Ror1 car t-cells
A sequence and amino acid technology, applied in the field of chimeric antigen receptors, can solve problems such as limited tumor scope
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Embodiment 1
[0230] Materials and methods
[0231] molecular biology
[0232] DNA cloning was performed using standard laboratory protocols. Restriction enzymes, Phusion Taq polymerase, Quick ligase and DH5α competent cells were obtained from New England Biolabs. DNA was run on a 1-2% TBE agarose gel according to the expected band size and stained with ethidium bromide (Sigma-Aldrich), SybrSafe gel stain (Life Technologies) or nucleic acid gel stain (Lonza) . Gel extraction and PCR purification were performed using the SV Wizard Gel and Purification Kit (Promega).
[0233] Bacteria were grown in Lennox Broth or Terrific Broth (Fisher Scientific); minipreps, midipreps and megapreps plasmid purification kits were from Mancherey Nagel, while large preps used Qiagen kits according to the manufacturer's instructions. DNA concentration was assessed by Nanodrop (Thermo Scientific) and sequenced by SourceBioscience or Beckman Coulter Genomics. Oligonucleotide primers and G-Block oligonucleoti...
Embodiment 2
[0257] ROR1 is expressed on primary CLL cells
[0258] Primary CLL cells from peripheral blood of newly diagnosed and treated patients were analyzed for ROR1 expression by flow cytometry. ROR1 was detectable in all samples analyzed (Biolegend Clone 2A2). Antigen density was assessed by Qifikit (Dako, Agilent Technologies). ROR1 had a median antigen binding capacity (ABC) of 2304 molecules / cell, with a range of 800-4828, and CD19 was expressed at a higher level with a median of 12583 (range, 5894-23652). See Table 1 below.
[0259]
Embodiment 3
[0261] Rat immunization and ROR1 antibody production
[0262] After immunizing 3 rats with full-length human ROR1 protein and DNA, we obtained 38 oligoclonal hybridomas. Seventeen of these were solved using 5' RACE to identify the variable regions of the heavy and light chains. We obtained sequences encoding 13 new antibodies (4 clones resulted in identical sequences), 10 of which combined in single-chain variable fragment (ScFv) format. (Cloning of hybridoma cDNA by RACE, Andrew Bradbury) See Table 2 below.
[0263] Table 2:
[0264]
[0265] As can be seen above, clone F binds the coiled domain. All other clones (except V) incorporated immunoglobulin domains. Prior art antibodies R12 and 4A5 also bind immunoglobulin domains. Thus, clone F showed different and differentiated binding properties compared to prior art antibodies R12 and 4A5.
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