Use of Fc-engineered antibodies as clearing agents to increase contrast during PET
Use of Fc-engineered antibodies as clearing agents to increase contrast during PET
Despite promise for the use of antibodies as molecular imaging agents in PET, their long in vivo half-lives result in poor contrast and radiation damage to normal tissue. This study describes an approach to overcome these limitations. Methods: Mice bearing human epidermal growth factor receptor type 2 (HER2)-overexpressing tumors were injected with radiolabeled (124I, 125I) HER2-specific antibody (pertuzumab). Pertuzumab injection was followed 8 h later by the delivery of an engineered, antibody-based inhibitor of the receptor, FcRn. Biodistribution analyses and PET were performed at 24 and 48 h after pertuzumab injection. Results: The delivery of the engineered, antibody-based FcRn inhibitor (or Abdeg, for antibody that enhances IgG degradation) results in improved tumor-to-blood ratios, reduced systemic exposure to radiolabel, and increased contrast during PET. Conclusion: Abdegs have considerable potential as agents to stringently regulate antibody dynamics in vivo, resulting in increased contrast during molecular imaging with PET. COPYRIGHT
Breast cancer, Engineered antibodies, FcRn, PET
1204-1207
Swiercz, Rafal
30beab68-d405-405d-a401-e53f83eece6e
Chiguru, Srinivas
bb584e20-9bfb-4403-970f-18eefa85b79d
Tahmasbi, Amir
5a377bd3-4578-434f-919a-87804245791e
Ramezani, Saleh M.
6cf23f5d-92ad-402a-ac04-7d2141822ba5
Hao, Guiyang
f35004eb-e264-48c5-b250-2f5836ab7ee7
Challa, Dilip K.
433af413-17a0-4c55-b86f-21e4e5cedd6f
Lewis, Matthew A.
a0c61e4f-b42c-4dd2-881d-1dcde38b2a38
Kulkarni, Padmakar V.
a8cb6a00-f1a9-4f92-acfa-7ab9fda8bac1
Sun, Xiankai
b56022ad-53ef-4b9b-b248-f7ce4d25a34b
Ober, Raimund J.
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36
Mason, Ralph P.
e2909e92-8c39-4d5d-be1b-cfb9005e7b57
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
1 July 2014
Swiercz, Rafal
30beab68-d405-405d-a401-e53f83eece6e
Chiguru, Srinivas
bb584e20-9bfb-4403-970f-18eefa85b79d
Tahmasbi, Amir
5a377bd3-4578-434f-919a-87804245791e
Ramezani, Saleh M.
6cf23f5d-92ad-402a-ac04-7d2141822ba5
Hao, Guiyang
f35004eb-e264-48c5-b250-2f5836ab7ee7
Challa, Dilip K.
433af413-17a0-4c55-b86f-21e4e5cedd6f
Lewis, Matthew A.
a0c61e4f-b42c-4dd2-881d-1dcde38b2a38
Kulkarni, Padmakar V.
a8cb6a00-f1a9-4f92-acfa-7ab9fda8bac1
Sun, Xiankai
b56022ad-53ef-4b9b-b248-f7ce4d25a34b
Ober, Raimund J.
31f4d47f-fb49-44f5-8ff6-87fc4aff3d36
Mason, Ralph P.
e2909e92-8c39-4d5d-be1b-cfb9005e7b57
Ward, E. Sally
b31c0877-8abe-485f-b800-244a9d3cd6cc
Swiercz, Rafal, Chiguru, Srinivas, Tahmasbi, Amir, Ramezani, Saleh M., Hao, Guiyang, Challa, Dilip K., Lewis, Matthew A., Kulkarni, Padmakar V., Sun, Xiankai, Ober, Raimund J., Mason, Ralph P. and Ward, E. Sally
(2014)
Use of Fc-engineered antibodies as clearing agents to increase contrast during PET.
Journal of Nuclear Medicine, 55 (7), .
(doi:10.2967/jnumed.113.136481).
Abstract
Despite promise for the use of antibodies as molecular imaging agents in PET, their long in vivo half-lives result in poor contrast and radiation damage to normal tissue. This study describes an approach to overcome these limitations. Methods: Mice bearing human epidermal growth factor receptor type 2 (HER2)-overexpressing tumors were injected with radiolabeled (124I, 125I) HER2-specific antibody (pertuzumab). Pertuzumab injection was followed 8 h later by the delivery of an engineered, antibody-based inhibitor of the receptor, FcRn. Biodistribution analyses and PET were performed at 24 and 48 h after pertuzumab injection. Results: The delivery of the engineered, antibody-based FcRn inhibitor (or Abdeg, for antibody that enhances IgG degradation) results in improved tumor-to-blood ratios, reduced systemic exposure to radiolabel, and increased contrast during PET. Conclusion: Abdegs have considerable potential as agents to stringently regulate antibody dynamics in vivo, resulting in increased contrast during molecular imaging with PET. COPYRIGHT
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e-pub ahead of print date: 27 May 2014
Published date: 1 July 2014
Keywords:
Breast cancer, Engineered antibodies, FcRn, PET
Identifiers
Local EPrints ID: 423652
URI: http://eprints.soton.ac.uk/id/eprint/423652
ISSN: 0161-5505
PURE UUID: 017f1977-2313-4b22-9917-3d9a5a5c6a71
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Date deposited: 27 Sep 2018 16:30
Last modified: 16 Mar 2024 04:37
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Contributors
Author:
Rafal Swiercz
Author:
Srinivas Chiguru
Author:
Amir Tahmasbi
Author:
Saleh M. Ramezani
Author:
Guiyang Hao
Author:
Dilip K. Challa
Author:
Matthew A. Lewis
Author:
Padmakar V. Kulkarni
Author:
Xiankai Sun
Author:
Ralph P. Mason
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