Longitudinal Dynamics of the SARS-CoV-2 Antibody Repertoire after SARS-CoV-2 Delta and Omicron Breakthrough Infections in Patients with Immune-Mediated Inflammatory Diseases DOI
Eileen W Stalman, Luuk Wieske, Jim Keijser

et al.

Published: Jan. 1, 2023

Background: Despite impaired humoral responses after SARS-CoV-2 vaccination, the incidence and severity of breakthrough infections is not increased in patients with immune-mediated inflammatory diseases (IMID) on immunosuppressants (ISPs). This could be explained by preserved recall but data are lacking. study aimed to investigate longitudinal dynamics response delta omicron IMID ISPs compared controls.Methods: a sub-study ongoing national Target-to-B! (T2B!) study, focusing vaccination patients. We included controls (IMID healthy individuals) who had completed primary vaccinations reported between July 1, 2021, April 2022, during prevalence variants. Antibody titers against wild-type RBD, S, RBD were measured at various time points post-infection assess responses. Dynamics assessed for separately, different controls.Findings: 480 participants. comparable following or infections. However, anti-CD20 therapy S1P modulators showed greatly those anti-TNF moderately greater decline antibodies than controls.Interpretations: Most do influence infections, exception modulators, lesser extent anti-TNF, which shows more rapid antibody decay.Funding: was supported ZonMw (The Netherlands Organization Health Research Development, grant 10430072010007). The sponsor no role design, analyses reporting study.Declaration Interest: F Eftimov T Kuijpers report (governmental) grants from immune SARS-Cov2 auto-immune diseases. also reports Prinses Beatrix Spierfonds, CSL Behring, Kedrion, Terumo BCT, Grifols, Takeda Pharmaceutical Company, GBS-CIDP Foundation; consulting fees UCB Pharma Behring; honoraria Grifols. AJ van der Kooi Behring participation an advisory board Argen-X. M Löwenberg Galapagos related this Bristol Myers Squibb, Pfizer, Takeda, Tillotts. Ph I Spuls involved performing clinical trials many pharmaceutical industries that manufacture drugs used treatment e.g. psoriasis atopic dermatitis, financial compensation paid department/hospital chief investigator TREAT NL registry taskforce SECURE-AD registry. M.W. Bekkenk secretary Dutch Experimental Dermatology Board head pigmentary disorders group within Board, Sanofi, Novartis Fondation René Touraine. J Killestein has speaking relationships Merck Serono, Biogen Idec, TEVA, Genzyme, Roche Novartis; Amsterdam UMC, location VUmc, MS Center received support research activities Bayer Shcering Pharma, GlaxoSmithKline, Roche, Teva, Novartis. B Horváth unpaid positions as medical advisor several patient groups, position ERN-SKIN, associate editor British Journal Dermatology; Abbvie, Akari Therapeutics, Celgene, Janssen-Cilag; Abbvie. J.J.G.M. Verschuuren Argenx, Alexion NMD Pharma; coinventor patent applications based MuSK-related research. DJ Hijnen AstraZeneca, Janssen, LEO Galderma, Lilly, Sanofi BIOMAP IMI. P.A. Doorn participated Octapharma. P. Paassen GSK; GSK Vifor boards. G.R.A.M. D'Haens Agomab, AM AMT, Arena Pharmaceuticals, Meiers Boehringer Ingelheim, Celltrion, Eli Exeliom Biosciences, Exo Biologics, Galapagos, Index Kaleido, Gilead, Glaxo Smith Kline, Gossamerbio, Immunic, Johnson Johnson, Origo, Polpharma, Procise Diagnostics, Prometheus laboratories, Progenity, Protagonist; Arena, BMS, Takeda; boards Seres Health, AstraZeneca. R.B. Takkenberg Sobi Norgine Norgine. SH Goedee member Society Clinical Neurophysiology (unpaid), speaker Shire/Takeda. AH Zwinderman safety monitoring Torrent Ltd Foresee Pharmaceuticals Co. No other disclosures reported.Ethical Approval: ethical committee AMC (2020.194) approved study.

Language: Английский

mRNA-1273 vaccinated inflammatory bowel disease patients receiving TNF inhibitors develop broad and robust SARS-CoV-2-specific CD8+ T cell responses DOI Creative Commons
Jet van den Dijssel,

Mariël C Duurland,

Veronique A. L. Konijn

et al.

Journal of Autoimmunity, Journal Year: 2024, Volume and Issue: 144, P. 103175 - 103175

Published: Feb. 21, 2024

SARS-CoV-2-specific CD8

Language: Английский

Citations

4

T cell activation markers CD38 and HLA-DR indicative of non-seroconversion in anti-CD20-treated patients with multiple sclerosis following SARS-CoV-2 mRNA vaccination DOI Creative Commons
Niels J. M. Verstegen, Ruth R Hagen,

Christine Kreher

et al.

Journal of Neurology Neurosurgery & Psychiatry, Journal Year: 2024, Volume and Issue: 95(9), P. 855 - 864

Published: March 28, 2024

Background Messenger RNA (mRNA) vaccines provide robust protection against SARS-CoV-2 in healthy individuals. However, immunity after vaccination of patients with multiple sclerosis (MS) treated ocrelizumab (OCR), a B cell-depleting anti-CD20 monoclonal antibody, is not yet fully understood. Methods In this study, deep immune profiling techniques were employed to investigate the response induced by mRNA untreated MS (n=21), OCR-treated (n=57) and individuals (n=30). Results Among MS, 63% did produce detectable levels antibodies (non-seroconverted), those who have lower spike receptor-binding domain-specific IgG responses compared MS. Before vaccination, no discernible immunological differences observed between non-seroconverted seroconverted received overall more OCR infusions, had shorter intervals since their last infusion displayed higher serum concentrations at time initial vaccination. Following two vaccinations, smaller cell compartments but instead exhibited activation general CD4 + CD8 T compartments, as indicated upregulation CD38 HLA-DR surface expression, when patients. Conclusion These findings highlight importance optimising treatment regimens scheduling for maximise humoral cellular responses. This study provides valuable insights strategies including identification potential markers explore vaccine efficacy non-seroconverting

Language: Английский

Citations

4

Long-Term Immune Response Profiles to SARS-CoV-2 Vaccination and Infection in People with Multiple Sclerosis on Anti-CD20 Therapy DOI Creative Commons
Christina Woopen, Marie Dunsche, Georges Katoul Al Rahbani

et al.

Vaccines, Journal Year: 2023, Volume and Issue: 11(9), P. 1464 - 1464

Published: Sept. 7, 2023

Our objective was to analyze longitudinal cellular and humoral immune responses severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination in people with multiple sclerosis (pwMS) on B-cell depleting treatment (BCDT) compared pwMS without immunotherapy. We further evaluated the impact of COVID-19 infection timing. PwMS (n = 439) BCDT (ocrelizumab, rituximab, ofatumumab) or immunotherapy were recruited for this prospective cohort study between June 2021 2022. SARS-CoV-2 spike-specific antibodies interferon-γ release CD4 CD8 T-cells upon stimulation spike protein peptide pools analyzed at different timepoints (after primary vaccination, 3 6 months after booster booster). Humoral response consistently lower whereas T-cell higher patients controls. Cellular decreased over time increased again significantly antibody titers than both untreated B-cell-depleted pwMS. led a significant increase SARS-CoV-2-specific responses. Despite attenuated responses, third seems recommendable, since least partial protection can be expected from strong response. Moreover, our data show that an assessment may helpful evaluate efficacy vaccination.

Language: Английский

Citations

7

Single‐cell multi‐omics analysis of COVID‐19 patients with pre‐existing autoimmune diseases shows aberrant immune responses to infection DOI Creative Commons
Anis Barmada,

Louis‐François Handfield,

Gerard Godoy‐Tena

et al.

European Journal of Immunology, Journal Year: 2023, Volume and Issue: 54(1)

Published: Oct. 6, 2023

Abstract In COVID‐19, hyperinflammatory and dysregulated immune responses contribute to severity. Patients with pre‐existing autoimmune conditions can therefore be at increased risk of severe COVID‐19 and/or associated sequelae, yet SARS‐CoV‐2 infection in this group has been little studied. Here, we performed single‐cell analysis peripheral blood mononuclear cells from patients three major diseases (rheumatoid arthritis, psoriasis, or multiple sclerosis) during infection. We observed compositional differences between the disease groups coupled altered patterns gene expression, transcription factor activity, cell–cell communication that substantially shape response under While enrichment HLA‐DRlow CD14+ monocytes was all groups, type‐I interferon signaling as well inflammatory T cell monocyte varied widely patients. Our results reveal disturbed autoimmunity, highlighting important considerations for treatment follow‐up.

Language: Английский

Citations

7

Ocrelizumab Concentration Is a Good Predictor of SARS‐CoV‐2 Vaccination Response in Patients with Multiple Sclerosis DOI Creative Commons
Zoé L. E. van Kempen, Laura Hogenboom, Alyssa A Toorop

et al.

Annals of Neurology, Journal Year: 2022, Volume and Issue: 93(1), P. 103 - 108

Published: Oct. 17, 2022

Ocrelizumab, an anti-CD20 monoclonal antibody, counteracts induction of humoral immune responses after severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) vaccinations in patients with multiple sclerosis (MS). We aimed to assess if serum ocrelizumab concentration measured at the time vaccination could predict response SARS-CoV-2 vaccination. In 52 MS, we found be a good predictor for IgG anti-RBD titers (comparable B-cell count). As course may predicted using pharmacokinetic models, this superior biomarker guide optimal timing depleted MS. ANN NEUROL 2023;93:103-108.

Language: Английский

Citations

12

Primary SARS-CoV-2 infection in patients with immune-mediated inflammatory diseases: long-term humoral immune responses and effects on disease activity DOI Creative Commons
Koos P J van Dam, Adriaan Volkers, Luuk Wieske

et al.

BMC Infectious Diseases, Journal Year: 2023, Volume and Issue: 23(1)

Published: May 17, 2023

Abstract Background Patients with immune-mediated inflammatory diseases (IMIDs) on immunosuppressants (ISPs) may have impaired long-term humoral immune responses and increased disease activity after SARS-CoV-2 infection. We aimed to investigate against a primary infection in unvaccinated IMID patients ISPs. Methods active treatment ISPs controls (i.e. not ISP healthy controls) confirmed before first vaccination were included from an ongoing prospective cohort study (T2B! study). Clinical data infections registered using electronic surveys health records. A serum sample was collected measure anti-receptor-binding domain (RBD) antibodies. Results In total, 193 113 included. Serum samples 185 participants available, median time of 173 days between collection. The rate seropositive 78% compared 100% ( p < 0.001). Seropositivity rates lowest anti-CD20 (40.0%) anti-tumor necrosis factor (TNF) agents (60.5%), as other 0.001 0.001, respectively). Increased reported by 68 260 (26.2%; 95% CI 21.2–31.8%), leading intensification 6 out these (8.8%). Conclusion showed reduced infection, which mainly attributed anti-TNF agents. commonly, but mostly mild. Trial registration NL74974.018.20, ID: NL8900. Registered 9 September 2020.

Language: Английский

Citations

6

SARS-CoV-2 mRNA vaccine-induced immune responses in rheumatoid arthritis DOI Creative Commons

Marc-André Limoges,

Audrey Lortie,

Élodie Demontier

et al.

Journal of Leukocyte Biology, Journal Year: 2023, Volume and Issue: 114(4), P. 358 - 367

Published: July 20, 2023

Our objective was to characterize T and B cell responses vaccination with SARS-CoV-2 antigens in immunocompromised rheumatoid arthritis (RA) patients. In 22 RA patients, clinical biological variables were analyzed before 4 weeks after each of 3 messenger RNA (mRNA) vaccine doses compared unmatched healthy individuals. Sequentially sampled peripheral blood mononuclear cells sera collected determine immune profiles analyze the response a spike peptide pool specificity receptor-binding domain (RBD). Anti-spike antibodies detectable 6 patients 1 dose increasing titers booster dose, although overall lower that control Responding first more likely have higher baseline proportion circulating follicular cells. mRNA elicited robust CD4+ following second doses. Consistent serologies, RBD-specific exhibited modest increase resulted marked increases only fraction both ancestral omicron RBD. results highlight importance multidose COVID-19 develop protective humoral response. However, these rapidly specific responses, despite delayed responses.

Language: Английский

Citations

6

T follicular helper cell responses to SARS‐CoV ‐2 vaccination among healthy and immunocompromised adults DOI Creative Commons
Mollie Ailie Acheson Boyd,

Alexandra Carey Hoppé,

Anthony D. Kelleher

et al.

Immunology and Cell Biology, Journal Year: 2023, Volume and Issue: 101(6), P. 504 - 513

Published: Feb. 24, 2023

Abstract The worldwide rollout of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) vaccinations in the last years has produced a multitude studies investigating T‐cell responses peripheral blood and limited number secondary lymphoid tissues. As key component to an effective immune response, vaccine‐specific T follicular helper (Tfh) cells are localized draining lymph node (LN) assist selection highly specific B‐cell clones for production neutralizing antibodies. While these have been noted as circulating Tfh (cTfh) cells, they not often taken into consideration when examining CD4 + responses, particularly immunocompromised groups. Furthermore, site‐specific analyses locations such LN recently become attractive area investigation. This is mainly result improved sampling methods via ultrasound‐guided fine‐needle biopsy (FNB)/fine‐needle aspiration (FNA), which less invasive than excision able be performed longitudinally. undertaken healthy individuals, data from groups lacking. review will focus on both cTfh after SARS‐CoV‐2 vaccination individuals. investigation could identify characteristics successful response required prevention infection viral clearance. furthermore may highlight that fine‐tuned improve vaccine efficacy within at risk more disease.

Language: Английский

Citations

5

Impact of methotrexate on humoral and cellular immune responses to SARS-CoV-2 mRNA vaccine in patients with rheumatoid arthritis DOI
Masahiro Shirata, Isao Ito, Masao Tanaka

et al.

Clinical and Experimental Medicine, Journal Year: 2023, Volume and Issue: 23(8), P. 4707 - 4720

Published: Aug. 16, 2023

Language: Английский

Citations

5

Impact of methotrexate treatment on vaccines immunogenicity in adult rheumatological patients – Lessons learned from the COVID-19 pandemic DOI Creative Commons
Jakub Wroński, Marzena Ciechomska, Ewa Kuca-Warnawin

et al.

Biomedicine & Pharmacotherapy, Journal Year: 2023, Volume and Issue: 165, P. 115254 - 115254

Published: Aug. 3, 2023

Despite the development of new biological and synthetic targeted therapies, methotrexate remains one most commonly used immunomodulatory drugs in rheumatology. However, its effect on immunogenicity vaccines has been studied only to a limited extent until recently, resulting lack clear guidelines use during vaccination. Significant progress was made COVID-19 pandemic due dynamic research vaccines, including patients with autoimmune inflammatory rheumatic diseases. In following literature review, we present summary what know so far impact post-vaccination response adult rheumatology patients, taking into account lessons learned from pandemic. Studies influenza, pneumococcal, herpes zoster, tetanus/diphtheria/pertussis, hepatitis A, yellow fever, are described detail, humoral cellular individual vaccines. The available evidence for recommendations withholding period is presented. Lastly, an overview potential immunological mechanisms through which MTX modulates vaccinations also provided.

Language: Английский

Citations

2