A Rauscher1, M Frindel1, C Maurel1, M Maillasson2, P Le Saëc1, H Rajerison1, J-F Gestin1, J Barbet1, A Faivre-Chauvet1, M Mougin-Degraef3. 1. Centre de Recherche en Cancérologie Nantes-Angers (CRCNA), UMR 892 - Inserm/6299 CNRS/Université de Nantes, Institut de Recherche en Santé de l'Université de Nantes, 8 quai Moncousu, BP 70721, 44007 Nantes Cedex 1, France. 2. Centre de Recherche en Cancérologie Nantes-Angers (CRCNA), UMR 892 - Inserm/6299 CNRS/Université de Nantes, Institut de Recherche en Santé de l'Université de Nantes, 8 quai Moncousu, BP 70721, 44007 Nantes Cedex 1, France; Plateforme Interactome & Puces à Protéines Biogenouest; Institut de Recherche en Santé de l'Université de Nantes, 8 quai Moncousu, BP 70721, 44007 Nantes Cedex 1, France. 3. Centre de Recherche en Cancérologie Nantes-Angers (CRCNA), UMR 892 - Inserm/6299 CNRS/Université de Nantes, Institut de Recherche en Santé de l'Université de Nantes, 8 quai Moncousu, BP 70721, 44007 Nantes Cedex 1, France. Electronic address: marie.degraef@univ-nantes.fr.
Abstract
INTRODUCTION: This paper proposes liposomes as a potential new tool for radioimmunotherapy in solid tumours with a two step targeting system. Tumour pretargeting is obtained by using a monoclonal bispecific antibody (BsmAb, anti CEA x anti-DTPA-In) and pegylated liposomes containing lipid-hapten (DSPE-DTPA-In or DSPE-PEG-DTPA-In). To optimise at the same time in vivo behaviour and specific targeting, the study focuses on the liposome formulation in order to determine more precisely the role of pegylation on both the blood half-life and the specific recognition with the BsmAb. METHODS: Different liposome formulations containing two PEG length (1000 and 2000) in varying amount (1.5-6 mol%) were prepared with DTPA directly coupled to DSPE or at the end of the PEG chain (DSPE-DTPA or DSPE-PEG-DTPA). Liposomes were immobilized on an L1 chip to measure by SPR (Surface Plasmon Resonance) the effect of pegylation on the BsmAb recognition of the DTPA-In hapten. Pharmacokinetic studies were performed in mice. Tumour targeting was studied in nude mice xenografted with human colorectal adenocarcinoma cells that express CEA, and doubly radiolabelled liposomes (with (111)In and (125)I) injected 24h after the BsmAb. RESULTS: The best in vitro apparent dissociation constant was obtained with liposomes bearing DTPA at the end of the PEG chain (KD=6.3 nM), which showed significant specific tumour uptake after BsmAb injection (8.6 ± 2.4% ID/g at 24h versus 4.5 ± 0.5%ID/g for passive targeting, α=0.01). All tumour/organ ratios were superior to 1 at 24h for this formulation, except for the spleen. CONCLUSION: The feasibility of specific tumour targeting in mice with a BsmAb and radiolabelled liposomes was demonstrated and the interest of SPR to predict their targeting performance in vivo was highlighted. This original and new approach provides promising prospects for the radioimmunotherapy of solid tumours.
INTRODUCTION: This paper proposes liposomes as a potential new tool for radioimmunotherapy in solid tumours with a two step targeting system. Tumour pretargeting is obtained by using a monoclonal bispecific antibody (BsmAb, anti CEA x anti-DTPA-In) and pegylated liposomes containing lipid-hapten (DSPE-DTPA-In or DSPE-PEG-DTPA-In). To optimise at the same time in vivo behaviour and specific targeting, the study focuses on the liposome formulation in order to determine more precisely the role of pegylation on both the blood half-life and the specific recognition with the BsmAb. METHODS: Different liposome formulations containing two PEG length (1000 and 2000) in varying amount (1.5-6 mol%) were prepared with DTPA directly coupled to DSPE or at the end of the PEG chain (DSPE-DTPA or DSPE-PEG-DTPA). Liposomes were immobilized on an L1 chip to measure by SPR (Surface Plasmon Resonance) the effect of pegylation on the BsmAb recognition of the DTPA-In hapten. Pharmacokinetic studies were performed in mice. Tumour targeting was studied in nude mice xenografted with humancolorectal adenocarcinoma cells that express CEA, and doubly radiolabelled liposomes (with (111)In and (125)I) injected 24h after the BsmAb. RESULTS: The best in vitro apparent dissociation constant was obtained with liposomes bearing DTPA at the end of the PEG chain (KD=6.3 nM), which showed significant specific tumour uptake after BsmAb injection (8.6 ± 2.4% ID/g at 24h versus 4.5 ± 0.5%ID/g for passive targeting, α=0.01). All tumour/organ ratios were superior to 1 at 24h for this formulation, except for the spleen. CONCLUSION: The feasibility of specific tumour targeting in mice with a BsmAb and radiolabelled liposomes was demonstrated and the interest of SPR to predict their targeting performance in vivo was highlighted. This original and new approach provides promising prospects for the radioimmunotherapy of solid tumours.
Authors: Christina L Parker; Morgan D McSweeney; Andrew T Lucas; Timothy M Jacobs; Daniel Wadsworth; William C Zamboni; Samuel K Lai Journal: Nanomedicine Date: 2019-08-05 Impact factor: 5.307
Authors: Cecilia Yamil Chain; María Antonieta Daza Millone; José Sebastián Cisneros; Eduardo Alejandro Ramirez; María Elena Vela Journal: Front Chem Date: 2021-01-07 Impact factor: 5.221