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Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy

Human T-cell leukemia virus type 1 (HTLV-1), a retrovirus, causes adult T-cell leukemia-lymphoma, HTLV-1 associated myelopathy/tropical spastic paraparesis, and HTLV-1 uveitis. Currently, no antiretroviral therapies or vaccines are available for HTLV-1 infection. This study aimed to develop an antib...

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Autores principales: Hatayama, Yasuyoshi, Yamaoka, Yutaro, Morita, Takeshi, Jeremiah, Sundararaj Stanleyraj, Miyakawa, Kei, Nishi, Mayuko, Kimura, Yayoi, Mitsunaga, Makoto, Iwase, Tadayuki, Kimura, Hirokazu, Yamamoto, Naoki, Takaori-Kondo, Akifumi, Hasegawa, Hideki, Ryo, Akihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608601/
https://www.ncbi.nlm.nih.gov/pubmed/36298708
http://dx.doi.org/10.3390/v14102153
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author Hatayama, Yasuyoshi
Yamaoka, Yutaro
Morita, Takeshi
Jeremiah, Sundararaj Stanleyraj
Miyakawa, Kei
Nishi, Mayuko
Kimura, Yayoi
Mitsunaga, Makoto
Iwase, Tadayuki
Kimura, Hirokazu
Yamamoto, Naoki
Takaori-Kondo, Akifumi
Hasegawa, Hideki
Ryo, Akihide
author_facet Hatayama, Yasuyoshi
Yamaoka, Yutaro
Morita, Takeshi
Jeremiah, Sundararaj Stanleyraj
Miyakawa, Kei
Nishi, Mayuko
Kimura, Yayoi
Mitsunaga, Makoto
Iwase, Tadayuki
Kimura, Hirokazu
Yamamoto, Naoki
Takaori-Kondo, Akifumi
Hasegawa, Hideki
Ryo, Akihide
author_sort Hatayama, Yasuyoshi
collection PubMed
description Human T-cell leukemia virus type 1 (HTLV-1), a retrovirus, causes adult T-cell leukemia-lymphoma, HTLV-1 associated myelopathy/tropical spastic paraparesis, and HTLV-1 uveitis. Currently, no antiretroviral therapies or vaccines are available for HTLV-1 infection. This study aimed to develop an antibody against the HTLV-1 envelope protein (Env) and apply it to a near-infrared photoimmuno-antimicrobial strategy (NIR-PIAS) to eliminate HTLV-1 infected cells. We established mouse monoclonal antibodies (mAbs) against HTLV-1 Env by immunization with a complex of liposome and the recombinant protein. Detailed epitope mapping revealed that one of the mAbs bound to the proline-rich region of gp46 and exhibited no obvious neutralizing activity to inhibit viral infection. Instead, the mAb was rarely internalized intracellularly and remained on the cell surface of HTLV-1-infected cells. The antibody conjugated to the photosensitive dye IRDye700Dx recognized HTLV-1 infected cells and killed them following NIR irradiation. These results suggest that the novel mAb and NIR-PIAS could be developed as a new targeted therapeutic tool against HTLV-1 infected cells.
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spelling pubmed-96086012022-10-28 Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy Hatayama, Yasuyoshi Yamaoka, Yutaro Morita, Takeshi Jeremiah, Sundararaj Stanleyraj Miyakawa, Kei Nishi, Mayuko Kimura, Yayoi Mitsunaga, Makoto Iwase, Tadayuki Kimura, Hirokazu Yamamoto, Naoki Takaori-Kondo, Akifumi Hasegawa, Hideki Ryo, Akihide Viruses Article Human T-cell leukemia virus type 1 (HTLV-1), a retrovirus, causes adult T-cell leukemia-lymphoma, HTLV-1 associated myelopathy/tropical spastic paraparesis, and HTLV-1 uveitis. Currently, no antiretroviral therapies or vaccines are available for HTLV-1 infection. This study aimed to develop an antibody against the HTLV-1 envelope protein (Env) and apply it to a near-infrared photoimmuno-antimicrobial strategy (NIR-PIAS) to eliminate HTLV-1 infected cells. We established mouse monoclonal antibodies (mAbs) against HTLV-1 Env by immunization with a complex of liposome and the recombinant protein. Detailed epitope mapping revealed that one of the mAbs bound to the proline-rich region of gp46 and exhibited no obvious neutralizing activity to inhibit viral infection. Instead, the mAb was rarely internalized intracellularly and remained on the cell surface of HTLV-1-infected cells. The antibody conjugated to the photosensitive dye IRDye700Dx recognized HTLV-1 infected cells and killed them following NIR irradiation. These results suggest that the novel mAb and NIR-PIAS could be developed as a new targeted therapeutic tool against HTLV-1 infected cells. MDPI 2022-09-29 /pmc/articles/PMC9608601/ /pubmed/36298708 http://dx.doi.org/10.3390/v14102153 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hatayama, Yasuyoshi
Yamaoka, Yutaro
Morita, Takeshi
Jeremiah, Sundararaj Stanleyraj
Miyakawa, Kei
Nishi, Mayuko
Kimura, Yayoi
Mitsunaga, Makoto
Iwase, Tadayuki
Kimura, Hirokazu
Yamamoto, Naoki
Takaori-Kondo, Akifumi
Hasegawa, Hideki
Ryo, Akihide
Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title_full Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title_fullStr Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title_full_unstemmed Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title_short Development of a Monoclonal Antibody Targeting HTLV-1 Envelope gp46 Glycoprotein and Its Application to Near-Infrared Photoimmuno-Antimicrobial Strategy
title_sort development of a monoclonal antibody targeting htlv-1 envelope gp46 glycoprotein and its application to near-infrared photoimmuno-antimicrobial strategy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608601/
https://www.ncbi.nlm.nih.gov/pubmed/36298708
http://dx.doi.org/10.3390/v14102153
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