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Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan

BACKGROUND: Autoimmune inflammatory rheumatic disease (AIRD) patients are at high risk of the coronavirus disease 2019 (COVID-19), but the medium-term effects of immunosuppressants on vaccine efficacy are unknown. We investigated the duration of humoral responses against severe acute respiratory syn...

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Autores principales: Yamaguchi, Yuta, Nameki, Shinichiro, Kato, Yasuhiro, Saita, Ryotaro, Sato, Tomoharu, Nagao, Sayaka, Murakami, Teruaki, Yoshimine, Yuko, Amiya, Saori, Morita, Takayoshi, Okita, Yasutaka, Kawasaki, Takahiro, Fujimoto, Jun, Ueda, Yasutaka, Maeda, Yuichi, Watanabe, Akane, Takamatsu, Hyota, Nishida, Sumiyuki, Shima, Yoshihito, Narazaki, Masashi, Kumanogoh, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763057/
https://www.ncbi.nlm.nih.gov/pubmed/36569794
http://dx.doi.org/10.1016/j.lanwpc.2022.100661
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author Yamaguchi, Yuta
Nameki, Shinichiro
Kato, Yasuhiro
Saita, Ryotaro
Sato, Tomoharu
Nagao, Sayaka
Murakami, Teruaki
Yoshimine, Yuko
Amiya, Saori
Morita, Takayoshi
Okita, Yasutaka
Kawasaki, Takahiro
Fujimoto, Jun
Ueda, Yasutaka
Maeda, Yuichi
Watanabe, Akane
Takamatsu, Hyota
Nishida, Sumiyuki
Shima, Yoshihito
Narazaki, Masashi
Kumanogoh, Atsushi
author_facet Yamaguchi, Yuta
Nameki, Shinichiro
Kato, Yasuhiro
Saita, Ryotaro
Sato, Tomoharu
Nagao, Sayaka
Murakami, Teruaki
Yoshimine, Yuko
Amiya, Saori
Morita, Takayoshi
Okita, Yasutaka
Kawasaki, Takahiro
Fujimoto, Jun
Ueda, Yasutaka
Maeda, Yuichi
Watanabe, Akane
Takamatsu, Hyota
Nishida, Sumiyuki
Shima, Yoshihito
Narazaki, Masashi
Kumanogoh, Atsushi
author_sort Yamaguchi, Yuta
collection PubMed
description BACKGROUND: Autoimmune inflammatory rheumatic disease (AIRD) patients are at high risk of the coronavirus disease 2019 (COVID-19), but the medium-term effects of immunosuppressants on vaccine efficacy are unknown. We investigated the duration of humoral responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) wild-type and Omicron variant in AIRD patients administered with two doses of the BNT162b2 (Pfizer–BioNTech) vaccine. METHODS: Serum-neutralizing antibody (NAb) and anti-receptor-binding domain (RBD)/spike antibody levels were measured. Short- and medium-term effects of immunosuppressants were analyzed pre-vaccination (Term 1) and 14–42 days (Term 2) and 100–200 days (Term 3) after the second vaccination. FINDINGS: From Feb 1, 2021, to Feb 28, 2022, 439 AIRD patients and 146 healthy controls were investigated. The seropositivity rate and log(10)-NAb titers were significantly lower in AIRD patients than in controls at Terms 2 and 3. In rheumatoid arthritis patients, tumor necrosis factor-α inhibitors (TNFis) at Term 3, and older age, glucocorticoids, and abatacept at Terms 2 and 3 were risk factors for reduced responses. Anti-Omicron RBD/spike IgG levels strongly correlated with NAb titers. INTERPRETATION: Glucocorticoids, TNFis, and abatacept treatments negatively affect the longevity of humoral responses to SARS-CoV-2, including Omicron, after two vaccine doses. These findings may inform the timing of additional vaccination for AIRD patients. FUNDING: Cloud Funding of Peace Winds Japan; 10.13039/501100009033Center of Innovation Program from the 10.13039/501100001700Ministry of Education, Culture, Sports, Science and Technology of Japan; 10.13039/501100001691Japan Society for the Promotion of Science KAKENHI; 10.13039/100009619Japan Agency for Medical Research and Development; 10.13039/100020408Kansai Economic Federation; Mitsubishi Zaidan; and Research Grant from 10.13039/100009619Japan Agency for Medical Research and Development—10.13039/501100003382Core Research for Evolutional Science and Technology.
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spelling pubmed-97630572022-12-20 Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan Yamaguchi, Yuta Nameki, Shinichiro Kato, Yasuhiro Saita, Ryotaro Sato, Tomoharu Nagao, Sayaka Murakami, Teruaki Yoshimine, Yuko Amiya, Saori Morita, Takayoshi Okita, Yasutaka Kawasaki, Takahiro Fujimoto, Jun Ueda, Yasutaka Maeda, Yuichi Watanabe, Akane Takamatsu, Hyota Nishida, Sumiyuki Shima, Yoshihito Narazaki, Masashi Kumanogoh, Atsushi Lancet Reg Health West Pac Articles BACKGROUND: Autoimmune inflammatory rheumatic disease (AIRD) patients are at high risk of the coronavirus disease 2019 (COVID-19), but the medium-term effects of immunosuppressants on vaccine efficacy are unknown. We investigated the duration of humoral responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) wild-type and Omicron variant in AIRD patients administered with two doses of the BNT162b2 (Pfizer–BioNTech) vaccine. METHODS: Serum-neutralizing antibody (NAb) and anti-receptor-binding domain (RBD)/spike antibody levels were measured. Short- and medium-term effects of immunosuppressants were analyzed pre-vaccination (Term 1) and 14–42 days (Term 2) and 100–200 days (Term 3) after the second vaccination. FINDINGS: From Feb 1, 2021, to Feb 28, 2022, 439 AIRD patients and 146 healthy controls were investigated. The seropositivity rate and log(10)-NAb titers were significantly lower in AIRD patients than in controls at Terms 2 and 3. In rheumatoid arthritis patients, tumor necrosis factor-α inhibitors (TNFis) at Term 3, and older age, glucocorticoids, and abatacept at Terms 2 and 3 were risk factors for reduced responses. Anti-Omicron RBD/spike IgG levels strongly correlated with NAb titers. INTERPRETATION: Glucocorticoids, TNFis, and abatacept treatments negatively affect the longevity of humoral responses to SARS-CoV-2, including Omicron, after two vaccine doses. These findings may inform the timing of additional vaccination for AIRD patients. FUNDING: Cloud Funding of Peace Winds Japan; 10.13039/501100009033Center of Innovation Program from the 10.13039/501100001700Ministry of Education, Culture, Sports, Science and Technology of Japan; 10.13039/501100001691Japan Society for the Promotion of Science KAKENHI; 10.13039/100009619Japan Agency for Medical Research and Development; 10.13039/100020408Kansai Economic Federation; Mitsubishi Zaidan; and Research Grant from 10.13039/100009619Japan Agency for Medical Research and Development—10.13039/501100003382Core Research for Evolutional Science and Technology. Elsevier 2022-12-20 /pmc/articles/PMC9763057/ /pubmed/36569794 http://dx.doi.org/10.1016/j.lanwpc.2022.100661 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Yamaguchi, Yuta
Nameki, Shinichiro
Kato, Yasuhiro
Saita, Ryotaro
Sato, Tomoharu
Nagao, Sayaka
Murakami, Teruaki
Yoshimine, Yuko
Amiya, Saori
Morita, Takayoshi
Okita, Yasutaka
Kawasaki, Takahiro
Fujimoto, Jun
Ueda, Yasutaka
Maeda, Yuichi
Watanabe, Akane
Takamatsu, Hyota
Nishida, Sumiyuki
Shima, Yoshihito
Narazaki, Masashi
Kumanogoh, Atsushi
Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title_full Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title_fullStr Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title_full_unstemmed Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title_short Persistence of SARS-CoV-2 neutralizing antibodies and anti-Omicron IgG induced by BNT162b2 mRNA vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in Japan
title_sort persistence of sars-cov-2 neutralizing antibodies and anti-omicron igg induced by bnt162b2 mrna vaccine in patients with autoimmune inflammatory rheumatic disease: an explanatory study in japan
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763057/
https://www.ncbi.nlm.nih.gov/pubmed/36569794
http://dx.doi.org/10.1016/j.lanwpc.2022.100661
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