.029), but was not different in PMR patients on treatment. Similar levels of VZV-IgG were found in GCA and PMR patients at baseline, compared to HCs.ConclusionThe finding of a decreased cell-mediated immunity to VZV, known to be of great importance in defense to the virus, indicates an increased herpes zoster risk in GCA patients compared to an already at-risk elderly population. Herpes zoster vaccination is, therefore, of special importance in GCA patients, and would ideally be administered at time of diagnosis. Interestingly, as VZV was suggested to be the trigger in GCA pathogenesis, similar levels of VZV-IgG were found in GCA patients at time of diagnosis and age-matched HCs, indicating that GCA patients did not experience herpes zoster substantially more often in the months preceding diagnosis than controls. |
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spelling | doaj.art-a48a25e391b94fc392d6eebb1b333a832022-12-21T16:53:55ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-10-01810.3389/fimmu.2017.01377294335Decreased Immunity to Varicella Zoster Virus in Giant Cell ArteritisChristien Rondaan0Kornelis S. M. van der Geest1Elisabeth Eelsing2Annemieke M. H. Boots3Nicolaas A. Bos4Johanna Westra5Elisabeth Brouwer6Department of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen, NetherlandsIntroductionHerpes zoster, which can have a major impact on quality of life, results from reactivation of a latent varicella zoster virus (VZV) infection. We hypothesized that giant cell arteritis (GCA) patients are at increased risk of herpes zoster because of treatment with high-dose glucocorticoids and advanced age. Aim of the study, therefore, was to determine cell-mediated and humoral immunity to VZV in patients with GCA, patients with closely related disease polymyalgia rheumatica (PMR; treated with lower doses of glucocorticoids) and healthy controls (HCs).MethodsCell-mediated immunity to VZV was determined by performing interferon-γ (IFNγ) enzyme-linked immunospot and intracellular cytokine flow cytometry measurements in 11 GCA and 15 PMR patients and in 26 age/sex-matched HCs. Immunoglobulin G antibodies to VZV glycoprotein (VZV-IgG) were measured in serum samples of 35 GCA and 26 PMR patients at different times of follow-up and in 58 age and sex-matched HCs by an enzyme-linked immunosorbent assay.ResultsThe number of VZV-specific IFNγ spot-forming cells was significantly lower in GCA patients on treatment, than in age-matched HCs (p = 0.029), but was not different in PMR patients on treatment. Similar levels of VZV-IgG were found in GCA and PMR patients at baseline, compared to HCs.ConclusionThe finding of a decreased cell-mediated immunity to VZV, known to be of great importance in defense to the virus, indicates an increased herpes zoster risk in GCA patients compared to an already at-risk elderly population. Herpes zoster vaccination is, therefore, of special importance in GCA patients, and would ideally be administered at time of diagnosis. Interestingly, as VZV was suggested to be the trigger in GCA pathogenesis, similar levels of VZV-IgG were found in GCA patients at time of diagnosis and age-matched HCs, indicating that GCA patients did not experience herpes zoster substantially more often in the months preceding diagnosis than controls.http://journal.frontiersin.org/article/10.3389/fimmu.2017.01377/fullgiant cell arteritispolymyalgia rheumaticavaricella zoster virusherpes zostercell-mediated immunityhumoral immunity |
spellingShingle | Christien Rondaan Kornelis S. M. van der Geest Elisabeth Eelsing Annemieke M. H. Boots Nicolaas A. Bos Johanna Westra Elisabeth Brouwer Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis Frontiers in Immunology giant cell arteritis polymyalgia rheumatica varicella zoster virus herpes zoster cell-mediated immunity humoral immunity |
title | Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis |
title_full | Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis |
title_fullStr | Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis |
title_full_unstemmed | Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis |
title_short | Decreased Immunity to Varicella Zoster Virus in Giant Cell Arteritis |
title_sort | decreased immunity to varicella zoster virus in giant cell arteritis |
topic | giant cell arteritis polymyalgia rheumatica varicella zoster virus herpes zoster cell-mediated immunity humoral immunity |
url | http://journal.frontiersin.org/article/10.3389/fimmu.2017.01377/full |
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