METHOD OF TARGETING ONCOLYTIC VIRUSES TO TUMORS

Description

CROSS REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of U.S. Provisional Application Serial No. 62/396,604, filed Sep. 19, 2016, which is hereby incorporated by reference herein in its entirety, including any figures, tables, nucleic acid sequences, amino acid sequences, or drawings.

BACKGROUND OF THE INVENTION

Lung cancers remain the leading cause worldwide of cancer-related mortality in both men and women (National Comprehensive Cancer Network). Deaths due to lung cancers exceed the combined number of deaths from the leading types of carcinoma (breast, prostate and colon cancer), and account for 6% of all deaths within the US (1). Lung cancer patients often present with locally advanced or disseminated disease. Such aggressive lung cancers are difficult to treat due to drug-induced toxicity, as a result ~ 6 out of 10 people die within one year of diagnosis. Available treatment options have limited therapeutic success in non-small cell lung cancer (NSCLC), constituting ~85% of all lung cancer patients, as it becomes resistant to therapy. This is partly due to the tumor itself, a heterogeneous mixture of cells depending on different survival pathways. This heterogeneity allows some of the drug-sensitive cancer cells to eventually acquire resistance to treatment. Radiotherapy, alone or in combination with surgery or chemotherapy, is useful in the management of NSCLC (2). Radiotherapy can be problematic for NSCLC treatment due to tumor radio-resistance before treatment and acquired radio-resistance during radiotherapy, which has been linked with specific genes, such as p53 (3), EGFR (4), and TNNC1 (calcium signaling pathway) (5). Thus, despite progress in surgery, chemotherapy, radiation therapy and development of tumor-specific monoclonal antibodies, advanced or metastatic NSCLC remains difficult-to-treat (6). Such development of resistance to classical chemo- and radio-therapies, underscore the need for development of novel, non-palliative therapeutic strategies.

These challenges have led to the re-emergence of oncolytic viro-therapy (7), a strategy using either naturally occurring or genetically modified viruses to selectively target and lyse tumor cells or kill them by apoptosis while leaving surrounding non-malignant cells unharmed. Despite clinical trials with a few viruses that showed promise in terms of safety and tolerability (8), there remain formidable challenges (9), which include: 1) the vulnerability of viruses to host immune system including complements, neutralizing Abs and macrophages, which rapidly clears the virus from circulation (10); 2) non-specific uptake by other tissues, e.g., by spleen and liver and suboptimal viral escape from the vascular compartment decreases virus reaching the tumor target (9); and 3) targeting the virus specifically to tumor, not healthy tissue. Particularly, for lung cancers, the development of oncolytic virotherapy has been very limited. Also, targeting oncolytic viruses to tumors and tumor cells in the lung remains a major unmet need.

BRIEF SUMMARY OF THE INVENTION

The present invention pertains to a strategy of selectively targeting oncolytic virotherapy, using either naturally occurring or genetically modified viruses by packaging them in mesenchymal stem cells (MSCs), such as human MSCs (hMSCs). Such tumoritropic targeting of the virus, specifically lyse tumor cells or kill them by apoptosis, while leaving surrounding non-malignant cells unharmed. In one embodiment of the invention, hMSCs were found to be almost 100% infected by respiratory syncytial virus (RSV) in cultures. However, such infection also increased the expression of IDO, that inhibits anti-tumor immunity, which is known to have immunosuppressive property. In another embodiment, hMSCs rendered IDO-negative using the CRISP/R method lost their immunosuppressive function. These IDO-deficient hMSCs were found to be capable of being infected by RSV and the infected cells retained their ability to migrate to the tumor sites. In another embodiment, RSV was shown to infect lung cancer cells such as the LLC1 cells in both monolayer and tumoroid cultures.

One aspect of the invention concerns a mesenchymal stem cell (MSC) that is: (a) infected with a naturally occurring or genetically modified oncolytic virus, or (b) is indoleamine 2,3-dioxygenase (IDO)-deficient, or both (a) and (b).

Another aspect of the invention concerns a composition comprising an MSC as described herein, and a pharmaceutically acceptable carrier or diluent, which is useful for the treatment of cancer. Optionally, the composition may include one or more adjuvants.

Another aspect of the invention concerns a method for treating cancer, comprising administering an effective amount of the MSCs described herein to a human or non-human animal subject in need thereof.

Another aspect of the invention concerns a method for lysing or inducing apoptosis of cancer cells in vitro or in vivo, comprising contacting the cancer cells in vitro or in vivo with, or bringing into close proximity, an effective amount of MSC as described herein.

Another aspect of the invention concerns a method for producing an oncolytic agent, comprising: providing an MSC; and infecting the MSC with an oncolytic virus. Optionally, the infected MSC may be combined as a composition with a pharmaceutically acceptable carrier or diluent. Optionally, the composition may include one or more adjuvants.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.

FIGS. 1A-1E. RSV infects and replicates in hMSCs. (1A) hMSCs were infected with RSV (MOI=1), immunostained at 48 or 72 h p.i. with a mAb to GFP-RSV, Evan’s blue dye (red) and DAPI (blue) and visualized by confocal microscopy (mag 200X or 1000X). (1B) RSV nucleocapsid (RSVN) transcripts detected in MSCs at 6, 12, 24 and 72 hours p.i. normalized to mock. (1C) RSV titers (PFU/ml) isolated from the culture medium of infected MSCs. Results representative of at least duplicate experiments. *p< 0.05, ** p< 0.01, ***p<0.001. qPCR analysis of interferon-β (1D) and IDO (1E) expression in RSV-infected NHBE and MSCs compared to mock-infected cells (n=6) by 72 h p.i., *p<0.05, **p<0.01.

FIGS. 2A-2F: (2A) IDO antagonists abrogate proliferative inhibition by RSV-infected MSC CM. CFSE labeled PBMCs were treated with CM from uninfected (mock) or RSV-infected hMSC cultures in the presence or absence of 1 mM 1-MT and 10 µM of vitamin K3 cultured (triplicate) for 5 days with the mitogen PHA. Cell proliferation analyzed by flow cytometry. (2B-2C) RSV infection (2B) and kynurenine levels (2C) in 1-MT or vitamin K3 treated human MSCs. (2D-2F) RSV infection in IDO-deficient mice. Wild type and IDO-knockout mice were infected intranasally with 3 × 10⁶ pfu RSV, euthanized 5 days p.i. and lungs were examined for RSV infection (2D), RSVN- (2E) and IFN-β- (2F) transcripts by qPCR. * p<0.05, *** p<0.001 & **** p<0.0001

FIGS. 3A-3C: IDO-deficient hMSCs remained susceptible to RSV infection. Human MSCs were transduced with lentiviral (Lv) particles containing the pCRISPR-LvSG03 expression plasmid for mCherry, CRISPR associated protein 9 (Cas9), and one of two human IDO-specific single guide (sg) RNAs (LvA and LvB) or a scrambled control (LvS) (GeneCopoeia) in the presence of 10 µg per mL polybrene for 12 hours, per manufacturer’s instructions. The cells were incubated for 48 hours prior to infection with rgRSV. (3A) Lentiviral transduction and RSV infection were visualized by fluorescent microscopy for mCherry (red) and GFP (green) respectively. (3B) Knockout of IDO eliminates the immune regulatory effect of RSV-infected MSCs. Proliferation of PBMCs treated with conditioned media from MSCs was detected by CFSE, n=3, **** p < 0.0001 vs. PHA control, ‡ p < 0.0001 vs. LvS. (3C) RSV infection quantified by real-time PCR (I) *p<0.05 vs. LvS-R.

FIGS. 4A-4B: LLC1 tumoroids were cultured with hMSCs in the presence or absence of 1MT in transwell insert. Migrated MSCs were counted after 24 h. Each group was done in triplicates. (4A) Representative images and (4B) means ± SD of migrated MSCs are shown.

FIGS. 5A-1, 5A-2, 5B, 5C, 5D, 5E, 5F: Susceptibility of LLC1 monolayer (5A-1 and 5A-2) and tumoroids (5B) to RSV infection. A representative picture is shown. (5C) Establishment of orthotopic lung tumors. After incision of the skin overlying the left chest wall in the mid-axillary line, LLC1 (~10⁶ cells/mouse) cells were injected into the left lung. Two weeks after inoculation, lungs were harvested, fixed and sectioned H&E stained. (5D) Tumor tropism of hMSC. I.V. administered PKH26-labeled hMSC to tumor bearing GFP-C57BL/6 mouse lungs (left) detected by IVIS imaging, 24 hrs post injection. Right: control tumor bearing GFP-C57BL/6 mouse. (5E-5F) RSV detection in mouse lung tumors 5 days post infection of RSV-loaded hMSC via i.n. route. (5E) Immunostaining with a anti-RSV antibody (Abcam), (5F) RSV N transcripts by q-PCR * p<0.05.

BRIEF DESCRIPTION OF THE SEQUENCES

SEQ ID NO:1 - Human IDO amino acid sequence (UniProt accession number P14902).

SEQ ID NO:2 - Human IDO nucleic acid sequence (NCBI Accession number NM_002164, version NM_002164.5).

DETAILED DESCRIPTION OF THE INVENTION

The inventors have extensively studied RSV for the last decade in relation to its immunobiology and its interaction with diverse host cells including A549 lung carcinoma epithelial cells and normal human bronchial epithelial cells (NHBE) (11-14) and have shown that RSV-induced IFN-β to be important to apoptosis. Wild-type (wt) RSV was shown to be oncolytic when delivered locally to prostate cancer xenograft tumors (15); however, it cannot be given locally to all tumors. Thus, there is a need to administer viruses systemically, and to target the virus to the tumors. Also, the inventors found that lung cancer cells did not show a cytopathic effect (CPE) when infected with wt-RSV presumably because RSV primarily infects cells that are poor producers of IFN-β, e.g., NHBE cells (16).

Although RSV commonly infects the apical airway epithelial cells, only about 40% of cells in a culture get infected. An error in cell handling in the inventors’ lab led to the finding that human MSCs (hMSCs) are highly susceptible to RSV. Since MSCs are known to target to tumors (17), the inventors hypothesized that RSV-infected hMSCs might be useful to develop targeted oncolytic virotherapy. However, initial studies showed that RSV-infected hMSCs upregulate IDO expression and activity, which could suppress anti-tumor immunity. Thus, the inventors produced IDO-negative MSCs, which provide targeted delivery of RSV-based oncolytic therapy, and which may be used to deliver other oncolytic virotherapies.

The MSC may be a human MSC or a non-human animal MSC. In some embodiments, the subject receiving the MSC is human and the MSC is a human MSC.

The MSC may be autologous, allogeneic, or xenogeneic to the subject to which the MSCs are administered.

The oncolytic virus should be oncolytic for the cancer cell type. Examples of oncolytic viruses include, but are not limited to, respiratory syncytial virus (RSV), herpes simplex virus, vesicular stomatitis virus, poliovirus, reovirus, senecavirus, and RIGVIR. In some embodiments, the virus is RSV. In some embodiments, the virus is RSV and the cancer is lung cancer.

The virus may be engineered or genetically modified, for example, by attenuation (e.g., deleting viral genes or gene regions to eliminate viral functions that are expendable in tumor cells, but not in normal cells, thus making the virus safer and more tumor-specific); tumor targeting (e.g., transductional targeting or non-transductional targeting); inclusion of reporter genes (e.g., green fluorescent protein (GFP)); improvement of oncolytic activity (e.g., inclusion of suicide genes, suppression of angiogenesis by addition of anti-angiogenic genes, radioiodine (accumulation of iodine by addition of the sodium-iodide symporter (NIS) gene)).

The MSCs may be administered to the subject, or brought into contact or proximity to the target cancer cells in vitro or in vivo, in an isolated state and, optionally, combined with a pharmaceutically acceptable carrier or diluent, as a pharmaceutical composition. Optionally, the composition can further include one or more additional biologically active agents, such as an adjuvant, chemotherapeutic, immunotherapeutic, etc.

Optionally, MSCs can be co-administered, simultaneously or consecutively, with one or more other agents to a subject. Anti-cancer agents that may be administered include but are not limited to those listed Table 1.

Co-administration can be carried out simultaneously (in the same or separate formulations) or consecutively with the additional agent administered before and/or after one or more compounds disclosed herein.

Thus, the MSCs, whether administered separately, or as a pharmaceutical composition, can include various other components. Examples of acceptable components or adjuncts which can be employed in relevant circumstances include antioxidants, free radical scavenging agents, peptides, growth factors, antibiotics, bacteriostatic agents, immunosuppressives, anticoagulants, buffering agents, anti-inflammatory agents, anti-angiogenics, anti-pyretics, time-release binders, anesthetics, steroids, and corticosteroids. Such components can provide additional therapeutic benefit, act to affect the therapeutic action of the MSCs, or act towards preventing any potential side effects which may be posed as a result of administration of the MSCs or other agents.

In some embodiments, the compositions of the invention include at least one additional anti-cancer agent (e.g., a chemotherapeutic agent). In some embodiments of the methods of the invention, at least one additional anti-cancer agent is administered with the MSCs.

In some embodiments, the compositions can include, and the methods can include administration of, one or more proteasome inhibitors (e.g., bortezomib), inhibitors of autophagy (e.g., chloroquine), alkylating agents (e.g., melphalan, cyclophosphamide), MEK inhibitors (e.g., PD98509), FAK/PYK2 inhibitors (e.g., PF562271), or EGFR inhibitors (e.g., erlotinib, gefitinib, cetuximab, panitumumab, zalutumumab, nimotuzumab, matuzumab), or a combination of two or more of the foregoing.

Thus, immunotherapeutics, whether administered separately, or as a pharmaceutical composition, can include various other components as additives. Examples of acceptable components or adjuncts which can be employed in relevant circumstances include antioxidants, free radical scavenging agents, peptides, growth factors, antibiotics, bacteriostatic agents, immunosuppressives, anticoagulants, buffering agents, anti-inflammatory agents, anti-angiogenics, anti-pyretics, time-release binders, anesthetics, steroids, and corticosteroids. Such components can provide additional therapeutic benefit, act to affect the therapeutic action of the MSCs or other agents, or act towards preventing any potential side effects which may be posed as a result of administration of the MSCs or other agents. The immunotherapeutic agent can be conjugated to a therapeutic agent or other agent, as well.

As used herein, the term “immunotherapy” refers to the treatment of disease via the stimulation, induction, subversion, mimicry, enhancement, augmentation or any other modulation of a subject’s immune system to elicit or amplify adaptive or innate immunity (actively or passively) against cancerous or otherwise harmful proteins, cells or tissues. Immunotherapies (i.e., immunotherapeutic agents) include cancer vaccines, immunomodulators, monoclonal antibodies (e.g., humanized monoclonal antibodies), immunostimulants, dendritic cells, and viral therapies, whether designed to treat existing cancers or prevent the development of cancers or for use in the adjuvant setting to reduce likelihood of recurrence of cancer. Examples of cancer vaccines include GVAX, Stimuvax, DCVax and other vaccines designed to elicit immune responses to tumor and other antigens including MUC1, NY-ESO-1, MAGE, p53 and others. Examples of immunomodulators include 1MT, Ipilimumab, Tremelimumab and/or any drug designed to de-repress or otherwise modulate cytotoxic or other T cell activity against tumor or other antigens, including, but not restricted to, treatments that modulate T-Reg cell control pathways via CTLA-4, CD80, CD86, MHC, B7-DC, B7-H1, B7-H2, B7-H3, B7-H4, CD28, other TCRs, PD-1, PDL-1, CD80, ICOS and their ligands, whether via blockade, agonist or antagonist. Examples of immunostimulants include corticosteroids and any other anti- or pro-inflammatory agent, steroidal or non-steroidal, including, but not restricted to, GM-CSF, interleukins (e.g., IL-2, IL-7, IL-12), cytokines such as the interferons, and others. Examples of dendritic cell (DC) therapies include modified dendritic cells and any other antigen presenting cell, autologous or xeno, whether modified by multiple antigens, whole cancer cells, single antigens, by mRNA, phage display or any other modification, including but not restricted to ex vivo-generated, antigen-loaded dendritic cells (DCs) to induce antigen-specific T-cell immunity, ex vivo gene-loaded DCs to induce humoral immunity, ex vivo-generated antigen-loaded DCs induce tumour-specific immunity, ex vivo-generated immature DCs to induce tolerance, including but not limited to Provenge and others. Examples of viral therapies include oncolytic viruses or virus-derived genetic or other material designed to elicit anti-tumor immunity and inhibitors of infectious viruses associated with tumor development, such as drugs in the Prophage series. Examples of monoclonal antibodies include Alemtuzumab, Bevacizumab, Cetuximab, Gemtuzumab ozogamicin, Rituximab, Trastuzumab, Radioimmunotherapy, Ibritumomab tiuxetan, Tositumomab/iodine tositumomab regimen. An immunotherapy may be a monotherapy or used in combination with one or more other therapies (one or more other immunotherapies or non-immunotherapies).

As used herein, the term “cytotoxic agent” refers to a substance that inhibits or prevents the function of cells and/or causes destruction of cells in vitro and/or in vivo. The term is intended to include radioactive isotopes (e.g., At²¹¹, I¹³¹, I¹²⁵, Y⁹⁰, Re¹⁸⁶, Re¹⁸⁸, Sm¹⁵³, Bi²¹², P³², and radioactive isotopes of Lu), chemotherapeutic agents, toxins such as small molecule toxins or enzymatically active toxins of bacterial, fungal, plant or animal origin, and antibodies, including fragments and/or variants thereof.

As used herein, the term “chemotherapeutic agent” is a chemical compound useful in the treatment of cancer, such as, for example, taxanes, e.g., paclitaxel (TAXOL, BRISTOL-MYERS SQUIBB Oncology, Princeton, N.J.) and doxetaxel (TAXOTERE, Rhone-Poulenc Rorer, Antony, France), chlorambucil, vincristine, vinblastine, antiestrogens including for example tamoxifen, raloxifene, aromatase inhibiting 4(5)-imidazoles, 4-hydroxytamoxifen, trioxifene, keoxifene, LY117018, onapristone, and toremifene (FARESTON, GTx, Memphis, TN), and anti-androgens such as flutamide, nilutamide, bicalutamide, leuprolide, and goserelin, etc. Examples of anti-cancer agents, including chemotherapeutic agents, that may be used in conjunction with the compositions and methods of the invention are listed in Table 1. In some embodiments, the chemotherapeutic agent is one or more anthracyclines. Anthracyclines are a family of chemotherapy drugs that are also antibiotics. The anthracyclines act to prevent cell division by disrupting the structure of the DNA and terminate its function by: (1) intercalating into the base pairs in the DNA minor grooves; and (2) causing free radical damage of the ribose in the DNA. The anthracyclines are frequently used in leukemia therapy. Examples of anthracyclines include daunorubicin (CERUBIDINE), doxorubicin (ADRIAMYCIN, RUBEX), epirubicin (ELLENCE, PHARMORUBICIN), and idarubicin (IDAMYCIN).

TABLE 1

Examples of Anti-Cancer Agents
13-cis-Retinoic Acid	Mylocel
2-Amino-6-Mercaptopurine	Letrozole
Neosar
2-CdA	Neulasta
2-Chlorodeoxyadenosine	Neumega
5-fluorouracil	Neupogen
5-FU	Nilandron
6 - TG	Nilutamide
6 - Thioguanine	Nitrogen Mustard
6-Mercaptopurine	Novaldex
6-MP	Novantrone
Accutane	Octreotide
Actinomycin-D	Octreotide acetate
Adriamycin	Oncospar
Adrucil	Oncovin
Agrylin	Ontak
Ala-Cort	Onxal
Aldesleukin	Oprevelkin
Alemtuzumab	Orapred
Alitretinoin	Orasone
Alkaban-AQ	Oxaliplatin
Alkeran	Paclitaxel
All-transretinoic acid	Pamidronate
Alpha interferon	Panretin
Altretamine	Paraplatin
Amethopterin	Pediapred
Amifostine	PEG Interferon
Aminoglutethimide	Pegaspargase
Anagrelide	Pegfilgrastim
Anandron	PEG-INTRON
Anastrozole	PEG-L-asparaginase
Arabinosylcytosine	Phenylalanine Mustard
Ara-C	Platinol
Aranesp	Platinol-AQ
Aredia	Prednisolone
Arimidex	Prednisone
Aromasin	Prelone
Arsenic trioxide	Procarbazine
Asparaginase	PROCRIT
ATRA	Proleukin
Avastin	Prolifeprospan 20 with Carmustine implant
BCG	Purinethol
BCNU	Raloxifene
Bevacizumab	Rheumatrex
Bexarotene	Rituxan
Bicalutamide	Rituximab
BiCNU	Roveron-A (interferon alfa-2a)
Blenoxane	Rubex
Bleomycin	Rubidomycin hydrochloride
Bortezomib	Sandostatin
Busulfan	Sandostatin LAR
Busulfex	Sargramostim
C225	Solu-Cortef
Calcium Leucovorin	Solu-Medrol
Campath	STI-571
Camptosar	Streptozocin
Camptothecin-11	Tamoxifen
Capecitabine	Targretin
Carac	Taxol
Carboplatin	Taxotere
Carmustine	Temodar
Carmustine wafer	Temozolomide
Casodex	Teniposide
CCNU	TESPA
CDDP	Thalidomide
CeeNU	Thalomid
Cerubidine	TheraCys
cetuximab	Thioguanine
Chlorambucil	Thioguanine Tabloid
Cisplatin	Thiophosphoamide
Citrovorum Factor	Thioplex
Cladribine	Thiotepa
Cortisone	TICE
Cosmegen	Toposar
CPT-11	Topotecan
Cyclophosphamide	Toremifene
Cytadren	Trastuzumab
Cytarabine	Tretinoin
Cytarabine liposomal	Trexall
Cytosar-U	Trisenox
Cytoxan	TSPA
Dacarbazine	VCR
Dactinomycin	Velban
Darbepoetin alfa	Velcade
Daunomycin	VePesid
Daunorubicin	Vesanoid
Daunorubicin hydrochloride	Viadur
Vinblastine
Daunorubicin liposomal	Vinblastine Sulfate
DaunoXome	Vincasar Pfs
Decadron	Vincristine
Delta-Cortef	Vinorelbine
Deltasone	Vinorelbine tartrate
Denileukin diftitox	VLB
DepoCyt	VP-16
Dexamethasone	Vumon
Dexamethasone acetate	Xeloda
dexamethasone sodium phosphate	Zanosar
Zevalin
Dexasone	Zinecard
Dexrazoxane	Zoladex
DHAD	Zoledronic acid
DIC	Zometa
Diodex	Gliadel wafer
Docetaxel	Glivec
Doxil	GM-CSF
Doxorubicin	Goserelin
Doxorubicin liposomal	granulocyte - colony stimulating factor
Droxia	Granulocyte macrophage colony stimulating factor
DTIC
DTIC-Dome	Halotestin
Duralone	Herceptin
Efudex	Hexadrol
Eligard	Hexalen
Ellence	Hexamethylmelamine
Eloxatin	HMM
Elspar	Hycamtin
Emcyt	Hydrea
Epirubicin	Hydrocort Acetate
Epoetin alfa	Hydrocortisone
Erbitux	Hydrocortisone sodium phosphate
Erwinia L-asparaginase	Hydrocortisone sodium succinate
Estramustine	Hydrocortone phosphate
Ethyol	Hydroxyurea
Etopophos	Ibritumomab
Etoposide	Ibritumomab Tiuxetan
Etoposide phosphate	Idamycin
Eulexin	Idarubicin
Evista	Ifex
Exemestane	IFN-alpha
Fareston	Ifosfamide
Faslodex	IL - 2
Femara	IL - 11
Filgrastim	Imatinib mesylate
Floxuridine	Imidazole Carboxamide
Fludara	Interferon alfa
Fludarabine	Interferon Alfa-2b (PEG conjugate)
Fluoroplex	Interleukin - 2
Fluorouracil	Interleukin-11
Fluorouracil (cream)	Intron A (interferon alfa-2b)
Fluoxymesterone	Leucovorin
Flutamide	Leukeran
Folinic Acid	Leukine
FUDR	Leuprolide
Fulvestrant	Leurocristine
G-CSF	Leustatin
Gefitinib	Liposomal Ara-C
Gemcitabine	Liquid Pred
Gemtuzumab ozogamicin	Lomustine
Gemzar	L-PAM
Gleevec	L-Sarcolysin
Lupron	Meticorten
Lupron Depot	Mitomycin
Matulane	Mitomycin-C
Maxidex	Mitoxantrone
Mechlorethamine	M-Prednisol
Mechlorethamine Hydrochlorine	MTC
MTX
Medralone	Mustargen
Medrol	Mustine
Megace	Mutamycin
Megestrol	Myleran
Megestrol Acetate	Iressa
Melphalan	Irinotecan
Mercaptopurine	Isotretinoin
Mesna	Kidrolase
Mesnex	Lanacort
Methotrexate	L-asparaginase
Methotrexate Sodium	LCR
Methylprednisolone

One or more adjuvants may be administered with the MSCs, within the same composition as the MSCs, or in a separate composition before, during, and/or after administration of the MSCs. The adjuvant may be of any class such as alum salts and other mineral adjuvants, bacterial, products or bacteria-derived adjuvants, tensoactive agents (e.g., saponins), oil-in-water (o/w) and water-in-oil (w/o) emulsions, liposome adjuvants, cytokines (e.g., IL-2, GM-CSP, IL-12, and IFNgamma), and alpha-galactosylceramide analogs. Nonlimiting examples of adjuvants include Montanide emulsions, QS21, Freund’s complete or incomplete adjuvant, aluminum phosphate, aluminum hydroxide, Bacillus Calmette-Guerin (BCG), and alum.

The MSCs may be administered in a composition that is adapted for an appropriate route of administration, such as enteral, parenteral, intravenous, intramuscular, topical, subcutaneous, and so forth. The MSCs can be administered at continuous or at distinct intervals, as can be determined by a person of ordinary skill in the art.

In some embodiments, the MSCs are administered to the subject systemically. In some embodiments, the MSCs are administered to the subject at an anatomical location remote from the site of a cancer. In some embodiments, the MSCs are administered locally, at the site of a cancer. In some embodiments, the MSCs are administered intranasally. In some embodiments, the MSCs are administered intravascularly (e.g., intravenously).

Various methods may be used to induce transient or sustained indoleamine 2,3-dioxygenase (IDO)-deficiency in the MSC. For example, gene deletion or gene silencing may be used to eliminate or reduce IDO expression in the MSC before, during, or after, infection with the oncolytic virus, such as homologous recombination, RNA interference (RNAi), transcription activator-like effector nucleases (TALENs), and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) mechanism (see, for example, (22), (23), and (24), which are each incorporated herein by reference in their entireties. In some embodiments, a CRISPR/Cas9 system is used (see Example 3). The deficiency in IDO function and/or expression may be complete (100%) or partial (e.g., 90%, 80%, 70%, 60%, 50%).

The nucleic acid and amino acid sequences of human IDO are known (NCBI accession number NM_002164, version NM_002164.5 GI:323668304; UniProt accession number P14902, which are incorporated herein by reference in their entirety).

SEQ ID NO:1 - Human IDO amino acid sequence:

MAHAMENSWTISKEYHIDEEVGFALPNPQENLPDFYNDWMFIAKHLPDLI

ESGQLRERVEKLNMLSIDHLTDHKSQRLARLVLGCITMAYVWGKGHGDVR

KVLPRNIAVPYCQLSKKLELPPILVYADCVLANWKKKDPNKPLTYENMDV

LFSFRDGDCSKGFFLVSLLVEIAAASAIKVIPTVFKAMQMQERDTLLKAL

LEIASCLEKALQVFHQIHDHVNPKAFFSVLRIYLSGWKGNPQLSDGLVYE

GFWEDPKEFAGGSAGQSSVFQCFDVLLGIQQTAGGGHAAQFLQDMRRYMP

PAHRNFLCSLESNPSVREFVLSKGDAGLREAYDACVKALVSLRSYHLQIV

TKYILIPASQQPKENKTSEDPSKLEAKGTGGTDLMNFLKTVRSTTEKSLL

KEG

(UniProt accession number P14902)

SEQ ID NO:2 - Human IDO nucleic acid sequence:

1 aatttctcac tgcccctgtg ataaactgtg gtcactggct gtggcagcaa ctattataag

61 atgctctgaa aactcttcag acactgaggg gcaccagagg agcagactac aagaatggca

121 cacgctatgg aaaactcctg gacaatcagt aaagagtacc atattgatga agaagtgggc

181 tttgctctgc caaatccaca ggaaaatcta cctgattttt ataatgactg gatgttcatt

241 gctaaacatc tgcctgatct catagagtct ggccagcttc gagaaagagt tgagaagtta

301 aacatgctca gcattgatca tctcacagac cacaagtcac agcgccttgc acgtctagtt

361 ctgggatgca tcaccatggc atatgtgtgg ggcaaaggtc atggagatgt ccgtaaggtc

421 ttgccaagaa atattgctgt tccttactgc caactctcca agaaactgga actgcctcct

481 attttggttt atgcagactg tgtcttggca aactggaaga aaaaggatcc taataagccc

541 ctgacttatg agaacatgga cgttttgttc tcatttcgtg atggagactg cagtaaagga

601 ttcttcctgg tctctctatt ggtggaaata gcagctgctt ctgcaatcaa agtaattcct

661 actgtattca aggcaatgca aatgcaagaa cgggacactt tgctaaaggc gctgttggaa

721 atagcttctt gcttggagaa agcccttcaa gtgtttcacc aaatccacga tcatgtgaac

781 ccaaaagcat ttttcagtgt tcttcgcata tatttgtctg gctggaaagg caacccccag

841 ctatcagacg gtctggtgta tgaagggttc tgggaagacc caaaggagtt tgcagggggc

901 agtgcaggcc aaagcagcgt ctttcagtgc tttgacgtcc tgctgggcat ccagcagact

961 gctggtggag gacatgctgc tcagttcctc caggacatga gaagatatat gccaccagct

1021 cacaggaact tcctgtgctc attagagtca aatccctcag tccgtgagtt tgtcctttca

1081 aaaggtgatg ctggcctgcg ggaagcttat gacgcctgtg tgaaagctct ggtctccctg

1141 aggagctacc atctgcaaat cgtgactaag tacatcctga ttcctgcaag ccagcagcca

1201 aaggagaata agacctctga agacccttca aaactggaag ccaaaggaac tggaggcact

1261 gatttaatga atttcctgaa gactgtaaga agtacaactg agaaatccct tttgaaggaa

1321 ggttaatgta acccaacaag agcacatttt atcatagcag agacatctgt atgcattcct

1381 gtcattaccc attgtaacag agccacaaac taatactatg caatgtttta ccaataatgc

1441 aatacaaaag acctcaaaat acctgtgcat ttcttgtagg aaaacaacaa aaggtaatta

1501 tgtgtaatta tactagaagt tttgtaatct gtatcttatc attggaataa aatgacattc

561 aataaataaa aatgcataag atatattctg tcggctgggc gcggtggctc acgcctgtaa

1621 tcccagcact ttgggaggcc gaggcgggcg gatcacaagg tcaggagatc gagaccatct

1681 tggctaacac ggtgaaaccc cgtctctact aaaaatacaa aaaattagcc gggcgcggtg

1741 gcgggcacct gtagtcccag ctactcggga ggctgaggca ggagaatggc gtgaacctgg

1801 gaggcggagc ttgcagtgag ccaagattgt gccactgcaa tccggcctgg gctaaagagc

1861 gggactccgt ctcaaaaaaa aaaaaaaaaa gatatattct gtcataataa ataaaaatgc

1921 ataagatata aaaaaaaaaa aaaa

(NCBI Accession number NM_002164, version NM_002164.5 GI:323668304; Yeung Aw et al., “Role of indoleamine 2,3-dioxygenase in health and disease”, Clin. Sci. 129 (7), 601-672 (2015), which is incorporated herein by reference in its entirety).

As indicated above, initial studies showed that RSV-infected MSCs upregulate IDO expression and activity, which could potentially have the undesisirable effect of suppressing anti-tumor immunity. One approach to avoid this is to use IDO-deficient MSCs, as described above. Another approach is to utilize inhibitors of indoleamine 2,3-dioxygenase (IDO inhibitors). Optionally, one or more IDO inhibitors may be administered to the subject, or brought into contact or proximity to the target cancer cells in vitro or in vivo. IDO inhibitors may be administered by appropriates routes of administration, such as enteral, parenteral, intravenous, intramuscular, topical, subcutaneous, and so forth. Administration can be continuous or at distinct intervals, as can be determined by a person of ordinary skill in the art. IDO inhibitors may be administered to a subject within the same composition as the MSCs, or administered in a separate composition before, during, or after administration of the MSCs.

The IDO inhibitors may be administered to the subject with MSCs having normal IDO function, or the IDO inhibitors may be administered with IDO-deficient MSCs in order to inhibit IDO endogenously. IDO is an immunoregulatory enzyme that suppresses T-cell responses and promotes immune tolerance. IDO catabolizes tryptophan and is believed to help tumor cells escape the immune system at least in part by depleting Trp in the tumor microenvironment. IDO helps create a tolerogenic milieu within the tumor and the associated tumor-draining lymph nodes. IDO directly suppresses the proliferation and differentiation of effector T cells, and markedly enhances the suppressor activity of Tregs. IDO inhibitors include, for example, hydroxyamidines such as INCB023843 and INCB024360 (WO 2006122150) and tryptophan analogs such as 1-methyl tryptophan, dextro-1-methyl tryptophan (D-1MT). Other IDO inhibitors are described in WO2014159248, US20120277217, US20140315962, and US20140323740, which are incoporated herein by reference in their entireties.

The IDO inhibitor may have one or more mechanisms of action ((21); the contents of which is incorporated herein by reference in its entirety). The IDO inhibitor may be an IDO1 inhibitor, an IDO2 inhibitor, or both. The IDO inhibitor may be any class of molecule, such as a small molecule or a biologic such as a nucleic acid (such as interfering RNA specific for IDO 1 and/or IDO2), protein or peptide, antibody or antibody fragment. Examples of IDO inhibitors include, but are not limited to, D-1MT (a tryptophan mimetic, D isoform of MT; and transcriptional suppressor of IDO), L-1MT (a tryptophan mimetic, L isoform of MT, and selective IDO1 inhibitor), MTH-Trp ( tryptophan mimetic and transcriptional suppressor of IDO), β-carbolines (a tryptophan mimetic, and IDO and TDO inhibitor), Naphthoquinone-based inhibitor (a pharmacophore of natural product annulin B; indole mimetic; and an IDO inhibitor), S-allyl-brassinin (a phytoalexin and indole mimetic), S-benzyl-brassinin (a phytoalexin and indole mimetic), 5-Bromo-brassinin (a phytoalexin and indole mimetic), phenylimidazole-based inhibitor (a computationally designed synthetic IDO inhibitor), 4-phenylimidazole (a heme ligand in IDO enzyme), Exiguamine A (a non-tryptophan analogue, and NSC401366 a (a non-indolic IDO inhibitor). IDO inhibitors undergoing clinical development include, for example, INCB024360 (Incyte), indoximod (NewLink Genetics), an IDO peptide vaccine (Copenhagen University), and NLG919 (NewLink Genetics).

Exemplified Embodiments

Embodiment 1. A mesenchymal stem cell (MSC) that is: (a) infected with a naturally occurring or genetically modified oncolytic virus, or (b) is indoleamine 2,3-dioxygenase (IDO)-deficient, or both (a) and (b).

Embodiment 2. The MSC of embodiment 1, wherein the MSC is infected with a naturally occurring or genetically modified oncolytic virus.

Embodiment 3. The MSC of embodiment 1, wherein the MSC is IDO-deficient.

Embodiment 4. The MSC of embodiment 1, wherein the MSC is infected with a naturally occurring or genetically modified oncolytic virus, and wherein the MSC is IDO-deficient.

Embodiment 5. The MSC of any one of embodiments 1 to 4, wherein the oncolytic virus is respiratory syncytial virus (RSV).

Embodiment 6. The MSC of any one of embodiments 1 to 5, wherein the MSC is a human MSC.

Embodiment 7. The MSC of any preceding embodiment, wherein the MSC is rendered IDO-deficient by CRISPR-mediated knockout of IDO.

Embodiment 8. A method for treating cancer, comprising administering an effective amount of the MSC of any one of embodiments 1 to 7 to a human or non-human animal subject in need thereof.

Embodiment 9. The method of embodiment 8, wherein the cancer is lung cancer.

Embodiment 10. The method of embodiment 9, wherein the lung cancer is non-small cell lung cancer (NSCLC).

Embodiment 11. The method of any one of embodiments 8 to 10 further comprising administering an inhibitor of indoleamine 2,3-dioxygenase (IDO inhibitor) to the subject.

Embodiment 12. A method for producing an oncolytic agent, comprising: providing an MSC; and infecting the MSC with an oncolytic virus.

Embodiment 13. The method of embodiment 12, wherein the MSC is indoleamine 2,3-dioxygenase (IDO)-deficient at the time of infection.

Embodiment 14. The method of embodiment 12, further comprising rendering the MSC indoleamine 2,3-dioxygenase (IDO)-deficient before or after said infecting.

Embodiment 15. A method for lysing or inducing apoptosis of cancer cells in vitro or in vivo, comprising contacting the cancer cells in vitro or in vivo with, or bringing into close proximity, an effective amount of MSC of any one of embodiments 1 to 7.

Embodiment 16. The method of embodiment 15, wherein the cancer cells are lung cancer cells.

Embodiment 17. The method of embodiment 16, wherein the lung cancer cells are non-small cell lung cancer (NSCLC).

Embodiment 18. The method of any one of embodiments 15 to 17, further comprising contacting the cancer cells in vitro or in vivo with an inhibitor of indoleamine 2,3-dioxygenase (IDO inhibitor).

Embodiment 19. A composition comprising an MSC of any one of embodiment 1 to 4; and a pharmaceutically acceptable carrier or diluent.

Embodiment 20. The composition of embodiment 19, further comprising an adjuvant.

Further Definitions

The terms “cancer” and “malignancy” are used herein interchangeably to refer to or describe the physiological condition in mammals that is typically characterized by unregulated cell growth. The cancer may be drug-resistant or drug-sensitive. The cancer may be primary or metastatic. The cancer may represent early, middle, or late stage disease, and be acute or chronic. In some embodiments, the cancer is lung cancer. In some embodiments, the cancer is non-small cell lung cancer (NSCLC) or small-cell lung cancer.

Examples of cancer include but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia. More particular examples of such cancers include breast cancer, prostate cancer, colon cancer, squamous cell cancer, small-cell lung cancer, non-small cell lung cancer, gastrointestinal cancer, pancreatic cancer, cervical cancer, ovarian cancer, peritoneal cancer, liver cancer, e.g., hepatic carcinoma, bladder cancer, colorectal cancer, endometrial carcinoma, kidney cancer, and thyroid cancer. In some embodiments, the cancer is melanoma, MDS, ovarian cancer, breast cancer, or multiple myeloma.

Other non-limiting examples of cancers are basal cell carcinoma, biliary tract cancer; bone cancer; brain and CNS cancer; choriocarcinoma; connective tissue cancer; esophageal cancer; eye cancer; cancer of the head and neck; gastric cancer; intra-epithelial neoplasm; larynx cancer; lymphoma including Hodgkin’s and Non-Hodgkin’s lymphoma; melanoma; myeloma; neuroblastoma; oral cavity cancer (e.g., lip, tongue, mouth, and pharynx); retinoblastoma; rhabdomyosarcoma; rectal cancer; cancer of the respiratory system; sarcoma; skin cancer; stomach cancer; testicular cancer; uterine cancer; cancer of the urinary system, as well as other carcinomas and sarcomas. Examples of cancer types that may be treated with the compositions and methods of the invention are listed in Table 2.

TABLE 2

Examples of Cancer Types
Acute Lymphoblastic Leukemia, Adult	Hairy Cell Leukemia
Acute Lymphoblastic Leukemia, Childhood	Head and Neck Cancer
Acute Myeloid Leukemia, Adult	Hepatocellular (Liver) Cancer, Adult (Primary)
Acute Myeloid Leukemia, Childhood	Hepatocellular (Liver) Cancer, Childhood (Primary)
Adrenocortical Carcinoma	Hodgkin’s Lymphoma, Adult
Adrenocortical Carcinoma, Childhood	Hodgkin’s Lymphoma, Childhood
AIDS-Related Cancers	Hodgkin’s Lymphoma During Pregnancy
AIDS-Related Lymphoma	Hypopharyngeal Cancer
Anal Cancer	Hypothalamic and Visual Pathway Glioma, Childhood
Astrocytoma, Childhood Cerebellar	Intraocular Melanoma
Astrocytoma, Childhood Cerebral	Islet Cell Carcinoma (Endocrine Pancreas)
Basal Cell Carcinoma	Kaposi’s Sarcoma
Bile Duct Cancer, Extrahepatic	Kidney (Renal Cell) Cancer
Bladder Cancer	Kidney Cancer, Childhood
Bladder Cancer, Childhood	Laryngeal Cancer
Bone Cancer, Osteosarcoma/Malignant	Laryngeal Cancer, Childhood
Fibrous Histiocytoma	Leukemia, Acute Lymphoblastic, Adult
Brain Stem Glioma, Childhood	Leukemia, Acute Lymphoblastic, Childhood
Brain Tumor, Adult	Leukemia, Acute Myeloid, Adult
Brain Tumor, Brain Stem Glioma, Childhood	Leukemia, Acute Myeloid, Childhood
Brain Tumor, Cerebellar Astrocytoma, Childhood	Leukemia, Chronic Lymphocytic
Brain Tumor, Cerebellar Astrocytoma, Childhood	Leukemia, Chronic Myelogenous
Brain Tumor, Cerebral	Leukemia, Hairy Cell
Astrocytoma/Malignant Glioma, Childhood	Lip and Oral Cavity Cancer
Brain Tumor, Ependymoma, Childhood	Liver Cancer, Adult (Primary)
Brain Tumor, Medulloblastoma, Childhood	Liver Cancer, Childhood (Primary)
Brain Tumor, Supratentorial Primitive	Lung Cancer, Non-Small Cell
Neuroectodermal Tumors, Childhood	Lung Cancer, Small Cell
Brain Tumor, Visual Pathway and	Lymphoma, AIDS-Related
Hypothalamic Glioma, Childhood	Lymphoma, Burkitt’s
Brain Tumor, Childhood	Lymphoma, Cutaneous T-Cell, see Mycosis
Breast Cancer	Fungoides and Sézary Syndrome
Breast Cancer, Childhood	Lymphoma, Hodgkin’s, Adult
Breast Cancer, Male	Lymphoma, Hodgkin’s, Childhood
Bronchial Adenomas/Carcinoids, Childhood	Lymphoma, Hodgkin’s During Pregnancy
Burkitt’s Lymphoma	Lymphoma, Non-Hodgkin’s, Adult
Carcinoid Tumor, Childhood	Lymphoma, Non-Hodgkin’s, Childhood
Carcinoid Tumor, Gastrointestinal	Lymphoma, Non-Hodgkin’s During
Carcinoma of Unknown Primary	Pregnancy
Central Nervous System Lymphoma, Primary	Lymphoma, Primary Central Nervous System
Cerebellar Astrocytoma, Childhood	Macroglobulinemia, Waldenström’s
Cerebral Astrocytoma/Malignant	Malignant Fibrous Histiocytoma of Bone/Osteosarcoma
Glioma, Childhood	Medulloblastoma, Childhood
Cervical Cancer	Melanoma
Childhood Cancers	Melanoma, Intraocular (Eye)
Chronic Lymphocytic Leukemia	Merkel Cell Carcinoma
Chronic Myelogenous Leukemia	Mesothelioma, Adult Malignant
Chronic Myeloproliferative Disorders	Mesothelioma, Childhood
Colon Cancer	Metastatic Squamous Neck Cancer with
Colorectal Cancer, Childhood Cutaneous T-Cell Lymphoma, see Mycosis Fungoides and Sézary Syndrome	Occult Primary
Endometrial Cancer	Multiple Endocrine Neoplasia Syndrome, Childhood
Ependymoma, Childhood	Multiple Myeloma/Plasma Cell Neoplasm Mycosis Fungoides
Esophageal Cancer	Myelodysplastic Syndromes
Esophageal Cancer, Childhood	Myelodysplastic/Myeloproliferative Diseases
Ewing’s Family of Tumors	Myelogenous Leukemia, Chronic
Extracranial Germ Cell Tumor, Childhood	Myeloid Leukemia, Adult Acute
Extragonadal Germ Cell Tumor	Myeloid Leukemia, Childhood Acute
Extrahepatic Bile Duct Cancer	Myeloma, Multiple
Eye Cancer, Intraocular Melanoma	Myeloproliferative Disorders, Chronic
Eye Cancer, Retinoblastoma	Nasal Cavity and Paranasal Sinus Cancer
Gallbladder Cancer	Nasopharyngeal Cancer
Gastric (Stomach) Cancer	Nasopharyngeal Cancer, Childhood
Gastric (Stomach) Cancer, Childhood	Neuroblastoma
Gastrointestinal Carcinoid Tumor	Non-Hodgkin’s Lymphoma, Adult
Germ Cell Tumor, Extracranial, Childhood	Non-Hodgkin’s Lymphoma, Childhood
Germ Cell Tumor, Extragonadal	Non-Hodgkin’s Lymphoma During Pregnancy
Germ Cell Tumor, Ovarian	Non-Small Cell Lung Cancer
Gestational Trophoblastic Tumor	Oral Cancer, Childhood
Glioma, Adult	Oral Cavity Cancer, Lip and
Glioma, Childhood Brain Stem	Oropharyngeal Cancer
Glioma, Childhood Cerebral Astrocytoma	Osteosarcoma/Malignant Fibrous
Glioma, Childhood Visual Pathway and Hypothalamic	Histiocytoma of Bone
Skin Cancer (Melanoma)	Ovarian Cancer, Childhood
Skin Carcinoma, Merkel Cell	Ovarian Epithelial Cancer
Small Cell Lung Cancer	Ovarian Germ Cell Tumor
Small Intestine Cancer	Ovarian Low Malignant Potential Tumor
Soft Tissue Sarcoma, Adult	Pancreatic Cancer
Soft Tissue Sarcoma, Childhood	Pancreatic Cancer, Childhood
Squamous Cell Carcinoma, see Skin	Pancreatic Cancer, Islet Cell
Cancer (non-Melanoma)	Paranasal Sinus and Nasal Cavity Cancer
Squamous Neck Cancer with Occult	Parathyroid Cancer
Primary, Metastatic	Penile Cancer
Stomach (Gastric) Cancer	Pheochromocytoma
Stomach (Gastric) Cancer, Childhood	Pineoblastoma and Supratentorial Primitive
Supratentorial Primitive	Neuroectodermal Tumors, Childhood
Neuroectodermal Tumors, Childhood	Pituitary Tumor
T-Cell Lymphoma, Cutaneous, see Mycosis Fungoides and Sézary Syndrome	Plasma Cell Neoplasm/Multiple Myeloma
Testicular Cancer	Pleuropulmonary Blastoma
Thymoma, Childhood	Pregnancy and Breast Cancer
Thymoma and Thymic Carcinoma	Pregnancy and Hodgkin’s Lymphoma
Thyroid Cancer	Pregnancy and Non-Hodgkin’s Lymphoma
Thyroid Cancer, Childhood	Primary Central Nervous System Lymphoma Prostate Cancer
Transitional Cell Cancer of the Renal Pelvis and Ureter	Rectal Cancer
Trophoblastic Tumor, Gestational	Renal Cell (Kidney) Cancer
Unknown Primary Site, Carcinoma of, Adult	Renal Cell (Kidney) Cancer, Childhood
Unknown Primary Site, Cancer of, Childhood	Renal Pelvis and Ureter, Transitional Cell
Unusual Cancers of Childhood Ureter and Renal Pelvis, Transitional Cell Cancer	Cancer
Urethral Cancer	Retinoblastoma
Uterine Cancer, Endometrial	Rhabdomyosarcoma, Childhood
Uterine Sarcoma	Salivary Gland Cancer
Vaginal Cancer	Salivary Gland Cancer, Childhood
Visual Pathway and Hypothalamic Glioma, Childhood	Sarcoma, Ewing’s Family of Tumors
Vulvar Cancer	Sarcoma, Kaposi’s
Waldenström’s Macroglobulinemia Wilms’ Tumor	Sarcoma, Soft Tissue, Adult
	Sarcoma, Soft Tissue, Childhood
	Sarcoma, Uterine
	Sezary Syndrome
	Skin Cancer (non-Melanoma)
	Skin Cancer, Childhood

As used herein, the term “tumor” refers to all neoplastic cell growth and proliferation, whether malignant or benign, and all pre-cancerous and cancerous cells and tissues. For example, a particular cancer may be characterized by a solid mass tumor. The solid tumor mass, if present, may be a primary tumor mass. A primary tumor mass refers to a growth of cancer cells in a tissue resulting from the transformation of a normal cell of that tissue. In most cases, the primary tumor mass is identified by the presence of a cyst, which can be found through visual or palpation methods, or by irregularity in shape, texture or weight of the tissue. However, some primary tumors are not palpable and can be detected only through medical imaging techniques such as X-rays (e.g., mammography), or by needle aspirations. The use of these latter techniques is more common in early detection. Molecular and phenotypic analysis of cancer cells within a tissue will usually confirm if the cancer is endogenous to the tissue or if the lesion is due to metastasis from another site. The term “tumor” is inclusive of solid tumors and non-solid tumors.

In the case of cancers, positive clinical outcomes that may result from the methods of the invention that involve treatment include, but are not limited to, alleviation of one or more symptoms of the cancer, diminishment of extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state, remission (whether partial or total), whether detectable or undetectable, tumor regression, inhibition of tumor growth, inhibition of tumor metastasis, reduction in cancer cell number, inhibition of cancer cell infiltration into peripheral organs, improved time to disease progression (TTP), improved response rate (RR), prolonged overall survival (OS), prolonged time-to-next-treatment (TNTT), or prolonged time from first progression to next treatment, or a combination of two or more of the foregoing.

The terms “comprising”, “consisting of” and “consisting essentially of” are defined according to their standard meaning. The terms may be substituted for one another throughout the instant application in order to attach the specific meaning associated with each term.

The term “effective amount” also means an amount of the agent (e.g., MSC or compositions of the invention) that will elicit the desired biological response within a subject or from a target cancer cell, such as alleviation of one or more symptoms of cancer, or cancer cell lysing or induction of cancer cell apoptosis.

The terms “isolated” or “biologically pure” refer to material that is substantially or essentially free from components which normally accompany the material as it is found in its native state. Thus, MSCs in accordance with the invention preferably do not contain materials normally associated with the MSC in their in situ environment, i.e., are administered in an isolated or purified form. However, the MSCs may be administered to a subject in a non-isolated or non-purified form, e.g., as a tissue.

As used in this specification, the singular forms “a”, “an”, and “the” include plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to “a cell”, e.g., an MSC, includes more than one such cell. A reference to “a compound” includes more than one such compound, and so forth.

Mammalian species which benefit from the disclosed MSC, compositions, and methods include, but are not limited to, primates, such as apes, chimpanzees, orangutans, humans, monkeys; domesticated animals (e.g., pets) such as dogs, cats, guinea pigs, hamsters, Vietnamese pot-bellied pigs, rabbits, and ferrets; domesticated farm animals such as cows, buffalo, bison, horses, donkey, swine, sheep, and goats; exotic animals typically found in zoos, such as bear, lions, tigers, panthers, elephants, hippopotamus, rhinoceros, giraffes, antelopes, sloth, gazelles, zebras, wildebeests, prairie dogs, koala bears, kangaroo, opossums, raccoons, pandas, hyena, seals, sea lions, elephant seals, otters, porpoises, dolphins, and whales. Other species that may benefit from the disclosed methods include fish, amphibians, avians, and reptiles. As used herein, the terms “patient”, “subject”, and “individual” are used interchangeably and are intended to include such human and non-human species unless specified to be human or non-human.

Subjects in need of treatment using the methods of the present invention (e.g., having a cancer) can be identified using standard techniques known to those in the medical or veterinary professions, as appropriate. A subject having a cancer may be symptomatic or asymptomatic.

Optionally, the MSCs and compositions of the invention may be administered prophylactically to a subject without cancer, to prevent or delay the onset of cancer or its recurrence.

The practice of the present invention can employ, unless otherwise indicated, conventional techniques of molecular biology, microbiology, recombinant DNA technology, electrophysiology, and pharmacology that are within the skill of the art. Such techniques are explained fully in the literature (see, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989); DNA Cloning, Vols. I and II (D. N. Glover Ed. 1985); Perbal, B., A Practical Guide to Molecular Cloning (1984); the series, Methods In Enzymology (S. Colowick and N. Kaplan Eds., Academic Press, Inc.); Transcription and Translation (Hames et al. Eds. 1984); Gene Transfer Vectors For Mammalian Cells (J. H. Miller et al. Eds. (1987) Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.); Scopes, Protein Purification: Principles and Practice (2nd ed., Springer-Verlag); and PCR: A Practical Approach (McPherson et al. Eds. (1991) IRL Press)), each of which are incorporated herein by reference in their entirety.

All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.

Following are examples that illustrate procedures for practicing the invention. These examples should not be construed as limiting. All percentages are by weight and all solvent mixture proportions are by volume unless otherwise noted.

Example 1. MSCs Are Highly Susceptible to RSV Infection

RSV commonly infects the apical airway epithelial cells, but also may infect various immune cells of blood and bone marrow (17-19). An error in cell handling in the inventors’ lab led to the finding that human MSCs (hMSCs) are highly susceptible to RSV (FIG. 1). RSV readily and aggressively replicates in MSCs infecting ~90% of cells within 72 h p.i. (FIGS. 1 A-C). High expression levels of IFN-β and IDO were found in RSV-infected MSCs compared to mock (FIGS. 1D-E). Also, these cells exhibit expression of IL-1β, IL-6, IL-8, prostaglandin D2 (PGD2) and CXCR4, (not shown).

Example 2. IDO Deficient MSCs Are Equally Susceptible to RSV Infection

To examine the immunological consequences of RSV-infected MSCs, the inventors isolated fresh human peripheral blood mononuclear cells (PBMCs) and treated them with conditioned medium (CM) from MSCs. PBMCs were stained with 5,6-carboxyfluorescein diacetate succinimidyl ester (CFSE) and treated with CM collected from the MSC culture infected with RSV in the presence or absence of IDO inhibitors, 1-methyltryptophan (1-MT) and vitamin K₃. As expected, IDO secreted in the MSC culture supernatant inhibited lymphocyte proliferation (FIG. 2A) whereas treatment of RSV-infected MSCs with 1-MT or vitamin K₃ reduced kynurenine levels (FIG. 2C) and abolished the negative effect on PBMC proliferation measured by CFSE dye dilution by flow cytometry (FIG. 2A). However, 1-MT or vitamin K₃ treatment did not reduce RSV infection as determined by viral titers (FIG. 2B). The inventors also examined the susceptibility of wt and IDO knockout mice to RSV infection. RSV infected and replicated in wt and IDO knockout mice and there was no statistical difference in the numbers of PFUs or RSV nucleocapsid (RSVN) transcript (FIG. 2E) or IFN-β transcript (FIG. 2F) found in the lungs of wt versus IDO-knockout mice.

Example 3. CRISPR-Mediated Knockout of IDO Prevents Anti-Proliferative Effects of RSV-Infected MSCs but Retained Susceptibility to RSV Infection

As an alternative method to the use of IDO inhibitors, which may have off-target effects, the inventors utilized the CRISPR/Cas9 system to knockout the IDO gene from the hMSCs prior to infection with RSV. Two separate plasmids expressing different IDO-specific guide RNAs (LvA and LvB) as well as a control plasmid expressing a non-targeted scrambled guide RNA (LvS) (GeneCopoeia) were transfected individually into hMSCs. Expression of the plasmid was evident by fluorescent microscopy for mCherry (red) in cells (FIG. 3A). Similarly, infection with rgRSV was observed by GFP (green) fluorescence (FIG. 3A). Conditioned media from IDO-knockout and control hMSCs was used in to treat PBMCs during a CFSE proliferation assay, as described in FIG. 2A. Media from control hMSCs (LvS) resulted in a similar reduction in PBMC proliferation as had been seen in FIG. 2A, however PBMC treatment with media from each of the two IDO-knockout constructs (LvA and LvB) showed no RSV-associated reduction in proliferation (FIG. 3B), suggesting that these hMSCs lacked IDO expression. However, IDO-deficient hMSCs retained their susceptibility to RSV infection (FIG. 3C).

Example 4. IDO Inhibitor Does Not Affect hMSC Migration

To test the effect of 1-MT on the migratory capacity of hMSCs the inventors used a Boyden chamber invasion assay with Lewis lung carcinoma (LLC1) cells in the bottom chamber to produce trophic factors. MSCs were seeded on the top of a matrigel layer above a PET membrane with 8.0 µm pores (BD Bioscience) and treated with control MSC media or media containing 1MT. Cells were cocultured for 24 hours before fixation in 4% paraformaldehyde in PBS. Upper matrigel layer was removed by cue tip and migrant cells were visualized and counted by Giemsa staining. Results shown in FIG. 4 suggest that IDO inhibitor did not inhibit migration of hMSC towards LLC1 cells.

Example 5. RSV Infection in LLC1 Cells in Vitro and in Vivo

LLC1 cells were infected with 1 and 5 MOI of rA2-KL19F strain expressing a red fluorescent marker, mKate2 (14), and cells were examined using fluorescent microscope. Forty-eight hrs after infection, majority of cells were found to be infected with RSV (FIG. 5A). The inventors further examined the potential of conditioned medium of RSV-infected hMSCs (FIG. 2) to infect LLC1 tumoroids. LLC1 tumoroids were cultured in the presence of conditioned medium of rgRSV-infected MSCs for 90 mins and cells were examined 72 hrs after infection by confocal microscopy. Results show that LLC1 tumoroids were readily infected by rgRSV (FIG. 5B), suggesting the potential of this platform to screen oncolytic potential of genetically engineered RSV ex vivo. hMSCs are known to have tumor tropism. Further, tumor tropism of human MSCs to mouse tumors have been demonstrated before (20). Consistent with this, RSV-loaded hMSCs when administered intranasally or i.v. (FIG. 5D) homed to the lungs of tumor bearing (orthotopic LLC1 inoculated) C57BL/6 mouse (FIG. 5C). Moreover, RSV-loaded hMSCs when administered intranasally to LLC1 tumor bearing mice, hMSC survived and RSV replicated in the tumor cells (FIGS. 5E-F).

It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and the scope of the appended claims. In addition, any elements or limitations of any invention or embodiment thereof disclosed herein can be combined with any and/or all other elements or limitations (individually or in any combination) or any other invention or embodiment thereof disclosed herein, and all such combinations are contemplated with the scope of the invention without limitation thereto.

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