SARS-CoV-2 spike protein antibody titers 6 months after SARS-CoV-2 mRNA vaccination among patients undergoing hemodialysis in Japan

Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination is shown to prevent severe illness and death in hemodialysis (HD) patients, but the immune response to vaccines is reduced in this population. This study compared SARS-CoV-2 spike protein antibody titers between HD p...

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Veröffentlicht in:Clinical and experimental nephrology 2022-10, Vol.26 (10), p.988-996
Hauptverfasser: Kanai, Daisuke, Wakui, Hiromichi, Haze, Tatsuya, Azushima, Kengo, Kinguchi, Sho, Tsukamoto, Shunichiro, Kanaoka, Tomohiko, Urate, Shingo, Toya, Yoshiyuki, Hirawa, Nobuhito, Kato, Hideaki, Watanabe, Fumimasa, Hanaoka, Kanako, Hanaoka, Masaaki, Mitsuhashi, Hiroshi, Yamaguchi, Satoshi, Ohnishi, Toshimasa, Tamura, Kouichi
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Sprache:eng
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Zusammenfassung:Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination is shown to prevent severe illness and death in hemodialysis (HD) patients, but the immune response to vaccines is reduced in this population. This study compared SARS-CoV-2 spike protein antibody titers between HD patients and healthy controls in Japan for up to 6 months following vaccination. Methods A multi-institutional retrospective study at five clinics in Japan was conducted using 412 HD patients and 156 healthy controls who received two doses of the BNT162b2 (Pfizer-BioNTech) mRNA vaccine. Anti-SARS-CoV-2 spike protein S1 IgG antibody titers were measured at 1, 3, and 6 months after the second dose. The attenuation speed was calculated as slope (i.e., – β ) using a linear mixed-effects model toward the log-transformed antibody titers. Results The HD group had significantly lower month 1 antibody titers (Ab-titer-1) than the controls, and these remained lower through month 6 (95% CI: 2617.1 (1296.7, 5240.8) vs. 7285.4 (4403.9, 11,000.0) AU/mL at Ab-titer-1, and 353.4 (178.4, 656.3) vs. 812.0 (498.3, 1342.7) AU/mL at Ab-titer-6 ( p  
ISSN:1342-1751
1437-7799
1437-7799
DOI:10.1007/s10157-022-02243-8