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Radionuclide Therapy of HER2-Expressing Human Xenografts Using Affibody-Based Peptide Nucleic Acid-Mediated Pretargeting : In Vivo Proof of Principle

Authors :
Westerlund, Kristina
Altai, Mohamed
Mitran, Bogdan
Konijnenberg, Mark
Oroujeni, Maryam
Atterby, Christina
de Jong, Marion
Orlova, Anna
Mattsson, Johanna Sofia Margareta
Micke, Patrick
Eriksson Karlström, Amelie
Tolmachev, Vladimir
Westerlund, Kristina
Altai, Mohamed
Mitran, Bogdan
Konijnenberg, Mark
Oroujeni, Maryam
Atterby, Christina
de Jong, Marion
Orlova, Anna
Mattsson, Johanna Sofia Margareta
Micke, Patrick
Eriksson Karlström, Amelie
Tolmachev, Vladimir
Publication Year :
2018

Abstract

Affibody molecules are small proteins engineered using a nonanti-body scaffold. Radiolabeled Affibody molecules are excellent imaging probes, but their application to radionuclide therapy has been prevented by high renal reabsorption. The aim of this study was to test the hypothesis that Affibody-based peptide nucleic acid (PNA)-mediated pretargeted therapy of human epidermal growth factor receptor 2 (HER2)-expressing cancer extends survival without accompanying renal toxicity. Methods: A HER2-targeting Affibody molecule ligated with an AGTCGTGATGTAGTC PNA hybridization probe (Z(HER2:342)-SR-HP1) was used as the primary pretargeting agent. A complementary AGTCGTGATGTAGTC PNA conjugated to the chelator DOTA and labeled with the radionuclide Lu-177 (Lu-177-HP2) was used as the secondary agent. The influence of different factors on pretargeting was investigated. Experimental radionuclide therapy in mice bearing SKOV-3 xenografts was performed in 6 cycles separated by 7 d. Results: Optimal tumor targeting was achieved when 16 MBq/3.5 mu g (0.65 nmol) of Lu-177-HP2 was injected 16 h after injection of 100 mu g (7.7 nmol) of Z(HER2:342)-SR-HP1. The calculated absorbed dose to tumors was 1,075 mGy/MBq, whereas the absorbed dose to kidneys was 206 mGy/MBq and the absorbed dose to blood (surrogate of bone marrow) was 4 mGy/MBq. Survival of mice was significantly longer (P < 0.05) in the treatment group (66 d) than in the control groups treated with the same amount of Z(HER2:342)-SR-HP1 only (37 d), the same amount and activity of Lu-177-HP2 only (32 d), or phosphate-buffered saline (37 d). Conclusion: The studied pretargeting system can deliver an absorbed dose to tumors appreciably exceeding absorbed doses to critical organs, making Affibody-based PNA-mediated pretargeted radionuclide therapy highly attractive.<br />Kristina Westerlund and Mohamed Altai contributed equally. Amelie Eriksson Karlström and Vladimir Tolmachev contributed equally.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235211280
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.2967.jnumed.118.208348