Objectives: To characterize the kinetics of humoral and T-cell responses in rheumatoid arthritis (RA)-patients followed up to 4-6 weeks (T3) after the SARS-CoV-2 vaccine booster dose. Methods: Health care workers (HCWs, n = 38) and patients with RA (n = 52) completing the messenger RNA vaccination schedule were enrolled at T3. In each cohort, 25 subjects were sampled after 5 weeks (T1) and 6 months (T2) from the first vaccine dose. The humoral response was assessed by measuring anti-receptor-binding domain (RBD) and neutralizing antibodies, the T-cell response by interferon-γ-release assay (IGRA), T cell cytokine production, and B cell phenotype at T3 by flow cytometry. Results: Patients with RA showed a significant reduction of antibody titers from T1 to T2 and a significant increase at T3. T-cell response by IGRA persisted over time in patients with RA, whereas it increased in HCWs. Most patients with RA scored positive for anti-RBD, neutralizing antibody and T-cell responses, although the magnitude was lower than HCWs. The spike-specific-cytokine response was mainly clusters of differentiation (CD)4+ T cells restricted in both cohorts and significantly lower with reduced interleukin-2 response and CD4-antigen-responding naïve T cells in patients with RA. Unswitched memory B cells were reduced in patients with RA compared with HCWs independently of vaccination. Conclusion: COVID-19 vaccine booster strengthens the humoral immunity in patients with RA even with a reduced cytokine response.

Booster dose of SARS-CoV-2 mRNA vaccines strengthens the specific immune response of patients with rheumatoid arthritis: a prospective multicenter longitudinal study / Farroni, Chiara; Aiello, Alessandra; PICCHIANTI DIAMANTI, Andrea; Lagana', Bruno; Petruccioli, Elisa; Agrati, Chiara; Rosa Garbuglia, Anna; Meschi, Silvia; Lapa, Daniele; Cuzzi, Gilda; Petrone, Linda; Vanini, Valentina; Salmi, Andrea; Altera, ANNA MARIA GERARDA; Repele, Federica; Grassi, Germana; Bettini, Aurora; Vita, Serena; Andrea, Mariano; Damiani, Arianna; Infantino, Maria; Grossi, Valentina; Manfredi, Mariangela; Niccoli, Laura; Puro, Vincenzo; DI ROSA, Roberta; Salemi, Simonetta; Sesti, Giorgio; Scolieri, Palma; Bruzzese, Vincenzo; Benucci, Maurizio; Cantini, Fabrizio; Nicastri, Emanuele; Goletti, Delia. - In: INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES. - ISSN 1201-9712. - (2022). [10.1016/j.ijid.2022.10.035]

Booster dose of SARS-CoV-2 mRNA vaccines strengthens the specific immune response of patients with rheumatoid arthritis: a prospective multicenter longitudinal study

Alessandra Aiello
Co-primo
;
Andrea Picchianti Diamanti;Bruno Laganà;Elisa Petruccioli;Linda Petrone;Anna Maria Gerarda Altera;Federica Repele;Germana Grassi;Aurora Bettini;Serena Vita;Andrea Mariano;Mariangela Manfredi;Roberta Di Rosa;Giorgio Sesti;Emanuele Nicastri
Penultimo
;
2022

Abstract

Objectives: To characterize the kinetics of humoral and T-cell responses in rheumatoid arthritis (RA)-patients followed up to 4-6 weeks (T3) after the SARS-CoV-2 vaccine booster dose. Methods: Health care workers (HCWs, n = 38) and patients with RA (n = 52) completing the messenger RNA vaccination schedule were enrolled at T3. In each cohort, 25 subjects were sampled after 5 weeks (T1) and 6 months (T2) from the first vaccine dose. The humoral response was assessed by measuring anti-receptor-binding domain (RBD) and neutralizing antibodies, the T-cell response by interferon-γ-release assay (IGRA), T cell cytokine production, and B cell phenotype at T3 by flow cytometry. Results: Patients with RA showed a significant reduction of antibody titers from T1 to T2 and a significant increase at T3. T-cell response by IGRA persisted over time in patients with RA, whereas it increased in HCWs. Most patients with RA scored positive for anti-RBD, neutralizing antibody and T-cell responses, although the magnitude was lower than HCWs. The spike-specific-cytokine response was mainly clusters of differentiation (CD)4+ T cells restricted in both cohorts and significantly lower with reduced interleukin-2 response and CD4-antigen-responding naïve T cells in patients with RA. Unswitched memory B cells were reduced in patients with RA compared with HCWs independently of vaccination. Conclusion: COVID-19 vaccine booster strengthens the humoral immunity in patients with RA even with a reduced cytokine response.
2022
antibody response; COVID-19 vaccine; immunosuppressive therapy; rheumatoid arthritis; SARS-CoV-2; T-cell response
01 Pubblicazione su rivista::01a Articolo in rivista
Booster dose of SARS-CoV-2 mRNA vaccines strengthens the specific immune response of patients with rheumatoid arthritis: a prospective multicenter longitudinal study / Farroni, Chiara; Aiello, Alessandra; PICCHIANTI DIAMANTI, Andrea; Lagana', Bruno; Petruccioli, Elisa; Agrati, Chiara; Rosa Garbuglia, Anna; Meschi, Silvia; Lapa, Daniele; Cuzzi, Gilda; Petrone, Linda; Vanini, Valentina; Salmi, Andrea; Altera, ANNA MARIA GERARDA; Repele, Federica; Grassi, Germana; Bettini, Aurora; Vita, Serena; Andrea, Mariano; Damiani, Arianna; Infantino, Maria; Grossi, Valentina; Manfredi, Mariangela; Niccoli, Laura; Puro, Vincenzo; DI ROSA, Roberta; Salemi, Simonetta; Sesti, Giorgio; Scolieri, Palma; Bruzzese, Vincenzo; Benucci, Maurizio; Cantini, Fabrizio; Nicastri, Emanuele; Goletti, Delia. - In: INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES. - ISSN 1201-9712. - (2022). [10.1016/j.ijid.2022.10.035]
File allegati a questo prodotto
File Dimensione Formato  
Farroni_Booster dose_2022.pdf

accesso aperto

Note: Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Creative commons
Dimensione 3.24 MB
Formato Adobe PDF
3.24 MB Adobe PDF

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1674333
Citazioni
  • ???jsp.display-item.citation.pmc??? 15
  • Scopus 18
  • ???jsp.display-item.citation.isi??? ND
social impact