A 3-Step Pretargeting Strategy to Image Infection

Journal of Nuclear Medicine

Frans H.M. Corstens¹  Wim J.G. Oyen¹  Julliette van Eerd¹  Otto C. Boerman¹ 

[1] Department of Nuclear Medicine, University Hospital Nijmegen, Nijmegen, The Netherlands Department of Nuclear Medicine, University Hospital Nijmegen, Nijmegen, The Netherlands Department of Nuclear Medicine, University Hospital Nijmegen, Nijmegen, The Netherlands

关键词: pretargeting;    infection imaging;    bivalent hapten;    anti-DTPA antibody;   

DOI  :  

学科分类：医学（综合）

来源: Society of Nuclear Medicine

【 摘 要 】

A new 3-step approach to imaging infectious and inflammatory foci was developed and optimized in a rat model. The approach relies on the nonspecific localization of an anti-diethylenetriaminepentaacetic acid (DTPA) antibody in inflamed tissue. In this study, the 3-step strategy was optimized by selecting the most suitable radiolabeled hapten and tuning the dosing schedule. Methods: Wistar rats with Staphylococcus aureus infection in the left calf muscle were primed with the anti-DTPA antibody DTIn-1 (0.67, 2, or 6 nmol per rat). In the second step (1–24 h later), the anti-DTPA activity in the circulation was blocked with unlabeled bovine serum albumin DTPA-In (0.3, 1, or 3 nmol per rat). In the third step (5–30 min later), the radiolabeled hapten (monovalent or bivalent 111In-DTPA) was administered. The in vivo distribution of the radiolabel was monitored by scintigraphic imaging and by ex vivo counting of dissected tissues. Results: Scatchard analysis revealed that the affinity of DTIn-1 for bivalent DTPA-111In (111In-diDTPA) was 6 times higher than the affinity for monovalent 111In-DTPA (Ka = 0.87 × 10−9 mol/L vs. 5.3 × 10−9 mol/L). The uptake of the bivalent chelate in the abscess was 2.5-fold higher than that of monovalent 111In-DTPA. Most important, the bivalent chelate was completely retained in the abscess over time. Using the bivalent chelate, the optimal dosing scheme was determined with respect to the DTIn-1 dose (2 nmol per rat), the blocking agent dose (1 nmol per rat), and radiolabeled chelate dose (40 pmol per rat). The procedure was rapid; the infectious focus was clearly visualized 1 h after injection of the 111In-labeled diDTPA, which was 5 h after administration of the anti-DTPA antibody. The nontargeted radiolabel rapidly cleared to the urine, only being retained in the abscess and the kidneys (4–6 percentage injected dose). Finally, an N2S2 core was attached to the diDTPA compound, allowing the use of 99mTc. Conclusion: This 3-step approach enables rapid imaging of infectious foci with minimal uptake in noninflamed tissues.

【 授权许可】

Unknown