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Correspondence on ‘Immunogenicity and safety of anti-SARS-CoV-2 mRNA vaccines in patients with chronic inflammatory conditions and immunosuppressive therapy in a monocentric cohort’
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  1. Larissa Valor-Méndez1,
  2. Koray Tascilar1,
  3. David Simon1,
  4. Joerg Distler1,
  5. Arnd Kleyer2,
  6. Georg Schett2,
  7. Juergen Rech1
  1. 1Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany
  2. 2Internal Medicine 3, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany
  1. Correspondence to Dr Larissa Valor-Méndez, Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander University Erlangen-Nuremberg, 91054 Erlangen, Germany; larissa.valormendez{at}uk-erlangen.de

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We read with interest the work by Geisen and colleagues1 on the efficacy and safety of anti-SARS-CoV-2 mRNA vaccine in patients with rheumatic diseases. While substantial data on the efficacy and safety of SARS-CoV-2 vaccination have been created during the last months, it is currently unclear whether the vaccination is efficacious and safe in patients with autoinflammatory diseases (AIDs). These patients present with exacerbated innate immune responses associated with enhanced production of interleukin (IL)-1.2

Testing the immune response to SARS-CoV-2 vaccination in patients with AIDs is of interest, as IL-1 has been involved in the pathogenesis of COVID-19; thus, IL-1 expression is massively increased in patients with severe COVID-19.3–5 Furthermore, COVID-19 has shown to trigger an increased inflammatory disease activity in patients with AIDs.6 7 In addition, IL-1 inhibition has been applied in the treatment of COVID-19 and while initial uncontrolled studies revealed promising results,8 a randomised controlled trial showed no improvement of COVID-19 on IL-1 blockade.9 While current data suggest the immune response to SARS-CoV-2 vaccination may be reduced in certain diseases, such as rheumatoid arthritis,10 and certain treatments such as methotrexate,11 such data cannot be applied to AID or to IL-1 inhibitors as the underlying pathophysiology is fundamentally different. Hence, we aimed to investigate SARS-CoV-2 vaccination responses in patients with AIDs treated with IL-1 inhibitors and compared them with healthy controls (HCs).

Ten patients with AIDs, four with adult-onset Still’s disease, three with familial Mediterranean fever (FMF) and each one with gout, systemic AID and tumour necrosis factor receptor-associated periodical syndrome were investigated (online supplemental table 1). Their mean age was 33±10 years, eight were women and two men. All patients with AIDs were treated with IL-1 inhibitors, eight with canakinumab and two with anakinra, administered regularly and at standard dosages of 150 mg/300 mg every 4 weeks and 100 mg/day, respectively. Two patients with FMF were additionally treated with 1 mg colchicine. None of the patients received glucocorticoids. In addition, 10 HCs were examined. All patients with AIDs and HCs received the BNT162b2 vaccine (Pfizer/BioNTech). None of the patients with AIDs and HCs did have COVID-19 before, nor did they have a positive anti-SARS-CoV-2 antibody test before vaccination.

IgG antibodies against the S1 domain of the spike protein of SARS-CoV-2 were tested by CE-certified ELISA (Euroimmun, Lübeck, Germany).12 To assess neutralisation activity of antibodies, a CE-certified SARS-CoV-2 surrogate virus neutralisation assay (cPASS, Medac, Wedel, Germany) was used. A cut-off of 30% inhibition was considered as positive, according to the manufacturer’s instructions.13 We compared binary response status of antibody levels and neutralising activity using Fisher’s exact test. ODs and per cent neutralising activity of the antibodies were compared using Mann-Whitney U tests. Two-sided p values were considered significant when <0.05. Analyses were performed using the open-source R software V.4.0.1 (R Foundation for Statistical Computing, Vienna, Austria).

Nine out of 10 patients with AIDs and all HCs developed SARS-CoV-2-specific IgG antibodies (OD >0.8 units). The time course of the antibody response in patients and controls was very similar (figure 1A). SARS-CoV-2-specific IgG antibodies were even higher in patients with AIDs than in HCs (figure 1B). Respective median (IQR) ODs were 7.0 (6.6 to 7.4) in HCs and 8.4 (7.3 to 8.9) in patients with AIDs (p=0.00.19, Wilcoxon rank-sum test). The neutralising activity of receptor-binding domain binding to ACE2 was 96.4% (95.4% to 97.2%) in HCs and 95.3% (87.2% to 96.2%) in patients with AIDs, respectively (p=0.21, Wilcoxon rank-sum test). Vaccination was tolerated well in all patients and controls.

Figure 1

(A) Time course of anti-SARS-CoV-2 antibody response in patients with autoinflammatory disease receiving interleukin (IL)-1 blockade and healthy controls. Horizontal dashed line indicates the cut-off at OD 0.8. Shaded area represents the period during which second vaccine dose was administered. Dots connected by lines indicate antibody measurements from the same participants after the first and second vaccine dose. (B) Optical densities after the second vaccination, horizontal dashed line indicates the OD cut-off of 0.8. P value by Wilcoxon rank-sum test. (C) Neutralising activity of the antibodies after second vaccination. Horizontal dashed line indicates the cut-off at 30%. P value by Wilcoxon rank-sum test.

These data show good responses to SARS-CoV-2 vaccination in patients with AIDs treated with IL-1 inhibitors. They support previous anecdotal reports that IL-1 inhibitors may not impair the immune response in the context of COVID-19.14 Importantly, both IgG levels as well as neutralising capacity of the anti-SARS-CoV-2 antibodies were comparable in patients with AIDs and HCs. Only one patient with gout and chronic renal failure undergoing haemodialysis did not respond to SARS-CoV-2 vaccination. The data also showed that there is no overshooting inflammatory response to SARS-CoV-2 vaccination in patients with AID. Taken together, these data support the current American College of Rheumatology guidelines for SARS-CoV-2 vaccination in patients with rheumatic diseases, including AIDs.15

In summary, SARS-CoV-2 vaccination in patients with AIDs receiving IL-1 inhibition is efficacious and well tolerated.

Ethics statements

Ethics approval

Based on ethics approval #157_20 B and the TARDA Database.

Acknowledgments

The authors thankfully acknowledge Mrs Silke Winkler for her technical assistance.

References

Supplementary materials

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Footnotes

  • Collaborators Silke Winkler.

  • Contributors JR conceived the original idea. JR, KT and LV-M designed the study and wrote the manuscript. All authors provided critical feedback and helped shape the research and analysis, and contributed to the final version of the manuscript.

  • Funding This study was supported by the Schreiber Foundation and the German Research Council (CRC1181 and FOR2886 Mascara).

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; internally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.

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