TY - JOUR
T1 - Impact of COVID-19 and vaccination campaign on 1,755 systemic sclerosis patients during first three years of pandemic. Possible risks for individuals with impaired immunoreactivity to vaccine, ongoing immunomodulating treatments, and disease-related lung involvement during the next pandemic phase
AU - Ferri, Clodoveo
AU - Raimondo, Vincenzo
AU - Giuggioli, Dilia
AU - Gragnani, Laura
AU - Lorini, Serena
AU - Dagna, Lorenzo
AU - Bosello, Silvia Laura
AU - Foti, Rosario
AU - Riccieri, Valeria
AU - Guiducci, Serena
AU - Cuomo, Giovanna
AU - Tavoni, Antonio
AU - De Angelis, Rossella
AU - Cacciapaglia, Fabio
AU - Zanatta, Elisabetta
AU - Cozzi, Franco
AU - Murdaca, Giuseppe
AU - Cavazzana, Ilaria
AU - Romeo, Nicoletta
AU - Codullo, Veronica
AU - Pellegrini, Roberta
AU - Varcasia, Giuseppe
AU - De Santis, Maria
AU - Selmi, Carlo
AU - Abignano, Giuseppina
AU - Caminiti, Maurizio
AU - L'Andolina, Massimo
AU - Olivo, Domenico
AU - Lubrano, Ennio
AU - Spinella, Amelia
AU - Lumetti, Federica
AU - De Luca, Giacomo
AU - Ruscitti, Piero
AU - Urraro, Teresa
AU - Visentini, Marcella
AU - Bellando-Randone, Silvia
AU - Visalli, Elisa
AU - Testa, Davide
AU - Sciascia, Gabriella
AU - Masini, Francesco
AU - Pellegrino, Greta
AU - Saccon, Francesca
AU - Balestri, Eugenia
AU - Elia, Giusy
AU - Ferrari, Silvia Martina
AU - Tonutti, Antonio
AU - Dall'Ara, Francesca
AU - Pagano Mariano, Giuseppa
AU - Pettiti, Giorgio
AU - Zanframundo, Giovanni
AU - Brittelli, Raffaele
AU - Aiello, Vincenzo
AU - Dal Bosco, Ylenia
AU - Foti, Roberta
AU - Di Cola, Ilenia
AU - Scorpiniti, Daniela
AU - Fusaro, Enrico
AU - Ferrari, Tommaso
AU - Gigliotti, Pietro
AU - Campochiaro, Corrado
AU - Francioso, Francesca
AU - Iandoli, Carlo
AU - Caira, Virginia
AU - Zignego, Anna Linda
AU - D'Angelo, Salvatore
AU - Franceschini, Franco
AU - Matucci-Cerinic, Marco
AU - Giacomelli, Roberto
AU - Doria, Andrea
AU - Santini, Stefano Angelo
AU - Fallahi, Poupak
AU - Iannone, Florenzo
AU - Antonelli, Alessandro
PY - 2023
Y1 - 2023
N2 - Introduction: The impact of COVID-19 pandemic represents a serious challenge for ‘frail’ patients' populations with inflammatory autoimmune systemic diseases such as systemic sclerosis (SSc). We investigated the prevalence and severity of COVID-19, as well the effects of COVID-19 vaccination campaign in a large series of SSc patients followed for the entire period (first 38 months) of pandemic. Patients and method: This prospective survey study included 1755 unselected SSc patients (186 M, 1,569F; mean age 58.7 ± 13.4SD years, mean disease duration 8.8 ± 7.3SD years) recruited in part by telephone survey at 37 referral centers from February 2020 to April 2023. The following parameters were carefully evaluated: i. demographic, clinical, serological, and therapeutical features; ii. prevalence and severity of COVID-19; and iii. safety, immunogenicity, and efficacy of COVID-19 vaccines. Results: The prevalence of COVID-19 recorded during the whole pandemic was significantly higher compared to Italian general population (47.3 % vs 43.3 %, p < 0.000), as well the COVID-19-related mortality (1.91 % vs 0.72 %, p < 0.001). As regards the putative prognostic factors of worse outcome, COVID-19 positive patients with SSc-related interstitial lung involvement showed significantly higher percentage of COVID-19-related hospitalization compared to those without (5.85 % vs 1.73 %; p < 0.0001), as well as of mortality rate (2.01 % vs 0.4 %; p = 0.002). Over half of patients (56.3 %) received the first two plus one booster dose of vaccine; while a fourth dose was administered to 35.6 %, and only few of them (1.99 %) had five or more doses of vaccine. Of note, an impaired seroconversion was recorded in 25.6 % of individuals after the first 2 doses of vaccine, and in 8.4 % of patients also after the booster dose. Furthermore, the absence of T-cell immunoreactivity was observed in 3/7 patients tested by QuantiFERON® SARSCoV-2 Starter Set (Qiagen). The efficacy of vaccines, evaluated by comparing the COVID-19-related death rate recorded during pre- and post-vaccination pandemic periods, revealed a quite stable outcome in SSc patients (death rate from 2.54 % to 1.76 %; p = ns), despite the significant drop of mortality observed in the Italian general population (from 2.95 % to 0.29 %; p < 0.0001). Conclusions: An increased COVID-19 prevalence and mortality rate was recorded in SSc patients; moreover, the efficacy of vaccines in term of improved outcomes was less evident in SSc compared to Italian general population. This discrepancy might be explained by concomitant adverse prognostic factors: increased rate of non-responders to vaccine in SSc series, low percentage of individuals with four or more doses of vaccine, ongoing immunomodulating treatments, disease-related interstitial lung disease, and/or reduced preventive measures in the second half of pandemic. A careful monitoring of response to COVID-19 vaccines together with adequate preventive/therapeutical strategies are highly recommendable in the near course of pandemic in this frail patients’ population.
AB - Introduction: The impact of COVID-19 pandemic represents a serious challenge for ‘frail’ patients' populations with inflammatory autoimmune systemic diseases such as systemic sclerosis (SSc). We investigated the prevalence and severity of COVID-19, as well the effects of COVID-19 vaccination campaign in a large series of SSc patients followed for the entire period (first 38 months) of pandemic. Patients and method: This prospective survey study included 1755 unselected SSc patients (186 M, 1,569F; mean age 58.7 ± 13.4SD years, mean disease duration 8.8 ± 7.3SD years) recruited in part by telephone survey at 37 referral centers from February 2020 to April 2023. The following parameters were carefully evaluated: i. demographic, clinical, serological, and therapeutical features; ii. prevalence and severity of COVID-19; and iii. safety, immunogenicity, and efficacy of COVID-19 vaccines. Results: The prevalence of COVID-19 recorded during the whole pandemic was significantly higher compared to Italian general population (47.3 % vs 43.3 %, p < 0.000), as well the COVID-19-related mortality (1.91 % vs 0.72 %, p < 0.001). As regards the putative prognostic factors of worse outcome, COVID-19 positive patients with SSc-related interstitial lung involvement showed significantly higher percentage of COVID-19-related hospitalization compared to those without (5.85 % vs 1.73 %; p < 0.0001), as well as of mortality rate (2.01 % vs 0.4 %; p = 0.002). Over half of patients (56.3 %) received the first two plus one booster dose of vaccine; while a fourth dose was administered to 35.6 %, and only few of them (1.99 %) had five or more doses of vaccine. Of note, an impaired seroconversion was recorded in 25.6 % of individuals after the first 2 doses of vaccine, and in 8.4 % of patients also after the booster dose. Furthermore, the absence of T-cell immunoreactivity was observed in 3/7 patients tested by QuantiFERON® SARSCoV-2 Starter Set (Qiagen). The efficacy of vaccines, evaluated by comparing the COVID-19-related death rate recorded during pre- and post-vaccination pandemic periods, revealed a quite stable outcome in SSc patients (death rate from 2.54 % to 1.76 %; p = ns), despite the significant drop of mortality observed in the Italian general population (from 2.95 % to 0.29 %; p < 0.0001). Conclusions: An increased COVID-19 prevalence and mortality rate was recorded in SSc patients; moreover, the efficacy of vaccines in term of improved outcomes was less evident in SSc compared to Italian general population. This discrepancy might be explained by concomitant adverse prognostic factors: increased rate of non-responders to vaccine in SSc series, low percentage of individuals with four or more doses of vaccine, ongoing immunomodulating treatments, disease-related interstitial lung disease, and/or reduced preventive measures in the second half of pandemic. A careful monitoring of response to COVID-19 vaccines together with adequate preventive/therapeutical strategies are highly recommendable in the near course of pandemic in this frail patients’ population.
KW - COVID-19
KW - COVID-19 vaccine
KW - Systemic sclerosis
KW - SARS-CoV-2
KW - Scleroderma
KW - Interstitial lung disease
KW - COVID-19
KW - COVID-19 vaccine
KW - Systemic sclerosis
KW - SARS-CoV-2
KW - Scleroderma
KW - Interstitial lung disease
UR - http://hdl.handle.net/10807/265034
U2 - 10.1016/j.jtauto.2023.100212
DO - 10.1016/j.jtauto.2023.100212
M3 - Article
SN - 2589-9090
VL - 7
SP - N/A-N/A
JO - Journal of Translational Autoimmunity
JF - Journal of Translational Autoimmunity
ER -