Next Article in Journal
The Implementation of Mass-Vaccination against SARS-CoV-2: A Systematic Review of Existing Strategies and Guidelines
Next Article in Special Issue
Association between Antiviral Prophylaxis and Cytomegalovirus and Epstein–Barr Virus DNAemia in Pediatric Recipients of Allogeneic Hematopoietic Stem Cell Transplant
Previous Article in Journal
BNT162b2 Vaccine Encoding the SARS-CoV-2 P2 S Protects Transgenic hACE2 Mice against COVID-19
Previous Article in Special Issue
Factors Associated with Post-Transplant Active Epstein-Barr Virus Infection and Lymphoproliferative Disease in Hematopoietic Stem Cell Transplant Recipients: A Systematic Review and Meta-Analysis
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Vaccines
Volume 9
Issue 4
10.3390/vaccines9040325
vaccines-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Brief Report

Humoral Immunity to Varicella Zoster Virus in Patients with Systemic Lupus Erythematosus and Rheumatoid Arthritis Compared to Healthy Controls

by
Marco Krasselt
1,*,
Christoph Baerwald
1,
Uwe G. Liebert
2 and
Olga Seifert
1
1
Rheumatology Unit, Clinic for Endocrinology, Nephrology and Rheumatology, Department of Internal Medicine, Neurology and Dermatology, University of Leipzig, Liebigstr. 20, 04103 Leipzig, Germany
2
Institute for Virology, University of Leipzig, Johannisallee 30, 04103 Leipzig, Germany
*
Author to whom correspondence should be addressed.
Vaccines 2021, 9(4), 325; https://doi.org/10.3390/vaccines9040325
Submission received: 8 March 2021 / Revised: 22 March 2021 / Accepted: 29 March 2021 / Published: 1 April 2021
(This article belongs to the Special Issue Herpesvirus-Specific Immunomonitoring in Patient Groups of Increased Risk)
Browse Figures
Versions Notes

Abstract

:
Background: The prevalence of herpes zoster (HZ) is high in patients with rheumatic diseases. Systemic lupus erythematosus (SLE) doubles the risk for developing HZ. However, little is known about natural humoral immunity against varicella zoster virus (VZV) in patients with SLE. Hence, we compared VZV IgG antibody concentrations in a group of SLE patients with healthy controls and patients with rheumatoid arthritis (RA). Methods: n = 56 patients with SLE, n = 54 patients with RA, and n = 56 healthy controls were included in this study. The VZV IgG antibody concentration was measured using an enzyme-linked immunosorbent assay (ELISA). The antibody concentrations were compared between the groups. Results: Overall IgG antibody titers for VZV in SLE patients were comparable to healthy controls but higher when compared to patients with rheumatoid arthritis (p = 0.0012). In consequence, antibody levels in controls were higher than in RA patients (p = 0.0097). Stratification by age revealed highest titers among SLE patients in the fourth life decade (p = 0.03 for controls, p = 0.0008 for RA patients) whereas RA patients in their sixth decade had the lowest antibody concentration (p = 0.03 for controls, p = 0.04 for SLE patients). Regarding the individual HZ history, antibody levels of SLE patients with a positive history exceeded all other groups. Conclusions: Although humoral VZV immunity in SLE patients is comparable to healthy controls it seems to be pronounced in young SLE patients between 30 and 39. The lowest VZV IgG levels were found in RA patients. HZ seems to induce antibody production, particularly in patients with SLE. Immunological processes might contribute to VZV antibody levels in SLE patients, but further investigations are needed to substantiate this hypothesis. Even though the increased HZ prevalence seems to be independent of humoral immunity in SLE patients, reduced humoral immunity might contribute to HZ in RA patients. The available HZ subunit vaccination might be an appropriate way to reduce the HZ risk in patients with rheumatic diseases.

1. Introduction

With a lifetime risk of 20–30% in general and up to 50% in people reaching 85 years of age [1], herpes zoster (HZ, shingles) is a relevant clinical problem. Current investigations show an overall incidence of 9.9/1.000 person-years [2]. HZ is the result of an endogenous reactivation of a latent varicella zoster virus (VZV) infection, persisting in the sensory ganglia [3]. The most important complication of HZ is postherpetic neuralgia (PHN), a neuropathic pain syndrome that can persist for years and is often intractable [3]. The relevance of HZ is particularly high in patients with inflammatory rheumatic diseases. Within this large group, patients with systemic lupus erythematosus (SLE, relative risk (RR) up to 4.11) and rheumatoid arthritis (RA, RR up to 2.4) show a particularly increased risk for acquiring HZ [4,5,6]. This increased risk leads to high incidences of up to 91/1.000 person-years in SLE and 12/1.000 person-years in RA patients [5,7]. To date, two different vaccines have been approved to prevent HZ: a live-attenuated vaccine in 2006 and a subunit vaccine in 2017/2018. Increasing use of the available vaccines might reduce the striking incidence in inflammatory rheumatic diseases in the future. Nevertheless, the knowledge concerning humoral VZV immunity in SLE and RA patients is limited. We therefore compared VZV IgG antibodies in patients with SLE to both RA patients and controls.

2. Methods and Study Design

Consecutive patients with SLE or RA (≥18 years), matched for age and sex, were recruited from our outpatient clinic for participation in this study. SLE patients fulfilled the American College of Rheumatology (ACR) criteria for SLE [8], and RA patients the 2010 criteria of the ACR/European League Against Rheumatism (EULAR) [9]. Herpes zoster history was taken during the visit or was available from the existing medical records.
To compare the VZV antibody titers, controls without any history of inflammatory rheumatic or other relevant autoimmune diseases were randomly selected from the University Hospital of Leipzig and were age- and sex-matched. VZV IgG antibody concentrations were measured with an IgG enzyme-linked immunosorbent assay (ELISA) employing highly purified whole virus lysate strain Ellen.
The ethics committee of the University of Leipzig approved the design of the study, and written informed consent was obtained from each participant before study enrollment.

Biostatistical Analysis

To report continuous data in this study, mean and standard deviation were used. Categorical data were described by absolute or relative frequencies. Fisher’s exact test was performed to compare frequencies of categorical variables. For the comparison of continuous data, either student’s t test or the Mann–Whitney U test was used after performing the Kolmogorov–Smirnov normality test. Holm-Šidák’s correction for multiple comparisons was applied for the subgroup analysis. Correlation between two parameters was analyzed with either Pearson’s product–moment correlation or Spearman, depending on the data distribution. A significant statistical difference was assumed when the p-value was below 0.05. Statistical analysis and figure preparation was conducted using GraphPad PRISM Version 8 for Mac (GraphPad Software Inc., San Diego, CA, USA).

3. Results

In total, 56 SLE (mean age 49.8 ± 15.9 years) and 54 RA patients (mean age 51.3 ± 13.4 years) were enrolled in this study. Furthermore, 56 controls (mean age 51.9 ± 14.8 years) were randomly selected from the diagnostic in-house routine. None of the participants had an HZ vaccination. There were no significant differences in age and sex between the patient groups and the healthy control group.
Details on the included patients and controls can be obtained from Table 1, and the medication of the patients is presented in Table 2.

3.1. VZV IgG Concentrations in SLE Patients Are Comparable to Healthy Controls but Higher Than in RA Patients

When comparing the VZV IgG levels between the three groups (Figure 1), the levels in SLE patients were comparable to controls but significantly higher than in RA patients (p = 0.0012). Furthermore, titers were higher in controls than in RA patients (p = 0.0097). No correlation between the individual medication and antibody levels was found within the two patient groups. Looking at all patients (SLE and RA), though, the use of azathioprine was positively correlated with the antibody titer (r = 0.274, p = 0.004). The meaning of this finding is limited by the fact that only one RA patient was receiving azathioprine.

3.2. Young SLE Patients Show the Highest VZV Titers

A stratification by age revealed the VZV IgG titers to be highest in SLE patients between 30 and 39 years (n = 6) compared to both controls (n = 5, p = 0.03) and RA patients (n = 7, p = 0.0008). Interestingly, RA patients between 50 and 59 years (n = 12) had significantly lower levels than the controls (n = 16, p = 0.03) and SLE patients (n = 13, p = 0.04). Beyond the age of 60, no difference in VZV IgG levels was found throughout the three groups (Figure 2).

3.3. History of Herpes Zoster in SLE Patients Is Associated with Higher Antibody Levels

The mean age at developing HZ was 33.5 ± 12.4 years (SLE) and 36.7 ± 12.4 years (RA) in our cohort. The HZ frequency was comparable in both patient groups (30.4 vs. 25.9% in SLE and RA patients, respectively). The mean time from onset of the rheumatic disease to HZ was shorter in SLE patients (6.8 ± 5.9 vs. 15.2 ± 10.2 years, p = 0.04, Table 1). When comparing the VZV IgG levels between SLE patients with positive HZ history and any other group (including SLE patients without HZ history, but also RA patients and controls), SLE patients show higher titers after at least one episode of HZ (Figure 3, statistical significances as indicated). No other inter-group differences were found in that regard. HZ history was not available for the controls. Furthermore, in both patient groups, no correlation between the age at HZ and the antibody level was revealed. Among SLE patients, prednisolone use (regardless the dose) was associated with a higher risk for HZ (p = 0.01).

4. Discussion

The aim of this study was to compare humoral immunity against VZV in SLE patients to patients with RA and healthy controls. Patients with inflammatory rheumatic diseases, in particular with SLE and RA, have an increased risk of developing herpes zoster (HZ) during their lifetime [4,5,6,10,11]. Age, use of immunosuppressives (including small molecules such as baricitinib), and glucocorticoid therapy increase that risk further [12,13,14]. In our cohort, an association between HZ and glucocorticoid use was evident in SLE patients only.
Both SLE and RA have a different and complex pathophysiology. SLE is often referred to as the prototype autoimmune disease with B-/T-cell exaggeration, autoantibody production, and immune complex deposition. RA, however, involves synovitis with infiltration of mononuclear cells and disease perpetuation is driven by cytokines such as tumor necrosis factor (TNF) [15].
The knowledge on immunity against VZV in inflammatory rheumatic diseases is scarce, mostly focusing on cellular rather than humoral immunity [7,16,17,18,19]. Of particular interest is our observation that young SLE patients in their fourth decade of life harbored higher titers than both controls and RA patients. Other researchers found higher overall titers of VZV IgG in SLE patients (n = 38) compared to healthy controls, independent of their age [7]. The authors speculated that SLE flares could be responsible for subclinical virus reactivations and therefore lead to increased VZV antibody levels. Of importance, no individual HZ history was available in that study [7]. A further investigation showed no connection between SLE disease activity and VZV antibody levels [20], making increased VZV titers due to subclinical reactivations in SLE flares unlikely [7,20]. Our results lead to the assumption that at least one episode of HZ is related to higher VZV titers in SLE patients. This finding is in line with the report of Nagasawa et al., who measured antibodies using a neutralization test [21]. Polyclonal hypergammaglobulinemia is frequently seen in patients with SLE [16,22,23,24], most likely due to B-cell activation [25]. Therefore, polyclonal IgG elevation was believed to be a possible explanation for high VZV IgG levels in SLE patients [21,26]. This assumption was questioned when IgG antibodies against diphtheria were found to be lower in SLE patients than in age-matched healthy controls, while VZV IgG antibodies were increased in the same SLE cohort [7]. Hypergammaglobulinemia as a consequence of polyclonal B-cell activation is also known in RA patients [24,27,28]. Antibodies against VZV, however, were lowest in RA patients in our cohort. Furthermore, we previously demonstrated that VZV antibody avidity is decreased in RA patients compared to matched controls [29]. Reactivation of VZV (either with HZ disease or subclinical) is thought to stimulate production of VZV IgG antibodies [30], a process called endogenous boosting [31]. However, VZV IgG levels in SLE patients with a positive HZ history not only exceeded those in SLE patients without a HZ history, but also those in RA patients regardless of their HZ history. Furthermore, antibody levels of SLE patients with a positive history were also higher than in controls. Although these findings emphasize the impact of a prior HZ on the VZV antibody levels in SLE patients, they also imply the existence of SLE-specific reasons. In a recent trial, combined therapy targeting B-cells with rituximab (CD20 antibody) and belimumab (B-cell activating factor (BAFF) antibody) in SLE patients led to a significant decrease of anti-VZV IgG, whereas both anti-tetanus IgG and anti-rubella IgG remained stable [32]. The authors speculated that autoreactive B-cells might have an increased BAFF dependence due to the continuous (auto-)antigen presence. In our cohort, only one SLE patient was under rituximab therapy, not allowing us to draw meaningful conclusions in that regard. Nevertheless, this speculation could explain the impact on VZV antibodies since VZV persists in the cranial nerve and dorsal root sensory ganglia after primary infection [32,33]. Indeed, high BAFF levels result in an enhanced humoral immunity and are associated with an increased SLE risk [34]. Therefore, the high levels of VZV antibodies in SLE patients might be the combined consequence of both autoreactive B-cells and prior HZ.
Despite the increased VZV antibodies, HZ incidence was high in SLE patients. The elevated VZV levels in the SLE patients in our cohort in their fourth decade of life might also be explained by the peak frequency of HZ at this age (mean age 33.5 ± 12.4 years). RA patients in our cohort had a similar mean age when developing HZ (36.7 ± 12.4 years), but lower antibody levels, emphasizing the suggested SLE-related reasons discussed above. An explanation for the particularly reduced antibody concentrations among RA patients in their sixth decade, probably hampering VZV immunity, might be premature immunosenescence, as discussed elsewhere [29,35].
During the last years, evidence accumulated that cell-mediated rather than humoral immunity is likely to be of utmost importance for controlling VZV reactivation. Cell-mediated immunity (measured using the VZV skin test) inversely correlates with both the severity of HZ skin lesions and pain [36,37]. In this context, the incidence of PHN might be associated with the decline of VZV-specific cell-mediated immunity [38]. However, humoral immunity, i.e., an antibody level increase, correlates with vaccine efficacy [39]. We previously showed that humoral VZV immunity seems to be reduced in RA patients [29]. The results at hand confirm this finding. Unfortunately, HZ vaccination indication in patients with rheumatic diseases remain unclear and reported vaccination rates are generally low [40,41,42,43,44]. The EULAR recommends HZ vaccination in patients with inflammatory rheumatic diseases “at high risk” only [45], and the ACR recommends a vaccination (live vaccine) for RA patients under treatment with disease-modifying antirheumatic drugs excluding any biologic therapy [46]. German vaccination guidelines, however, recommend HZ vaccination using the subunit vaccine for all patients with SLE or RA ≥ 50 years [47]. This recommendation is based on the pivotal subunit vaccine trials [48,49] and investigations on the efficacy and safety in other immunocompromised patient groups (e.g., patients after peripheral stem cell transplantation or renal transplant recipients) [50,51,52,53,54]. Although the live vaccine was shown to be effective and well tolerated in stable SLE patients in a randomized trial [55] and retrospective analyses also indicated a reduced incidence of HZ for other individuals under immunosuppressive medication, including RA patients [56,57], its effectiveness is limited and reduced in the elderly (<70 years 63.9%, ≥70 years 37.6%) [3]. The subunit vaccine, however, demonstrated a high efficacy of 97.2 and 89.8%, respectively (patients ≥ 50 and ≥70 years) [48,49]. Recently published post-marketing safety data are promising [58,59]. Data on effectiveness and safety in patients with inflammatory rheumatic diseases, however, are still scarce, except for preliminary data focusing on RA patients [60,61].
Our study has several limitations. Most importantly, no HZ history was available from the controls, limiting the subgroup analysis to both of the patient groups. On the other hand, we were able to compare the four subgroups of the two rheumatic entities to a healthy control group, gaining insight into humoral immunity of both SLE and RA patients. In addition, the sample size is relatively small, but comparable to other investigations in that context. Nevertheless, we believe that our results may contribute to furthering our understanding of VZV immunity, particularly in patients with rheumatic diseases.

5. Conclusions

HZ is a relevant clinical problem in patients with inflammatory rheumatic diseases. Incidence is highest in SLE patients despite increased antibody levels in young patients. Clinicians should therefore not rely on high antibody levels, suggesting proper immunity. Besides prior HZ episodes, BAFF might be involved in the seemingly adequate humoral immunity in SLE patients, but clearly further studies including cell-mediated VZV immunity are needed to underline this speculation. Vaccination against HZ should be considered in patients with rheumatic diseases, particularly in SLE and RA patients, who are both at a high risk.

Author Contributions

M.K.: statistical analysis, data interpretation, and manuscript drafting. C.B.: contribution to data interpretation and manuscript drafting. U.G.L.: antibody titer measurement and contribution to manuscript drafting. O.S.: data collection and contribution to statistical analysis as well as manuscript preparation. All authors have read and agreed to the published version of the manuscript.

Funding

We acknowledge support from Leipzig University for Open Access Publishing.

Institutional Review Board Statement

All procedures performed in this survey were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Data obtained in this study did not interfere with the course of treatment for patients included.

Informed Consent Statement

Informed consent was obtained from all participants.

Data Availability Statement

The data presented in this study are available on reasonable request from the corresponding author. The data are not publicly available due to privacy reasons.

Conflicts of Interest

M.K., U.G.L. and O.S. have nothing to declare. C.B. received lecture fees from Merck, MSD, Mundipharma, and Pfizer.

References

  1. Thomas, S.L.; Hall, A.J. What Does Epidemiology Tell Us About Risk Factors for Herpes Zoster? Lancet Infect. Dis. 2004, 4, 26–33. [Google Scholar] [CrossRef]
  2. Tseng, H.F.; Bruxvoort, K.; Ackerson, B.; Luo, Y.; Tanenbaum, H.; Tian, Y.; Zheng, C.; Cheung, B.; Patterson, B.J.; Van Oorschot, D.; et al. The epidemiology of herpes zoster in immunocompetent, unvaccinated adults >/= 50 years old: Incidence, complications, hospitalization, mortality, and recurrence. J. Infect. Dis. 2020, 222, 798–806. [Google Scholar] [CrossRef]
  3. Oxman, M.N.; Levin, M.J.; Johnson, G.R.; Schmader, K.E.; Straus, S.E.; Gelb, L.D.; Arbeit, R.D.; Simberkoff, M.S.; Gershon, A.A.; Davis, L.E.; et al. A vaccine to prevent herpes zoster and postherpetic neuralgia in older adults. N. Engl. J. Med. 2005, 352, 2271–2284. [Google Scholar] [CrossRef] [Green Version]
  4. Forbes, H.J.; Bhaskaran, K.; Thomas, S.L.; Smeeth, L.; Clayton, T.; Langan, S.M. Quantification of risk factors for herpes zoster: Population based case-control study. Br. Med. J. 2014, 348, g2911. [Google Scholar] [CrossRef] [Green Version]
  5. Veetil, B.M.A.; Myasoedova, E.; Matteson, E.L.; Gabriel, S.E.; Green, A.B.; Crowson, C.S. Incidence and time trends of herpes zoster in rheumatoid arthritis: A population-based cohort study. Arthritis Care Res. 2013, 65, 854–861. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Hata, A.; Kuniyoshi, M.; Ohkusa, Y. Risk of herpes zoster in patients with underlying diseases: A retrospective hospital-based cohort study. Infection 2011, 39, 537–544. [Google Scholar] [CrossRef] [Green Version]
  7. Rondaan, C.; De Haan, A.; Horst, G.; Hempel, J.C.; Van Leer, C.; Bos, N.A.; Van Assen, S.; Bijl, M.; Westra, J. Altered cellular and humoral immunity to varicella-zoster virus in patients with autoimmune diseases. Arthritis Rheumatol. 2014, 66, 3122–3128. [Google Scholar] [CrossRef]
  8. Tan, E.M.; Cohen, A.S.; Fries, J.F.; Masi, A.T.; McShane, D.J.; Rothfield, N.F.; Schaller, J.G.; Talal, N.; Winchester, R.J. The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheumatol. 1982, 25, 1271–1277. [Google Scholar] [CrossRef] [PubMed]
  9. Aletaha, D.; Neogi, T.; Silman, A.J.; Funovits, J.; Felson, D.T.; Bingham, C.O., 3rd; Birnbaum, N.S.; Burmester, G.R.; Bykerk, V.P.; Cohen, M.D. 2010 rheumatoid arthritis classification criteria: An American College of Rheumatology/European League against Rheumatism collaborative initiative. Ann. Rheum. Dis. 2010, 69, 1580–1588. [Google Scholar] [CrossRef] [PubMed]
  10. Smitten, A.L.; Choi, H.K.; Hochberg, M.C.; Suissa, S.; Simon, T.A.; Testa, M.A.; Chan, K.A. The risk of herpes zoster in patients with rheumatoid arthritis in the United States and the United Kingdom. Arthritis Rheumatol. 2007, 57, 1431–1438. [Google Scholar] [CrossRef]
  11. Kawai, K.; Yawn, B.P. Risk factors for herpes zoster: A systematic review and meta-analysis. Mayo Clin. Proc. 2017, 92, 1806–1821. [Google Scholar] [CrossRef] [Green Version]
  12. Pappas, D.A.; Hooper, M.M.; Kremer, J.M.; Reed, G.; Shan, Y.; Wenkert, D.; Greenberg, J.D.; Curtis, J.R. Herpes zoster reactivation in patients with rheumatoid arthritis: Analysis of disease characteristics and disease-modifying antirheumatic drugs. Arthritis Care Res. 2015, 67, 1671–1678. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Liao, T.-L.; Chen, Y.-M.; Liu, H.-J.; Chen, D.-Y. Risk and severity of herpes zoster in patients with rheumatoid arthritis receiving different immunosuppressive medications: A case-control study in Asia. Br. Med. J. Open 2017, 7, e014032. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Bechman, K.; Subesinghe, S.; Norton, S.; Atzeni, F.; Galli, M.; Cope, A.P.; Winthrop, K.L.; Galloway, J.B. A Systematic review and meta-analysis of infection risk with small molecule jak inhibitors in rheumatoid arthritis. Rheumatology 2019, 58, 1755–1766. [Google Scholar] [CrossRef] [PubMed]
  15. Firestein, G.; Budd, R.; Sherine, E.G.; Iain, B.M.; O′Dell, J. Firestein & Kelley′s Textbook of Rheumatology-E-Book; Elsevier: London, UK, 2020. [Google Scholar]
  16. Blaese, R.; Grayson, J.; Steinberg, A.D. Increased immunoglobulin-secreting cells in the blood of patients with active systemic lupus erythematosus. Am. J. Med. 1980, 69, 345–3450. [Google Scholar] [CrossRef]
  17. Krasselt, M.; Baerwald, C. Sex, symptom severity, and quality of life in rheumatology. Clin. Rev. Allergy Immunol. 2017, 26, 1214–1221. [Google Scholar] [CrossRef]
  18. Levin, M.J.; Oxman, M.N.; Zhang, J.H.; Johnson, G.R.; Stanley, H.; Hayward, A.R.; Caulfield, M.J.; Irwin, M.R.; Smith, J.G.; Clair, J.; et al. Varicella-zoster virus-specific immune responses in elderly recipients of a herpes zoster vaccine. J. Infect. Dis. 2008, 197, 825–835. [Google Scholar] [CrossRef] [Green Version]
  19. Levin, M.J.; Smith, J.G.; Kaufhold, R.M.; Barber, D.; Hayward, A.R.; Chan, C.Y.; Chan, I.S.; Li, D.J.; Wang, W.; Keller, P.M.A. Decline in varicella-zoster virus (Vzv)-Specific cell-mediated immunity with increasing age and boosting with a high-dose Vzv vaccine. J. Infect. Dis. 2003, 188, 1336–1344. [Google Scholar] [CrossRef] [Green Version]
  20. Rondaan, C.; Van Leer, C.C.; Van Assen, S.; Bootsma, H.; De Leeuw, K.; Arends, S.; Bos, N.A.; Westra, J. Longitudinal analysis of varicella-zoster virus-specific antibodies in systemic lupus erythematosus: No association with subclinical viral reactivations or lupus disease activity. Lupus 2018, 27, 1271–1278. [Google Scholar] [CrossRef] [Green Version]
  21. Nagasawa, K.; Yamauchi, Y.; Tada, Y.; Kusaba, T.; Niho, Y.; Yoshikawa, H. High incidence of herpes zoster in patients with systemic Lupus erythematosus: An immunological analysis. Ann. Rheumatol. Dis. 1990, 49, 630–633. [Google Scholar] [CrossRef] [Green Version]
  22. Fauci, A.S.; Moutsopoulos, H.M. Polyclonally yriggered B cells in the peripheral blood and bone marrow of normal individuals and in patients with systemic Lupus erythematosus and primary Sjogren’s syndrome. Arthritis Rheumatol. 1981, 24, 577–5783. [Google Scholar] [CrossRef]
  23. Cuadrado, M.J.; Calatayud, I.; Urquizu-Padilla, M.; Wijetilleka, S.; Kiani-Alikhan, S.; Karim, M.Y. Immunoglobulin abnormalities are frequent in patients with Lupus nephritis. BMC Rheumatol. 2019, 3, 30. [Google Scholar] [CrossRef] [PubMed]
  24. Hassan, A.B.; Rönnelid, J.; Gunnarsson, I.; Karlsson, G.; Berg, L.; Lundberg, I. Increased serum levels of immunoglobulins, C-reactive protein, type 1 and type 2 cytokines in patients with mixed connective tissue disease. J. Autoimmun. 1998, 11, 503–508. [Google Scholar] [CrossRef]
  25. Kay, R.A.; Wood, K.J.; Bernstein, R.M.; Holt, P.J.; Pumphrey, R.S. An igg subclass imbalance in connective tissue disease. Ann. Rheumatol. Dis. 1988, 47, 536–541. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Draborg, A.H.; Duus, K.; Houen, G. Epstein-barr virus and systemic Lupus erythematosus. Clin. Dev. Immunol. 2012, 2012, 370516. [Google Scholar] [CrossRef] [Green Version]
  27. Kelly, C.; Sykes, H. Rheumatoid arthritis, malignancy, and paraproteins. Ann. Rheum. Dis. 1990, 49, 657–659. [Google Scholar] [CrossRef] [Green Version]
  28. Scarsi, M.; Paolini, L.; Ricotta, D.; Pedrini, A.; Piantoni, S.; Caimi, L.; Tincani, A.; Airò, P. Abatacept reduces levels of switched memory B cells, autoantibodies, and immunoglobulins in patients with rheumatoid arthritis. J. Rheumatol. 2014, 41, 666–672. [Google Scholar] [CrossRef] [Green Version]
  29. Krasselt, M.; Baerwald, C.; Liebert, U.G.; Seifert, O. Humoral immunity to varicella zoster virus is altered in patients with rheumatoid arthritis. Clin. Rheumatol. 2019, 38, 2493–2500. [Google Scholar] [CrossRef]
  30. Arvin, A.M. Humoral and cellular immunity to varicella-zoster virus: An overview. J. Infect. Dis. 2008, 197, S58–S60. [Google Scholar] [CrossRef] [Green Version]
  31. Harpaz, R. How little we know herpes zoster. J. Infect. Dis. 2020, 222, 708–711. [Google Scholar] [CrossRef]
  32. Kraaij, T.; Arends, E.J.; Van Dam, L.S.; Kamerling, S.W.A.; Van Daele, P.L.A.; Bredewold, O.W.; Ray, A.; Bakker, J.A.; Scherer, H.U.; Huizinga, T.J.W.; et al. Long-Term effects of combined B-cell immunomodulation with rituximab and belimumab in severe, refractory systemic Lupus erythematosus: 2-year results. Nephrol. Dial. Transpl. 2020. online ahead of print. [Google Scholar] [CrossRef] [PubMed]
  33. Reichelt, M.; Zerboni, L.; Arvin, A.M. Mechanisms of varicella-zoster virus neuropathogenesis in human dorsal root ganglia. J. Virol. 2008, 82, 3971–3983. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Korn, T.; Oukka, M. A baffling association between malaria resistance and the risk of multiple sclerosis. N. Engl. J. Med. 2017, 376, 1680–1681. [Google Scholar] [CrossRef]
  35. Weyand, C.M.; Fujii, H.; Shao, L.; Goronzy, J.J. Rejuvenating the immune system in rheumatoid arthritis. Nat. Rev. Rheumatol. 2009, 5, 583–588. [Google Scholar] [CrossRef]
  36. Asada, H. Vzv-specific cell-mediated immunity, but not humoral immunity, correlates inversely with the incidence of herpes zoster and the severity of skin symptoms and zoster-associated pain: The Shez study. Vaccine 2019, 37, 6776–6781. [Google Scholar] [CrossRef] [PubMed]
  37. Asada, H.; Nagayama, K.; Okazaki, A.; Mori, Y.; Okuno, Y.; Takao, Y.; Miyazaki, Y.; Onishi, F.; Okeda, M.; Yano, S.; et al. An inverse correlation of Vzv skin-test reaction, but not antibody, with severity of herpes zoster skin symptoms and zoster-associated pain. J. Derm. Sci. 2013, 69, 243–249. [Google Scholar] [CrossRef]
  38. Imoto, K.; Okazaki, A.; Onishi, F.; Miyazaki, Y.; Okeda, M.; Yano, S.; Takao, Y.; Gomi, Y.; Ishikawa, T.; Okuno, Y.; et al. Vzv skin-test reaction, but not antibody, is an important predictive factor for postherpetic neuralgia. J. Derm. Sci. 2015, 79, 235–240. [Google Scholar] [CrossRef] [PubMed]
  39. Gilbert, P.B.; Gabriel, E.E.; Miao, X.; Li, X.; Su, S.-C.; Parrino, J.; Chan, I.S.F. Fold rise in antibody titers by measured by glycoprotein-based enzyme-linked immunosorbent assay is an excellent correlate of protection for a herpes zoster vaccine, demonstrated via the vaccine efficacy curve. J. Infect. Dis. 2014, 210, 1573–1581. [Google Scholar] [CrossRef] [Green Version]
  40. Mok, C.C. Herpes zoster vaccination in systemic lupus erythematosus: The current status. Hum. Vaccin. Immunother. 2019, 15, 45–48. [Google Scholar] [CrossRef]
  41. Krasselt, M.; Ivanov, J.-P.; Baerwald, C.; Seifert, O. Low vaccination rates among patients with rheumatoid arthritis in a german outpatient clinic. Rheumatol Int. 2017, 37, 229–237. [Google Scholar] [CrossRef]
  42. Krasselt, M.; Baerwald, C.; Seifert, O. Insufficient vaccination rates in patients with systemic Lupus erythematosus in a german outpatient clinic. Z. Rheumatol. 2018, 77, 727–734. [Google Scholar] [CrossRef]
  43. Schmedt, N.; Schiffner-Rohe, J.; Sprenger, R.; Walker, J.; Von Eiff, C.; Häckl, D. Pneumococcal vaccination rates in immunocompromised patients—A cohort study based on claims data from more than 200.000 patients in Germany. PLoS ONE 2019, 14, e0220848. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Chehab, G.; Richter, J.G.; Brinks, R.; Fischer-Betz, R.; Winkler-Rohlfing, B.; Schneider, M. Vaccination coverage in systemic Lupus erythematosus—A cross-sectional analysis of the German long-term study (Lula Cohort). Rheumatology 2018, 57, 1439–1447. [Google Scholar] [CrossRef] [Green Version]
  45. Furer, V.; Rondaan, C.; Heijstek, M.W.; Agmon-Levin, N.; Van Assen, S.; Bijl, M.; Breedveld, F.C.; D’Amelio, R.; Dougados, M.; Kapetanovic, M.C.; et al. 2019 update of eular recommendations for vaccination in adult patients with autoimmune inflammatory rheumatic diseases. Ann. Rheumatol. Dis. 2020, 79, 39–52. [Google Scholar] [CrossRef]
  46. Singh, J.A.; Furst, D.E.; Bharat, A.; Curtis, J.R.; Kavanaugh, A.F.; Kremer, J.M.; Moreland, L.W.; O’Dell, J.; Winthrop, K.L.; Beukelman, T.; et al. 2012 update of the 2008 American College of Rheumatology recommendations for the use of disease-modifying antirheumatic drugs and biologic agents in the treatment of rheumatoid arthritis. Arthritis Care Res. 2012, 64, 625–639. [Google Scholar] [CrossRef] [Green Version]
  47. RKI. StäNdige Impfkommission: Empfehlungen Der StäNdigen Impfkommission; Robert Koch-Institut: Berlin, Germany, 2020; pp. 1–68. [Google Scholar]
  48. Cunningham, A.L.; Lal, H.; Kovac, M.; Chlibek, R.; Hwang, S.-J.; Díez-Domingo, J.; Godeaux, O.; Levin, M.J.; McElhaney, J.E.; Puig-Barberà, J.; et al. Efficacy of the herpes zoster subunit vaccine in adults 70 years of age or older. N. Engl. J. Med. 2016, 375, 1019–1032. [Google Scholar] [CrossRef]
  49. Lal, H.; Cunningham, A.L.; Godeaux, O.; Chlibek, R.; Diez-Domingo, J.; Hwang, S.-J.; Levin, M.J.; McElhaney, J.E.; Poder, J.P.-B.A.; Puig-Barberà, J.; et al. Efficacy of an adjuvanted herpes zoster subunit vaccine in older adults. N. Engl. J. Med. 2015, 372, 2087–2096. [Google Scholar] [CrossRef]
  50. Berkowitz, E.M.; Moyle, G.; Stellbrink, H.J.; Schurmann, D.; Kegg, S.; Stoll, M.; El Idrissi, M.; Oostvogels, L.; Heineman, T.C.; Zoster-015 HZ/su Study Group. Safety and immunogenicity of an adjuvanted herpes zoster subunit candidate vaccine in hiv-infected adults: A phase 1/2a randomized, placebo-controlled study. J. Infect. Dis. 2015, 211, 1279–1287. [Google Scholar] [CrossRef] [Green Version]
  51. Bastidas, A.; de la Serna, J.; El Idrissi, M.; Oostvogels, L.; Quittet, P.; Lopez-Jimenez, J.; Vural, F.; Pohlreich, D.; Zuckerman, T.; Issa, N.C. Effect of recombinant zoster vaccine on incidence of herpes zoster after autologous stem cell transplantation: A randomized clinical trial. J. Am. Med. Assoc. 2019, 322, 123–133. [Google Scholar] [CrossRef] [Green Version]
  52. Stadtmauer, E.A.; Sullivan, K.M.; Marty, F.M.; Dadwal, S.S.; Papanicolaou, G.A.; Shea, T.C.; Mossad, S.B.; Andreadis, C.; Young, J.A.; Buadi, F.K. A phase 1/2 study of an adjuvanted varicella-zoster virus subunit vaccine in autologous hematopoietic cell transplant recipients. Blood 2014, 124, 2921–2929. [Google Scholar] [CrossRef] [Green Version]
  53. Vink, P. Immunogenicity and safety of a candidate subunit adjuvanted herpes zoster vaccine (Hz/Su) in adults post renal transplant: A phase iii randomized clinical trial. Open Forum Infect. Dis. 2017, 4, S417–S418. [Google Scholar] [CrossRef] [Green Version]
  54. Wagner, N.; Assmus, F.; Arendt, G.; Baum, E.; Baumann, U.; Bogdan, C.; Burchard, G.; Foll, D.; Garbe, E.; Hecht, J.; et al. Impfen bei Immundefizienz. Bundesgesundheitsbl. 2019, 62, 494–515. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Mok, C.C.; Chan, K.H.; Ho, L.Y.; Fung, Y.F.; Fung, W.F.; Woo, P.C.Y. Safety and immune response of a live-attenuated herpes zoster vaccine in patients with systemic lupus erythematosus: A randomised placebo-controlled trial. Ann. Rheumatol. Dis. 2019, 78, 1663–1668. [Google Scholar] [CrossRef]
  56. Zhang, J.; Xie, F.; Delzell, E.; Chen, L.; Winthrop, K.L.; Lewis, J.D.; Saag, K.G.; Baddley, J.W.; Curtis, J.R. Association between vaccination for herpes zoster and risk of herpes zoster infection among older patients with selected immune-mediated diseases. J. Am. Med. Assoc. 2012, 308, 43–49. [Google Scholar] [CrossRef] [Green Version]
  57. Zhang, J.; Delzell, E.; Xie, F.; Baddley, J.W.; Spettell, C.; Mcmahan, R.M.; Fernandes, J.; Chen, L.; Winthrop, K.; Curtis, J.R. The use, safety, and effectiveness of herpes zoster vaccination in individuals with inflammatory and autoimmune diseases: A longitudinal observational study. Arthritis Res. Ther. 2011, 13, R174. [Google Scholar] [CrossRef] [Green Version]
  58. Tavares-Da-Silva, F.; Co, M.M.; Dessart, C.; Hervé, C.; López-Fauqued, M.; Mahaux, O.; Van Holle, L.; Stegmann, J.-U. Review of the initial post-marketing safety surveillance for the recombinant zoster vaccine. Vaccine 2020, 38, 3489–3500. [Google Scholar] [CrossRef]
  59. Dagnew, A.F.; Rausch, D.; Hervé, C.; Zahaf, T.; Levin, M.J.; Schuind, A. Efficacy and serious adverse events profile of the adjuvanted recombinant zoster vaccine in adults with pre-existing potential immune-mediated diseases: A pooled post hoc analysis on two parallel randomized trials. Rheumatology 2021, 60, 1226–1233. [Google Scholar] [CrossRef]
  60. Acharya, S.; Raza, S.; Pattanaik, D.; Howard, A. Safety of adjuvanted herpes zoster subunit vaccine (Hz/Su, Shingrix) among patients with autoimmune inflammatory diseases. In Arthritis & Rheumatology; Wiley: Hoboken, NJ, USA, 2019; Volume 71. [Google Scholar]
  61. Källmark, H.; Gullstrand, B.; Nagel, J.; Einarsson, J.; Jönsson, G.; Kahn, F.; Kahn, R.; Bangtsson, A.; Bergström, T.; Kapetanovic, M. Immunogenicity of adjuvanted herpes zoster subunit vaccine in rheumatoid arthritis patients treated with janus kinase inhibitors and controls: Preliminary results. In Arthritis & Rheumatology; Wiley: Hoboken, NJ, USA, 2020; Volume 72. [Google Scholar]
Vaccines 09 00325 g001 550
Figure 1. Varicella zoster virus (VZV) IgG antibody concentration among the three groups (healthy controls—black bar, SLE—light grey bar, RA—dark grey bar). Boxplots depict median with whiskers from the 5th to 95th percentile.
Figure 1. Varicella zoster virus (VZV) IgG antibody concentration among the three groups (healthy controls—black bar, SLE—light grey bar, RA—dark grey bar). Boxplots depict median with whiskers from the 5th to 95th percentile.
Vaccines 09 00325 g001
Vaccines 09 00325 g002 550
Figure 2. VZV antibody concentration stratified by age (healthy controls—black bars, SLE—light grey bars, RA—dark grey bars). Boxplots show median and whiskers from minimum to maximum. Additionally, all individual values (each symbol represents one participant) are superimposed to illustrate the size of each group. ** p < 0.01; * p < 0.05.
Figure 2. VZV antibody concentration stratified by age (healthy controls—black bars, SLE—light grey bars, RA—dark grey bars). Boxplots show median and whiskers from minimum to maximum. Additionally, all individual values (each symbol represents one participant) are superimposed to illustrate the size of each group. ** p < 0.01; * p < 0.05.
Vaccines 09 00325 g002
Vaccines 09 00325 g003 550
Figure 3. Comparison of VZV antibody titers between the three groups (SLE—light grey bars, n = 17 vs. 39; RA—dark grey bars, n = 14 vs. 40; controls—black bars, n = 56) after stratification by history of herpes zoster. Please note that there is no HZ history available for the controls. All depicted significances are related to SLE patients with positive HZ history (first light grey bar). No other inter-group differences were found. The boxplots are depicted using median and Tukey’s method. *** p < 0.001; ** p < 0.01; * p < 0.05.
Figure 3. Comparison of VZV antibody titers between the three groups (SLE—light grey bars, n = 17 vs. 39; RA—dark grey bars, n = 14 vs. 40; controls—black bars, n = 56) after stratification by history of herpes zoster. Please note that there is no HZ history available for the controls. All depicted significances are related to SLE patients with positive HZ history (first light grey bar). No other inter-group differences were found. The boxplots are depicted using median and Tukey’s method. *** p < 0.001; ** p < 0.01; * p < 0.05.
Vaccines 09 00325 g003
Table
Table 1. Epidemiology of patients and controls. Given are mean and standard deviation (SD).
Table 1. Epidemiology of patients and controls. Given are mean and standard deviation (SD).
SLE Patients
N = 56		RA Patients
N = 54		Controls
N = 56
Mean age, years49.8 ± 15.951.3 ± 13.451.9 ± 14.8
Female, n (%)54 (96.4)47 (87)53 (94.6)
Subjects with positive HZ history, n (%)17 (30.4)14 (25.9)n.a.
Mean age at HZ, years33.5 ± 12.436.7 ± 12.4 n.a.
Mean time from disease onset to HZ, years6.8 ± 5.915.2 ± 10.2n.a.
Table
Table 2. Medication of the studied patients with SLE and RA (n = 56 and 54, respectively).
Table 2. Medication of the studied patients with SLE and RA (n = 56 and 54, respectively).
CharacteristicsSLERA
Medication, n (%)
All immunosuppressives38 (67.9)50 (92.6)
Prednisolone44 (78.6)44 (81.5)
Hydroxychloroquine13 (23.2)0 (0)
Azathioprine18 (32.1)1 (1.9)
Mycofenolat-mofetil17 (30.4)0 (0)
Cyclophosphamide1 (1.8)0 (0)
Methotrexate1 (1.8)33 (61.1)
Leflunomide0 (0)5 (9.3)
Sulfasalazine0 (0)1 (1.9)
bDMARDs, n (%)
Adalimumab0 (0)12 (22.2)
Etanercept0 (0)6 (11.1)
Abatacept0 (0)4 (7.4)
Rituximab1 (1.8)2 (3.7)
Certolizumab0 (0)2 (3.7)
tsDMARDs, n (%)
Tofacitinib0 (0)2 (3.7)
Given are numbers (%). bDMARD—biological disease-modifying antirheumatic drug; tsDMARD—targeted synthetic disease-modifying antirheumatic drug.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Krasselt, M.; Baerwald, C.; Liebert, U.G.; Seifert, O. Humoral Immunity to Varicella Zoster Virus in Patients with Systemic Lupus Erythematosus and Rheumatoid Arthritis Compared to Healthy Controls. Vaccines 2021, 9, 325. https://doi.org/10.3390/vaccines9040325

AMA Style

Krasselt M, Baerwald C, Liebert UG, Seifert O. Humoral Immunity to Varicella Zoster Virus in Patients with Systemic Lupus Erythematosus and Rheumatoid Arthritis Compared to Healthy Controls. Vaccines. 2021; 9(4):325. https://doi.org/10.3390/vaccines9040325

Chicago/Turabian Style

Krasselt, Marco, Christoph Baerwald, Uwe G. Liebert, and Olga Seifert. 2021. "Humoral Immunity to Varicella Zoster Virus in Patients with Systemic Lupus Erythematosus and Rheumatoid Arthritis Compared to Healthy Controls" Vaccines 9, no. 4: 325. https://doi.org/10.3390/vaccines9040325

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop