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Novel single‐chain variant of antibody against mesothelin established by phage library

Mesothelin (MSLN) shows increased expression in various cancer cells. For clinical application of antibodies as a positron emission tomography (PET) imaging reagent, a human shortened antibody is essential both for avoiding redundant immune responses and for providing rapid imaging. Therefore, we cl...

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Autores principales: Yakushiji, Hiromasa, Kobayashi, Kazuko, Takenaka, Fumiaki, Kishi, Yoshiro, Shinohara, Midori, Akehi, Masaru, Sasaki, Takanori, Ohno, Eiji, Matsuura, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726835/
https://www.ncbi.nlm.nih.gov/pubmed/31461572
http://dx.doi.org/10.1111/cas.14150
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author Yakushiji, Hiromasa
Kobayashi, Kazuko
Takenaka, Fumiaki
Kishi, Yoshiro
Shinohara, Midori
Akehi, Masaru
Sasaki, Takanori
Ohno, Eiji
Matsuura, Eiji
author_facet Yakushiji, Hiromasa
Kobayashi, Kazuko
Takenaka, Fumiaki
Kishi, Yoshiro
Shinohara, Midori
Akehi, Masaru
Sasaki, Takanori
Ohno, Eiji
Matsuura, Eiji
author_sort Yakushiji, Hiromasa
collection PubMed
description Mesothelin (MSLN) shows increased expression in various cancer cells. For clinical application of antibodies as a positron emission tomography (PET) imaging reagent, a human shortened antibody is essential both for avoiding redundant immune responses and for providing rapid imaging. Therefore, we cloned a single‐chain fragment of variable regions (scFv) from a human‐derived gene sequence. This was achieved through the construction of a naïve phage library derived from human tonsil lymphocytes. Using a column with human recombinant MSLN, we carried out bio‐panning of phage‐variants by colony formation. We first obtained 120 clones that were subjected to selection in an ELISA using human recombinant MSLN as a solid phase antigen, and 15 phage clones of scFv with a different sequence were selected and investigated by flow cytometry (FCM). Then, six variants were selected and the individual scFv gene was synthesized in the V(L) and V(H) domains and expressed in Chinese hamster ovary cells. Mammalian cell‐derived human‐origin scFv clones were analyzed by FCM again, and one MSLN highly specific scFv clone was established. PET imaging by (89)Zr‐labeled scFv was done in mice bearing xenografts with MSLN‐expressing cancer cells, and tumor legions were successfully visualized. The scFv variant established in the present study may be potentially useful for cancer diagnosis by PET imaging.
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spelling pubmed-67268352019-09-10 Novel single‐chain variant of antibody against mesothelin established by phage library Yakushiji, Hiromasa Kobayashi, Kazuko Takenaka, Fumiaki Kishi, Yoshiro Shinohara, Midori Akehi, Masaru Sasaki, Takanori Ohno, Eiji Matsuura, Eiji Cancer Sci Original Articles Mesothelin (MSLN) shows increased expression in various cancer cells. For clinical application of antibodies as a positron emission tomography (PET) imaging reagent, a human shortened antibody is essential both for avoiding redundant immune responses and for providing rapid imaging. Therefore, we cloned a single‐chain fragment of variable regions (scFv) from a human‐derived gene sequence. This was achieved through the construction of a naïve phage library derived from human tonsil lymphocytes. Using a column with human recombinant MSLN, we carried out bio‐panning of phage‐variants by colony formation. We first obtained 120 clones that were subjected to selection in an ELISA using human recombinant MSLN as a solid phase antigen, and 15 phage clones of scFv with a different sequence were selected and investigated by flow cytometry (FCM). Then, six variants were selected and the individual scFv gene was synthesized in the V(L) and V(H) domains and expressed in Chinese hamster ovary cells. Mammalian cell‐derived human‐origin scFv clones were analyzed by FCM again, and one MSLN highly specific scFv clone was established. PET imaging by (89)Zr‐labeled scFv was done in mice bearing xenografts with MSLN‐expressing cancer cells, and tumor legions were successfully visualized. The scFv variant established in the present study may be potentially useful for cancer diagnosis by PET imaging. John Wiley and Sons Inc. 2019-08-28 2019-09 /pmc/articles/PMC6726835/ /pubmed/31461572 http://dx.doi.org/10.1111/cas.14150 Text en © 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Yakushiji, Hiromasa
Kobayashi, Kazuko
Takenaka, Fumiaki
Kishi, Yoshiro
Shinohara, Midori
Akehi, Masaru
Sasaki, Takanori
Ohno, Eiji
Matsuura, Eiji
Novel single‐chain variant of antibody against mesothelin established by phage library
title Novel single‐chain variant of antibody against mesothelin established by phage library
title_full Novel single‐chain variant of antibody against mesothelin established by phage library
title_fullStr Novel single‐chain variant of antibody against mesothelin established by phage library
title_full_unstemmed Novel single‐chain variant of antibody against mesothelin established by phage library
title_short Novel single‐chain variant of antibody against mesothelin established by phage library
title_sort novel single‐chain variant of antibody against mesothelin established by phage library
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6726835/
https://www.ncbi.nlm.nih.gov/pubmed/31461572
http://dx.doi.org/10.1111/cas.14150
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