The role of neutralizing antibodies by sVNT after two doses of BNT162b2 mRNA vaccine in a cohort of Italian healthcare workers

Author:

Infantino Maria1,Manfredi Mariangela1,Stacchini Lorenzo2,Cosma Claudia2,Grossi Valentina1,Lari Barbara1,Russo Edda3,Amedei Amedeo3,Benucci Maurizio4,Veneziani Francesca5,Casprini Patrizia5,Catalano Cateno Mario6,Cirrincione Giuseppe6,Bonaccorsi Guglielmo2,Pompetti Adolfo7

Affiliation:

1. Immunology and Allergology Laboratory Unit , S. Giovanni di Dio Hospital , Florence , Italy

2. Department of Health Science , University of Florence , Florence , Italy

3. Department of Experimental and Clinical Medicine , University of Florence , Florence , Italy

4. Rheumatology Unit , S. Giovanni di Dio Hospital , Florence , Italy

5. Clinical Pathology Laboratory Unit , S. Giovanni di Dio Hospital , Florence , Italy

6. Department of Technical Health Services, Preventive Medicine , S. Giovanni di Dio Hospital , Florence , Italy

7. SOC Clinical Assistance Governance, SOS Preventive Medicine Unit , S. Giovanni di Dio Hospital , Florence , Italy

Abstract

Abstract Objectives Evaluating anti-SARS-CoV-2 antibody levels is a current priority to drive immunization, as well as to predict when a vaccine booster dose may be required and for which priority groups. The aim of our study was to investigate the kinetics of anti-SARS-CoV-2 Spike S1 protein IgG (anti-S1 IgG) antibodies and neutralizing antibodies (NAbs) in an Italian cohort of healthcare workers (HCWs), following the Pfizer/BNT162b2 mRNA vaccine, over a period of up to six months after the second dose. Methods We enrolled 57 HCWs, without clinical history of COVID-19 infection. Fluoroenzyme-immunoassay was used for the quantitative anti-S1 IgG antibodies at different time points T1 (one month), T3 (three months) and T6 (six months) following the second vaccine shot. Simultaneously, a commercial surrogate virus neutralization test (sVNT) was used for the determination of NAbs, expressed as inhibition percentage (% IH). Results Median values of anti-S1 IgG antibodies decreased from T1 (1,452 BAU/mL) to T6 (104 BAU/mL) with a percent variation of 92.8% while the sVNT showed a percent variation of 34.3% for the same time frame. The decline in anti-S1 IgG antibodies from T1 to T6 was not accompanied by a loss of the neutralizing capacity of antibodies. In fact at T6 a neutralization percentage <20% IH was observed only in 3.51% of HCWs. Conclusions Our findings reveal that the decrease of anti-S1 IgG levels do not correspond in parallel to a decrease of NAbs over time, which highlights the necessity of using both assays to assess vaccination effectiveness.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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