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Clin Microbiol Infect ; 2022 Sep 20.
Article in English | MEDLINE | ID: covidwho-2233652

ABSTRACT

OBJECTIVES: Some vaccinated individuals fail to acquire an adequate immune response against infection. We aimed to determine whether mRNA severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination could induce a sufficient immune response against SARS-CoV-2 in low responders to other vaccinations. METHODS: Using data from health-care workers who received two doses of the BNT162b2 vaccine (BioNTech/Pfizer), we conducted a single-centre, cross-sectional study to determine whether low responders to measles, rubella, and hepatitis B virus (HBV) vaccinations could acquire sufficient antibodies after SARS-CoV-2 vaccination. From May 2021 to June 2021, participants were tested for anti-SARS-CoV-2 spike (anti-S) IgG antibodies at least 2 weeks after the second dose of BNT162b2. The association between a low response to measles, rubella, and HBV vaccinations and the post-vaccination anti-S IgG titre was evaluated using the multivariable linear regression analysis. RESULTS: All 714 participants were positive for the anti-S IgG titre (≥50.0 AU/mL) after two doses of BNT162b2 (median, 7126.8 AU/mL; interquartile range, 4496.2-11 296.8). There were 323 (45.2%), 131 (18.3%), and 43 (6.0%) low responders to measles, rubella, and HBV vaccinations, respectively. In the multivariable linear regression analysis, low responders to rubella vaccination had significantly low acquisition of the anti-S IgG titre after two doses of the BNT162b2 vaccine (standardized coefficient ß, -0.110; 95% CI, -0.175 to -0.044). CONCLUSIONS: A low response to rubella vaccination is a potential predictor of a reduced response to SARS-CoV-2 vaccination. Further studies are needed to determine whether a low response to rubella vaccination is associated with the durability of SARS-CoV-2 vaccination-induced immune response.

2.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases ; 2022.
Article in English | EuropePMC | ID: covidwho-2034222

ABSTRACT

Objectives Some vaccinated individuals fail to acquire an adequate immune response against infection. We aimed to determine whether messenger-RNA severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination could induce sufficient immune response against SARS-CoV-2 in low responders to other vaccinations. Methods Using data from healthcare workers who received two doses of the BNT162b2 vaccine (BioNTech, Pfizer), we conducted a single-centre cross-sectional study to determine whether low responders to measles, rubella, and hepatitis B virus (HBV) vaccinations could acquire sufficient antibodies after SARS-CoV-2 vaccination. From May 2021 to June 2021, participants were tested for anti-SARS-CoV-2 spike immunoglobulin G (anti-S IgG) antibody at least two weeks after the second dose of BNT162b2. The association between low response to measles, rubella, and HBV vaccinations and the post-vaccination anti-S IgG titre was evaluated using multivariable linear regression analysis. Results All 714 participants were positive for the anti-S IgG titre (≥50.0 AU/mL) after two doses of BNT162b2 (median: 7,126.8 AU/mL, interquartile range: 4,496.2–11,296.8). There were 323 (45.2%), 131 (18.3%), and 43 (6.0%) low responders to measles, rubella, and HBV vaccinations, respectively. In the multivariable linear regression analysis, low responders to rubella vaccination had a significantly low acquisition of anti-S IgG titre after two doses of the BNT162b2 vaccine (standardised coefficient β = −0.110: 95% confidence interval: −0.175 to −0.044). Conclusions Low response to rubella vaccination is a potential predictor of reduced response to SARS-CoV-2 vaccination. Further studies are needed to determine whether a low response to rubella vaccination is associated with the durability of SARS-CoV-2 vaccination-induced immune response.

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