The Effect of Exposure to SARS-CoV-2 Vaccination and Infection on Humoral and Cellular Immunity in a Cohort of Patients with Immune-Mediated Diseases: A Pilot Study

Author:

Costanzo Giulia Anna Maria Luigia1ORCID,Sanna Giuseppina2ORCID,Pes Francesco1,Deiana Carla Maria1ORCID,Ledda Andrea Giovanni1,Perra Andrea3ORCID,Palmas Vanessa2,Manca Valeria2,Miglianti Michela1,Coghe Ferdinando4,Manzin Aldo2ORCID,Del Giacco Stefano1,Chessa Luchino1ORCID,Firinu Davide1ORCID

Affiliation:

1. Department of Medical Sciences and Public Health, University of Cagliari, 09100 Cagliari, Italy

2. Microbiology and Virology Unit, Department of Biomedical Sciences, University of Cagliari, 09042 Monserrato, Italy

3. Oncology and Molecular Pathology Unit, Department of Biomedical Sciences, University of Cagliari, 09100 Cagliari, Italy

4. Laboratory Clinical Chemical Analysis and Microbiology, University Hospital of Cagliari, 09042 Monserrato, Italy

Abstract

Immunization against COVID-19 is needed in patients with immune-mediated inflammatory diseases (IMIDs). However, data on long-term immunity kinetics remain scarce. This study aimed to compare the humoral and cellular response to COVID-19 in patients with immune-mediated inflammatory diseases (IMIDs) compared to healthy controls. We compared the humoral and cellular response to SARS-Cov-2 elicited by vaccination and/or infection in a prospective cohort of 20 IMID patients compared with a group of 21 healthcare workers (HCWs). We assessed immunity before and after the third and fourth dose of BNT162b2 or after COVID-19 infection using quantitative IgG anti-SARS-CoV-2 Spike antibody (anti-S-IgG), neutralization assay, and specific interferon-gamma (IFN-g) release assay (IGRA). The responses were compared with those of healthy controls. The two groups were similar in age and total exposure, becoming infected for the first time, mainly after the third dose. Neutralizing antibodies and IGRA were negative in 9.5% of IMID patients but not in any HCWs. No significant difference was found between neutralization titers to BA.1 in the IMID and the HCW groups. The study highlights the SARS-CoV-2 immunological responses in healthy controls and IMID patients, suggesting that the combined stimuli of vaccination and infection in IMID patients could promote a more profound immunological response.

Funder

Fondazione di Sardegna

NextGeneration EU-MUR PNRR Extended Partnership initiative on Emerging Infectious Diseases

Associazione per l’Avanzamento della Ricerca per i Trapianti O.D.V.

Publisher

MDPI AG

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