DOTA-Functionalized Polylysine: A High Number of DOTA Chelates Positively Influences the Biodistribution of Enzymatic Conjugated Anti-Tumor Antibody chCE7agl

作者：Gruenberg Juergen; Jeger Simone; Sarko Dikran; Dennler Patrick; Zimmermann Kurt; Mier Walter; Schibli Roger^*

来源：PLos One, 2013, 8(4): e60350.

DOI：10.1371/journal.pone.0060350

Site-specific enzymatic reactions with microbial transglutaminase (mTGase) lead to a homogenous species of immunoconjugates with a defined ligand/antibody ratio. In the present study, we have investigated the influence of different numbers of 1,4,7,10-tetraazacyclododecane-N-N'-N ''-N'''-tetraacetic acid (DOTA) chelats coupled to a decalysine backbone on the in vivo behavior of the chimeric monoclonal anti-L1CAM antibody chCE7agl. The enzymatic conjugation of (DOTA)(1)-decalysine, (DOTA)(3)-decalysine or (DOTA)(5)-decalysine to the antibody heavy chain (via Gln295/297) gave rise to immunoconjugates containing two, six or ten DOTA moieties respectively. Radiolabeling of the immunoconjugates with Lu-177 yielded specific activities of approximately 70 MBq/mg, 400 MBq/mg and 700 MBq/mg with increasing numbers of DOTA chelates. Biodistribution experiments in SKOV3ip human ovarian cancer cell xenografts demonstrated a high and specific accumulation of radioactivity at the tumor site for all antibody derivatives with a maximal tumor accumulation of 43.6 +/- 4.3% ID/g at 24 h for chCE7agl-[(DOTA)-decalysine](2), 30.6 +/- 12.0% ID/g at 24 h for chCE7agl-[(DOTA)(3)-decalysine](2) and 49.9 +/- 3.1% ID/g at 48 h for chCE7agl-[(DOTA)(5)-decalysine)](2). The rapid elimination from the blood of chCE7agl-[(DOTA)decalysine](2) (1.0 +/- 0.1% ID/g at 24 h) is associated with a high liver accumulation (23.2 +/- 4.6% ID/g at 24 h). This behavior changed depending on the numbers of DOTA moieties coupled to the decalysine peptide with a slower blood clearance (5.1 +/- 1.0 (DOTA)(3) versus 11.7 +/- 1.4% ID/g (DOTA)(5), p<0.005 at 24 h) and lower radioactivity levels in the liver (21.4 +/- 3.4 (DOTA)(3) versus 5.8 +/- 0.7 (DOTA)(5), p<0.005 at 24 h). We conclude that the site-specific and stoichiometric uniform conjugation of the highly DOTA-substituted decalysine ((DOTA) 5-decalysine) to an anti-tumor antibody leads to the formation of immunoconjugates with high specific activity and excellent in vivo behavior and is a valuable option for radioimmunotherapy and potentially antibody-drug conjugates (ADCs).

• 出版日期2013-4-2