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Antibody responses and SARS-CoV-2 infection after BNT162b2 mRNA booster vaccination among healthcare workers in Japan.
Igari, Hidetoshi; Asano, Haruna; Murata, Shota; Yoshida, Toshihiko; Kawasaki, Kenji; Kageyama, Takahiro; Ikeda, Key; Koshikawa, Hiromi; Okuda, Yoshio; Urushihara, Misao; Chiba, Hitoshi; Yahaba, Misuzu; Taniguchi, Toshibumi; Matsushita, Kazuyuki; Yoshino, Ichiro; Yokote, Koutaro; Nakajima, Hiroshi.
  • Igari H; Department of Infection Control, Chiba University Hospital, Japan; COVID-19 Vaccine Center, Chiba University Hospital, Japan. Electronic address: igari_h@chiba-u.jp.
  • Asano H; Division of Laboratory Medicine, Chiba University Hospital, Japan. Electronic address: ha-asano@chiba-u.jp.
  • Murata S; Division of Laboratory Medicine, Chiba University Hospital, Japan. Electronic address: aeya4511@chiba-u.jp.
  • Yoshida T; Division of Laboratory Medicine, Chiba University Hospital, Japan. Electronic address: yoshidat@chiba-u.jp.
  • Kawasaki K; Division of Laboratory Medicine, Chiba University Hospital, Japan. Electronic address: kawaken@chiba-u.jp.
  • Kageyama T; Department of Allergy and Clinical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan. Electronic address: t.kageyama@chiba-u.jp.
  • Ikeda K; Department of Allergy and Clinical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan. Electronic address: K.Ikeda@faculty.chiba-u.jp.
  • Koshikawa H; Department of Infection Control, Chiba University Hospital, Japan. Electronic address: koshikawah@chiba-u.jp.
  • Okuda Y; Department of Infection Control, Chiba University Hospital, Japan. Electronic address: adha5658@chiba-u.jp.
  • Urushihara M; Department of Infection Control, Chiba University Hospital, Japan.
  • Chiba H; Department of Infection Control, Chiba University Hospital, Japan. Electronic address: aaka5237@chiba-u.jp.
  • Yahaba M; Department of Infection Control, Chiba University Hospital, Japan. Electronic address: mis_misuzu@yahoo.co.jp.
  • Taniguchi T; Department of Infection Control, Chiba University Hospital, Japan. Electronic address: tosh-tanig@chiba-u.jp.
  • Matsushita K; Division of Laboratory Medicine, Chiba University Hospital, Japan. Electronic address: kmatsu@faculty.chiba-u.jp.
  • Yoshino I; Department of General Thoracic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan. Electronic address: iyoshino49@icloud.com.
  • Yokote K; Department of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, Japan. Electronic address: kyokote@faculty.chiba-u.jp.
  • Nakajima H; COVID-19 Vaccine Center, Chiba University Hospital, Japan; Department of Allergy and Clinical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan. Electronic address: nakajimh@faculty.chiba-u.jp.
J Infect Chemother ; 28(11): 1483-1488, 2022 Nov.
Article in English | MEDLINE | ID: covidwho-1936797
ABSTRACT

INTRODUCTION:

Vaccine effectiveness against SARS-CoV-2 infections decreases due to waning immunity, and booster vaccination was therefore introduced. We estimated the anti-spike antibody (AS-ab) recovery by booster vaccination and analyzed the risk factors for SARS-CoV-2 infections.

METHODS:

The subjects were health care workers (HCWs) in a Chiba University Hospital vaccination cohort. They had received two doses of vaccine (BNT162b2) and a booster vaccine (BNT162b2). We retrospectively analyzed AS-ab titers and watched out for SARS-CoV-2 infection for 90 days following booster vaccination.

RESULTS:

AS-ab titer eight months after two-dose vaccinations had decreased to as low as 587 U/mL (median, IQR (interquartile range) 360-896). AS-ab titer had then increased to 22471 U/mL (15761-32622) three weeks after booster vaccination. There were no significant differences among age groups. A total of 1708 HCWs were analyzed for SARS-CoV-2 infection, and 48 of them proved positive. SARS-CoV-2 infections in the booster-vaccinated and non-booster groups were 1.8% and 4.0%, respectively, and were not significant. However, when restricted to those 20-29 years old, SARS-CoV-2 infections in the booster-vaccinated and non-booster groups were 2.9% and 13.6%, respectively (p = 0.04). After multivariate logistic regression, COVID-19 wards (adjusted odds ratio (aOR)2.9, 95% confidence interval (CI) 1.5-5.6) and those aged 20-49 years (aOR9.7, 95%CI 1.3-71.2) were risk factors for SARS-CoV-2 infection.

CONCLUSIONS:

Booster vaccination induced the recovery of AS-ab titers. Risk factors for SARS-CoV-2 infection were HCWs of COVID-19 wards and those aged 20-49 years. Increased vaccination coverage, together with implementing infection control, remains the primary means of preventing HCWs from SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccines / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Humans / Young adult Country/Region as subject: Asia Language: English Journal: J Infect Chemother Journal subject: Microbiology / Drug Therapy Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccines / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Humans / Young adult Country/Region as subject: Asia Language: English Journal: J Infect Chemother Journal subject: Microbiology / Drug Therapy Year: 2022 Document Type: Article