Patent Application
20190015493
The Sequence Listing is concurrently submitted herewith with the specification as an ASCII formatted text file via EFS-Web with a file name of Sequence Listing.txt with a creation date of May 15, 2017, and a size of 13.0 kilobytes. The Sequence Listing filed via EFS-Web is part of the specification and is hereby incorporated in its entirety by reference herein.
The present invention relates to Hela-CD19 cell line that stably express CD19 (cluster of differentiation 19), which is a marker of hematopoietic cancers.
Hela cell line was derived from cervical cancer cells taken on Feb. 8, 1951 from Henrietta Lacks, who died of cancer on Oct. 4, 1951 [Ghorashian et al. Br J Haematol 2015, 169, 463-478.] The cell line was found to be remarkably durable and extensively used in scientific research.
CD19 is a marker of hematopoietic cancers. B-lymphocyte antigen CD19, also known as CD19 (cluster of differentiation 19), is a protein that in humans is encoded by the CD19 gene. It is found on the surface of B-cells and overexpressed in leukemia and lymphoma and effectively targeted with CD19-CAR-T cells (Kochenderfer et al., Blood 2013, 122, 4129-4139, Scherer et al., J Exp Med 1953, 97, 695-710). There are many other hematological cancer tumor antigens such as CD4, CD5, CD7, CD8, CD10, CD20, CD22, CD23, CD24, CD33, CD38, CD47, CD56, CD57, CD123, CD138, BCMA and other which can be overexpressed on cancer cell surfaces and can be targeted by target-specific-CAR-T cells.
As used herein, a “chimeric antigen receptor (CAR)” means a fused protein comprising an extracellular domain capable of binding to an antigen, a transmembrane domain derived from a polypeptide different from a polypeptide from which the extracellular domain is derived, and at least one intracellular domain. The “chimeric antigen receptor (CAR)” is sometimes called a “chimeric receptor”, a “T-body”, or a “chimeric immune receptor (CIR).” The “extracellular domain capable of binding to an antigen” means any oligopeptide or polypeptide that can bind to a certain antigen. The “intracellular domain” means any oligopeptide or polypeptide known to function as a domain that transmits a signal to cause activation or inhibition of a biological process in a cell.
As used herein, a FLAG-tag, or FLAG octapeptide, or FLAG epitope, is a polypeptide protein tag that can be added to a protein using recombinant DNA technology, having the sequence motif DYKDDDDK (SEQ ID NO: 1). It can be fused to the C-terminus or the N-terminus of a protein, or inserted within a protein.
As used herein, a “domain” means one region in a polypeptide which is folded into a particular structure independently of other regions.
As used herein, a “single chain variable fragment (scFv)” means a single chain polypeptide derived from an antibody which retains the ability to bind to an antigen. An example of the scFv includes an antibody polypeptide which is formed by a recombinant DNA technique and in which Fv regions of immunoglobulin heavy chain (H chain) and light chain (L chain) fragments are linked via a spacer sequence. Various methods for preparing an scFv are known to a person skilled in the art.
As used herein, a “tumor antigen” means a biological molecule having antigenicity, expression of which causes cancer.
The present invention is directed to a transduced adherent cell line that stably expresses a leukemia tumor antigen; it is a solid tumor cell line expressing a hematopoietic cancer marker. The adherent cells suitable in the present invention include those that are negative for hematologic markers and are durable; for example, cervical cancer cells such as Hela, breast cancer cells such as MCF-7, ovarian cancer cells such as A1747, pancreatic cancer cells such as PANC-1, lung cancer cells such as A549, and glioblastoma cells such as U87 or other type of solid cancer (prostate, colon, lung). A preferred cell line is Hela.
The hematological tumor antigen that can be expressed in the transduced adherent cell line of the present invention include CD (Cluster of Differentiation)19, CD4, CD5, CD7, CD8, CD10, CD20, CD22, CD23, CD24, CD33, CD38, CD47, CD56, CD57, CD123, CD138, BCMA and other
In one embodiment, the present invention is directed to a transduced Hela cell line that stably expresses CD19 (Hela-CD19). The Hela-CD19 cell line is greater than 90% positive, preferrably greater than 95%, greater than 98%, or greater than 99%, for expressing CD19.
The transduced adherent cell line of the present invention is useful for many pre-clinical applications. In one embodiment, the transduced adherent cell line is useful for real time cytotoxicity assay with CD19-CAR-T cells, CD2O-CAR-T cells, CD22-CAR-T cells, CD23-CAR-T cells, or CD24-CAR-T cells, or CD4, CD5, CD7, CD8, CD10, CD33, CD38, CD47, CD56, CD57, CD123, CD138, BCMA and other CAR-T cells targeting each specific tumor antigen.
The Hela-CD19 cell line can be used in xenograft mice studies to test the effect of CD19-CAR-T cells.
The transduced cell line of the present invention is a solid cancer cell line that allows to study tumor microenvironment and signaling of solid tumors in vivo. Because it is an adherent cell line, it allows to perform different assays such as RTCA (real time cytotoxicity assay) where adherent properties of cells are used for quantification. The transduced cell line expresses tumor markers of leukemia, which can be used to study targeting of leukemia markers and tumor antigens.
The following examples further illustrate the present invention. These examples are intended merely to be illustrative of the present invention and are not to be construed as being limiting.
The nucleic acid sequence of human CD19 is shown in SEQ ID NO: 2, which starts with start codon, ATG and finishes with stop codon TGA. The NCI Accession number of human CD19 is NM_001770. This human CD19 was inserted into Xba I and EcoR I sites of lentiviral vector (Lenti CMV-MCS-EF1a-puro, obtained from Systems Bioscience).
DNAs encoding CD19 cDNA were synthesized and subcloned into a third-generation lentiviral vector, Lenti CMV-MCS-EF1a-puro by Syno Biological (Beijing, China). All lentiviral constructs were sequenced in both directions to confirm the construct sequence and used for lentivirus production. Ten million growth-arrested HEK293FT cells (Thermo Fisher) were seeded into T75 flasks and cultured overnight, then transfected with the pPACKH1 Lentivector Packaging mix (System Biosciences, Palo Alto, Calif.) and 10 μg of each lentiviral vector using the CalPhos Transfection Kit (Takara, Mountain View, Calif.). The next day the medium was replaced with fresh medium, and 48 h later the lentivirus-containing medium was collected. The medium was cleared of cell debris by centrifugation at 2100 g for 30 min. The virus particles were collected by centrifugation at 112,000 g for 100 min, suspended in DMEM or AIM V medium, aliquoted and frozen at −80° C. The titers of the virus preparations were determined by quantitative RT-PCR using the Lenti-X qRT-PCR kit (Takara) according to the manufacturer's protocol and the 7900HT thermal cycler (Thermo Fisher). The lentiviral titers were >1×108 pfu/ml.
CD19-lentivirus of Example 2 were thawed on ice. To each well of 1×106 Hela cells, 5×106 CD19-lentivirus, and 2 μL/mL of media of Transplus (Alstem, Richmond, Calif.) (a final dilution of 1:500) were added. Cells were incubated for an additional 24 hr before repeating addition of lentivirus.
The Hela cells were transduced with lentiviral construct containing CD19 DNA, and puromycin was added to the medium to select stable Hela-CD19 cells. Puromycin was added 1 μg/ml to DMEM with 10% FBS medium, and fresh medium was changed with puromycin 1 μg/ml every 3 days.
Hela cells were then grown in the continued presence of fresh medium with puromycin for a period of 12-14 days. The stable clone of Hela-CD19 cells were isolated and grown until confluence. The expression of CD19 was confirmed by FACS analysis with CD19 antibody.
The Hela-CD19 stable cell line was received on May 31, 2017, and deposited on Jun. 1, 2017 with American Type Culture Collection (ATCC) under ATCC deposit number HeLa-CD19, under the Budapest Treaty provisions.
Sequence of CD19-CD28-CD3 zeta was described in [Kochenderfer et al. J Immunother 2009, 32, 689-702]. CD19 scFv and CD28-transmembrane and activation domains and CD3 zeta were subcloned into a third-generation lentiviral vector, Lenti CMV-MCS-EF1a-puro by Syno Biological (Beijing, China). All CAR lentiviral constructs were sequenced in both directions to confirm CAR sequence and used for lentivirus production.
The lentiviruses were generated in 293T cells, titer was established by RT-PCR, and was used for transduction of T cells according to protocol described in Example 2 of Berahovich et al Front Biosci (Landmark Ed). 22:1644-1654 (2017).
CAR-T cells (CD19ScFv-CD28-CD3zeta) were generated similarly as described for Hela cells in Example 3, but without selection of stable cell clones. No puromycin treatment was performed to preserve higher cell number. The CAR-T were used for cytotoxicity assay (Example 5) with target Hela-CD19 cells.
The cytotoxicity was performed using ACEA machine according to manufacturer's protocol listed below.
Adherent target cells (HeLa or HeLa-CD19) were seeded into 96-well E-plates (Acea Biosciences, San Diego, Calif.) at 1×104 cells per well and monitored in culture overnight with the impedance-based real-time cell analysis (RTCA) iCELLigence system (Acea Biosciences). The next day, the medium was removed and replaced with AIM V-AlbuMAX medium containing 10% FBS ±1×105 effector cells (CAR-T cells or non-transduced T cells), in triplicate. The cells in the E-plates were monitored for another 2-3 days with the RTCA system, and impedance was plotted over time. Cytolysis was calculated as (impedance of target cells without effector cells—impedance of target cells with effector cells)×100/impedance of target cells without effector cells.
To measure CAR expression, 0.5 million cells were suspended in 100 μl of buffer (PBS containing 0.5% BSA) and incubated on ice with 1 μl of human serum (Jackson Immunoresearch, West Grove, Pa.) for 10 min. The anti-CD19-PE or its isotype control PE-labelled antibody were added, and the cells were incubated on ice for 30 min. The cells were rinsed with 3 ml of buffer, then suspended in buffer and acquired on a FACSCalibur (BD Biosciences).
Hela cells are negative for CD19. In Example 3, the Hela cells were stably transduced with CD19, and the resulting Hela-CD19 cells express CD19, as verified by flow cytometry with CD19-PE antibody (
We used Hela-CD19 cells (Example 3), T cells, and CD19-CD28-CD3-zeta CAR-T (CD19scFv CAR-T, Example 4) cells in this Experiment.
The same result was obtained with CD19-NK (natural killer) cells (
To test that Hela-CD19 cells can be used with hematological cancer targets, we developed a novel xenograft tumor model using the HeLa-CD19 cell line. Immunodeficient NSG mice were injected subcutaneously on each flank with 2×106 HeLa-CD19 cells, and the sizes of the tumors were monitored for 36 days. The tumors injected intratumorally with CD19 and CD19-FLAG CAR-T cells (average 285 mm3) were significantly smaller than the control tumors injected with non-transduced T cells (average 935 mm3).
To characterize the effect of CD19-FLAG CAR-T cells in the HeLa-CD19 solid tumor model, a second study was conducted with earlier, intravenous application of the CD19-FLAG CAR-T cells. In this study, the CD19-FLAG CAR-T cells almost completely blocked tumor growth (see
The results show that solid cancer Hela cell line with stably overexpressed leukemia antigen can be used as a model of solid cancer to study hematological targets in the solid tumor microenvironment allowing to study solid tumor biology, signaling and effect of hematological market targeting.
Examples 9-12 shows the nucleotide sequences of CD20, CD22, CD23, and CD24. The same approach as described above are used to generate solid tumor cell lines such as stable Hela or other stable cancer cell lines, which stably expressing these leukemia tumor antigens.
CD20 (Membrane-Spanning 4-Domains Subfamily A Member 1), nucleotide sequence is shown as SEQ ID NO: 4 (NCBI Accesion number, NM_021950.3),
CD22, nucleotide sequence is shown as SEQ ID NO: 5; Gen Bank Accession Number, X52785.1.
CD23 (other name: Fc Fragment Of IgE, Low Affinity II, Receptor For (CD23) is shown as SEQ ID NO: 6; Accesion number: AC008763.
CD24, (Accession NCBI number: NM_001291737.1
NM_001291738.1, NM_001291739.1, NM_013230.3, SEQ ID NO: 7
CD4, CD5, CD7, CD8, CD10, CD33, CD38, CD47, CD56, CD57, CD123, CD138, BCMA and other nucleotide sequences are available from NCBI or Uniprot databases, respectively (www.uniprot.org).
The same approach as described above are used to generate solid tumor cell lines such as stable Hela or other stable cancer cell lines, which stably expressing these leukemia tumor antigens.
It is to be understood that the foregoing describes preferred embodiments of the present invention and that modifications may be made therein without departing from the scope of the present invention as set forth in the claims.
This application is a continuation of U.S. application Ser. No. 15/610,419, filed May 31, 2017, which claims the priority of U.S. Provisional Application No. 62/343,976, dated Jun. 1, 2016. The above applications are incorporated herein by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| 62343976 | Jun 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15610419 | May 2017 | US |
| Child | 16148974 | US |
