Patent Grant
11426460
The instant application contains a Sequence Listing which has been filed electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Mar. 28, 2019, is named 115872-0707_SL.txt and is 1,823 bytes in size.
The present invention relates generally to the fields of oncology, virology and immunotherapy. More particularly, it concerns the use of poxviruses, specifically inactivated modified vaccinia Ankara virus (“inactivated-MVA”) which is infection-competent but nonreplicative and which has been further modified for example by heat or ultraviolet light (UV) irradiation. This inactivated MVA can be used as an immunotherapeutic agent for the treatment of cancer either as monotherapy or as a combination therapy in combination with immune checkpoint blockade therapies.
Immune System and Cancer
Malignant tumors are inherently resistant to conventional therapies and present significant therapeutic challenges. Immunotherapy has become an evolving area of research and an additional option for the treatment of certain types of cancers. The immunotherapy approach rests on the rationale that the immune system may be stimulated to identify tumor cells, and target them for destruction.
Numerous studies support the importance of the differential presence of immune system components in cancer progression [1]. Clinical data suggest that high densities of tumor-infiltrating lymphocytes are linked to improved clinical outcome [2]. The correlation between a robust lymphocyte infiltration and patient survival has been reported in various types of cancer, including melanoma, ovarian, head and neck, breast, urothelial, colorectal, lung, hepatocellular, gallbladder, and esophageal cancer [3]. Tumor immune infiltrates include macrophages, dendritic cells (DC), mast cells, natural killer (NK) cells, naïve and memory lymphocytes, B cells and effector T cells (T lymphocytes), primarily responsible for the recognition of antigens expressed by tumor cells and subsequent destruction of the tumor cells by T cells.
Despite presentation of antigens by cancer cells and the presence of immune cells that could potentially react against tumor cells, in many cases the immune system does not get activated. Key to this phenomenon is the ability of tumors to protect themselves from immune response by coercing cells of the immune system to inhibit other cells of the immune system. For example, CD4+ T cells possess the ability to differentiate into T regulatory (Treg) cells, which have the ability to inhibit activated T cells. Additionally, cancer cells can impair CDS+ T cell effector function, leading to the evasion of anti-tumor immune response. Finally, the local immunosuppressive nature of the tumor microenvironment, along with immune editing, can lead to the escape of cancer cell subpopulations that do not express the target antigens. This, finding a method to that would allow for the preservation and/or restoration of anti-tumor activities of the immune system is of paramount importance.
It has been established that type I IFN plays important roles in host antitumor immunity [4]. IFNAR1-deficent mice are more susceptible to developing tumors after implantation of tumor cells. Spontaneous tumor-specific T cell priming is also defective in IFNAR1-deficient mice [5, 6]. More recent studies have shown that the cytosolic DNA-sensing pathway is important in the recognition of tumor-derived DNA by the innate immune system. In turn, this leads to the development of antitumor CD8+ T cell immunity [7]. This pathway also plays an important role in radiation-induced antitumor immunity [8].
Melanoma
Melanoma, one of the deadliest cancers, is the fastest growing cancer in the US and worldwide. Its incidence has increased by 50% among young Caucasian women since 1980, primarily due to excess sun exposure and the use of tanning beds. According to the American Cancer Society, approximately 76,380 people in the US will be diagnosed with melanoma and 10,130 people (or one person per hour) are expected to die of melanoma in 2016. In most cases, advanced melanoma is resistant to conventional therapies, including chemotherapy and radiation. As a result, people with metastatic melanoma have a very poor prognosis, with a life expectancy of only 6 to 10 months. The discovery that about 50% of melanomas have mutations in BRAF (a key tumor-promoting gene) opened the door for targeted therapy in this disease. Early clinical trials with BRAF inhibitors showed remarkable, but unfortunately not sustainable responses in patients with melanomas with BRAF mutations. Therefore, alternative treatment strategies for these patients, as well as patients with melanoma without BRAF mutations, are urgently needed.
Human pathological data indicate that the presence of T-cell infiltrates within melanoma lesions correlates positively with longer patient survival [9]. The importance of the immune system in protection against melanoma is further supported by partial success of immunotherapies, such as the immune activators IFN-α2b and IL-2 [10] as well as the unprecedented clinical responses of patients with metastatic melanoma to immune checkpoint blockade therapy, including anti-CTLA-4 and anti-PD-1/PD-L1 used either individually or in combination [11-17]. However, many patients fail to respond to immune checkpoint blockade therapy alone. The addition of virotherapy might overcome resistance to immune checkpoint blockade, which is supported by animal tumor models [18].
Poxviruses
Poxviruses, such as engineered vaccinia viruses, are in the forefront as oncolytic therapy for metastatic cancers [19]. Vaccinia viruses are large DNA viruses, which have a rapid life cycle [20]. Poxviruses are well suited as vectors to express multiple transgenes in cancer cells and thus to enhance therapeutic efficacy [21]. Preclinical studies and clinical trials have demonstrated efficacy of using oncolytic vaccinia viruses and other poxviruses for treatment of advanced cancers refractory to conventional therapy [22-24]. Poxvirus-based oncolytic therapy has the advantage of killing cancer cells through a combination of cell lysis, apoptosis, and necrosis. It also triggers the innate immune sensing pathway that facilitates the recruitment of immune cells to the tumors and the development of anti-tumor adaptive immune responses. The current oncolytic vaccinia strains in clinical trials (JX-594, for example) use wild-type vaccinia with deletion of thymidine kinase to enhance tumor selectivity, and with expression of transgenes such as granulocyte macrophage colony stimulating factor (GM-CSF) to stimulate immune responses [21]. Many studies have shown however that wild-type vaccinia has immune suppressive effects on antigen presenting cells (APCs) [25-28] and thus adds to the immunosuppressive and immunoevasive effects of the tumors themselves.
Poxviruses are extraordinarily adept at evading and antagonizing multiple innate immune signaling pathways by encoding proteins that interdict the extracellular and intracellular components of those pathways [29]. Modified vaccinia virus Ankara (MVA) is an attenuated vaccinia virus that was developed through serial passaging in chicken embryonic fibroblasts. MVA has a 31-kb deletion of the parental vaccinia genome and was used successfully as a vaccine during the WHO-sponsored smallpox eradication campaign [30-32]. MVA has been investigated intensively as a vaccine vector against HIV, tuberculosis, malaria, influenza, and coronavirus, as well as cancers [33-38].
MVA has deletions or truncations of several intracellular immunomodulatory genes including K1L, N1L, and A52R, which have been implicated in regulating innate immune responses [39-46]. On the other hand, MVA retains the E3L gene encoding a bifunctional Z-DNA/dsRNA binding protein, a key vaccinia virulence factor [47-55]. It has been shown that MVA infection of human monocyte-derived dendritic cells causes DC activation [56]. Waibler et al. [57] reported that MVA infection of murine Flt3L-DC triggered a TLR-independent type I IFN response. In addition, MVA infection of human macrophages triggers type I IFN and pro-inflammatory cytokines and chemokines via a TLR2/TLR6/MyD88 and MDAS/MAVS-dependent pathways [58].
The sensing of DNA in the cytosol triggers a cascade of events leading to the production of type I IFN and cytokines as well as cellular stress responses. STING (stimulator of IFN genes) was identified as an important adaptor for the cytosolic DNA-sensing pathway [59-61]. The nature of the DNA sensors remained elusive until the discovery of cyclic GMP-AMP synthase (cGAS) as the critical DNA sensor, and its product cyclic GMP-AMP, which contains an unanticipated 2′,5′ linkage at the GpA step and standard 3′,5′ linkage at the ApG step [62-68] Subsequent research confirmed STING as the key adaptor activated by cGAMP, thereby mediating the cascade of downstream events involving kinases and transcription factors that lead to the interferon response [66, 68, 69]. We reported that MVA infection of murine conventional dendritic cells induces type I IFN via a cytosolic DNA-sensing pathway mediated by cytosolic DNA sensor cGAS, its adaptor STING, and transcription factors IRF3 and IRF7. By contrast, wild-type vaccinia virus fails to activate this pathway. Intravenous inoculation of MVA via tail-vein injection induced type I IFN secretion in WT mice, which was diminished in STING or IRF3-deficient mice [70]. Furthermore, we showed that vaccinia virulence factors E3 and N1 play inhibitory roles in the cytosolic DNA-sensing pathway [70].
In one aspect, the present disclosure provides a method for treating a subject afflicted with one or more solid malignant tumors, the method comprising delivering to cells of the tumor inactivated modified vaccinia Ankara (inactivated MVA) and thereby treating the tumor.
In another aspect, a method is provided for treating a solid malignant tumor in a subject comprising delivering to tumor cells of the subject an amount of inactivated-MVA effective to induce the immune system of the subject to mount an immune response against the tumor.
In yet another aspect, the disclosure provides a method for treating a malignant tumor in a subject, the method comprising a combination of delivering to tumor cells of the subject inactivated-MVA in an amount effective to induce the immune system of the subject to mount an immune response against the tumor and conjointly administering to the subject a second amount of an immune checkpoint blocking agent effective to block an immune checkpoint expressed by the tumor, thereby treating the tumor. As used herein, “delivering” means “administering;” the former is mostly used in connection with inactivated MVA, the latter in connection with immune checkpoint blocking agents.
It will be understood that unless stated explicitly to the contrary, the embodiments described below shall pertain to each of the foregoing aspects and that features of further or more specific embodiments may be presented individually within a particular aspect or one or more of them may be combined.
In some embodiments, the amount of inactivated MVA is effective to accomplish one or more of the following:
In some embodiments, the treated tumor includes tumor located at the site of inactivated MVA delivery, or tumor located both at said site and elsewhere in the body of the subject. In other words, the effect of MVA delivery is systemic even though the inactivated MVA may be delivered to only one or only a plurality of solid tumors of the subject.
In more specific embodiments, the immune response comprises on or more of the following:
In some embodiments, the tumor is primary or metastatic melanoma or primary or metastatic colon carcinoma.
In some embodiments, the subject is a human.
In some embodiments, the delivery of the inactivated MVA is repeated in spaced apart time intervals; in more specific embodiments, the repeated delivery continues for several weeks, months or years or indefinitely as long as benefits persist or a maximum tolerated dose is reached; in further embodiments, the delivery of inactivated MVA is repeated with a frequency within the range from once per month to two times per week; in some more specific embodiments, the delivery is repeated once weekly.
In some embodiments, delivery of the inactivated MVA is by parenteral route; in more specific embodiments by intratumor injection or intravenous injection.
In some embodiments, the inactivated-MVA is delivered at a dosage per administration within the range of about 105-1010 plaque-forming units (pfu); in more specific embodiments, it is delivered at a dosage per administration within the range of about 106 to about 109 plaque-forming units (pfu).
In some embodiments, the inactivated MVA is UV-inactivated MVA; in other embodiments, it is heat-inactivated MVA; in yet other embodiments, a combination of heat- and UV-inactivated MVA.
In some embodiments, the induction and activation of effector T cells is accompanied by a reduction of regulatory CD4+ cells in said tumor; in some embodiments, the inactivated-MVA induces maturation of dendritic cells infiltrating said tumor through induction of type I IFN; in some embodiments, the inactivated MVA induces the expression of MEW Class I and the induction of one or more of type I interferon and other inflammatory cytokines and chemokines in infected tumor cells.
In some embodiments, the induced immune response effects or contributes to one or more of the following: reduction of the size of the tumor, eradication of the tumor, inhibition of tumor or metastatic growth. Again, the tumor is not confined to the tumor injected with inactivated MVA.
Specific embodiments within the third aspect mentioned above include the foregoing and additional ones as follows:
In some embodiments, the delivery of the inactivated MVA is by intratumoral injection and the administration of the immune checkpoint blocking agents by intravenous route; in other embodiments, both the delivery and the administration are by intravenous route; in yet other embodiments, both the delivery and the administration are by intratumoral injection. In some embodiments, the immune checkpoint blocking agent is selected from the group consisting of anti-PD-1 inhibitors, PD-L1, inhibitors and CTLA4 inhibitors, which in specific embodiments are antibodies
In some embodiments, the inactivated MVA is delivered and the immune checkpoint blocking agents administered each according to its own administration schedule of spaced apart intervals. In some embodiments, the delivery and administration occur in parallel during the same overall period of time.
In some embodiments, a first dose of the inactivated MVA is delivered first and after a lapse of time, for example a week, a first dose of the immune checkpoint blocking agent is administered. In some embodiments, one or both of the inactivated MVA and the immune checkpoint blocking agent are respectively delivered and administered during a period of time of several weeks, months or years, or indefinitely as long as benefits persist and a maximum tolerated dose is not reached.
In some embodiments, the immune checkpoint blocking agent and the inactivated MVA are administered simultaneously; in some embodiments, they are administered in the same composition; in some embodiments, they are both delivered intratumorally. In some embodiments, simultaneous delivery permits a lower dose of the immune check point blocking agent to be employed and the combined effect of the two active agents can be synergistic.
Any feature or combination of features of any embodiment or chosen among multiple embodiments that is or are disclosed may be excluded.
Definitions:
As used herein the following terms shall have the meanings ascribed to them below unless the context clearly indicates otherwise:
“Cancer” refers to a class of diseases of humans and animals characterized by uncontrolled cellular growth. Unless otherwise explicitly indicated, the term “cancer” may be used herein interchangeably with the terms “tumor,” (which in turn includes both primary and metastatic tumors) “malignancy,” “hyperproliferation” and “neoplasm(s);” the term “cancer cell(s)” is interchangeable with the terms “tumor cell(s),” “malignant cell(s),” “hyperproliferative cell(s),” and “neoplastic cell(s)”.
“Melanoma” refers to a malignant neoplasm originating from cells that are capable of producing melanin. The term melanoma is synonymous with “malignant melanoma”. Melanoma metastasizes widely, involving a patient's lymph nodes, skin, liver, lungs and brain tissues.
“Solid tumor” refers to all neoplastic cell growth and proliferation, primary or metastatic, and all pre-cancerous and cancerous cells and tissues, except for hematologic cancers such as lymphomas, leukemias and multiple myeloma. Examples of solid tumors include, but are not limited to: fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms' tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, melanoma, neuroblastoma, and retinoblastoma. Some of the most common solid tumors for which the compositions and methods of the present disclosure would be useful include: head-and-neck cancer, rectal adenocarcinoma, glioma, medulloblastoma, urothelial carcinoma, pancreatic adenocarcinoma, endometrial cancer, ovarian cancer, prostate adenocarcinoma, non-small cell lung cancer (squamous and adenocarcinoma), small cell lung cancer, melanoma, breast carcinoma, renal cell carcinoma, and hepatocellular carcinoma.
“Metastasis” refers to the spread of cancer from its primary site to neighboring tissues or distal locations in the body. Cancer cells can break away from a primary tumor, penetrate into lymphatic and blood vessels, circulate through the bloodstream, and grow in in normal tissues elsewhere in the body. Metastasis is a sequential process, contingent on tumor cells (or cancer stem cells) breaking off from the primary tumor, traveling through the bloodstream or lymphatics, and stopping at a distant site. Once at another site, cancer cells re-penetrate through the blood vessels or lymphatic walls, continue to multiply, and eventually form a new tumor (metastatic tumor). In some embodiments, this new tumor is referred to as a metastatic (or secondary) tumor.
“Immune response” refers to the action of one or more of lymphocytes, antigen presenting cells, phagocytic cells, granulocytes, and soluble macromolecules produced by the above cells or the liver (including antibodies, cytokines, and complement) that results in selective damage to, destruction of, or elimination from the human body of cancerous cells, metastatic tumor cells, etc. An immune response may include a cellular response, such as a T cell response that is an alteration (modulation, e.g., significant enhancement, stimulation, activation, impairment, or inhibition) of cellular function, i.e., a T cell function. A T cell response may include generation, proliferation or expansion, or stimulation of a particular type of T cell, or subset of T cells, for example, effector CD4+, cytotoxic CD8+, or natural killer (NK) cells. Such T cell subsets may be identified by detecting one or more cell receptors or cell surface molecules (e.g., CD or cluster of differentiation molecules). A T cell response may also include altered expression (statistically significant increase or decrease) of a cellular factor, such as a soluble mediator (e.g., a cytokine, lymphokine, cytokine binding protein, or interleukin) that influences the differentiation or proliferation of other cells. For example, Type I interferon (IFN-α/β) is a critical regulator of the innate immunity [71]. Animal and human studies have shown a role for IFN-α/β in directly influencing the fate of both CD4+ and CD8+T cells during the initial phases of antigen recognition anti-tumor immune response. Type I IFN is induced in response to activation of dendritic cells, in turn a sentinel of the innate immune system.
“Tumor immunity” refers to the process by which tumors evade recognition and clearance by the immune system. Thus, as a therapeutic concept, tumor immunity is “treated” when such evasion is attenuated or eliminated, and the tumors are recognized and attacked by the immune system. An example of tumor recognition is tumor binding, and examples of tumor attack are tumor reduction (in number, size or both) and tumor clearance.
“T cell” refers to a thymus derived lymphocyte that participates in a variety of cell-mediated adaptive immune reactions.
“Helper T cell” refers to a CD4+ T cell; helper T cells recognize antigen bound to MHC Class II molecules. There are at least two types of helper T cells, Th1 and Th2, which produce different cytokines.
“Cytotoxic T cell” refers to a T cell that usually bears CD8 molecular markers on its surface (CD8+) and that functions in cell-mediated immunity by destroying a target cell having a specific antigenic molecule on its surface. Cytotoxic T cells also release Granzyme, a serine protease that can enter target cells via the perforin-formed pore and induce apoptosis (cell death). Granzyme serves as a marker of Cytotoxic phenotype. Other names for cytotoxic T cell include CTL, cytolytic T cell, cytolytic T lymphocyte, killer T cell, or killer T lymphocyte. Targets of cytotoxic T cells may include virus-infected cells, cells infected with bacterial or protozoal parasites, or cancer cells. Most cytotoxic T cells have the protein CD8 present on their cell surfaces. CD8 is attracted to portions of the Class I MHC molecule. Typically, a cytotoxic T cell is a CD8+ cell.
“Tumor-infiltrating lymphocytes” refers to white blood cells of a subject afflicted with a cancer (such as melanoma), that are resident in or otherwise have left the circulation (blood or lymphatic fluid) and have migrated into a tumor.
“Immune checkpoint inhibitor(s)” or “immune checkpoint blocking agent” refers to molecules that completely or partially reduce, inhibit, interfere with or modulate the activity of one or more checkpoint proteins. Checkpoint proteins regulate T-cell activation or function. Checkpoint proteins include, but are not limited to CTLA-4 and its ligands CD80 and CD86; PD-1 and its ligands PDL1 and PDL2; LAG3, B7-H3, B7-H4, TIM3, ICOS, and BTLA [72].
“Parenteral” when used in the context of administration of a therapeutic substance includes any route of administration other than administration through the alimentary tract. Particularly relevant for the methods disclosed herein are intravenous (including for example through the hepatic portal vein), intratumoral or intrathecal administration.
“Antibody” refers to an immunoglobulin molecule which specifically binds to an antigen or to an antigen-binding fragment of such a molecule. Thus, antibodies can be intact immunoglobulins derived from natural sources or from recombinant sources and can be immunoreactive (antigen-binding) fragments or portions of intact immunoglobulins. The antibodies may exist in a variety of forms including, for example, polyclonal antibodies, monoclonal antibodies, Fv, Fab and F(ab)2, as well as single chain antibodies (scFv) humanized antibodies, chimeric antibodies, human recombinant antibodies and bi- and tri-specific antibodies.
“Oncolytic virus” refers to a virus that preferentially infects cancer cells, replicates in such cells, and induces lysis of the cancer cells through its replication process. Nonlimiting examples of naturally occurring oncolytic viruses include vesicular stomatitis virus, reovirus, as well as viruses engineered to be oncoselective such as adenovirus, Newcastle disease virus and herpes simplex virus [19, 73-75]. Vaccinia virus infects many types of cells but replicates preferentially in tumor cells due to the fact that tumor cells have a metabolism that favors replication, exhibit activation of certain pathways that also favor replication and create an environment that evades the innate immune system, which also favors viral replication. Heat-inactivated MVA does not fit the definition of oncolytic virus.
“MVA” means “modified vaccinia Ankara” and refers to a highly attenuated strain of vaccinia derived from the Ankara strain and developed for use as a vaccine and vaccine adjuvant. The original MVA was isolated from the wild-type Ankara strain by successive passage through chicken embryonic cells. Treated thus, it lost about 15% of the genome of wild-type vaccinia including its ability to replicate efficiently in primate (including human) cells [76]. The smallpox vaccination strain MVA: marker, genetic structure, experience gained with the parenteral vaccination and behavior in organisms with a debilitated defense mechanism. MVA is considered an appropriate candidate for development as a recombinant vector for gene or vaccination delivery against infectious diseases or tumors [77]. MVA has a genome of 178 kb in length and a sequence first disclosed in Antoine, G et al [78]. Sequences are also disclosed in Genbank U94848.1. Clinical grade MVA is commercially and publicly available from Bavarian Nordic A/S Kvistgaard, Denmark. Additionally, MVA is available from ATCC, Rockville, Md. and from CMCN (Institut Pasteur Collection Nationale des Microorganismes) Paris, France. Mutant MVA E3L knockout (ΔE3L-MVA) and its preparation have been described for example in U.S. Pat. No. 7,049,145.
“Heat-inactivated MVA” or “heat MVA” means MVA which has been further treated by exposure to heat under conditions that do not destroy its immunogenicity or its ability to enter target cells (tumor cells) but remove residual replication ability of the virus as well as factors that inhibit the host's immune response (for example, such factors as inhibit the induction of IFN Type I in infected cells). An example of such conditions is exposure to a temperature within the range of about 50 to about 60° C. for a period of time of about an hour. Other times and temperatures can be determined with routine experimentation and IFN Type I induction in infected cDC's can be compared to the Heat-MVA used in experiments described herein and should be higher than that of MVA. In one experiment conducted by the present inventors, infection of cDCs by MVA treated with a combination of 65° C. and 1-hour exposure failed to induce IFN Type I. This combination of safety and strong immunogenicity makes Heat-MVA particularly attractive compared to WT vaccinia and even MVA.
“UV-inactivated MVA” or “UV-MVA” means MVA that has been inactivated by exposure to UV under conditions that do not destroy its immunogenicity or its ability to enter target cells (tumor cells) but remove residual replication ability of the virus. An example of such conditions, which can be useful in the present methods, is exposure to UV using for example a 365 nm UV bulb for a period of about 30 min to about 1 hour [56, 79]. Again, as explained for Heat-MVA above, the limits of these conditions of UV wavelength and exposure can be determined by routine experimentation by determining Type I IFN induced by UV-MVA having received a given exposure and comparing it to the Type I IFN induced by UV-MVA used in the experiments below and to untreated MVA. UV-MVA is similarly safe to Heat-MVA and also induces significant Type I IFN.
Accordingly, “inactivated MVA” shall be used as a generic term comprising heat-inactivated MVA and UV-inactivated MVA which are infective, nonreplicative and do not suppress IFN Type I production in infected DC cells. MVA inactivated by a combination of heat and UV radiation is also within the scope of the present disclosure.
“Subject” means any animal (mammalian, human or other) patient that can be afflicted with cancer.
“Therapeutically effective amount” or “effective amount” refers to a sufficient amount of an agent when administered at one or more dosages and for a period of time sufficient to provide a desired biological result in alleviating, curing or palliating a disease. In the present disclosure, an effective amount of the inactivated-MVA is an amount that (administered for a suitable period of time and at a suitable frequency) reduces the number of cancer cells; or reduces the tumor size or eradicates the tumor; or inhibits (i.e., slows down or stops) cancer cell infiltration into peripheral organs; inhibits (i.e., slows down or stops) metastatic growth; inhibits (i.e., stabilizes or arrests) tumor growth; allows for treatment of the tumor, and/or induces an immune response against the tumor. An appropriate therapeutic amount in any individual case may be determined by one of ordinary skill in the art using routine experimentation in light of the present disclosure. Such determination will begin with amounts found effective in vitro and amounts found effective in animals. The therapeutically effective amount will be initially determined based on the concentration or concentrations found to confer a benefit to cells in culture. Effective amounts can be extrapolated from data within the cell culture and can be adjusted up or down based on factors such as detailed herein. An example of an effective amount range is from 105 viral particles to about 1012 viral particles per administration.
With particular reference to the viral-based immunostimulatory agents disclosed herein, “therapeutically effective amount” or “effective amount” refers to an amount of a composition comprising inactivated MVA sufficient to reduce, inhibit, or abrogate tumor cell growth, thereby reducing or eliminating the tumor, or sufficient to inhibit, reduce or abrogate metastatic spread either in vitro or in a subject or to elicit an immune response against the tumor that will eventually result in one or more of reduction, inhibition and/or abrogation as the case may be. The reduction, inhibition, or eradication of tumor cell growth may be the result of necrosis, apoptosis, or an immune response or a combination of two or more of the foregoing. The amount that is therapeutically effective may vary depending on such factors as the particular inactivated MVA used in the composition, the age and condition of the subject being treated, the extent of tumor formation, the presence or absence of other therapeutic modalities, and the like. Similarly, the dosage of the composition to be administered and the frequency of its administration will depend on a variety of factors, such as the potency of the active ingredient, the duration of its activity once administered, the route of administration, the size, age, sex and physical condition of the subject, the risk of adverse reactions and the judgment of the medical practitioner. The compositions are administered in a variety of dosage forms, such injectable solutions.
With particular reference to combination therapy with an immune checkpoint inhibitor, “therapeutically effective amount” for an immune checkpoint blocking agent” shall mean an amount of an immune checkpoint blocking agent sufficient to block an immune checkpoint from averting apoptosis response in tumor cells of the subject being treated. There are several immune checkpoint blocking agents approved, in clinical trials or still otherwise under development including CD28 inhibitors such as CTL4 inhibitors (e.g., ipilimumab), PD-1 inhibitors (e.g., nivolumab, pembrolizumab, pidilizumab, lambrolizumab) PD-L1 inhibitors (MPDL3280A, BMS-936559, MEDI4736, MSB 00107180) ICOS and BTLA or decoy molecules of them. Dosage ranges of the foregoing are known in or readily within the skill in the art as several dosing clinical trials have been completed, making extrapolation to other agents possible.
Preferably, the tumor expresses the particular checkpoint but this is not strictly necessary as immune checkpoint blocking agents block more generally immune suppressive mechanisms within the tumors, elicited by tumor cells, stromal cell, and tumor infiltrating immune cells.
For example, the CTLA4 inhibitor ipilimumab, when administered as adjuvant therapy after surgery in melanoma is administered at 1-2 mg/mL over 90 minutes for a total infusion amount of 3 mg/kg every three weeks for a total of 4 doses. This therapy is often accompanied by severe even life-threatening immune-mediated adverse reactions, which limits the tolerated dose as well as the cumulative amount that can be administered. It is anticipated that it will be possible to reduce the dose and/or cumulative amount of ipilimumab when it is administered conjointly with inactivated MVA. In particular, in light of the experimental results set forth below, it is anticipated that it will be further possible to reduce the CTLA4 inhibitor's dose if it is administered directly to the tumor simultaneously or sequentially with inactivated MVA. Accordingly, the amounts provided above for ipilimumab will be a starting point for determining the particular dosage and cumulative amount to be given to a patient in conjoint administration but dosing studies will be required to determine optimum amounts.
Pembrolizumab is prescribed for administration as adjuvant therapy in melanoma diluted to 25 mg/mL is administered at a dosage of 2 mg/kg over 30 minutes every three weeks.
Nivolumab is prescribed for administration at 3 mg/kg as an intravenous infusion over 60 minutes every two weeks.
“Pharmaceutically acceptable excipient” includes pharmaceutically acceptable carriers or diluents, such as any and all solvents, dispersion media, coatings, isotonic and absorption delaying agents and the like. It also includes preservatives and antibacterial and antifungal agents. The use of such media and agents for biologically active substances is well known in the art. Further details of excipients are provided below.
“Delivering” used in connection with depositing the inactivated-MVA of the present disclosure in the tumor microenvironment whether this is done by local administration to the tumor or by systemic administration, for example intravenous route. The term focuses on inactivated-MVA that reaches the tumor itself.
“Conjoint administration” herein refers to administration of a second therapeutic modality in combination with inactivated MVA for example an immune checkpoint blocking agent administered and in close temporal proximity with the inactivated MVA. For example, a PD-1/PDL-1 inhibitor and/or a CTLA4 inhibitor (in more specific embodiments, an antibody) can be administered simultaneously with the heat-inactivated MVA (by intravenous or intratumoral injection when the inactivated-MVA is administered intratumorally or systemically as stated above) or before or after the inactivated-MVA administration. If the inactivated MVA administration and the immune checkpoint blocking agent are administered 1-7 days apart or even up to three weeks apart, this would be within “close temporal proximity” as stated herein.
In one embodiment, the present disclosure relates to a method for eliciting an antitumor immune response in subjects with tumors comprising delivering to the tumor an amount of inactivated MVA effective to bring about one or more of the following:
increase cytotoxic CD8+ T cells within the tumor and/or in tumor-draining lymph nodes;
induce maturation of dendritic cells infiltrating said tumor through induction of type I IFN;
induce effector T cells in the subject recognizing tumor cells within the tumor and/or in tumor draining lymph nodes;
reduce immune suppressive (regulatory) CD4+ T cells within the tumor; and
induce cells of the tumor to express MHC Class I on their surface and to produce one or more of Type I IFN or other inflammatory cytokines or chemokines.
The present inventors have explored the mechanism of the immune response and concluded that it is initiated by the cytosolic DNA-sensing pathway mediated by cGAS/STING which mediates production of Type 1 IFN. Further insights into the mechanism and the immune cells that are recruited are provided in the Examples. The conclusions presented therein are not confined to the specific experimental milieu where these mechanisms are being elucidated.
In one embodiment, the present disclosure provides a method of treating a subject diagnosed with a solid tumor comprising delivering to the tumor a therapeutic effective amount of the Heat-MVA described herein.
In one embodiment, the present disclosure provides a method for inducing anti-tumor immunity in a subject diagnosed with cancer comprising administering to the subject a therapeutically effective amount of inactivated MVA. The methods of the present disclosure include induction of anti-tumor immunity that can reduce the size of the tumor, eradicate the tumor, inhibit growth of the tumor, or inhibit metastasis or metastatic growth of the tumor.
In another embodiment, the present disclosure provides a method for enhancing, stimulating, or eliciting, in a subject diagnosed with a solid malignant tumor, an anti-tumor immune response that may include an innate immune response and/or an adaptive immune response such as a T cell response by exposing the tumor to inactivated MVA in a therapeutically effective amount.
In specific embodiments, the present disclosure provides methods of eliciting an immune response that mediates adaptive immune responses both in terms of T-cell cytotoxicity directed against tumor cells and in terms of eliciting T helper cells also directed against tumor cells. The methods comprise administering to a subject intratumorally or intravenously a composition comprising a nonreplicative heat- or UV-inactivated MVA wherein administration of said composition results in a tumor-specific immune response against the tumor and, eventually, in reduction, inhibition or abrogation of tumor growth and/or in inhibition of metastatic growth. Indeed, the present inventors have shown that cancer cells are being killed and that the immune response can migrate to remote locations, as would be the case with metastases.
In some embodiments, the present disclosure provides methods of eliciting an immune response that mediates adaptive immune responses both in terms of T-cell cytotoxicity directed against tumor cells and in terms of eliciting T helper cells also directed against tumor cells. The methods comprise administering to a subject parenterally a composition comprising an inactivated-MVA wherein administration of said composition results in a tumor-specific immune response against the tumor and, eventually, in reduction, inhibition or eradication of tumor growth and/or in inhibition of metastatic growth. Indeed, the present inventors have shown that cancer cells are being killed and that the immune response can migrate to remote locations, as would be the case with metastases.
Because inactivated MVA is not replication competent, it does not exert its effect on the immune system the same way as replication competent vaccines or vectors. Thus, while it is believed that stimulation of the immune system is a barrier to efficacy for oncolysis [19], inactivated MVA is able to harness the innate immune system to stimulate adaptive immunity, both in terms of cytotoxicity and more broadly of T effector cell activation against the tumor.
The present disclosure thus provides a method for treating a solid malignant tumor, delivering to a tumor of the subject an amount of inactivated-MVA effective to bring an increase of cytotoxic CD8+ cells and reduction of regulatory CD4+ cells in the tumor and inducing an immune response in a subject diagnosed with solid tumor.
The present disclosure also provides a method for generating antitumor systemic immunity by treating a solid malignant tumor, comprising delivering to a tumor of the subject an amount of inactivated-MVA effective to bring about a considerable even dramatic increase in immune cells in the non-injected tumors, including CD103+ DCs, cytotoxic CD8+ cells and CD4+ effector cells, and thereby causing one or both of rejection of non-injected tumors in said subject and resistance to tumor metastasis (which the present inventors test by tumor rechallenge).
Modified Vaccinia Ankara (MVA)
Modified Vaccinia Ankara (MVA) virus is a member of the genera Orthopoxvirus in the family of Poxviridae. MVA was generated by approximately 570 serial passages on chicken embryo fibroblasts (CEF) of the Ankara strain of vaccinia virus (CVA) [80]. As a consequence of these long-term passages, the resulting MVA virus contains extensive genome deletions and is highly host cell restricted to avian cells [30]. It was shown in a variety of animal models that the resulting MVA is significantly avirulent [76].
The safety and immunogenicity of MVA has been extensively tested and documented in clinical trials, particularly against the human smallpox disease. These studies included over 120,000 individuals and have demonstrated excellent efficacy and safety in humans. Moreover, compared to other vaccinia based vaccines, MVA has weakened virulence (infectiousness) while it triggers a good specific immune response. Thus, MVA has been established as a safe vaccine vector, with the ability to induce a specific immune response.
Due to above mentioned characteristics, MVA became an attractive target for to the development of engineered MVA vectors, used for recombinant gene expression and vaccines. As a vaccine vector, MVA has been investigated against numerous pathological conditions, including HIV, tuberculosis and malaria, as well as cancer [33, 34].
It has been demonstrated that MVA infection of human monocyte-derived dendritic cells (DC) causes DC activation, characterized by the upregulation of co-stimulatory molecules and secretion of proinflammatory cytokines [56]. In this respect, MVA differs from standard wild type Vaccinia virus (WT-VAC), which fails to activate DCs. Dendritic cells can be classified into two main subtypes: conventional dendritic cells (cDCs) and plasmacytoid dendritic cells (pDCs). The former, especially the CD8+ subtype, are particularly adapted to presenting antigens to T cells; the latter are strong producers of Type I IFN.
Viral infection of human cells results in activation of an innate immune response (the first line of defense) mediated by type I interferons, notably interferon-alpha (α). This normally leads to activation of an immunological “cascade,” with recruitment and proliferation of activated T cells (both CTL and helper) and eventually with antibody production. However, viruses express factors that dampen immune responses of the host. MVA is a better immunogen than WT-VAC and replicates poorly in mammalian cells [81].
However, it is not entirely nonreplicative and, as the present inventors show, contains some immunosuppressive activity.
Immune Response
In addition to induction of the immune response by up-regulation of particular immune system activities (such as antibody and/or cytokine production, or activation of cell mediated immunity), immune responses may also include suppression, attenuation, or any other down-regulation of detectable immunity, so as to reestablish homeostasis and prevent excessive damage to the host's own organs and tissues. In some embodiments, an immune response that is induced according to the methods of the present disclosure generates cytotoxic CD8+ T cells or activated T helper cells or both that can bring about directly or indirectly the death, or loss of the ability to propagate, of a tumor cell.
Induction of an immune response by the methods of the present disclosure may be determined by detecting any of a variety of well-known immunological parameters [82, 83]. Induction of an immune response may therefore be established by any of a number of well-known assays, including immunological assays, Such assays include, but need not be limited to, in vivo, ex vivo, or in vitro determination of soluble immunoglobulins or antibodies; soluble mediators such as cytokines, chemokines, hormones, growth factors and the like as well as other soluble small peptides, carbohydrate, nucleotide and/or lipid mediators; cellular activation state changes as determined by altered functional or structural properties of cells of the immune system, for example cell proliferation, altered motility, altered intracellular cation gradient or concentration (such as calcium); phosphorylation or dephosphorylation of cellular polypeptides; induction of specialized activities such as specific gene expression or cytolytic behavior; cellular differentiation by cells of the immune system, including altered surface antigen expression profiles, or the onset of apoptosis (programmed cell death); or any other criterion by which the presence of an immune response may be detected. For example, cell surface markers that distinguish immune cell types may be detected by specific antibodies that bind to CD4+, CD8+, or NK cells. Other markers and cellular components that can be detected include but are not limited to interferon γ (IFN-γ), tumor necrosis factor (TNF), IFN-α, IFN-β, IL-6, and CCL5. Common methods for detecting the immune response include, but are not limited to flow cytometry, ELISA, immunohistochemistry. Procedures for performing these and similar assays are widely known and may be found, for example in Letkovits (Immunology Methods Manual: The Comprehensive Sourcebook of Techniques, Current Protocols in Immunology, 1998).
Pharmaceutical Compositions and Preparations
Pharmaceutical compositions comprising inactivated-MVA may contain one or more pharmaceutically acceptable excipients, such as a carrier or diluent. These are ingredients which do not interfere with activity or effectiveness of the vaccine components of the present disclosure and that are not toxic A carrier or diluent can be a solvent or dispersion medium containing, for example, water, dextrose solution, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), serum albumin, Ringer's solution, suitable mixtures thereof, and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants and/or wetting agents such as sodium lauryl sulfate or ethanol. The prevention of the action of microorganisms can be effected by various preservatives, antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, benzalcomium chloride, benzethonium chloride and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars like mannitol sorbitol, lactose or sodium or potassium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.
Pharmaceutical compositions and preparations comprising inactivated-MVA may be manufactured by means of conventional mixing, dissolving, emulsifying, or lyophilizing processes. Pharmaceutical viral compositions may be formulated in conventional manner using one or more physiologically acceptable carriers, diluents, excipients or auxiliaries that facilitate formulating virus preparations suitable for in vitro, in vivo, or ex vivo use. The compositions can be combined with one or more additional biologically active agents (for example parallel administration of GM-CSF) and may be formulated with a pharmaceutically acceptable carrier, diluent or excipient to generate pharmaceutical (including biologic) or veterinary compositions of the instant disclosure suitable for parenteral or intra-tumoral administration.
Many types of formulation are possible and well-known. The particular type chosen is dependent upon the route of administration chosen, as is well-recognized in the art. For example, systemic formulations will generally be designed for administration by injection, e.g., intravenous, as well as those designed for intratumoral administration Preferably, the systemic or intratumoral formulation is sterile.
Sterile injectable solutions are prepared by incorporating inactivated-MVA in the required amount of the appropriate solvent with various other ingredients enumerated herein, as required, followed by suitable sterilization means. Generally, dispersions are prepared by incorporating the active ingredients into a sterile vehicle that contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying techniques, which yield a powder of the inactive-MVA plus any additional desired ingredient from a previously sterile-filtered solution thereof.
In some embodiments, the inactivated-MVA compositions of the present disclosure may be formulated in aqueous solutions, or in physiologically compatible solutions or buffers such as Hanks's solution, Ringer's solution, mannitol solutions or physiological saline buffer. In certain embodiments, any of the inactivated-MVA compositions may contain formulator agents, such as suspending, stabilizing penetrating or dispersing agents, buffers, lyoprotectants or preservatives such as polyethylene glycol, polysorbate 80, 1-dodecylhexahydro-2H-azepin-2-one (laurocapran), oleic acid, sodium citrate, Tris HCl, dextrose, propylene glycol, mannitol , polysorbate polyethylenesorbitan monolaurate (Tween®-20), isopropyl myristate, benzyl alcohol, isopropyl alcohol, ethanol sucrose, trehalose and other such generally known in the art may be used in any of the compositions of the instant disclosure [84].
The biologic or pharmaceutical compositions of the present disclosure can be formulated to allow the virus contained therein to be available to infect tumor cells upon administration of the composition to a subject. The level of virus in serum, tumors, and if desired other tissues after administration can be monitored by various well-established techniques, such as antibody-based assays (e.g., ELISA, immunohistochemistry, etc.).
Dosage of Inactivated-MVA
In general, the subject is administered a dosage of inactivated-MVA in the range of about 105 to about 1010 plaque forming units (pfu), although a lower or higher dose may be administered as will be determined by a person of ordinary skill. In a preferred embodiment, dosage is about 106-109 pfu. This dosage can be formulated in unit dosage forms of about 1 to about 10 ml. The equivalence of pfu to virus particles can differ according to the specific pfu titration method used. Generally, pfu is equal to about 5 to 100 virus particles. A therapeutically effective amount of inactivated-MVA can be administered in one or more divided doses for a prescribed period of time and at a prescribed frequency of administration. For example, therapeutically effective amount of inactivated MVA in accordance with the present disclosure may vary according to factors such as the disease state, age, sex, weight, and general condition of the subject, the size of the tumor, the ability of inactivated-MVA to elicit a desired immunological response to a degree sufficient to combat the tumor in the particular subject and the ability of the immune system of the subject to mount such a response.
As is apparent to persons working in the field of cancer therapy, variation in dosage will necessarily occur depending for example on the condition of the subject being treated, route of administration and the subject's responsiveness to the therapy and the maximum tolerated dose for the subject. In delivering inactivated-MVA to a subject, the dosage will also vary depending upon such factors as the general medical condition, previous medical history, disease progression, tumor burden and the like.
It may be advantageous to formulate compositions of present disclosure in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect in association with the required pharmaceutically acceptable carrier.
Administration and Therapeutic Regimen of Inactivated-MVA
Administration of inactivated-MVA can be achieved using a combination of routes, including parenteral, for example intratumoral, or intravenous administration. In one embodiment, inactivated-MVA is administered directly into the tumor, e.g. by intratumoral injection, where a direct local reaction is desired. Additionally, administration routes of inactivated-MVA can vary, e.g., first administration using an intratumoral injection, and subsequent administration via an intravenous injection, or any combination thereof. A therapeutically effective amount of inactivated-MVA injection can be administered for a prescribed period of time and at a prescribed frequency of administration. In certain embodiments, inactivated-MVA can be used in conjunction with other therapeutic treatments. For example, inactivated-MVA can be administered in a neoadjuvant (preoperative) or adjuvant (postoperative) setting for subjects inflicted with bulky primary tumors. It is anticipated that such optimized therapeutic regimen will induce an immune response against the tumor, and reduce the tumor burden in a subject before and/or after primary therapy, such as surgery. Furthermore, inactivated-MVA can be administered in conjunction with other therapeutic treatments such as chemotherapy or radiation.
In certain embodiments, the inactivated-MVA virus is administered repeatedly at spaced apart intervals, for example at least once weekly or monthly but can be administered more often if needed, such as two times weekly for several weeks, months, years or even indefinitely as long as s persist. More frequent administrations are contemplated if tolerated and if they result in sustained or increased benefits. Benefits of the present methods include but are not limited to the following: reduction of the number of cancer cells, reduction of the tumor size, eradication of tumor, inhibition of cancer cell infiltration into peripheral organs, inhibition or stabilization of metastatic growth, inhibition or stabilization of tumor growth, and stabilization or improvement of quality of life. Furthermore, the benefits may include induction of an immune response against the tumor, activation of T helper cells, an increase of cytotoxic CDS+ T cells, or reduction of regulatory CD4+ cells. For example, in the context of melanoma or, a benefit may be a lack of recurrences or metastasis within one, two, three, four, five or more years of the initial diagnosis of melanoma. Similar assessments can be made for colon cancer and other solid tumors.
In certain other embodiments, the tumor mass or tumor cells are treated with inactivated-MVA in vivo, ex vivo, or in vitro.
Generally, reagents employed herein are from commercial sources or I, not, counterparts thereof are available commercially or publicly.
Viruses and Cell Lines
MVA viruses were kindly provided by Gerd Sutter (University of Munich), propagated in BHK-21 (baby hamster kidney cell, ATCC CCL-10) cells, but both materials are commercially and/or publicly available. Viruses were purified through a 36% sucrose cushion. B SC40 cells were maintained in Dulbecco's modified Eagle's medium (DMEM, can be purchased from Life Technologies, Cat#11965-092) supplemented with 5% fetal bovine serum (FBS), penicillin (100 units/ml), and streptomycin (100 μg/ml). BHK-21 were cultured in Eagle's Minimal Essential Medium (Eagle's MEM, can be purchased from Life Technologies, Cat#11095-080) containing 10% FBS, 0.1 mM nonessential amino acids (NEAA), and 50 mg/ml gentamycin. The murine melanoma cell line B16-F10 was originally obtained from I. Fidler (MD Anderson Cancer Center). B16-F10 cells were maintained in RPMI 1640 medium supplemented with 10% FBS, 100 Units/ml penicillin, 100 μg/ml streptomycin, 0.1 mM NEAA, 2 mM L-glutamine, 1 mM sodium pyruvate, and 10 mM HEPES buffer.
All cells were grown at 37.0 in a 5% CO2 incubator.
Heat-MVA was generated by incubating purified MVA virus at 55° C. for 1 hour. For generation of UV-MVA, MVA was UV irradiated in a Stratalinker 1800 UV cross-linker (Stratagene) with a 365 nm UV lamp for 15 min. Mice
Female C57BL/6J mice between 6 and 10 weeks of age were purchased from the Jackson Laboratory (Stock #000664) and were used for the preparation of bone marrow-derived dendritic cells and for in vivo experiments. These mice were maintained in the animal facility at the Sloan Kettering Institute. All procedures were performed in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institute of Health. The protocol was approved by the Committee on the Ethics of Animal Experiments of Sloan-Kettering Cancer Institute. cGAS−/−, IRF7−/−, IRF5−/−, Batf3−/−, and STINGGt/Gt mice were generated in the laboratories of Drs. Zhijian Chen (University of Texas Southwestern Medical Center; cGAS−/−), Tadatsugu Taniguchi (University of Tokyo; IRF3−/− and IRF7−/−), Tak Mak (University of Toronto; IRF5−/−); Kenneth Murphy (Washington University; Batf3−/−), and Russell Vance (University of California, Berkeley; STINGGt/Gt). IFNAR1−/− mice were provided by Dr. Eric Pamer (Sloan Kettering Institute); the mice were purchased from B&K Universal and were backcrossed with C57BL/6 mice for more than six generations. IRF5−/− mice were backcrossed to C57BL/6J mice for at least six generations in Dr. Paula M. Pitha's laboratory before they were transferred to Sloan Kettering Institute.
Commercial sources for the foregoing animals are as follows:
Generation of Bone Marrow-Derived Dendritic Cells
The bone marrow cells from the tibia and femur of mice were collected by first removing muscles from the bones, and then flushing the cells out using 0.5 cc U-100 insulin syringes (Becton Dickinson) with RPMI with 10% FCS. After centrifugation, cells were re-suspended in ACK Lysing Buffer (Lonza) for red blood cells lysis by incubating the cells on ice for 1-3 min. Cells were then collected, re-suspended in fresh medium, and filtered through a 40-μm cell strainer (BD Biosciences). The number of cells was counted. For the generation of GM-CSF-BMDCs, the bone marrow cells (5 million cells in each 15 cm cell culture dish) were cultured in CM in the presence of GM-CSF (30 ng/ml, produced by the Monoclonal Antibody Core facility at the Sloan Kettering Institute) for 10-12 days. CM is RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS), 100 Units/ml penicillin, 100 μg/ml streptomycin, 0.1 mM essential and nonessential amino acids, 2 mM L-glutamine, 1 mM sodium pyruvate, and 10 mM HEPES buffer. Cells were fed every 2 days by replacing 50% of the old medium with fresh medium and re-plated every 3-4 days to remove adherent cells. Only non-adherent cells were used for experiments.
RNA Isolation and Real-Time PCR
RNA was extracted from whole-cell lysates with an RNeasy Mini kit (Qiagen) and was reverse transcribed with a First Strand cDNA synthesis kit (Fermentas). Quantitative real-time PCR was performed in triplicate with SYBR Green PCR Mater Mix (Life Technologies) and Applied Biosystems 7500 Real-time PCR Instrument (Life Technologies) using gene-specific primers. Relative expression was normalized to the levels of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
The following primers were used for real-time PCR:
Relative expression was normalized to the levels of glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
Cytokine Assays
Cells were infected with various viruses at a MOI of 10 for 1 h or mock infected. The inoculum was removed and the cells were washed with PBS twice and incubated with fresh medium. Supernatants were collected at various times post infection. Cytokine levels were measured by using enzyme-linked immunosorbent essay (ELISA) kits for IFN-α/β (PBL Biomedical Laboratories), IL-6, CCL4, and CCLS (R & D systems).
Western Blot Analysis
BMDCs (1×106) from WT and KO mice were infected with MVA at a MOI (multiplicity of infection) of 10 or an equivalent amount of Heat-MVA, or UV-MVA. At various times post-infection, the medium was removed and cells were collected. Whole-cell lysates were prepared. Equal amounts of proteins were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the polypeptides were transferred to a nitrocellulose membrane. Phosphorylation of IRF3 was determined using a rabbit polyclonal antibody specific for phosphoserine-396 of IRF3 (Cell Signaling). The level of IRF3 was determined using a rabbit polyclonal antibody against IRF3 (Cell Signaling). Anti-STING antibodies were purchased from Cell Signaling. Vaccinia E3 protein level was determined by using anti-E3 monoclonal antibody (MAb 3015B2) kindly provided by Dr. Stuart N. Isaacs (University of Pennsylvania) [85]. Anti-glyceraldehyde-3-phosphate dehydrogenase (GADPH) or anti-β-actin antibodies (Cell Signaling) were used as loading controls.
B16-F10 melanoma cells were infected with MVA at a MOI of 10 or with an equivalent amount of Heat-MVA. Cell lysates were collected at various times post infection. Western blot analysis was performed using anti-phospho-IRF3, anti-IRF3, and anti-GAPDH antibodies as described above.
Unilateral Intradermal Tumor implantation and Intratumoral Injection with Viruses in the Presence or Absence of Systemic Administration of Immune Checkpoint Blockade
B16-F10 melanoma (1×105 cells in a volume of 50 μl) were implanted intradermally into the shaved skin on the right flank of STINGGt/Gt, or Batf3−/−, or age-matched WT C57BL/6J mice. After 10 to 12 days post implantation, tumor sizes were measured and tumors that are 3 mm in diameter or larger will be injected with Heat-MVA (equivalent to 2×107 pfu of MVA in a volume of 50 μl) or PBS when the mice were under anesthesia. Viruses were injected weekly or twice weekly as specified in each experiment. Mice were monitored daily and tumor sizes were measured twice a week. Tumor volumes were calculated according the following formula: l (length)×w (width)×h(height)/2. Mice were euthanized for signs of distress or when the diameter of the tumor reached 10 mm. Serum were collected when the mice were euthanized.
To evaluate the combination of Heat-MVA with immune checkpoint blockade, we treated the mice either with intratumoral injection of Heat-MVA or PBS in the presence or absence of anti-CTLA-4 antibody (100 μg in a volume of 100 μl) delivered intraperitoneally. The mice received virus and antibodies every 3-4 days (twice per week). The animals were monitored daily, and measured for tumor size every 3 days. Tumor volumes were calculated according the following formula: l (length)×w (width)×h(height)/2. Mice were euthanized for signs of distress or when the diameter of the tumor reached 10 mm.
In some cases, 1×105 MC38 colon adenocarcinoma cells were implanted intradermally on the right flank of shave mice. After 7 days, tumors were injected with either PBS, Heat-MVA, or UV-MVA at the same dose as described above twice weekly. The animals were monitored daily, and measured for tumor size every 3 days. Tumor volumes were calculated according the following formula: l (length)×w (width)×h(height)/2. Mice were euthanized for signs of distress or when the diameter of the tumor reached 10 mm.
Tumor Challenge to Assess the Development of Systemic Antitumor Immunity
For the B16-F10 murine melanoma model, tumors were implanted by injection of 1×105 cells (in a volume of 50 μl) on the right flank intradermally and treated with intratumoral delivery of PBS or Heat-MVA (an equivalent of heat-inactivated 2×107 pfu of MVA in a volume of 50 μl). The mice were monitored for tumor growth and survival for 30-80 days. The survived mice were rechallenged with either intradermally delivery of a lethal dose of B16-F10 (1×105 cells) at the contralateral side. Mice were monitored for 30-80 days for tumor growth. Alternatively, they were challenged by intravenous delivery of a lethal dose of B16-F10 (1×105 cells) and then euthanized at 3 weeks post rechallenge to evaluate the presence of tumors on the surface of lungs.
For the MC38 murine colon adenocarcinoma model, tumors were implanted by injection of 1×105 cells in the right flank intradermally and treated with intratumoral delivery of PBS, Heat-MVA, or UV-MVA (an equivalent of heat- or UV-inactivated 2×107 pfu of MVA). The mice were monitored for tumor growth and survival for 60 days. The survived mice were rechallenged with either intradermally delivery of a lethal dose of B16-F10 (1×105 cells) at the contralateral side. Mice were monitored for 60 days for tumor growth.
T Cell Depletion Experiment
B16-F10 murine melanoma cells (1×105 cells in a volume of 50 μl) were implanted intradermally into the right flank of shaved WT C57B/6 mice at 6-8 weeks of age. At 8 days post tumor implantation, the tumors were injected with either Heat-MVA (an equivalent dose of 2×107 pfu of MVA) or PBS twice weekly. Depletion antibodies for CD4+, CD8+ and NK cells (200 μg of GK1.5, 2.43, and PK136) (Monoclonal Antibody Core Facility, MSKCC) (ref, Avogadri et al., PloS One 2010) were injected intraperitoneally twice weekly starting one day prior to viral injection, and they were used until the animals either died, or were euthanized, or were completely clear of tumors. Mice were monitored daily and tumor sizes were measured. The depletion of targeted immune cells was validated by FACS of peripheral blood of mice after 4 doses of antibodies.
Bilateral Tumor Implantation Model and Intratumoral Injection with Viruses in the Presence or Absence of Systemic or Intratumoral Administration of Immune Checkpoint Blockade
Briefly, B16-F10 melanoma cells were implanted intradermally to the left and right flanks of C57B/6 mice (5×105 to the right flank and 1×105 to the left flank). 8 days after tumor implantation, we intratumorally inject 2×107 pfu of MVA or an equivalent amount of Heat-MVA to the larger tumors on the right flank. The tumor sizes were measured and the tumors were injected twice a week. The survival of mice was monitored.
In some experiments, MC38 colon adenocarcinoma cells were implanted intradermally to the left and right flanks of C57B/6 mice (5×105 to the right flank and 1×105 to the left flank).
In some experiments, STINGGt/Gt, Batf3−/− mice and WT age-matched controls were used for bilateral B16-F10 melanoma implantation, and treated with PBS or Heat-MVA to the larger tumors on the right flank of the mice.
In some experiments, the mice with bilateral tumors were treated with intratumoral injection of Heat-MVA to the larger tumors on the right flank and intraperitoneal delivery of immune checkpoint blockade antibodies, including anti-CTLA-4, anti-PD-1, or anti-PD-L1.
In some experiments, the mice with bilateral tumors were treated with intratumoral injection of both Heat-MVA and anti-CTLA-4 antibody (with one tenth of dose of as used for intraperitoneal delivery) to the larger tumors on the right flank. The sizes of both injected and non-injected tumors were measured and the survival of the mice was monitored.
Flow Cytometry Analysis of DC Maturation
For DC maturation analysis, BMDCs were generated from WT and STINGGt/Gt mice and infected with MVA at a MOI of 10 or with an equivalent amount of Heat-MVA. Cell were collected at 14 h post infection and were then fixed with Fix Buffer I (BD Biosciences) for 15 min at 37° C. Cells were washed, permeabilized with PermBuffer (BD Biosciences) for 30 min on ice, and stained with antibodies against MHC Class I, CD40, CD86, and CD80 for 30 min. Cells were analyzed using the LSRII Flow cytometer (BD Biosciences). Data were analyzed with FlowJo software (Treestar).
Flow Cytometry Analysis of Tumor Infiltrating Immune Cells
To analyze immune cell phenotypes and characteristics in the tumors or tumor draining lymph nodes, we generated cell suspensions prior to FACS analysis according to the following protocol (Zamarin et al., 2014). First we isolated injected and/or non-injected tumors using forceps and surgical scissors three days post second treatment and 7 days post first treatment with PBS, MVA or Heat-MVA. The tumors were then weighed. Tumors or tumor draining lymph nodes were minced prior to incubation with Liberase (1.67 Wunsch U/ml) and DNase (0.2 mg/ml) for 30 minutes at 37° C. Cell suspensions were generated by repeated pipetting, filtered through a 70-μm nylon filter, and then washed with complete RPMI prior to Ficoll purification to remove dead cells. Cells were processed for surface labeling with anti-CD3, CD45, CD4, and CD8 antibodies. Live cells are distinguished from dead cells by using fixable dye eFluor506 (eBioscience). They were further permeabilized using FoxP3 fixation and permeabilization kit (eBioscience), and stained for Ki-67, FoxP3, and Granzyme B. Data were acquired using the LSRII Flow cytometer (BD Biosciences). Data were analyzed with FlowJo software (Treestar).
Anti-Melanoma and Anti-Viral Antibody Measurement by ELISA
To determine anti-B16 melanoma antibody concentrations in the serum of the mice, 5×104 B16-F10 cells in 100 μl medium/well were add to 96 well culture plate and incubated overnight at 37° C. The plates were washed twice with PBST. Cells were treated with 10% buffered formalin (125 μl) and fixed for 15 min at room temperature. The plates were then washed three times with PBS. After blocking with PBS with 1% BSA (250 μl) at room temperature for 1 h, mouse serum diluted in PBS with 1% BSA (1:500) was added at 100 μl/well. The plate was washed with PBST five times. Incubate for 1 hr at 37° C. Then horseradish peroxidase (HRP)-conjugated anti-mouse IgG diluted in PBS with 1% BSA (1:2000) was added to the plate and incubated for 1 hr at 37° C. The plate was washed with PBS five times and incubated with substrate 3,3′,5,5′-Tetramethylbenzidine TMB (100 μl/well) at room temperature for 10 min. The reaction was terminated by adding sulfuric acid (2N, 50 μl/well). The optical density of each well was determined by using a microplate reader set to 450 nm.
To determine anti-vaccinia viral antibody concentrations in the serum of the mice, Heat-MVA (10 μg/ml) in 100 μl PBS/well were added to 96 well culture plate and incubated overnight at 37° C. The plates were washed twice with PBST. After blocking with PBS with 1% BSA (250 μl) at room temperature for 1 h, mouse serum diluted in PBS with 1% BSA (1:200) was added at 100 μl/well. The rest of the detection protocol is the same as stated above.
Reagents
The commercial sources for reagents were as follows: CpG oligodeoxynucleotide ODN2216 (Invitrogen); We used the following antibodies. Therapeutic anti-CTLA4 (clone 9H10 and 9D9), anti-PD1 (clone RMP1-14) were purchased from BioXcell; Antibodies used for flow cytometry were purchased from eBioscience (CD45.2 Alexa Fluor 700, CD3 PE-Cy7, CD4 APC-efluor780, CD8 PerCP-efluor710, FOXP3 Alexa Fluor 700, MHC Class I APC, CD40 APC, CD80 APC, CD86 APC), Invitrogen (CD4 QDot 605, Granzyme B PE-Texas Red, Granzyme B APC), BD Pharmingen (Ki-67-Alexa Fluor 488).
Statistics
Two-tailed unpaired Student's t test was used for comparisons of two groups in the studies. Survival data were analyzed by log-rank (Mantel-Cox) test. The p values deemed significant are indicated in the figures as follows: *, p<0.05; **, p<0.01; ***, p<0.001; ****, p<0.0001.
To test whether heat-inactivation of MVA (Heat-MVA) would result in higher levels of type I IFN induction than MVA, MVA was incubated at 55° C. for 1 h, which resulted in the reduction of infectivity by 1000-fold. Bone marrow-derived dendritic cells were cultured in the presence of GM-CSF (GM-CSF-BMDCs or cDCs) and infected with either MVA at a multiplicity of infection (MOI) of 10 or with an equivalent amount of Heat-MVA. Cells were harvested at 6 h post infection and quantitative real-time PCR analysis of RNA isolated from infected cells and mock-infected cells was performed. It was found that MVA infection of cDCs increased IFNA4 and IFNB mRNA levels by 4.8-fold and 148-fold, respectively, compared mock-infected cells. By contrast, infection of Heat-MVA dramatically increased IFNA4 and IFNB mRNA levels by 22.4-fold and 607-fold, respectively (
To assess the kinetics of induction of type I IFN secretion by Heat-MVA or MVA-infected cDCs, supernatants were collected at various times (0, 4, 8, 16, and 22 hours) post Heat-MVA or MVA infection, and the levels of secreted IFN-α and IFN-β were determined by ELISA. Heat-MVA strongly induced both IFN-α (1650 pg/ml) and IFN-β (1975 pg/ml) at 8 h post-infection, which were 10-fold and 6-fold higher than those induced by MVA at the same time point. Whereas MVA-induced IFN-α and IFN-β continued to rise between 8 h and 22 h post infection, Heat-MVA induced IFN-α levels increased modestly during this time frame, while Heat-MVA induced IFN-β peaked at 8 h post infection and leveled off thereafter (
To test whether Heat-MVA infection of cDCs triggers type I IFN induction via the cytosolic DNA-sensing pathway mediated by the cytosolic DNA sensor cGAS (cyclic GMP-AMP synthase) [62, 63], and its adaptor STING [59, 69], cDCs were generated from cGAS−/− [86] mice and age-matched WT controls and infected with Heat-MVA. Using quantitative real-time PCR analysis, it was found that Heat-MVA-induced IFNA4 and IFNB gene expression at 6 h post infection were both diminished in cGAS-deficient cells (
STING is a critical adaptor for the cytosolic DNA-sensing pathway [59, 69, 87, 88]. cDCs were also generated from STINGGt/Gt mice, which lack functional STING [89]. It was found that Heat-MVA induced type I IFN gene expression and that IFN-α/β secretion from the cDCs is also dependent on STING (
To test whether Heat-MVA-induction of type I IFN requires IRF3, IRF5 and IRF7, in addition to cGAS and STING, cDC were generated from IRF3−/−, IRF7−/− and age-matched WT mice, and infected with Heat-MVA. Heat-MVA-induced IFNA4 gene expression, and IFN-a protein production was dependent on IRF3 and IRF7, but independent of IRF5 (
To test whether Heat-MVA induces higher levels of type I IFN than MVA in vivo, Heat-MVA or MVA were inoculated into C57B/6 mice via tail vein injection, and serum was collected at 6 h post-infection. The levels of both IFN-α and IFN-β in the serum were significantly higher in Heat-MVA-treated mice than in MVA-treated mice (
To test whether Heat-MVA in vivo induction of type I IFN requires IFNAR1, intravenous (IV) inoculation of purified Heat-MVA via tail vein injection of IFNAR1−/− and WT age-matched control mice was performed. Heat-MVA infection of WT mice induced IFN-α and IFN-β production to the levels of 2256 pg/ml and 1901 pg/ml, which was reduced by 60% and 35%, respectively, in IFNAR1−/− mice (
Heat-MVA-induced IFN-α secretion was reduced by 89% in STINGGt/Gt mice compared with WT controls, whereas Heat-MVA-induced IFN-β secretion was abolished in STINGGt/Gt mice (
To test whether Heat-MVA infection of tumor cells triggers innate immune responses, B16-F10 melanoma cells were infected with MVA at an MOI of 10, or with equivalent amounts of Heat-MVA, and cells were collected at 6 h post infection and supernatants were collected at 22 h post infection. Quantitative real-time PCR analysis showed that Heat-MVA infection of B16-F10 cells induced higher levels of Ifna4, Ifnb, Ccl5, and Il6 gene expression than MVA (
To evaluate whether 55° C. is the optimal temperature for inactivating MVA, we incubated MVA at various different temperatures, including, 45° C., 50° C., 55° C., 60° C., and 65° C., for one hour. cDCs from WT mice were infected with these virus preparations and supernatants were collected at 22 h post infection. The concentrations of secreted IFN-α and IFN-β were measured by ELISA. We found that infection with MVA inactivated at 55° C. for one hour induced the highest levels of IFN-α and IFN-β secretion from cDCs (
The transplantable in vivo B16-F10 melanoma model involves the intradermal implantation of murine B16-F10 melanoma cells (1×105) on one side of the flank of C57B/6 mice. Ten days following tumor implantation, when the tumors were approximately 3 mm in diameter, Heat-MVA (with an equivalent of 2×107 pfu of MVA) or PBS were injected to the tumors weekly. Intratumoral injection of Heat-MVA resulted in tumor eradication and 100% survival of mice (
To test whether mice whose tumors were eradicated after intratumoral injection of Heat-MVA developed systemic anti-tumoral immunity, animals were challenged by intradermal implantation of a lethal dose of B16 melanoma cells (1×105) to the contralateral side 8 weeks after the eradication of initial tumors. Naïve mice that were never exposed to B16 melanoma cells or heat-MVA were used as a control. Animals were followed for 70 days after tumor challenge. 90% of heat-MVA-treated mice survived the tumor challenge, whereas all of the naïve mice developed growing tumors and were eventually euthanized (
To investigate the immunologic changes within the tumors induced by intratumoral injection of Heat-MVA, tumors were harvested at 3 days post intratumoral injection of Heat-MVA or PBS and the immune cell infiltrates were analyzed by FACS. The percentage of CD3+CD45+ T cells of live cells within the tumors increased from 6.5% in the PBS-treated tumors to 19.5% in the Heat-MVA-treated tumors (P=0.0002;
To test whether intratumoral injection of Heat-MVA causes immunological changes in TDLNs, TDLNs were isolated from Heat-MVA-treated or PBS-treated mice and analyzed by FACS. The percentage of Granzyme B+CD8+ T cells in TDLNs increased from 0.15% in mice treated with PBS to 3.04% in mice treated with Heat-MVA (P<0.0001;
Recent studies have shown that the STING-mediated cytosolic DNA-sensing pathway plays a role in spontaneous T cell responses against tumors as well as in radiation-induced antitumoral immunity [7, 8, 90]. BATF3 is a transcription factor that is critical for the development of CD8α+ lineage DCs, which play an important role in cross-presentation of viral and tumor antigens [91, 92]. Batf3-deficient mice were unable to reject highly immunogenic tumors [91]. To test whether STING or Batf3 plays a role in Heat-MVA-mediated tumor clearance, we implanted B16-F10 melanoma cells intradermally into the right flank of WT C57B/6, STINGGt/Gt, or Batf3−/− mice. At 11 days post tumor implantation, the tumors were injected with either Heat-MVA (an equivalent dose of 2×107 pfu) or PBS on a weekly basis as indicated (
To determine which immune cell type is required for the therapeutic effect of Heat-MVA, we performed an antibody depletion experiment. Briefly, we implanted B16-F10 melanoma cells (2×105) intradermally into the right flank of WT C57B/6 mice. At 8 days post tumor implantation, the tumors were injected with either Heat-MVA (an equivalent dose of 2×107 pfu) or PBS twice weekly basis as indicated (
Anti-tumor antibody production is an important aspect of adaptive immunity. To test whether Heat-MVA induces anti-melanoma antibody production, we performed ELISA to determine the serum concentration of anti-B16 melanoma antibodies in mice treated with Heat-MVA or mock-treated. We found that only Heat-MVA treated mice produced anti-melanoma antibodies (
To investigate whether intratumoral injection of Heat-MVA has the ability to enhance therapeutic effects of current immunotherapies, such as the blockade of immune checkpoints (for example anti-CTLA-4 antibody), tumor-bearing mice were treated with intratumoral injection of Heat-MVA in combination with intraperitoneal delivery of anti-CTLA-4 antibody. Briefly, we implanted B16-F10 melanoma cells (2×105) intradermally into the right flank of WT C57B/6 mice. Ten days following tumor implantation, when the tumors have grown larger than those in Example 7, 10 or 11, mice were treated with the following combinations: PBS+isotype control, PBS+anti-CTLA-4 antibody, Heat-MVA+isotype control, and Heat-MVA+anti-CTLA-4. As shown in
MVA is an attenuated vaccinia virus that is non-replicative in most mammalian cells. We found that MVA modestly replicates in B16 melanoma cells (
To understand the immune mechanisms underlying the superiority of Heat-MVA over MVA in the induction of systemic antitumor immunity, we investigated the immune cell infiltrates in the non-injected tumors in Heat-MVA or MVA-treated mice. Briefly, we intradermally implanted 2.5×105 B16-F10 melanoma cells to the left flank and 5×105 B16-F10 melanoma cells to the right flank of the mice. 7 days post implantation, we injected 2×107 pfu of MVA, or an equivalent amount of Heat-MVA, or PBS into the larger tumors on the right flank. The injection was repeated three days later. The non-injected tumors were harvested and cell suspensions were generated. The live immune cell infiltrates in the tumors were analyzed by FACS. We observed a dramatic increase of CD45+, CD103+, CD3+ and CD8+ immune cells in the non-injected tumors of mice treated with Heat-MVA compared with those in mice treated with MVA or PBS. Although MVA-treatment also resulted in the increase of these immune cells in the non-injected tumors compared with those in PBS-treated mice, MVA is less potent than Heat-MVA in the induction of immune cells in the non-injected tumors (
In example 10, we showed that intratumoral delivery of Heat-MVA is ineffective in eradicating B16-F10 melanoma in a unilateral implantation model. To further extend this study, we tested the efficacy of intratumoral delivery of Heat-MVA in a bilateral tumor implantation model. In PBS-treated group, all of the mice died with a median survival of 16 days due to rapid growth of the larger tumors on the right flank (
Given the importance of CD103+ DCs in Heat-MVA-induced antitumor immunity shown in Example 10 and 16, and the critical role of CD8+ and CD4+ T cells in Heat-MVA-mediated antitumor effects, we investigated whether there is a deficiency in the generation of antitumor CD4+ and CD8+ T cells in Batf3 KO mice in response to intratumoral injection of Heat-MVA using a bilateral tumor implantation model. Briefly, we intradermally implanted 2.5×105 B16-F10 melanoma cells to the left flank and 5×105 B16-F10 melanoma cells to the right flank of Batf3−/− mice and WT age-matched controls. 7 days post implantation, we injected either Heat-MVA or PBS into the larger tumors on the right flank. The injection was repeated three days later. The non-injected tumors were harvested on day 7 after first injection, and cell suspensions were generated. The live immune cell infiltrates in the injected and non-injected tumors were analyzed by FACS. Similar to Example 15, we observed a dramatic increase of CD3+ and CD8+ immune cells in both injected and non-injected tumors of mice treated with Heat-MVA compared with those in mice treated with PBS (
We then investigated whether intratumoral injection of Heat-MVA enhances therapeutic effects of immune checkpoint blockade therapy such as anti-CTLA-4, anti-PD-1, or anti-PD-L1 antibodies in a bilateral B16-F10 melanoma model, which simulates an individual with metastatic disease. Briefly, B16-F10 melanoma cells were implanted intradermally to the left and right flanks of C57B/6 mice (5×105 to the right flank and 1×105 to the left flank). 8 days after tumor implantation, we intratumorally injected Heat-MVA (heat-inactivated 2×107 pfu of MVA) or PBS to the larger tumors on the right flank twice weekly. Four groups of mice were treated with Heat-MVA, with each group receiving intraperitoneal delivery of either isotype control, or anti-CTLA-4, or anti-PD-1, or anti-PD-L1 antibodies (
Whereas the PBS-treated mice died quickly with increasing tumor growth over the next 20 days (
The ability to control the growth of non-injected distant tumors correlated with the improved survival in the combination group with Heat-MVA+immune checkpoint blockade compared with Heat-MVA+isotype control (
This experiment will be repeated to assess the longer term benefit of conjoint immune checkpoint blockade and inactivated MVA therapy.
We hypothesized that ultraviolet light inactivation of MVA may also result in an immune activating virus through activation of the STING-mediated cytosolic DNA-sensing pathway. To test this hypothesis, we infected cDCs from STINGGt/Gt and their age-matched WT control mice. Cells (1×106) were infected with MVA at a MOI of 10, or an equivalent amount of Heat-MVA, or UV-MVA. Supernatants were collected at 22 h post infection, and the concentrations of secreted IFN-α and IFN-β were determined by ELISA. Similar to Heat-MVA, UV-inactivated MVA also induces higher levels of type I IFN than MVA in WT cDCs (
Experimental studies disclosed in Example 7 and 14 showed that intratumoral injection of Heat-MVA leads to tumor eradication and systemic anti-tumoral immunity in a murine transplantable B16-F10 melanoma model. To test whether Heat-MVA or UV-MVA is capable of eradicating other solid tumors, we tested the anti-tumor effects of Heat-MVA or UV-MVA in a murine MC38 colon adenocarcinoma implantation model. Colon adenocarcinoma is representative of a solid tumor not related to melanoma but was otherwise an arbitrary choice. 5×105 MC38 colon carcinoma cells were intradermally implanted into the right flank of C57B/6 mice. Tumors were allowed to grow for 7 days, after which Heat-MVA or UV-MVA (through either heat or UV-inactivation of 2×107 pfu of MVA) or PBS control were intratumorally injected twice a week. Tumors were measured twice a week and tumor volumes were calculated according the following formula: l (length)×w (width)×h(height)/2. We found that all of the mice treated with PBS died due to tumor growth (
To test whether survived mice have developed systemic antitumor immunity, we challenged the mice with a lethal dose of MC38 cells (1×105) at the contralateral side and monitored survival. We found that whereas all of the naïve mice developed tumors and died, 100% of the Heat- or UV-MVA-treated mice rejected tumor challenge (
We further investigated whether intratumoral injection of Heat-MVA enhances therapeutic effects of immune checkpoint blockade therapy such as anti-CTLA-4, anti- or anti-PD-L1 antibodies in other bilateral tumor implantation model, which simulates an individual with metastatic disease. Briefly, MC38 colon adenocarcinoma cells were implanted intradermally to the left and right flanks of C57B/6 mice (5×105 to the right flank and 1×105 to the left flank). 8 days after tumor implantation, we intratumorally inject Heat-MVA (heat-inactivated 2×107 pfu of MVA) or PBS to the larger tumors on the right flank twice weekly. There are three groups of mice that were treated with PBS, with each group received intraperitoneal delivery of either PBS, or anti-CTLA-4, or anti-PD-L1 antibodies (
In Examples 13, 18, and 21, we showed that the combination of intratumoral injection of Heat-MVA with systemic (intraperitoneal) delivery of immune checkpoint blockade led to synergistic antitumor effects in both melanoma and colon adenocarcinoma models. Here we test whether the co-administration of Heat-MVA and anti-CTLA-4 antibody (at 1/10 of dose used for intraperitoneal delivery) would achieve antitumor effects in a stringent bilateral tumor implantation model. Briefly, B16-F10 melanoma cells were implanted intradermally to the left and right flanks of C57B/6 mice (5×105 to the right flank and 1×105 to the left flank). 8 days after tumor implantation, we intratumorally injected Heat-MVA (heat-inactivated 2×107 pfu of MVA) or PBS to the larger tumors on the right flank twice weekly. Three groups of mice were treated with Heat-MVA, with each group receiving: (i) intraperitoneal delivery of anti-CTLA-4 (100 μg/mouse) (ii) intratumoral delivery of isotype antibody (10 μg/mouse), or (iii) intratumoral delivery of anti-CTLA-4 antibody (10 μg/mouse) (
Given that the combination of anti-CTLA-4 and anti-PD-1 antibodies is more efficacious than either agent alone in PD-L1-negative tumors in a phase III clinical trials (Larkin et al., 2015), the inventors will deliver combined inactivated MVA and both anti-CTLA-4 and anti-PD-1/anti-PD-L1 (the blocking agents typically delivered at lower doses than monotherapy and lower doses than conjoint administration by different routes (intratumoral v. intravenous for example) will be delivered intratumorally. It is anticipated that this will result in additional augmentation of antitumor immunity and further improved survival with lower incidence of side effects. In addition, more recently developed immune checkpoint blockade antibodies will be included in such conjoint delivery such as anti-LAG-3, anti-TIM-3, and anti-TIGIT antibodies fin or the treatment of various solid tumors in pre-clinical models such as those described above.
The foregoing Examples are illustrative of the methods and features described herein and are not intended to be limiting. Moreover, they contain statements of general applicability to the present disclosure and such statements are not confined to the particular Example they appear in but constitute conclusions descriptions and expressions of broader implications of the experimental results described herein.
The contents of all cited references are incorporated by reference in their entirety as if fully transcribed herein for all purposes.
This application is a continuation of U.S. patent application Ser. No. 15/553,222, filed Aug. 24, 2017, which is a U.S. National Stage Application of PCT/US2016/019663, filed Feb. 25, 2016, which claims priority from U.S. Provisional Application No. 62/120,862, filed Feb. 25, 2015, each of which are incorporated herein by reference in their entireties.
This invention was made with government support under A1073736 and A1095692 awarded by the National Institutes of Health. The government has certain rights in the invention.
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| 20200237902 A1 | Jul 2020 | US |
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