A prospective multicenter study assessing humoral immunogenicity and safety of the mRNA SARS-CoV-2 vaccines in Greek patients with systemic autoimmune and autoinflammatory rheumatic diseases. Issue 125 (December 2021)
- Record Type:
- Journal Article
- Title:
- A prospective multicenter study assessing humoral immunogenicity and safety of the mRNA SARS-CoV-2 vaccines in Greek patients with systemic autoimmune and autoinflammatory rheumatic diseases. Issue 125 (December 2021)
- Main Title:
- A prospective multicenter study assessing humoral immunogenicity and safety of the mRNA SARS-CoV-2 vaccines in Greek patients with systemic autoimmune and autoinflammatory rheumatic diseases
- Authors:
- Tzioufas, Athanasios G.
Bakasis, Athanasios-Dimitrios
Goules, Andreas V.
Bitzogli, Kleopatra
Cinoku, Ilir I.
Chatzis, Loukas G.
Argyropoulou, Ourania D.
Venetsanopoulou, Aliki I.
Mavrommati, Maria
Stergiou, Ioanna E.
Pezoulas, Vasilis
Voulgari, Paraskevi V.
Katsimpari, Chaido
Katechis, Spyridon
Gazi, Souzana
Katsifis, Gkikas
Sfontouris, Charalampos I.
Georgountzos, Athanasios I.
Liossis, Stamatis-Nick
Papagoras, Charalampos
Fotiadis, Dimitrios I.
Skopouli, Fotini N.
Vlachoyiannopoulos, Panayiotis G.
Moutsopoulos, Haralampos M. - Abstract:
- Abstract: Objectives: To investigate humoral responses and safety of mRNA SARS-CoV-2 vaccines in systemic autoimmune and autoinflammatory rheumatic disease (SAARD) patients subjected or not to treatment modifications during vaccination. Methods: A nationwide, multicenter study, including 605 SAARD patients and 116 controls, prospectively evaluated serum anti-SARS-CoV-2 S1-protein IgG antibody titers, side-effects, and disease activity, one month after complete vaccination, in terms of distinct treatment modification strategies (none, partial and extended modifications). Independent risk factors associated with hampered humoral responses were identified by data-driven multivariable logistic regression analysis. Results: Patients with extended treatment modifications responded to vaccines similarly to controls as well as SAARD patients without immunosuppressive therapy (97.56% vs 100%, p = 0.2468 and 97.56% vs 97.46%, p > 0.9999, respectively). In contrast, patients with partial or without therapeutic modifications responded in 87.50% and 84.50%, respectively. Furthermore, SAARD patients with extended treatment modifications developed higher anti-SARS-CoV-2 antibody levels compared to those without or with partial modifications (median:7.90 vs 7.06 vs 7.1, p = 0.0003 and p = 0.0195, respectively). Mycophenolate mofetil (MMF), rituximab (RTX) and methotrexate (MTX) negatively affected anti-SARS-CoV-2 humoral responses. In 10.5% of vaccinated patients, mild clinicalAbstract: Objectives: To investigate humoral responses and safety of mRNA SARS-CoV-2 vaccines in systemic autoimmune and autoinflammatory rheumatic disease (SAARD) patients subjected or not to treatment modifications during vaccination. Methods: A nationwide, multicenter study, including 605 SAARD patients and 116 controls, prospectively evaluated serum anti-SARS-CoV-2 S1-protein IgG antibody titers, side-effects, and disease activity, one month after complete vaccination, in terms of distinct treatment modification strategies (none, partial and extended modifications). Independent risk factors associated with hampered humoral responses were identified by data-driven multivariable logistic regression analysis. Results: Patients with extended treatment modifications responded to vaccines similarly to controls as well as SAARD patients without immunosuppressive therapy (97.56% vs 100%, p = 0.2468 and 97.56% vs 97.46%, p > 0.9999, respectively). In contrast, patients with partial or without therapeutic modifications responded in 87.50% and 84.50%, respectively. Furthermore, SAARD patients with extended treatment modifications developed higher anti-SARS-CoV-2 antibody levels compared to those without or with partial modifications (median:7.90 vs 7.06 vs 7.1, p = 0.0003 and p = 0.0195, respectively). Mycophenolate mofetil (MMF), rituximab (RTX) and methotrexate (MTX) negatively affected anti-SARS-CoV-2 humoral responses. In 10.5% of vaccinated patients, mild clinical deterioration was noted; however, no differences in the incidence of deterioration were observed among the distinct treatment modification SAARD subgroups. Side-effects were generally comparable between SAARD patients and controls. Conclusions: In SAARD patients, mRNA SARS-CoV-2 vaccines are effective and safe, both in terms of side-effects and disease flares. Treatment with MMF, RTX and/or MTX compromises anti-SARS-CoV-2 antibody responses, which are restored upon extended treatment modifications without affecting disease activity. Highlights: Modifications in immunosuppressive treatment improve SARS-CoV-2 vaccine immunogenicity. Seroconversion is compromised by methotrexate, mycophenolate, and rituximab therapy. Overall disease activity remains stable and vaccination side-effects are mild. … (more)
- Is Part Of:
- Journal of autoimmunity. Issue 125(2021)
- Journal:
- Journal of autoimmunity
- Issue:
- Issue 125(2021)
- Issue Display:
- Volume 125, Issue 125 (2021)
- Year:
- 2021
- Volume:
- 125
- Issue:
- 125
- Issue Sort Value:
- 2021-0125-0125-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-12
- Subjects:
- mRNA SARS-COV-2 vaccine -- Systemic autoimmune rheumatic disease -- Immunosuppressive treatment -- Treatment modification -- Anti-SARS-CoV-2 antibody response
SAARD systemic autoimmune and autoinflammatory rheumatic diseases -- JAKi JAK inhibitors -- GC glucocorticoids -- MTX methotrexate -- RTX rituximab -- MMF mycophenolate mofetil -- GDPR General Data Protection Regulation -- EULAR European Alliance of Associations for Rheumatology -- ACR American College of Rheumatology -- OD optical density -- FCBF fast correlation based feature -- LR logistic regression -- TNFi tumor necrosis factor inhibitors
Autoimmunity -- Periodicals
Autoimmune diseases -- Periodicals
Autoantibodies -- Periodicals
Autoimmune Diseases -- Periodicals
Auto-immunité -- Périodiques
Maladies auto-immunes -- Périodiques
Electronic journals
616.978005 - Journal URLs:
- http://www.sciencedirect.com/science/journal/08968411 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/08968411 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jaut.2021.102743 ↗
- Languages:
- English
- ISSNs:
- 0896-8411
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- Legaldeposit
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