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Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms

BACKGROUND AND PURPOSE: Anti-CD20 monoclonal antibodies (MoAbs), rituximab (RIT), and obinutuzumab (OBZ) are the central components of immunochemotherapy for B-cell lymphoma (BCL). However, these agents potentially cause B-cell depletion, resulting in the impairment of antibody (Ab) production. Duri...

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Autores principales: Onishi, Akio, Matsumura-Kimoto, Yayoi, Mizutani, Shinsuke, Tsukamoto, Taku, Fujino, Takahiro, Miyashita, Akihiro, Nishiyama, Daichi, Shimura, Kazuho, Kaneko, Hiroto, Kawata, Eri, Takahashi, Ryoichi, Kobayashi, Tsutomu, Uchiyama, Hitoji, Uoshima, Nobuhiko, Nukui, Yoko, Shimura, Yuji, Inaba, Tohru, Kuroda, Junya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884434/
https://www.ncbi.nlm.nih.gov/pubmed/36721633
http://dx.doi.org/10.2147/IDR.S396271
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author Onishi, Akio
Matsumura-Kimoto, Yayoi
Mizutani, Shinsuke
Tsukamoto, Taku
Fujino, Takahiro
Miyashita, Akihiro
Nishiyama, Daichi
Shimura, Kazuho
Kaneko, Hiroto
Kawata, Eri
Takahashi, Ryoichi
Kobayashi, Tsutomu
Uchiyama, Hitoji
Uoshima, Nobuhiko
Nukui, Yoko
Shimura, Yuji
Inaba, Tohru
Kuroda, Junya
author_facet Onishi, Akio
Matsumura-Kimoto, Yayoi
Mizutani, Shinsuke
Tsukamoto, Taku
Fujino, Takahiro
Miyashita, Akihiro
Nishiyama, Daichi
Shimura, Kazuho
Kaneko, Hiroto
Kawata, Eri
Takahashi, Ryoichi
Kobayashi, Tsutomu
Uchiyama, Hitoji
Uoshima, Nobuhiko
Nukui, Yoko
Shimura, Yuji
Inaba, Tohru
Kuroda, Junya
author_sort Onishi, Akio
collection PubMed
description BACKGROUND AND PURPOSE: Anti-CD20 monoclonal antibodies (MoAbs), rituximab (RIT), and obinutuzumab (OBZ) are the central components of immunochemotherapy for B-cell lymphoma (BCL). However, these agents potentially cause B-cell depletion, resulting in the impairment of antibody (Ab) production. During the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, the optimal prediction of Ab response against anti–SARS-CoV-2 vaccination is critically important in patients with BCL treated by B-cell depletion therapeutics to prevent coronavirus disease 2019 (COVID-19). PATIENTS AND METHODS:  We investigated the effect of using RIT and/or OBZ on the Ab response in 131 patients with various types of BCL who received the second SARS-CoV-2 mRNA vaccine either after, during, or before immunochemotherapy containing B-cell–depleting moiety between June and November 2021 at seven institutes belonging to the Kyoto Clinical Hematology Study Group. The SARS-Cov-2 neutralizing Ab (nAb) was measured from 14 to 207 days after the second vaccination dose using the iFlash3000 automatic analyzer and the iFlash-2019-nCoV Nab kit. RESULTS: Among 86 patients who received the vaccine within 12 months after B-cell depletion therapy, 8 (9.3%) were seropositive. In 30 patients who received the vaccine after 12 months from B-cell depletion therapy, 22 (73%) were seropositive. In 15 patients who were subjected to B-cell depletion therapy after vaccination, 2 (13%) were seropositive. The multivariate analysis indicated that an interval of 12 months between B-cell depletion therapy and the subsequent vaccination was significantly associated with effective Ab production. Receiver operating characteristic curve analysis identified the optimal threshold period after anti-CD20 MoAb treatment, which determines the seropositivity against SARS-CoV-2, to be 342 days. CONCLUSION: The use of anti-CD20 MoAb within 12 months before vaccination is a critical risk for poor Ab response against anti–SARS-CoV-2 vaccination in patients with BCL.
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spelling pubmed-98844342023-01-30 Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms Onishi, Akio Matsumura-Kimoto, Yayoi Mizutani, Shinsuke Tsukamoto, Taku Fujino, Takahiro Miyashita, Akihiro Nishiyama, Daichi Shimura, Kazuho Kaneko, Hiroto Kawata, Eri Takahashi, Ryoichi Kobayashi, Tsutomu Uchiyama, Hitoji Uoshima, Nobuhiko Nukui, Yoko Shimura, Yuji Inaba, Tohru Kuroda, Junya Infect Drug Resist Original Research BACKGROUND AND PURPOSE: Anti-CD20 monoclonal antibodies (MoAbs), rituximab (RIT), and obinutuzumab (OBZ) are the central components of immunochemotherapy for B-cell lymphoma (BCL). However, these agents potentially cause B-cell depletion, resulting in the impairment of antibody (Ab) production. During the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, the optimal prediction of Ab response against anti–SARS-CoV-2 vaccination is critically important in patients with BCL treated by B-cell depletion therapeutics to prevent coronavirus disease 2019 (COVID-19). PATIENTS AND METHODS:  We investigated the effect of using RIT and/or OBZ on the Ab response in 131 patients with various types of BCL who received the second SARS-CoV-2 mRNA vaccine either after, during, or before immunochemotherapy containing B-cell–depleting moiety between June and November 2021 at seven institutes belonging to the Kyoto Clinical Hematology Study Group. The SARS-Cov-2 neutralizing Ab (nAb) was measured from 14 to 207 days after the second vaccination dose using the iFlash3000 automatic analyzer and the iFlash-2019-nCoV Nab kit. RESULTS: Among 86 patients who received the vaccine within 12 months after B-cell depletion therapy, 8 (9.3%) were seropositive. In 30 patients who received the vaccine after 12 months from B-cell depletion therapy, 22 (73%) were seropositive. In 15 patients who were subjected to B-cell depletion therapy after vaccination, 2 (13%) were seropositive. The multivariate analysis indicated that an interval of 12 months between B-cell depletion therapy and the subsequent vaccination was significantly associated with effective Ab production. Receiver operating characteristic curve analysis identified the optimal threshold period after anti-CD20 MoAb treatment, which determines the seropositivity against SARS-CoV-2, to be 342 days. CONCLUSION: The use of anti-CD20 MoAb within 12 months before vaccination is a critical risk for poor Ab response against anti–SARS-CoV-2 vaccination in patients with BCL. Dove 2023-01-25 /pmc/articles/PMC9884434/ /pubmed/36721633 http://dx.doi.org/10.2147/IDR.S396271 Text en © 2023 Onishi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Onishi, Akio
Matsumura-Kimoto, Yayoi
Mizutani, Shinsuke
Tsukamoto, Taku
Fujino, Takahiro
Miyashita, Akihiro
Nishiyama, Daichi
Shimura, Kazuho
Kaneko, Hiroto
Kawata, Eri
Takahashi, Ryoichi
Kobayashi, Tsutomu
Uchiyama, Hitoji
Uoshima, Nobuhiko
Nukui, Yoko
Shimura, Yuji
Inaba, Tohru
Kuroda, Junya
Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title_full Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title_fullStr Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title_full_unstemmed Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title_short Impact of Treatment with Anti-CD20 Monoclonal Antibody on the Production of Neutralizing Antibody Against Anti–SARS-CoV-2 Vaccination in Mature B-Cell Neoplasms
title_sort impact of treatment with anti-cd20 monoclonal antibody on the production of neutralizing antibody against anti–sars-cov-2 vaccination in mature b-cell neoplasms
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884434/
https://www.ncbi.nlm.nih.gov/pubmed/36721633
http://dx.doi.org/10.2147/IDR.S396271
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