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A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza

Radioprotective 105 (RP105) (also termed CD180) is an orphan and unconventional Toll-like receptor (TLR) that lacks an intracellular signaling domain. The agonistic anti-RP105 monoclonal antibody (mAb) can cross-link RP105 on B cells, resulting in the proliferation and activation of B cells. Anti-RP...

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Autores principales: Yamazaki, Tatsuya, Biswas, Mrityunjoy, Kosugi, Kouyu, Nagashima, Maria, Inui, Masanori, Tomono, Susumu, Takagi, Hidekazu, Ichimonji, Isao, Nagaoka, Fumiaki, Ainai, Akira, Hasegawa, Hideki, Chiba, Joe, Akashi-Takamura, Sachiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783388/
https://www.ncbi.nlm.nih.gov/pubmed/33414788
http://dx.doi.org/10.3389/fimmu.2020.606518
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author Yamazaki, Tatsuya
Biswas, Mrityunjoy
Kosugi, Kouyu
Nagashima, Maria
Inui, Masanori
Tomono, Susumu
Takagi, Hidekazu
Ichimonji, Isao
Nagaoka, Fumiaki
Ainai, Akira
Hasegawa, Hideki
Chiba, Joe
Akashi-Takamura, Sachiko
author_facet Yamazaki, Tatsuya
Biswas, Mrityunjoy
Kosugi, Kouyu
Nagashima, Maria
Inui, Masanori
Tomono, Susumu
Takagi, Hidekazu
Ichimonji, Isao
Nagaoka, Fumiaki
Ainai, Akira
Hasegawa, Hideki
Chiba, Joe
Akashi-Takamura, Sachiko
author_sort Yamazaki, Tatsuya
collection PubMed
description Radioprotective 105 (RP105) (also termed CD180) is an orphan and unconventional Toll-like receptor (TLR) that lacks an intracellular signaling domain. The agonistic anti-RP105 monoclonal antibody (mAb) can cross-link RP105 on B cells, resulting in the proliferation and activation of B cells. Anti-RP105 mAb also has a potent adjuvant effect, providing higher levels of antigen-specific antibodies compared to alum. However, adjuvanticity is required for the covalent link between anti-RP105 mAb and the antigen. This is a possible obstacle to immunization due to the link between anti-RP105 mAb and some antigens, especially multi-transmembrane proteins. We have previously succeeded in inducing rapid and potent recombinant mAbs in mice using antibody gene-based delivery. To simplify the covalent link between anti-RP105 mAb and antigens, we generated genetic constructs of recombinant anti-RP105 mAb (αRP105) bound to the transmembrane domain of the IgG-B cell receptor (TM) (αRP105-TM), which could enable the anti-RP105 mAb to link the antigen via the cell membrane. We confirmed the expression of αRP105-TM and the antigen hemagglutinin, which is a membrane protein of the influenza virus, on the same cell. We also found that αRP105-TM could activate splenic B cells, including both mature and immature cells, depending on the cell surface RP105 in vitro. To evaluate the adjuvanticity of αRP105-TM, we conducted DNA immunization in mice with the plasmids encoding αRP105-TM and hemagglutinin, followed by challenge with an infection of a lethal dose of an influenza virus. We then obtained partially but significantly hemagglutinin-specific antibodies and observed protective effects against a lethal dose of influenza virus infection. The current αRP105-TM might provide adjuvanticity for a vaccine via a simple preparation of the expression plasmids encoding αRP105-TM and of that encoding the target antigen.
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spelling pubmed-77833882021-01-06 A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza Yamazaki, Tatsuya Biswas, Mrityunjoy Kosugi, Kouyu Nagashima, Maria Inui, Masanori Tomono, Susumu Takagi, Hidekazu Ichimonji, Isao Nagaoka, Fumiaki Ainai, Akira Hasegawa, Hideki Chiba, Joe Akashi-Takamura, Sachiko Front Immunol Immunology Radioprotective 105 (RP105) (also termed CD180) is an orphan and unconventional Toll-like receptor (TLR) that lacks an intracellular signaling domain. The agonistic anti-RP105 monoclonal antibody (mAb) can cross-link RP105 on B cells, resulting in the proliferation and activation of B cells. Anti-RP105 mAb also has a potent adjuvant effect, providing higher levels of antigen-specific antibodies compared to alum. However, adjuvanticity is required for the covalent link between anti-RP105 mAb and the antigen. This is a possible obstacle to immunization due to the link between anti-RP105 mAb and some antigens, especially multi-transmembrane proteins. We have previously succeeded in inducing rapid and potent recombinant mAbs in mice using antibody gene-based delivery. To simplify the covalent link between anti-RP105 mAb and antigens, we generated genetic constructs of recombinant anti-RP105 mAb (αRP105) bound to the transmembrane domain of the IgG-B cell receptor (TM) (αRP105-TM), which could enable the anti-RP105 mAb to link the antigen via the cell membrane. We confirmed the expression of αRP105-TM and the antigen hemagglutinin, which is a membrane protein of the influenza virus, on the same cell. We also found that αRP105-TM could activate splenic B cells, including both mature and immature cells, depending on the cell surface RP105 in vitro. To evaluate the adjuvanticity of αRP105-TM, we conducted DNA immunization in mice with the plasmids encoding αRP105-TM and hemagglutinin, followed by challenge with an infection of a lethal dose of an influenza virus. We then obtained partially but significantly hemagglutinin-specific antibodies and observed protective effects against a lethal dose of influenza virus infection. The current αRP105-TM might provide adjuvanticity for a vaccine via a simple preparation of the expression plasmids encoding αRP105-TM and of that encoding the target antigen. Frontiers Media S.A. 2020-12-22 /pmc/articles/PMC7783388/ /pubmed/33414788 http://dx.doi.org/10.3389/fimmu.2020.606518 Text en Copyright © 2020 Yamazaki, Biswas, Kosugi, Nagashima, Inui, Tomono, Takagi, Ichimonji, Nagaoka, Ainai, Hasegawa, Chiba and Akashi-Takamura http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Yamazaki, Tatsuya
Biswas, Mrityunjoy
Kosugi, Kouyu
Nagashima, Maria
Inui, Masanori
Tomono, Susumu
Takagi, Hidekazu
Ichimonji, Isao
Nagaoka, Fumiaki
Ainai, Akira
Hasegawa, Hideki
Chiba, Joe
Akashi-Takamura, Sachiko
A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title_full A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title_fullStr A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title_full_unstemmed A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title_short A Novel Gene Delivery Vector of Agonistic Anti-Radioprotective 105 Expressed on Cell Membranes Shows Adjuvant Effect for DNA Immunization Against Influenza
title_sort novel gene delivery vector of agonistic anti-radioprotective 105 expressed on cell membranes shows adjuvant effect for dna immunization against influenza
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7783388/
https://www.ncbi.nlm.nih.gov/pubmed/33414788
http://dx.doi.org/10.3389/fimmu.2020.606518
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