Cargando…
(124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy
PURPOSE: The human monoclonal antibody (MAb) fragment L19-SIP is directed against extra domain B (ED-B) of fibronectin, a marker of tumour angiogenesis. A clinical radioimmunotherapy (RIT) trial with (131)I-L19-SIP was recently started. In the present study, after GMP production of (124)I and effici...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709218/ https://www.ncbi.nlm.nih.gov/pubmed/19259661 http://dx.doi.org/10.1007/s00259-009-1096-y |
_version_ | 1782169280987529216 |
---|---|
author | Tijink, Bernard M. Perk, Lars R. Budde, Marianne Stigter-van Walsum, Marijke Visser, Gerard W. M. Kloet, Reina W. Dinkelborg, Ludger M. Leemans, C. René Neri, Dario van Dongen, Guus A. M. S. |
author_facet | Tijink, Bernard M. Perk, Lars R. Budde, Marianne Stigter-van Walsum, Marijke Visser, Gerard W. M. Kloet, Reina W. Dinkelborg, Ludger M. Leemans, C. René Neri, Dario van Dongen, Guus A. M. S. |
author_sort | Tijink, Bernard M. |
collection | PubMed |
description | PURPOSE: The human monoclonal antibody (MAb) fragment L19-SIP is directed against extra domain B (ED-B) of fibronectin, a marker of tumour angiogenesis. A clinical radioimmunotherapy (RIT) trial with (131)I-L19-SIP was recently started. In the present study, after GMP production of (124)I and efficient production of (124)I-L19-SIP, we aimed to demonstrate the suitability of (124)I-L19-SIP immuno-PET for imaging of angiogenesis at early-stage tumour development and as a scouting procedure prior to clinical (131)I-L19-SIP RIT. METHODS: (124)I was produced in a GMP compliant way via (124)Te(p,n)(124)I reaction and using a TERIMO™ module for radioiodine separation. L19-SIP was radioiodinated by using a modified version of the IODO-GEN method. The biodistribution of coinjected (124)I- and (131)I-L19-SIP was compared in FaDu xenograft-bearing nude mice, while (124)I PET images were obtained from mice with tumours of <50 to ∼700 mm(3). RESULTS: (124)I was produced highly pure with an average yield of 15.4 ± 0.5 MBq/μAh, while separation yield was ∼90% efficient with <0.5% loss of TeO(2). Overall labelling efficiency, radiochemical purity and immunoreactive fraction were for (124)I-L19-SIP: ∼80 , 99.9 and >90%, respectively. Tumour uptake was 7.3 ± 2.1, 10.8 ± 1.5, 7.8 ± 1.4, 5.3 ± 0.6 and 3.1 ± 0.4%ID/g at 3, 6, 24, 48 and 72 h p.i., resulting in increased tumour to blood ratios ranging from 6.0 at 24 h to 45.9 at 72 h p.i.. Fully concordant labelling and biodistribution results were obtained with (124)I- and (131)I-L19-SIP. Immuno-PET with (124)I-L19-SIP using a high-resolution research tomograph PET scanner revealed clear delineation of the tumours as small as 50 mm(3) and no adverse uptake in other organs. CONCLUSIONS: (124)I-MAb conjugates for clinical immuno-PET can be efficiently produced. Immuno-PET with (124)I-L19-SIP appeared qualified for sensitive imaging of tumour neovasculature and for predicting (131)I-L19-SIP biodistribution. |
format | Text |
id | pubmed-2709218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-27092182009-07-14 (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy Tijink, Bernard M. Perk, Lars R. Budde, Marianne Stigter-van Walsum, Marijke Visser, Gerard W. M. Kloet, Reina W. Dinkelborg, Ludger M. Leemans, C. René Neri, Dario van Dongen, Guus A. M. S. Eur J Nucl Med Mol Imaging Original Article PURPOSE: The human monoclonal antibody (MAb) fragment L19-SIP is directed against extra domain B (ED-B) of fibronectin, a marker of tumour angiogenesis. A clinical radioimmunotherapy (RIT) trial with (131)I-L19-SIP was recently started. In the present study, after GMP production of (124)I and efficient production of (124)I-L19-SIP, we aimed to demonstrate the suitability of (124)I-L19-SIP immuno-PET for imaging of angiogenesis at early-stage tumour development and as a scouting procedure prior to clinical (131)I-L19-SIP RIT. METHODS: (124)I was produced in a GMP compliant way via (124)Te(p,n)(124)I reaction and using a TERIMO™ module for radioiodine separation. L19-SIP was radioiodinated by using a modified version of the IODO-GEN method. The biodistribution of coinjected (124)I- and (131)I-L19-SIP was compared in FaDu xenograft-bearing nude mice, while (124)I PET images were obtained from mice with tumours of <50 to ∼700 mm(3). RESULTS: (124)I was produced highly pure with an average yield of 15.4 ± 0.5 MBq/μAh, while separation yield was ∼90% efficient with <0.5% loss of TeO(2). Overall labelling efficiency, radiochemical purity and immunoreactive fraction were for (124)I-L19-SIP: ∼80 , 99.9 and >90%, respectively. Tumour uptake was 7.3 ± 2.1, 10.8 ± 1.5, 7.8 ± 1.4, 5.3 ± 0.6 and 3.1 ± 0.4%ID/g at 3, 6, 24, 48 and 72 h p.i., resulting in increased tumour to blood ratios ranging from 6.0 at 24 h to 45.9 at 72 h p.i.. Fully concordant labelling and biodistribution results were obtained with (124)I- and (131)I-L19-SIP. Immuno-PET with (124)I-L19-SIP using a high-resolution research tomograph PET scanner revealed clear delineation of the tumours as small as 50 mm(3) and no adverse uptake in other organs. CONCLUSIONS: (124)I-MAb conjugates for clinical immuno-PET can be efficiently produced. Immuno-PET with (124)I-L19-SIP appeared qualified for sensitive imaging of tumour neovasculature and for predicting (131)I-L19-SIP biodistribution. Springer-Verlag 2009-03-04 2009-08 /pmc/articles/PMC2709218/ /pubmed/19259661 http://dx.doi.org/10.1007/s00259-009-1096-y Text en © The Author(s) 2009 |
spellingShingle | Original Article Tijink, Bernard M. Perk, Lars R. Budde, Marianne Stigter-van Walsum, Marijke Visser, Gerard W. M. Kloet, Reina W. Dinkelborg, Ludger M. Leemans, C. René Neri, Dario van Dongen, Guus A. M. S. (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title | (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title_full | (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title_fullStr | (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title_full_unstemmed | (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title_short | (124)I-L19-SIP for immuno-PET imaging of tumour vasculature and guidance of (131)I-L19-SIP radioimmunotherapy |
title_sort | (124)i-l19-sip for immuno-pet imaging of tumour vasculature and guidance of (131)i-l19-sip radioimmunotherapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2709218/ https://www.ncbi.nlm.nih.gov/pubmed/19259661 http://dx.doi.org/10.1007/s00259-009-1096-y |
work_keys_str_mv | AT tijinkbernardm 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT perklarsr 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT buddemarianne 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT stigtervanwalsummarijke 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT vissergerardwm 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT kloetreinaw 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT dinkelborgludgerm 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT leemanscrene 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT neridario 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy AT vandongenguusams 124il19sipforimmunopetimagingoftumourvasculatureandguidanceof131il19sipradioimmunotherapy |