CA2986687A1 - Manufacturing multi-dose injection ready dendritic cell vaccines - Google Patents

Abstract

The present embodiments relate to an FDA- approved injectable multi-dose antigen pulsed dendritic cell (DC) vaccine. In one embodiment, the activated antigen-loaded DC vaccine comprises an initial immunizing dose and multiple "booster"doses. Also provided is a method of blocking both HER-2 and HER-3 as a treatment in causing permanent tumor senescence in HER-2 expressing breast cancers. Also provided is combination anti-estrogen therapy and anti-HER2 dendritic call vaccination for ERpos/HER2pos DCIS breast cancer patients.

Description

MANUFACTURING MULTI-DOSE INJECTION READY DENDRITIC CELL VACCINES
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a continuation-in-part application of Serial No.
PCT/US] 5/41022 filed July 17, 2015 which in turn claims priority and benefit from U.S.
Provisional Application Serial No. 62/025,673, filed July 17, 2014, U.S.
Provisional Application Serial No. 62/165,445, filed May 22, 2015, U.S. Provisional Application Serial No. 62/025,685, filed July 17, 2014, and U.S. Provisional Application Serial No.
62/028,774, flied July 24, 2014, the contents of each of which are incotporated by reference herein in their entireties.
ACKNOWLEDGMENT
The present invention was developed in part with government support under grant number ROI CA096997 awarded by the National Institutes of Ilealth.
The government has certain rights in this invention.
BACKGROUND
Dendrific cells (DCs) are white blood cells that acquire protein antigens from microbes or even cancerous cells and show, or "present" these antigens to T cells.
The T cells, thus activated by the DCs, then initiate systemic immune responses to challenge the threat Traditional vaccines against microbes contain additiv'es known as "adjuvants" that by a number of possible means enhance DC activity within the vaccinated individual and amplify vaccine-induced immune responses. 'fhe requirements of vaccines against cancer, however, present a number of unique problems. For example, traditional adjuvants do not provide the proper signals to Des that allow them to initiate optimal immunity against cancer. Also, the tumors themselves produce an environment that can affect the proper activation of DC's.
A popular solution to this problem is to extract DCs from cancer patients, load them with tumor allkeTIS in vitro, and then supply unique activation signals to the cells before re-administering them to the body. This ensures proper DC
activation removed from the influence of the tumor environment_ When returned to the body, the DCs can then interact with Teas and initiate powerful anti-tumor immunity.
Whereas the use of extra-corporealized'DCs has solved many efficacy issues, it has historically come at the price of practical limitations. For example, since the DC vaccines are comprised of living cells, a special cell processing and vaccine production facility has been required at the physical location of the medical center administering the therapy.
This is an expensive and inefficient way to deliver the therapy because every institution administering such treatment would have to build and maintain their own special-use Management of breast cancer currently relies on a combination of early diagnosis and aggressive treatment, which can include one or more treatments such as surgery, radiation therapy, chemotherapy, and hormone therapy. Herceptin (trastuzumab) was developed as a targeted therapy for HER2fErb-B2 positive breast cancer cells, often used in conjunction with other therapies, including the mitotic inhibitor paclitaxel (sold under the trademark Taxol).
The efficacy of Herceptin as a monotherapy is estimated to be. less than.
30%; combinatorial treatment with microtubtile stabilizing drugs such as paclitaxe-t.
increases efficacy to approximately 60% (Burris et al., 2000, Semin Oncol 27:
19-23).
Treatment with Herceptin results in accumulation of the Cdk inhibitor p27 and 20. subsequent GUS cell.cycle arrest, and paclita.xel stalls the entry Of mitosis which canlead to cell death: In spite of great promise, however, high doses- of Herceptin or paclitaxel result in undesirable side effects. Further, the cancer often develops resistance to Herceptin and/or paclitaxel.
Therefore, there remains an unmet need for compositions andefficient.
methods for producing maximal therapeutic DC vaccines and for new methods of treating cancer using :Herceptin. Accordingly, there is a need in the art to have additional immtmotherapeutic approaches for treating or preventing breast cancer and other Malignancies. The present embodiments fulfill this need.
BRIEF DESCRIPTION OF THE DRAWINGS

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The followMg detailed description of preferred embodiments will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the embodiments, there are shown in the drawings embodiments which are presently preferred. It should be understood, however, that the embodiments are not limited to the precise arrangements and instrumentalities of the embodiments shown in the drawings.
Figure us a chart showing the viability and yield of post-thawed ciyopreserved DC1. Recovery of cells was on average 89% and viability was 95%
when cells were directly thawed and counted.
Figure 2 is a chart showing that here was no significant difference in the viability (p-,4807), and recovery (p-.1220) of the cells.
Figure 3 is a chart showing that both populations had similar initial (7 hours post LPS addition) 1L-12 p70 secretion (v.0768). The populations continued to exhibit comparable secretion levels of IL-12 p70 over a 30 hour observation period with no significant differences between the populations.
Figure 4 is a chart showing that there was no significant difference between populations and production of IL-1p (p=0.7690), IL-In (v0.0841), Raines (p-0.902), MDC (V0.1514), 1L-8 (v0,7844); (p-.2673), IP-10 (v0.7366), IL-6 (p-0.24), TINF-u (p---4).8972); 1L-5 (p-0.0735),1L-15(p-0.8878), IL-10 (p-.1937), Nup-ip (p-A8.9217), Figure 5 is a chart showing production of1FN-f-froiri cryopreserved and non-cryopreserved DCs.
Figures 6A-6D show Th Icytokines TNF-a and IFN-y synergize to induce senescence in breast cancer cells and the doses required are in an inverse correlation with the LIER2 expression. Figure 6A shows results of studies in which SK-BR-3 breast cancer cells were incubated with 10 ngtml TNF-a and 100 Ii/m1IFN-7 for 5 days, cultured for 2 more passages in absence of crokines and then stained for SA-p-uaiactosidase (SA-0-gal) expression (senescence marker) and compared to untreated control cells. Only paired cytokines induced senescence. Top panel shows photographs of representative data horn I of 3 independent experiments. Bottom pariel.shows a histogram of densitometfic analysis. Data are presented as '.'4) of SA-0-gal-positive cells and presented as mean + S.D. (n=3). ). P- values were caleulated using a paired Students t-test. Statistical significance was determined at *P < 0.05. Figure 613 shows photographs of western blot analysis in which cell lysates of the cells described in Figure 6A were analyzed for p15INKb and p 1 6INK4a expression. Vinaulin was used as loading control.
Figure 6C shows results of studies in which 1-471) breast cancer cells were untreated (1) or incubated with the following concentrations of TNF-a and INF-y; 10 nglad and 100 U ml (2), 50:tigimi and 5001J:Iinl (3), 75 rigirtil and 750 U ml (4), and 100 tiginil and.
1000 .1.11m1 (5) for 5 days and i::ultured tot 2 more :passages in absence :.of cytokines. The cells were then stained for SA--gal and compared to control untreated cells or those treated with 8 u114. etoposide as a positive control (6). Top panel shows photographs of representative data from 1 of 3 independent experiments. Bottom panel shows a histogram of densitometric analysis of the 6 studies. Data are presented as %
of SA-0-gal-positive cells and presented as mean + S.D. (n=3). P-values were calculated using a paired Student's t-test. Statistical significance was determined at *P <0.05.
**P < 0.01, ***I' < 0.001. Figure 6D is a histogram showing remits of studies in which combination treatment with nil cytokines IFINI-1 and INF-ct resulted in greater senescence in SK-13R-3 (10 rig/nil TNF-a + 100 U.fml IFN,y) and1-47D (100 nglird NF-ci + 1000 -Ultril IFN-y) cells, compared with untreated controls; NIDA-MB-231 cells (200 nglinl TN.F-a +
2000 1.1/ml :IFN-y) remained largely unaffected by dual 1EN-7 + TNF-a.
treatment. Data are presented as % of SA-0-gal-positive cells and presented as mean + S.D.
(n=3). P-values were calculated using a paired Student's t-test. Statistical significance was determined at **,P < 0.01, ***P < 0,001.
Figures 7A-7B show HER2 induces senescence and apoptpsi lvIDA-MB-231 breast cancer cells, Figure 7A, left panel, is a histogram showing results of densitometric analysis in which SA-0-gal staining was performed in Mak-NI13-231 cells transfected with wt IHER2 (pcDNAHER2) or with empty vector (peDNA3) which were treated with the listed concentrations of TNF-a and IFN-y for 5 days and cultured for 2 more passages in absence of cytokines. Inset above the histogram are photographs of western blot analysis in which MDA-MB-231 cells transfected with pcDNAHER2 or pcDNA3 and probedwith HER2 specific antibody were analyzed for confirmation of.
expression or lack thereof VinCtiiin was used as loading control. Data are presented a % of SA-I3-ga1-positiv'e cells and presented as mean + S.D, P-values were calculated using a paired Student's t-test. Statistical significance was determined at **''`F <o= 0= Figure 7A, right panel, shows photographs of representative data from I
of 3 independent experiments. Figure 713 shows photographs of western blot analysis of the cell lysates of the cells described in Figure 7A for expression of p15INKb and cleaved caspase-3. Vinciilin was used as loading control.
Figures $,-sp show combined HER2 and HER blockage expression enhances h Icytokines TNE-a.-and lFN.y senescenceindoction and apoptoSisin 5K-I3R-3 breast cancer cells. Figure 8A shows results of studies in. which SA-13-gal staining was pertbrmed in SK-BR-3 cells transfected with non,target siRNA (siRNA mr.), siRNA, HER3 siRNA or a combination of HER2 and HER3 siRNA, and then treated with the concentrations listed of TNF-a and IFN-y for 5 days and cultured for

2 more passages in absence of cytokines. Left panel shows a histogram of den sitometric analysis. Data are presented as % of SA-0-gal-positive cells and presented as mean +
- SD. (r3), P-values were calculated using a paired .Student's mest.
Statistical significance as de.terthined at ***14 < 0.001. Inset shows photographs of western blot analysis of SK-BR-3 cells transfected with NT, HER2, or HER3 siRNA probed with HER and HER3 specific antibodies. Vinculin was used as loading control.
Similar results were observed in 3 independent experiments. Right panel shows photographs of representative data from 1 of 3 independent experiments. Figure 8B shows results of studies in which lysates of the cells described in Figure 8A were analyzed by western blotting for 0151NKb. and cleaved. easpase-3 expression Figures.9A-9C show combined HER2 inhibition and .HER2-HER3 dimerization inhibition enhances Thl cytokines rtkw.-a. and EFN-li senescence inditction and apoptosis in SK-BR-3 breast cancer cells. Figure 9A shows results of SA-13-gal staining performed in SK-BR-3 cells which were untreated (1) or treated with 10 ngluil TNF-a and 100 1.11m1 IFN-7 (2), or with 10 u.g/m1 of trastuzumab (Tan), pertuzumab (Per)(3), or with the combination of both treatments (4) for 5 days and cultured for 2 more passages in absence of the antibodies and the cytokines. Left panel is a histogram of densitometric analysis. Data are presented as % of SA--gal-positive cells and presented as mean + S.D. (n=3). ). P-values were calculated using a paired Student's t-test Statistical significance was determined at ***P <0.001. Right panel are photographs showing representative data from I of 3 independent experiments.
Figure 911 shows photographs of western blot analysis in which cell lysates of the cells described in Figure 9A were analyzed for p151NKb or cleaved caspase-3 expression. Vinculin was used as loading control. Similar results were observed in 3 independent.
experiments.
Figure 9C shows results of studies of induction of apoptosis of SK-BR-3 cells untreated or treated as described above performed by staining for annexin V and Pi and analyzed by flow cytometry_ Top panel shows plots of representative data from 1 of 3 independent experiments. Bottom panel, shows a histogram of densitometric analysis. Data are presented as average SEM of annexin V Pr cells from 3 independent experiments. P-values were calculated using a paired Student's t-test. Statistical significance was determined at **P <0.01.
Figures I0A-1013 show combined treatment with trastuzumab: and pertuzuniab enhance C1)4:' Thi -mediated Senescence and apoptosis of HE R2-ovexpressing human breast cancer cells. Figure 10A shows results of studies in which.
using a transwell system, 0.5x 105 SK-BR-3 cells were co-cultured with 5x I 03 CD4' T-cells alone (CD4' only), CD4' 1-cells + 05x10 each of HER2 Class :1:1 peptide (DC H)-or irrelevant Class B. BRAF or survivin peptides (DC B. or DC S)-pulsed type I
polarized mature DCs, and CD4' T-cells + HER2 (iDC 11)-pulsed immature DCs arx: H), with or without 10 rig nil of trastuzumab (Tztn).andpertuzumah(Per) for 5 days: The cells were then cultured for 2 more passages in absence of the blocking antibodies' and the immune system cells and then stained for SA-0-gal expression and compared to untreated control cells. Top panel is a histogram of densitometric analysis. Data are presented as SA-13-gal-positive cells and presented as mean + S.D. (n=3). P-values were calculated using a paired Students t-test. Statistical significance was determined at ***P <0.000L
Bottom panel shows photographs of representative data from I of 3 independent experiments. Figure 108 shows photographs of western blot analysis of cell lysates of SK-BR-3 cells co-cultured as indicated and analyzed for p15INK4b and cleaved caspace-

3 expression. Increased pl 5INK4b and cleaved caspase-3 expression is seen that suggests induced senescence and apoptosis of SK-BR-3 cells, respectively when co-cultured with the DC H/CD4'1.-cells in presence of trastuzumab and pertuzumab, but not 'front DC B, DC S. and-iDC 11 giNPS. Vint").din as used as iloading:control.
:Results are representative of 3 independent- experiments. photographs of western blot analysis in which cell tysates of the cells described in Figure 9A were analyzed for p15INKb or cleaved caspase-3 expression, Figures 11A-111) show. Thi cytokineS TM -a and IFNI sensitize trastuzumab and pertuzumab resistant breast cancer cellsita senescence and apoptosis induction, figure 11A shows results of SA:1)7gal staining performed in HCC-1419 and mwr- t cells respectively untreated (1) or treated with $0 rig ml INS4 and 500 11 nil IFNI (2), or treated with 10 rig/m1 of trastuzumab (Tzm), pertuzumab (Per) (3), or treated with the combination of the same concentrations of trastuzumab, pertuzumab and INF-a, IFN-y (4) for 5 days and cultured for 2 more passages in absence of the antibodies and the cytokines. Top panel is a histogram of densitometric analysis. Data are presented as % of SA-0-gal-positive cells and presented as mean + S.D.
P-values were calculated using a paired Student's t-test. Statistical significance was determined at **P <0.01. Bottom panel, top layer, shows photographs of representative data from I of 3 independent experiments in HC-1419 cells. Bottom panel, bottom layer, shows photographs of representative data from 1 of 3 independent experiments in JIMT- I cells, Figure 1111 shows results of cell lysates of the cells described in Figure 11A which were analyzed by western blotting for pi 5INKb or cleaved caspase-3 expression in HC-1419 (left panel) and .11MT-1 (right panel). Vinculin was used as loading control. Similar results were observed in 3 independent experiments.
Figure 12 shows 1FN-yRa and TNF-RI are expressed in Similar levels in breast cell lines independently from their -HER2 level. IFN-yRet, INF-RI and expression in immortalized MCF-I OA mammary epithelial cells and breast cancer cell lines (SK-BR-3, BT-474, MCF-7, T-47D and MDA-MB-231) as determined by Western blot. Vinculin was used as loading control. Similar results were observed in 3 independent experiments.
Figures 13A-13B show combined HER2 and FIER3 blockage expression enhances Tb 1cytokines INF-a and IFNI senescence and appptosis induction in MC

breast cancer cells. Figure 13A shows'results of studies in which SA43-gal staining Was performed in MICF-7 cells transfected with non-target .s.iRNA (siRNA NT), HER2 siRNA ora-combination of 11ER2 and HER3 sill:NA, and then treated with the concentrations listed of INF-a and UN-'y for 5 days and cultured for 2 more passages in absence of cytokines. Left panel shows a histogram of densitometrie analysis. Data are presented as % of SA-fl-gal-positive cells and presented as mean SD. (n-3), P-values were calculated using a paired Student's t-test, Statistical significance was determined at "*P < 0.001. Inset shows photographs of western blot analysis of MCF-7 cells transf.ected with NT. HER2 or HER3 or a combination of and HER3 sikNA probed with HER?. and HER3 specific antibodies. Vinculin was used as loading control. Similar results were observed in 3 independent experiments Right panel shows photographs of representative data from I of 3 independent experiments.
Figure 1311 shows results of studies in which cell lysates of the cells described in Figure 13A were analyzed by western blotting for p15INKb or cleaved caspase-3 expression.
***P <0.001. Inset shows photographs of western blot analysis of SK-BR-3 cells transfected with NT, HERZ, or HER.3 sikNA probed with HER and HER3 specific antibodies. Vineulin was used as loading control. Similar results were observed in 3.
independent experiments.
Figures 14A-I 413 show the effect of Th I-elaborated cytokines on SK-BR-3 senescence and apoptosis. Figure I4.Ashows the results of studies using a transwell system, whereby 0.5x105 SK-BR-3 cells were co-cultured with 5x] 05 CD4.' T-cells alone (CD4.i. only), CD4' 0.5x105 each of 11ER2 Class fl peptide (DC -H)- or irrelevant Class II BRAE peptide (DC B)7pulsed type 1:polariZed mature DC :s, and CD4'"
T-cells HE.R2 (iDC H)- or BRAF (iDC B)-pulsed immature DCs for 5 days. The cells were then cultured for 2 more passages in absence of immune system cells and then stained .for SA-0-gal expression and compared to untreated control cells, Compared with IgG isotype control, senescence induced in SK-BR-3 treated with CD4VDC H is partially rescued by neutralizing IFNI and TNF-a with specific antibodies (75.27 %
rescue). Top panel is a histogram of densitometric analysis. Data are presented as % of SA-13-gal-positive cells and presented as mean + S.D. (n3),). P-values were calculated using a paired Student's Hest. Bottom panel shows corresponding photographs of representative data from 1 of 3- independent experiments. Figure 1411 shows photographs Of western blots show tog pi 5INK4h and cleaved caspase 3-expressions which suggest CA 02986687 2017-11-21 =

senescence and apoptosis induction of SK-BR-3 cells µvhen co-cultured With Dell,"CD4*
T-cells compared with DC B, IDC H, and iDC B groups. Compared with IgG isotype control, senescence and apoptosis induced in SK-BR-3 treated with CD4"/DC H
were partially rescued by neutralizing IFN-7 and TNF-u specific antibodies.
Vinculin was used as loading control. Results are representative of 3 experiments.
Figure 15 shows the effect of trastuzumab and pertuzumab on AKT
activation by heregulin in breast cancer cell lines. Serum-starved T-47D, HCC-1419 and JIM`17-1 cells were treated with trastuzumab (Tzm) and pertuzumab (Per 10 uglini, 90 min) and then stimulated with (HRG, 20 ng/ml, 5 min). Top panel, shows representative data from 1 of 3 independent experiments. Data are expressed as % of the HRG
response in the absence of trastuzumab and pertuzumab and presented as mean S.D.
Figure 16 shows vaccination procedure_ Patients with biopsy diagnosed HER2P's DCIS were enrolled in the trial. Patient's monocytes were collected by leukapheresis and elutriation. The monocytes were rapidly matured into type 1 DC:s, and the pre-vaccination anti-HER2 CD4 nu immune response was measured. Patients underwent 4-6 weekly vaccinations (+/- anti-estrogen therapy). Patient's monocytes were collected again by a second leukapheresis and elutriation, and the post-vaccination anti-HER2 CD4 Thl immune response was measured_ Following vaccination, patients underwent surgical resection to cure them of residual disease. The clinical response was measured in the surgical specimen and the itrumme response was mugged in the Sentinel lymph noties(SLNS") When available.
Figures 17A-17B shows results of SKBR3 and MCF7 breast cancer cell lines treated with Thl eytokines (IFNy and INFO, a tamoxifen metabolite (l¨Ifydroxy-Tamoxifen, "4HT"), or both. SKBR3 (ER) (Figure 17A) increased anti-tumor activity in response to Thl cytokine treatment, but not in response to anti-estrogen treatment or the combination treatment. 1VICF7 (ER') (Figure 17B) did not increase anti-tumor activity in response to either Th I cytokine treatment or anti-estrogen treatment, but the combination reaulted in an increase in imetabolicaetiity Figure 18 shows patient distribution for the combination anti!-estrogen ("AE") therapy and anti-HER2 DC1 vaccination study. HER-2 positivity was defined as >5% of cells expression 2+ or 3+ intensity of the HER-2 protein on immunohistochemistry. AE therapy (Tamoxifen, LetrOzole, or Anastrozole) as gh,en concurrently with DC vaccination.
Figure 19 is a histogram showing pathologic complete response rate comparing patients by ER status and AE treatment. (ER "-% ER" W/0 AE; ER" w AE).
Figures 20A-20B shows subsequent breast events of the study patiets comparing patients by pathologic complete response ("pC1r) (Figure 20A) and ER
status and AE treatment (Figure 208).
Figures 21A-21C show C1)4+ systemic immune response measured in the peripheral blood. By each metric of Th I response (responsivity (Figure 21A);
response repertoire (Figure 218) and cumulative response (Figure 21C)), there was a significant increase in the immune response following anti-HER2 DC1 vaccination. However, the pre- and post-vaccination immune responses were similar across all three groups.
Figures 22A-22C show CD4 local regional immune response measured in patient sentinel lymph nodes. By each metric (responsivity (Figure 22A);
response repertoire (Figure 228) or cumulative response (Figure 22C)) the post-vaccination immune responses were higher in the ER patients who received AE compared to the EW'' patients who did not receive AE.
Figure 23 shows CD8' systemic immune response measured in the peripheral blood. Responsivity of patients with ElVeg status and those with ER
P' status with and without anti estrogen treatment (ER P"' wi`o AE; ER" wAE) are shown, Figure 24 shows BRAFwmE-DC1 vaccines overcome vemurafenib resistance in BRAF-mutant murine melanoma.
DETAILED :DESCRIPTION
The present embodiments provide compositions arid methods for producing an FDA-approved injectable multi-dose antigen pulsed dendrific cell vaccine for the personalized treatment and prevention of cancer or other disorders. In one entbodiment, the embodiments provide cotnpositiODS and methods for producing an FDA-approved injectable multi-dose antigen pulsed type I polarized dendritic cell vaccine (DC1).

In one embodiment, there is provided a method to ciyopreservedendritic cells in multiple-dose aliquots that are in an antigen-loaded, pre-activated state that is "syringe-ready", i.e. suitable for immediate injection into the patient without the necessity of any further cell processing that would require (e.g., by FDA
mandate) additional facilities and quality control/assurance steps.
In one embodiment, there is provided a method to efficiently produce injectable multi-dose antigen pulsed dendritic cell vaccine, preferably injectable multi-dose antigen pulsed type I polarized dendritic cell vaccine that exhibit maximal efficacy.
In one embodiment, an FDA-approved injectable multi-dose antigen pulsed dendritic cell vaccine is produced by collecting DCs in a single patient leukapheresis. Preferably, the leukapheresis and production of the dendritic cell vaccine is performed at a first location whereby the first location can be a centralized vaccine production facility where the DCs are manipulated to create an activated.
antigen-loaded DC vaecine comprised of an initial immunizing dose and multiple "booster doses thereof An advantage of the present embodiments is that all FDA mandated quality control/quality assurance steps would be performed at the central facility, and after completion and release, all vaccine doses are cryopreserved and shipped to remote medical centers for serial administration to the patient. In one embodiment., the FDA-approved injectable multi-dose antigen pulsed dendritic cell vaccine of the embodiments dOes not requirement any Mandated quality .control/quality assurance steps at the administration site In another aspect, the present embodiments are based on the discovery that an effective therapy to treat cancer includes changing the immune response in the tumor so that the immune cells in the tumor site are more effective in attacking the tumor cells.
hi some instances, the effective therapy includes improving the migration and activity of immune cells in the tumor site. Accordingly, the embodiments provide compositions and methods of using a dendritic cell vaccine in combination with a composition that inhibits one or moie Of KR-2 and. HER,3 trastwaLtriab, pertigOW), and the like) asia treatment regimen to treat cancer_ In one entodiment,. the treatment regimen comprises the use of dendritic cell vaccines, an inhibitor of HER-2, arid a chemokine modulator.

In one embodiment there is provided compositions and methods for using a dendritic cell vaccine in combination with blockage crone or more of HER-2 and HER-3 as a treatment regimen to treat cancer. En another embodiment, there is provided compositions and methods of using a dendritic cell vaccine in combination with blockage of HER-2 and HER-3 with the addition of TNE-ct and IFN-y. In another embodiment there is provided compositions and methods of blocking one or more of HER-2 and HER-3 with the addition of TNF-a. and .IFN-y as a treatment regimen to treat cancer.
In one embodiment the treatment regimen of the embodiments comprise a combination therapy of inducing an anti-oncodriver Thl immune response (e.g., INF-rx.
and IFN-y) and oncodriver blockade for one or more of HER-2 and HER-3 In one embodiment, the treatment regimen of the embodiments can be used to treat cancer and therefore can be considered as a type of anti-cancer therapy. In another embodiment, the treatment regimen of the embodiments can be used in combination with another anti-cancer therapy including but is not limited to surgery, chemotherapy, radiation therapy (e.g. X ray), gene therapy, immunotherapy, hormone therapy, viral therapy, DNA. therapy, RNA therapy, protein therapy, cellular therapy, nanotherapy, and the like.
En one embodiment, the treatment regimen of the embodiements is used prior to receiving the other anti-cancer therapy. In another embodiment, the treatment regimen of the embodiments is used concurrently with receiving the other anti-cancer therapy_ In another embodiment, the treatment regimen of the embodiments is used after receiving the other anti-cancer therapy, in another embodiment concurrent neoadjuvmut anti-estrogen therapy and anti-HER2 DC1 vaccination increases the immune response in the local sentinel lymph nodes and the rate of pathological complete response in HER21"VERI" DCIS
patients.
Definitions Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which these embodiments belong. Although any methods and materials similar or tClUiVaittit to those described herein can be used in the ptoc.tice ot testing of the present embodiments, the preferred methods and materials are described.
Generally, the nomenclature used herein and the laboratory procedures in cell culture, molecular genetics, organic chemistry, and nucleic acid chemistry and hybridization are those well-known and commonly employed in the art.
Standard techniques are used for nucleic acid and peptide synthesis. The techniques and procedures are generally performed according to conventional methods in the art and various general references (e,g,. Sambrook and Russell, 2012, Molecular Cloning, A Laboratory Approach, Cold Spring Harbor Press, Cold Spring Harbor, NY, and Ausubel et al., 2012, Current .Protocols in Molecular Biology, John Wiley & Sons, NY), which are provided throughout this document.
The nomenclature used herein and the laboratory procedures used in analytical chemistry and organic syntheses described below are those well-known and cc:Muni:m-1y -employed in the att. Standard techniques or modifications thereof are used for chemical syntheses and chemical analyses.
As used herein, each of the following terms has the Meaning- associated with it in this section.
The articles "a" and an arc used berein.to irefer to one or to more than one (i.e., to at least one) of the grammatical object of the article, By way of example an element" Means one element Or more than one element, "About" as used herein when referring to a measurable value, such as an amount, a temporal duration, and the like, is meant to encompass variations of 20%, or .-110%, or I.5%, or - 1%, or +0.1% from the specified value, as such variations are appropriate to perform the disclosed methods_ The term "abnormal" when used in the context of organisms, tissues, cells or components thereof, refers to those organisms, tissues, cells or components thereof that differ in at least one observable or detectable characteristic (e.g., age, treatment, time ad* etc.) from those OrganisinS, tissues, cells or components thereof that .display the "normal" (expected) respective characteristic. Characteristics which are normal or expected for one cell or tissue type, might be .abnormal for a different cell or tissue type.

Tho term 'antigen" or µat.)," as used herein is-defined:as a molecule that provokes an immune response. This immune response may involve either antibody production, or the activation of specific immunologically-competent cells, or both. The skilled artisan will understand that any macromolecule,- including virtually all proteins or peptides, can serve as an antigen. Furthermore, antigens can be derived from recombinant or genomic DNA. A skilled artisan will understand that any DNA, which comprises a nucleotide sequences or a partial nucleotide sequence encoding a protein that elicits an immune response therefore encodes an "antigen" as that term is used herein.
Furthermore, one skilled in the art will understand that an antigen need not be encoded solely by a full length nucleotide sequence of a gene. It is readily apparent that the present embodiments include, but are not limited to, the use of partial nucleotide sequences of more than one gene and that these nucleotide sequences are arranged in various combinations to elicit the desired immune response. Moreover, a skilled artisan will understand that an antigen need not be encoded by a "gene" at all. It is readily apparent that an antigen can be generated synthesized or can be derived from a biological sample. Such a biological sample can include, but is not limited to a tissue sample, a tumor sample, a cell or a biological fluid.
"An antigen presenting celr (APC) is :a cell that.arecapable.of aCtivating T cells, and includes, but is not limited to, monocytesimacrophages. B cells and denctritic cells (PCs): =
'Antigen-loaded APC." or.an "antigen-pulsed APC" includes an APC, which has been exposed to an antigen and activated by the antigen. For example, an APC
may become Ag-loaded in vitro, e.g., during culture in the presence of an antigen. The .APC may also be loaded in vivo by exposure to an antigen. An "antigen-loaded APC" is traditionally prepared in one of two ways: ( 1) small peptide fragments, known as antigenic peptides, are "pulsed" directly onto the outside of the APCs; or (2) the APC is incubated with whole proteins or protein particles which are then ingested by the APC.
These proteins are digested into small peptide .fragments by the APC and are eventually transported to and presented on the APC surface. In addition, the antigen-loaded APC can also be generated by introducing a wiyinicleotide encoding an antigen into the cell.

"Ann-HER2 response is the immune response specifically againstHER2 protein.
"Apoptosis" is the process of programmed cell death. Caspase-3 is a frequently activated death protease.
The term "autoimmune disease" as used herein is defined as a disorder that results from an autoimmune response. An atitthrIMUTIC disease is the result of an Inappropriate and excessive response to a self-antigen. Examples of autoimmune diseases include but are not limited to, Addision's disease, alopecia amata, ankylosing spondylitis, autoimmune hepatitis, autoimmune pm-otitis, Crohn's disease., diabetes (Type I), dystrophic epidermolysis bullosa, epididymitis, glomerulonephritis, Graves' disease, Guillain-Barr syndrome, Hashimoto's disease, hemolytic anemia, systemic lupus erythematosus, multiple sclerosis, myasthenia gravis, pemphigus vulgaris, psoriasis, rheumatic fever, rheumatoid arthritis, sarcoidosis, sclerodenna, Sjogren's syndrome, spondyloarthropathies, thyroiditis, vasculitis, vitiligo, myxedema, pernicious anemia, ulcerative colitis, among others.
As used herein, the term "autologous" is meant to refer to any material derived from the same individual to which it is later to be re-introduced into the individual.
The term "B cell" as used herein is defined as a cell derived from the bone marrow and/or spleen. B cells can develop into plasma. cells which produce antibodies_ The term "cancer" as used herein is defined as a hypetproliferation of cells whose unique trait--loss of normal control--results in unregulated growth, lack of differentiation, local tissue invasion, and/or metastasis, Examples include but are not limited to, breast cancer, prostate cancer, ovarian cancer, cervical cancer, skin cancer, pancreatic cancer, colorectal cancer, renal cancer and lung cancer.
"CD4 Thl cells," "Thl "CD4+ T-helper type !cells," "CD4+ T
cells," and the like are defined as a subtype of T-helper cells that express the surface protein CD4 and produce high levels of the cytokine &e also, "T-helper cells."

"Cumulative response" -means the combined immune response of a patient group:expressed as the total sum ofteactive spots (spot-forming cells "SFC"
per 10 cells from IFN-T:ELISPOT analysis) frorri all 6 MEC class II binding peptides from a given patient group.
The term "cryopreserved" or "clyopresmation7 as used herein refers to cells that have been resuspended in a freezing medium and frozen at a temperature of around -70 C or lower, "DC vaccination," -DC immunization," '"Del immunization," and the.
like refer to a strategy using autologous dendritic cells to harness the immune system to recognize specific molecules and mount specific responses against them.
The ternO'dendritie cell" (DC) is an antigen presenting cell existing in vivo, in vitro, ex -Vivo, or in a host or subject, or which can be derived from a hematopoietic stem cell or a monocyte. Death-itic cells and their precursors can be isolated from a variety of lymphoid organs, e.g., spleen, lymph nodes, as well as from bone marrow and peripheral blood. The DC has a characteristic morphology with thin sheets (lamellipodia) extending in multiple directions away from the dendritic cell body.
Typically, dendritic cells express high levels of MBE and costimulatory (e.g.,137-1 and B7,.2) molecules. Dendritic cellsean induce antigen specific differentiation of T cells in vitro, and are able. to .initiate primary T cell responses in vitro and in vivo.
As used herein, an "activated 'DC" is a DC that has been exposed to a Toll-like receptor ationist The activated DC may or may not be loaded with an antigen.
The term "mature -DC" as used herein, is defined as a dendritic cell that expresses molecules, including high levels ofMliC class Ti, CD80 (137.1) and (B7.2). In contrast, immature dendritic cells express low levels of MI-1C
class It, CD80 (117.1) and CD86 (137.2) molecules, yet can still take up an antigen. "Mature DC" also refers to an antigen presenting:cell existing in vivo, in vitro, ex vi.vp, or in a host or subject that is DC1-polatized.(i.e., folly capable. of promoting cell-mediated immapity).

A `4disease " is a state .of health at animal *herein the animal cannot maintain homeostasis, and-wherein if the disease is not ameliorated then the animal's health continues to deteriorate.
A "disorder" in an animal is a state of health in which the animal is able to maintain homeostasis, but in .which the animal s-state-of health is less favorable than it wonld be in the absence of the disorder: Left untreated, a disorder does not rie,cessatily cause a further decrease in the animal's state of health.
A disease or disorder is "alleviated" if the severity or frequency of at least one sign or symptom of the disease or disorder experienced by a patient is reduced.
"Effective amount" or "therapeutically effective amount" are used interchangeably herein, and refer to an amount of a. compound, formulation, material, or composition, as described herein effective to achieve a particular biological result. Such results may include, but are not limited to, the inhibition of virus infection as determined by any means suitable in the art.
As used herein "endogenous" refers to any material from or produced inside an organism, cell, tissue or system.
As used herein, the term "exogenous" refers to any material introduced from or produced outside an organism, cell, tissue or system.
"Estrogen receptor (ER) positive" cancer is cancer which tests positive for expression of ER. Conversely, "ER negative" cancer tests negative for such expressiOn.
Analysis of ER status can be performed by any method known in the art The term "freezing medium" as used herein refers to any medium mixed with a cell sample in preparation for freezing, such that at least some of cells within the cell sample can be recovered and remain viable after thawing.
"HER2" is a member of the human epidermal growth factor receptor ("EGER") family. HER2 is overexpressed in approximately 20-25% of human breast cancer and is expressed in many other cancers A "HER.reeeptor is a receptor poteio tyrOsitie kuase1.Vhich belongs to the HER receptor family and includes EGER (EibBl, HERO, HER2 (ErbB2), HER3 (Erb133) and HERA (Erb134) receptors. The HER receptor will generally comprise an extracellular domain, which may bind an HER ligand andfor dimerize with another HER

receptor mole-edit ;, a lipophilie transmenthrane domain; a conservedintracellular tyrosine kinase domain; and a carboxyl-terminal signaling domain harboring several tyrosine residues which can be phosphorylated. The HER receptor may be a "native sequence"
HER receptor or an "amino acid sequence variant" thereof Preferably the HER
receptor is a native sequence human HER receptor.
The "HER pathway" refers to the signaling network mediated by the HER
receptor family.
"HER activation" refers to activation, or phosphorylation, of any one or more HER receptors. Generally, HER activation results in signal transduction (e.g. that caused by an intracellular kinase domain of a HER receptor phosphorylating tyrosine residues in the HER receptor or a substrate polypeptide). HER activation may be mediated by HER ligand binding to a HER dimer comprising the HER receptor of interest. HER ligand binding to a HER dimer may activate a kinase domain of one or more of the HER receptors in the dimer and thereby results in phosphorylation of tyrosine residues in one or more of the HER receptors andlor phosphorylation of tyrosine residues in additional substrate polypeptides(s), such as Akt or MAPK intracellular kinases.
"HER2 binding peptides," "HER2 MHC: class IT binding peptides,"
"binding peptides," "HER2 peptides," "immunogenic MHC class II binding peptides,"
"antigen binding peptides," "HER2 epitopes," "reactive peptides," and the like as used herein refer to MFIC Class II peptides derived from Or: based on the sequence of the IIER2inen protein, a target found on approximately 20-25% of all human breast cancers and their equivalents. HER2 extracellular domain "ECD" refers to a domain of that is outside of a cell, either anchored to a cell membrane, or in circulation, including fragments thereof HER2 intracellular domain "IC!)" refers to a domain of the HER2ineu protein within the cytoplasm of a cell. According to a preferred embodiment HER2 epitopes or otherwise binding peptides comprise 6 HER2 binding peptides which include 3 HER2 ECD peptides and 3 HER2 [CD peptides.
Preferred HER2 ECD peptides comprise:
Peptide 42-56: EILDML,RHEYQGCQVNT (SEQ NO; 1);
30. Peptide 98-114: .RERIVRGTQLFEDNYAL (SEQ. ID NO: 2);-and Peptide 328.-345: TQRCEKCSKPCARVCYGL (SEQ ID NO; 3);:.

Preferred HERZ ICD peptides comprise:
Peptide 776-790: GVOSPYVSRLLGICL (SEQ ID NO: 4);
Peptide 927-941: PAREIPDLLEKGERL (SEQ ID NO: 5); and Peptide 1166-1180: TLERPKTLSPGKNGV (SEQ JO NO: 6).
:In embodiments where patients are FILA-A2P"9fbave A2.I blood type WIC class I
peptides or epitopes comprise:
Peptide 369-377:KIFGSLAFL (SEQ ID NO:7); and Peptide 689-697:RLLQETELV (SEQ ID NO:) "11ER2P"' is the classification or molecular subtype of a type of breast cancer as well as numerous other types of cancer. 1{EIt2 positivity is currently defined by gene amplification by FISH (fluorescent in situ hybridization) assay and 2+
or 3+ on intensity of pathological staining.
is defined by the lack of tame amplification by FISH and can encompass a range of pathologic staining from 0 to 2+ in most cases_ The term "hyperproliferative disease" is defined as a disease that results from a byperproliferation of cells. Exemplary hyperproliferative diseases include, but are not limited to, cancer or autoinmiune diseases. Other hyperproliferative diseases may include vascular occlusion, restenosis, atherosclerosis, or inflammatory bowel disease, for example.
The term "inhibit," as used herein, means to suppress or block an activity or function, for example about ten percept relative to a control value.
Preferably, the.
activity is suppressed or blocked by 50% compared to a control value, more preferably by 75%, and even More preferably by 95%. Inhibit," as used herein, also means to reduce a molecule, a reaction, an interaction, a gene, an mRNA, and/or a protein's expression, stability, function or activity by a measurable amount or to prevent entirely_ :Inhibitors are compounds that, e.g., bind to, partially or totally block stimulation, decrease, prevent, delay activation, inactivate, desensitize, or down regulate a protein, a gene, and an mRNA stability, expression, function and activity, e.g.,antagonists.

=

As used herein, an "instructional material" includes a publication, a recording, a. diagram, or any other medium of expression which can be used. to communicate the usefulness of the compositions and methods of the embodiments.
The instructional material of the kit of the embodiments may, for example, be affixed to a container, which contains the nucteicacid, peptide, and/or composition of the embodiments Or be shipped together with a container which contains the nucleic acid, peptide, and/or composition. Alternatively, the instructional material may be shipped separately from the container with the intention that the instructional material and the compound be used cooperatively by the recipient.
"Isolated" means altered or removed from the natural state. For example, a nucleic acid or a peptide naturally present in a living animal is not "isolated," but. the same nucleic acid or peptide partially or completely separated from the coexisting materials of its natural state is "isolated." An isolated nucleic acid or protein can exist in substantially purified form, or can exist in a non-native environment such as, for example, a host cell.
"Metrics" of CD4 Thl- responses (or-Thl responses) are defined for each subject group analyzed for anti-HER2 CD4' Thl immune response: (a) overall anti41ER2 responsivity (expressed as percent of subjects responding to ?1 reactive peptide); (b) response repertoire (expressed as mean number of reactive peptides (n) recognized by each subject grow); and (c) curtmlativ-e response (expressed as total Sum of -reactive spots (spot-fOrtning "S.FC" per 10' cells from IFNI, ELISPOT
analysis) from 6 MHC Class II binding peptides from each subject group.
By the term "modulating," as used herein, is meant mediating, a detectable increase or decrease in the level of a response in a subject compared with the level of a response in the subject in the absence of a treatment or compound, and/or compared with the level of a response in an otherwise identical but untreated subject. The term encompasses perturbing and/or affecting a native signal or response thereby mediating a beneficial therapeutic response in a subjeCt, preferably, a huntan.
"Neoadjimun therapy" for breast cancer as used herein refers to treatment given before primary therapy (i.e., surgery). "Adjuvant. therapy" is treatment given after primary therapy to increase the chance of long-term survival.

As used herein, a "populationr includes reference to an isolated culture comprising a homogenous, a substantially homogenous, or a heterogeneous culture of cells. Generally, a "population" may also be regarded as an "isolated" culture of cells.
As used herein, a "recombinant cell" is a host cell that comprises a recombinant polynucleotide.
"Responsivity" or "anti-HER2 responsivity" are used interchangeably herein to mean the percentage of subjects responding to at least 1 of 6 binding peptides.
"Response repertoire" is defined as the mean number ("n") of reactive peptides recognized by each subject group.
"Sample" or "biological sample" as used herein means a biological material from a subject, including but is not limited to organ, tissue, exosome, blood, plasma, saliva, urine and other body fluid. A sample can be any source of material obtained from a subject.
"Senescence" refers to cells no longer capable of dividing but which are still alive and metabolically active. Hallmarks of senescent cells include an essentially irreversible growth arrest, and expression of SA4-gal, P15INK
4B and pl6INK4a, "Signal I" as used herein generally referS to the first.biochemicatsignal passed from an activated DC to a T cell. Signal.] is provided by an antigen expressed. at the surface of the. DC and is sensed by the T cell through the T cell receptor%
Signal. 2" as used herein generally refers to the second signal provided by -DCs to T cells. Signal 2 is provided by "costimulatoty" molecules on the activated DC, usually CD80 and/or CD86 (although there are other co-stimulatory molecules known), and is sensed by the I cell through the surface receptor.CD28.
"Signal 3" as used herein generally refers to the signal generated from soluble proteins (usually cytokines) produced by the activated DC, These are sensed.
through receptors on the I lymphocyte. The 3rd signal instructs the T cell as to which phenotypical or functional features they Should ae4uire to best deal with-the current threat.

-BY the term "specifically binds," as used herein, is meant a molecule, such as an antibody, which recognizes and binds to another molecule or feature, but does not substantially recognize or bind other molecules or features in a sample.
The terms "subject," "patient," "individual," and the like are used interchangeably herein, and refer to any animal, or cells thereof whether in viim or in situ, amenable to the methods described herein. in certain non-limiting embodiments, the patient, subject or individual is a human.
"T/C" is defined as trastuzumab and chemotherapy. Tins -refers to patients that receive both trastuzumab and chemotherapy before/after surgery for breast cancer.
The term "T cell" as used herein is defined as a thymus-derived cell that participates in a variety of cell-mediated immune reactions.
The terms "T-helper cells," "helper I cells," "Th cells," and the like are used herein with reference to cells indicates a sub-group of lymphocytes (a type of white blood cell or leukocyte) including different cell types identifiable by a skilled person in the art. hi. particular, T-helper cells are effector T-cells (such as Th I, Th2 and Th17) whose primary function is to promote the activation and functions of other B and T
lymphocytes and/or macrophages. Helper T cells differentiate into two major subtypes of cells known as "Thl" or "Type 1" and "Th2" or "Type 2" phenotypes. These Th cells secrete cytokines, proteins, or peptides that stimulate or interact with other leukocytes.
"Thl "CD4.'. Thi "CD4 T;lielper type! "CD4'.I cell" and the like as used herein refer to a mature T-cell that has expressed the surface.
glycoprotein C04.
CD4* T-helper cells become activated when they are presented with peptide antigens by MEC class II molecules which are expressed on the surface of antigen-presenting peptides ("APCs") such as dendritic cells. Upon activation of a CD4j. T helper cell by the MHC-antigen complex, it secretes high levels of cytokines such as interferon-I
("IFN-y"). Such cells are thought to be highly effective against certain disease-causing microbes that live inside host cells, and are critical in antitumor response in human cancer.
"TM T cell" as used herein refers to a I cell that produces high levels 01'-the cytokine IFN-y and is thought to be highly effective against certain disease-causing microbes that live inside host cells, and cancer as well.
22 =

CA 02986687 2017-11-21 .

"1h17 T cell" as used herein refers to .a T cell that produces high levels of the cytokines IL-17 and 1L-22 and is thought to be highly effective against disease-causing microbes that live on mucousal surfaces.
"Therapeutically effective amount" is an amount of a compound of the embodiments, that when administered to a patient, ameliorates a symptom of the disease.
The amount of a compound of the embodiments which constitutes a "therapeutically effective amount" will vary depending on the compound, the disease state and its severity, the age of the patient to be treated, and the like. The therapeutically effective amount can be determined routinely by one of ordinary skill in the art having regard to his own knowledge and to this disclosure.
The terms "treat," "treating," and "treatment," refer to therapeutic or preventative measures described herein. The methods of "treatment" employ administration to a subject, in need of such treatment, a composition of the present embodiments, for example, a subject: afflicted a disease or disorder, or a subject who ultimately may acquire such a disease or disorder, in order to prevent, cure, delay, reduce the severity of, or ameliorate one or more symptoms of the disorder or recurring disorder, or in order to prolong the survival of a subject beyond that expected in the absence of such treatment.
The term "Toll like receptor", or "TLR" as used herein is defined as a 20. class of Proteins that play a:role in the innate-Mu-mine system. =TLRs are single-membrane-spanning, non-catalytic receptors that recognize structurally.
conserved molecules derived from microbes. TLRs activate immune cell responses upon .binding to a ligand.
The term "Toll like receptor agonists)% or "TLR. agonists'as used herein is defined as a ligand that binds to the TLR to activate immune cell response.
The term "vaccine" as used herein is defined as a material used to provoke an immune response after administration of the material to an animal, preferably a mammal, and more preferably a hunian. Upon introduction into a subject the vaceine Is able to provoke an immune response including, but notlimited to, the production of -antibodies, cytokines and/or other cellular responses.

Ranges : throughotnthis disclosure various aspects of the embodiments can be presented in a range format. It Should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the embodiments. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from I to 6 should be considered to have specifically disclosed subranges such as from I to 3, from I to 4, from I to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 22, 3, 4, 5, 53, and 6. This applies regardless of the breadth of the range.
Description The present embodiments include a preparation of DCs. In one embodiment, the DC preparations are greater than 90% pure. In another embodiment, the DC preparations are fully activated. For example, the DCs are activated with a cytokine and/or a Toll like receptor ligand, a state which is fully maintained by the cryopreservation technique of the embodiments. A benefit of the DC preparation of the embodiments is that the cells are efficiently cryopreserved from a single leukapheresis (patient collection) into an initial vaccine plus multiple "booster" doses (e.g., 10 or more) 20. that can be thawed as needed at remote treatment locations -without any specialized cell processing facilities or further required quality control testing.
As contemplated herein, the present embodiments provide a method for generating and cryopreseiving DCs with superior functionality in producing stronger signals to T cells, and thus resulting in a more potent DC-based vaccine. By effectively cryopreserving such cells, samples can be stored and thawed for later use, thereby reducing the need for repeated pheresis and elutriation processes during.
vaccine production. Being able to freeze DCs and then thaw them out later is an advantage because it means that ..4 single round . vaccine production can he divided into small.
parts, frozen away, and then administered one at a time to a patient over the course of weeks, months, or years to give "booster" vaccinations that strengthen immunity, In one embodiment, the present embodiments includes an FDA- approved injectable multi-dose antigen pulsed dendritic cell Vaccine produced by collecting DCs in a single patient letikapheresis. The FDA- approved injectable multi-dose antigen pulsed dendritic cell vaccine comprises an initial immunizing dose and multiple "booster" doses.
The FDA- approved injectable multi-dose antigen pulsed dendritic cell vaccine are mopreserved and can be shipped to remote medical centers for serial administration to the patient with no special requirements at the administration site (e.g., FDA
mandated QC/QA steps).
The present embodiments also relate to the cryopreservation of these activated DCs in a manner that retains their potency and functionality in presenting antigen as well as their production of various cytokines and chemokines after thawing, such that the cryopreserved and subsequently thawed activated DCs are as clinically effective as freshly harvested and activated DCs.
The present embodiments also relate to inducing tumor senescence and apoptosis in a cell by blocking one or more of HER-2 and HER-3 in combination with activating anti-HER-2 CD4 Thl cells. Accordingly, the embodiments include a combination and method for promoting an anti-oncodriver Th I immune response with an oncodiiver blockade for HER-2 in order to promote tumor senescent in HER-2 expressing breast cancers. in one embodiment, promoting an anti-oncodriver Thl 29 immune response comprises TNF-a. and IFN-y. In one embodiment, an oncodriver blockade for HER-2 includes an composition that blocks HER-2 including but is not limited to trastuzumab and pertuzumab.
In one embodiment, there are compositions and methods for the combination of blocking one or more of HER-2 and HER,3 together with the addition of TNF-0( and IFN-y for inducing senescence of HER-2 expressing breast cancer. In one embodiment, the INF-cL and IFN-y is secreted from CD4 Thl cells.
In one embodiment, HER2 is required in the mechanism of TNF-ct and IFN-y inducing senescence and apopwsis in breast cancer cells.
in one embodiment, INF-a and IFINI-7 restores the sensitivity to trastimonab and :pertnzurnab to breast cancer resistant cells In one embodiment, the Th cytokines,IFN-y and INE-a, revert the resistance to the therapeutic agents that is affecting cancer patients widely.
DC-Based Immunotherany Des are derived from pluripotent monocytes that serve as antigen-presenting cells (APCs), DCs are ubiquitous in peripheral tissues, \here they are prepared to capture antigens. Upon antigen capture, DCs process the antigen into small peptides and move towards secondary lymphoid organs. It is within the lymphoid organs that DCs present antigen peptides to naive T cells, thereby initiating a cascade of signals that polarizes I cell differentiation. Upon exposure, DCs present antigen molecules bound to either MHC class I or class 11 binding peptides and activate CD8 or CD4' T
cells, respectively (Steinman, 1991, Annu. Rev. Immunot 9:271-296; Banchereau et al., 1998, Nature392,245-252; Steinman, et al.õ 2007. Nature 449:419-426; Ginhoux et at, 2007, J. ap. Med. 204:3133-3146; Banerjee et al., 2006, Blood 108:2655-2661;
Sallusto et at, 1999, J. Exp. Med. 189:611-614; Reid et al., 2000, Cum Opin, Immuno1.12:114-121; Bykovskaia et al., 1999, J. Leukoc. Biol. 66:659-666;
Clark et at, 2000, Microbes infect, 2:257-272), DCs are responsible for the induction, c.00rdination and revilation of the adaptive immune response and also serve to orchestrate communication between effectors of the innate arm and the adaptiAT arm of the immune system. These features have made DCs strong candidates for immunotherapy, DCs have a unique capacity to sample the environment through macropinocytosis and receptor-mediated endocytosis (Gerner et al., 2008,3. immunoll 81:155-164; Stoitzner et al., 2008, Cancer Immunol.
Immunother 57:1665-1673; Lanzevecchia A., 1996, Curr_ Opin. Innnunol.8:348-354;
Delamarre et at, 2005, Science, 307(5715):1630-1634).
DCs also require maturation signals to enhance their antigen-presenting capacity. DCs upreaulate the expression of surface molecules, such as CD80 and (also known as second signal molecules) by providing additional maturation signals, such as TNF-a, CD401, or calcium signaling agents (Czerniecki et at, 1997,. J.
Immunol.159:3823-3837; IBedrosian et al. 2000, J. Immunother. 23:311-320;
Mailliard et at, 2004, Cancer Res.64,5934-5937; Brossart et at, 1998, Blood 92:4238-4247; Jin et CA 02986687 2017-11-21 =

al 2004, Hum. Irimitmol. 65:91-103). It has been established that 4 mixture of cytokines, including INF-,a, IL-6 and prostaglandin E2 (PGE2), have the ability- to mature DC (Jonuleit, et al., 2000, Arch. Derm. Res, 292:325-332). Des can also be matured with calcium ionophore prior to being pulsed with antigen.
:En addition to pathogen-recognition receptors, such as .PKR and MDA.-5 (Ka:lab et al., 2008, J. Immunol. 181:2694-2704; Nallagatla et al., 2008, RNA
Biol.
5(3):140-144), Des also contain a series of receptors, known as Toll-like receptors (lilts), that are also capable of sensing danger from pathogens. When these TLRs are triggered, a series of activational changes are induced in DCs, which lead to maturation and signaling of T cells (Boullart et al. 2008, Cancer Immunol. Immunother.
57(11):1589-1597; Kaisho et al., 2003, Curr. Mol. Med. 3(4)373-385; Pulendran et al., 2001, Science 293(5528):253-256; Napo! itani et al., 2005, Nat. Inummol.
6(8):769-776).
Des can activate and extend the various arms of the cell-mediated response, such as natural killer .-y-8 T and a-13 T cells and, once activated, Des retain their immunizing capacity (Steinman, 1991, Annu. Rev, Immunol. 9:271-296; Banchereau et al., 1998, Nature 392:245-252; Reid et al., 2000, CUM 0.pin. Immunol. 12:114-121;
Bykovskaia et al., 1999, J. Leukoc. Bio1,66:659-666; Clark et al., 2000, Microbes Infect.
2:257-272).
The present embodiments include mature, antigen loaded Des activated by Toll-like receptor agonists that induce clinically effective immune responses, 20. preferably \Ohen used earlier in the disease proCeSs. The Des of thepresemembodiments produce desirable levels of cytokines and chemokines, and further have the, capacity to induce apoptosis of tumor cells.
In one embodiment, there is provided a method of large scale production of antigen pulsed dendritic cell vaccine. In one embodiment, the method comprises rapidly maturing dendritic cells, cryopreserving the dendritic cells, and thawing the cryopresemed cells wherein the thawed dendritic cells produce an effective amount of at least one cytokine to generate a T cell response.
In one embodiment the maturation of dendritic cells eopriptie contacting the cells with IFN-gamma and LIPS.
In one embodiment, the thawed cells maintain DC1 phenotype to drive a ml polarized immune response.

In One etribodiment, the thawed cells maintain the ability to primarily sensitize T cells.
Generation of a loaded (pulsed) immune cell The present embodiments include a cell that has been exposed Or otherwise "pulsed" with an antigen. For example, an APC, such as a DC, may become Ag-loaded in vitro, e.g., by culture ex vivo in the presence of an antigen, OT
in vivo by exposure to an antigen.
A person skilled in the an would also readily understand that an APC can be "pulsed" in a manner that exposes the APC to an antigen for a time sufficient to promote presentation of that antigen on the surface of the APC. For example, an APC can be exposed to an antigen in the form of small peptide fragments, known as antigenic peptides, which are "pulsed" directly onto the outside of the APCs (Mehta-Damani el al., 1994); or APCs can be incubated with whole proteins or protein particles which are then ingested by the APCs. These whole proteins are digested into small peptide fragments by the APC and eventually carried to and presented on the APC surface (Cohen et at, 1994).
Antigen in peptide form may be exposed to the cell by standard "pulsing"
techniques described herein.
Without wishing to be bound by any particular theory, the antigen in the 20. form of a foreign- or an atitoantigen is processed by the APC of the embodiments in otclet to retain .the immunogenic form of The antigen. The immunogenic form of the antigen Implies processing of the antigen through fragmentation to produce a form of the antigen that can be recognized by and stimulate immune cells, for example I cells.
Preferably, such a foreign or an autoantigen is a protein which is processed into a peptide by the APC. The relevant peptide which is produced by the APC may be extracted and purified for use as an immunogenic composition. Peptides processed by the APC may also be used to induce tolerance to the proteins processed by the APC.
The antigen-loaded APC, Otherwise known as a "pulsed APC" of the embodiments, is produced by exposure of the APC to an antigen either in vitro or in. vivo, In the case where the APC is pulsed in vitro, the APC can be plated on a culture dish and exposed to an antigen in a sufficient amount and for a sufficient period of time to allow the antigen to bind to the APC. The amount and time necessary to achieve binding -of the antigen to the APC may be determined by using methods known in the art or otherwise disclosed herein. Other methods known to those of skill in the art, for example immunoassays or binding assays, may be used to detect the presence of antigen on the APC following exposure to the antigen.
In a further embodiment, the APC may be transfected with a vector which allows for the expression of a specific protein by the APC, The protein which is expressed by the APC may then be processed and presented on the cell surface.
The transfected APC may then be used as an immunogenic composition to produce an immune response to the protein encoded by the vector.
As discussed elsewhere herein, vectors may be prepared to include a specific polynucleotide which encodes and expresses a protein to which an immunogenic response is desired. Preferably, retroviral vectors are used to infect the cells. More preferably, adenoviml vectors are used to infect the cells.
In another embodiment, a vector may be targeted to an APC by modifying the viral vector to encode a protein or portions thereof that is recognized by a receptor on the APC, whereby occupation of the APC receptor by the vector will initiate endocytosis of the vector, allowing for processing and presentation of the antigen encoded by the nucleic acid of the viral vector. The nucleic acid which is delivered by the virus may be 20- rtati've to the virus, which When expressed on the APC encodes Vital proteinawhiehare then processed and presented on the MIIC receptor of the APC.
As contemplated herein, various methods can be used for transfecting a polytmeleotide into a host celL The methods include, but are not limited to, calcium phosphate precipitation, lipofection, particle bombardment, microinjection, electroporation, colloidal dispersion systems (i.e. macromolecule complexes, nanocapsules, microspheres, beads, and lipid-based systems including oil-in-water emulsions, micelles, mixed micelles, and liposomes). These methods are understood in the aft and are:described in published literature o as to enable one skilled in the art to perform these methods.
In another embodiment, a polynucleotide encoding an antigen can be cloned into an expression vector and the vector can be introduced into an APC
to otherwise generate a loaded APC. 'Various types of vectors and methods of introducing nucleic acids into a cell are discussed in the available published literature.
For example, the expression vector can be transferred into a host cell by physical, chemical or biological means. See, for example, Sambrook et al. (2001, Molecular Cloning:
A
Laboratory Manual, Cold Spring :Harbor Laboratory, New York), and in Ausubel et al.
(1997, Current Protocols in Molecular Biology, John Wiley & Sons, New York).
It is readily understood that the introduction of the expression vector comprising a polynucleotide encoding an antigen yields a pulsed cell.
The present embodiments include various methods for pulsing APCs including, but not limited to, loading APCs with whole antigen in the form of a protein, cDNA or mRNA. However, the embodiments should not be construed to be limited to the specific. form of the antigen used for pulsing the APC. Rather, the embodiments encompass other methods known in the art for generating an antigen loaded APC.

Preferably, the APC is tranfected with mRNA encoding a defined antigen. mRNA
corresponding to a gene product whose sequence is known can be rapidly generated in vitro using appropriate primers and reverse transcriptase-polymerase chain reaction (RT-PCR) coupled with transcription reactions. Transfection of an APC with an mRNA

provides an advantage over other antigen-loading techniques for generating a pulsed APC. For example, the ability to amplify RNA from a microscopic amount of tissue, i.e.
tumor tissue, extends the use of the APC for accip4tion to a large number of patients.
For an antigenic composition to be useful as a-vaccine, the antigenic composition must induce an immune response to the antigen in a cell, tissue or mammal (e.g., a human). As used herein, an "immunological composition" may comprise an antigen (e.g., a peptide or polypeptide), a nucleic acid encoding an antigen (e.g., an antigen expression vector), or a cell expressing or presenting an antigen or cellular component. In particular embodiments the antigenic composition comprises or encodes all or part of any antigen described herein, or an immunologically functional equivalent thereof In Other embodiments, the antigenic Cornposition is in a mixture that eomprises an additional immunostimnlatory agent or nucleic acids encoding such an agent.
Immtmostimulatoty agents include but are not limited to an additional antigen, an immunomodulator, an antigen presenting cell or an adjuvant. In other embodiments, one or more of the additional agent(s) is covalently bonded to the antigen or an.
immunostimulatory agent, in any combination, In certain embodiments, the antigenic composition is conjugated to or comprises an HLA anchor motif amino acids.
A vaccine, as contemplated herein, may vary in its composition of nucleic acid and/or cellular components. In a non-limiting example, a nucleic encoding an antigen might also be formulated with an adjuvant. Of course, it will be understood that various compositions described herein may further comprise additional components. For example, one or more vaccine components may be comprised in a lipid or liposome. In another non-limiting example, a vaccine may comprise one or more adjuvants. A.
vaccine of the present embodiments, and its various components, may be prepared and/or administered by any method disclosed herein or as would be known to one of ordinary skill in the art, in light of the present disclosure.
It is understood that an antigenic composition oldie present embodiments.
may be made by a method that is well known in the art, includingbutnOt limited to chemical synthesis by solid phase synthesis and purification away from the other products of the chemical reactions by HPLC, or production by the expression of a nucleic acid sequence (e.g., a DNA sequence) encoding a peptide or polypeptide comprising an antigen of the present embodiments in an in vitro translation system or in a living cell. In addition, an antigenic composition can comprise a cellular component isolated from a 20. biological sample. The antigenic composition isolated and extensively dialyzed to remove. one or more undesired small molecular weight molecules andlor lyophilized for more ready formulation into a desired vehicle. It is ftuther understood that additional amino acids, mutations, chemical modification and such like, its any, that are made in a vaccine component will preferably not substantially interfere with the antibody recognition of the epitopic sequence.
A peptide or polypeptide carresponding to one Of more antigenic determinants of the present embodiments should generally be at least five or six amino acid tesidnes in length, and may contain op to about. 10 about 15õ about 20, about 25, about 3.0, about 35õ about 40, about 45 or about 50 residues or so. A peptide sequence may be synthesized by methods known to those of ordinary skill in the art, such as, for example, peptide synthesis using automated peptide synthesis. machines, such as those available from Applied Biosystems, Inc., Foster City, CA (Foster City, CA).
Longer peptides or polypeptides also may be prepared, e.g., by recombinant means. in certain embodiments, a nucleic acid encoding an antigenic tompOsitiOli.andlor a component described herein may be used, for example, to produce an antigenic composition. in Om or in viva for the various compositions and methods of the present embodiments. For example, in certain embodiments, a nucleic acid encoding an antigen is comprised in, for example, a vector in a recombinant cell. The nucleic acid may be expressed to produce a peptide or polypeptide comprising an antigenic sequence.
The peptide or polypeptide may be secreted from the. cell, or comprised as part of or within the cell.
In certain embodiments, an immune response may be promoted by transfecting or inoculating a mammal with a nucleic acid encoding an antigen.
One or more ells comprised within a. target mammal then expresses the sequences encoded by the nucleic acid after administration of the nucleic acid to the mammal. A
vaccine may also be in the form, for example, of a nucleic acid (e.g., a cDNA or an RNA) encoding all or part of the peptide or polypeptide sequence of an antigen. Expression in viva by the nucleic acid may be, for example, by a plasmid type vector, a. viral vector, or a virallplasmid construct vector.
In another einbodiment, the 'nucleic acid comprises a coding region that encodes allor.part of the sequencesencoding an appropriate-antigen, or an immunologically functional equivalent thereof. Of course, the nucleic acid may comprise andior encode additional sequences, including hut not limited to those comprising one or more immunomodulators or adjuvants.
Antigens As contemplated herein, the present embodiments may include use of any antigen. Suitable for loading into an: APc to elicit an immune feVOLISe . In one embodiment, tumor antigens may be used. Timor antigens can be divided into two broad categories: shared tumor antigens; and unique tumor antigens. Shared antigens are expressed by many tumors, while unique tumor antigens can result from mutations induced through physical or chemical careinogens, and are therefore expressed only by individual tumors. In certain embodiments, shamd tumor antigens are loaded into the DCs of the present embodiments. In other embodiments, unique tumor antigens are loaded into the DCs of the present embodiments.
In the context of the present embodiments, "-tumor antigee refer to antigens that are common to specific hyperproliferative disorders in certain aspects, the hyperproliferative disorder antigens of the present embodiments are derived from cancers, including but not limited to, primary or metastatic melanoma, thymoma, lymphoma, sarcoma, lung cancer, liver cancer, non-Hodgkin's lymphoma, Hodgkins lymphoma, leukemias, uterine cancer, cervical cancer, bladder cancer, kidney cancer and adenocarcinomas such as breast cancer, prostate cancer, ovarian cancer, pancreatic cancer, and the like.
Malignant .tumors express a number of proteins that can serve as target antigens for an inmmtne -attack. These Molecules include, but are not limited to, tissue-specific antigens such as MART-1, tyrosinase and OP 100 in melanoma, and prostatic acid phosphatase (PAP) and prostate-specific antigen wsi-io in prostate cancer. Other target molecules belong to the group of transformation-related molecules, such as the oncogene HER-2/NeulErbB-2. Yet another group of target antigens are onco-fetal antigens, such as carcinoembryonic antigen (CEA). In B cell lymphoma, the tumor-specific idiotype immunoglobulin constitutes a Indy tumor-specific immtmoglobtilin antigen that is unique to the individual tumor, 13 cell differentiation antigens, such as CD! 9, CD20 and CD37, are other candidates for target antigens in B cell lymphoma.
Some of these antigens (CEA, HER-2, CD 19, CD20, idiotype) have been used as targets for passive inunwtotherapy with monoclonal antibodies with limited success.
The tumor antigen and the antigenic cancer epitopes thereof may be purified and isolated from natural sources such as from primary clinical isolates, cell lines and the like. The cancer peptides and their antigenic epitopes may also be obtained by chemical syntheSis or by recombinant DNA. tediniquesiknoNVii. in the arts.
Techniques for chemical synthesis are described in Steward et at (1-969);:-Bodansky et at (1974 Meienhofer (1983); and Schroder et at. (1965). Furthermore, as described in Renkvist et al. (2001), there are numerous antigens known in the art. Although analogs or artificially modified .epitopes:are not specifically described, a skilled artisan recognizes how to obtain or generate them by standard means in the art. Other antigens, identified by antibodies and as detected by the Serex technology (see Sahin et al. (1997) and Chen et al. (2000)), are identified in the database of the Ludwig Institute for Cancer Research.
In yet another embodiment, the present embodiments may include microbial antigens for presentation by the APCs. As contemplated herein, microbial antigens may be viral, bacterial, or fungal in origin. Examples of infectious virus include:
Retroviridae (e.g. human immunodeficiency viruses, such as HIV -1 (also referred to as HTLAT-Ill, LAY or HILN-III/LAY, or tifY411.; and other isolates, such as H1V-LP;
Picornaviridae (e.g. polio viruses, hepatitis A virus; enteroviruses, human coxsackie viruses, rhinoviruses, echoviruses); Calciviridae (e.g. strains that cause gastroenteritis);
Togaviridae (e.g. equine encephalitis viruses, rubella viruses); Flaviridae (e.g. dengue viruses, encephalitis viruses, yellow fever viruses); Coronaviridae (e.g.
corortaviruses);
Rhabdoviridae (e.g. vesicular stomatitis viruses, rabies viruses); Filoviridae (e.g. chola viruses); Paramyxoviridae (e.g. parainfluenza viruses, mumps virus, measles virus, respiratory syncytial virus); Orthomyxoviridae (e.g. influenza viruses);
Bungaviridae (e.g. Hantaan viruses, bunga viruses, phleboviruses and Naito viruses); Arena viridae (hemorrhagic fever viruses); Reoviridae (e.g. reoviruses, orbiviruses and rotaviruses);
Bimaviridae; Hepadnaviridae (Hepatitis B virus);1Parvovirida (parvoviruses);
20. Papovaviridae (Papilloma viruses, polyoma iruses); Adenovitidae (most adertoviruses);
Iletpesviridae (limes simplex virus (11W) I and 2, vaticella zoster virus, cytomegalovirus (CMV), herpes virus); Poxviridae (variola viruses, vaccinia viruses, pox viruses); and rridoviridae (e.g. African swine fever virus); and unclassified viruses (e.g.
the etiological agents of Spongiform encephalopathies, the agent of delta hepatitis (thought to be a defective satellite of hepatitis B virus), the agents of non-A, non-B
hepatitis (class 1.---internally transmitted; class 2--parenterally transmitted (i.e. Hepatitis C); Norwalk and related viruses, and astroviruses).
.ExaMples of infectious baCteria includet Helitobacter pyloriS,.E3orelia burgdorferi, Legionella pneumophilia, IMycobacteria sps (e :g, M.
tuberculosis, M. aviurn, M. intracellulare, M. kansasii, M. gordonae), Staphylococcus aureus, Neisseria gonorrboeae, Neisseria meningitidis, Listeria monocytogenes, Streptococcus pyogenes (Group A Streptococcus), Streptococcus agalactiae (Group 13 StreptococcuS), Streptococcus (viridans group), Streptococcus faecalis, Streptococcus bovis, Streptococcus (anaerobic sps.), Streptococcus pneumoniae, pathogenic Clunpylobacter sp., Enterococcus sp., Haemophilus influenzae, Bacillus anthracis, corynebacterium diphtheriae, corynebacterium sp., Etysipelothtix rhusiopathiae, Clostridium perfringens, Clostridium tetani, Enterobacter aemgenes, Klebsiella pneumoniae, PastureIla multocida, Bacteroides sp, Fusobacterium nucleatum, Streptobacillus moniliformis, Treponema Treponema pertenue, Leptospira, and Actinomyces israeilL
Examples of infectious fungi include: Cryptococcus neofbrmans, Histoplasma capsulatum, Coccidioides immitis, Blastornyces dermatitidis, Chlamydia trachomatis, Candida albicans. Other infectious organisms (i.e., protists) including:
Plasmodium falciparum and Toxoplasma Activation of DCs While traditional DC-based vaccines (that have previously dominated clinical trials) comprise of matured DCs generated from using a cytokine cocktail mixture including combinations of TNIF, 1L-6, PGE2 and 1L-113, which ultimately stimulate aseptic inflammation, the present embodiments instead utilize TLR agonists to mature the DCs and stimulate production of signal_ According to an aspect of the present embodiments, the stimulation of DCs. with a combination of TLR ligands leads to the production of increased amounts of 1L-12. Further, activation of DCs with a combination of TLR agonists can yield a more pronounced C1)4 and CDS T-cell response (Waraer et at., 2006, Blood 108:544-550).
Thus, the DCs of the present embodiments can secrete Th1 driving cytokines, such as IL-12, by exposure to these ligands that trigger ThRs. For example, the addition of poly(1:C), a TLR3 agonist to EL-1 13, INF-a, and IEN-y, can generate a potent type-I
polarized DC, characterized by robust levels of IL-12 production (Heifler et al., 1996, Eur. Inatutiol. 26 6 S9 -668) In CertainettiboditnOts, antigen can be loaded into. the DC prior to TLR agonist exposure. in other-embodiments, antigen can be loaded into the DC subsequent to MR agonist exposure.
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According to an aspect of the present .emhodinients, the injectable multi-dose antigen pulsed dendritic cell vaccine is produced by collecting DCs in a single patient leukapheresis whereby the cells are activated with biomolecules that simulate bacterial infection (e.g., LPS). This unique activation method endows the DCs with qualities not found in DCs that are matured with a cytokine cocktail of `INF, 11,6, .PGE2 and IL-1p (the "traditional maturation"), which also simulates aseptic inflammation (Lombardi et at.. 200, J. Immunol. 182:3372-3379).
In one embodiment, the DCs of the present embodiments can be activated with the combination of the TLR4 agonist, bacterial lipopolysa.ccharide (LPS), the TLR7/8 agonist, resimiquod (R848) andlor IFN-y (Amati et al., 2006, Curt.
Pharm. Des 12:4247-4254). By activating DCs with a TLR4 agonist and bacterial LPS, DCs are generated that are at least virtually identical (in phenotype) to DC1s generated via traditional maturation methods. These DCs have a high expression of surface molecules, Including CD83, (1)80, CD86 and IlLA-DR. In other embodiments, TI.,R2 agonists, such as lipotechoic acid (LTA), TLR3 agonists, such as poly( [:C), and/or other TLR4 agoitists, such as MPL, may be used. As contemplated herein, any TLR. agonist, or combination of TLR agonists, can be used to active DCs, provided such ligands stimulate the production of cytokine and chemokine signals by the activated:DC.s. Many other TLR
agonists are known in the art and can be found in the published literature for use with the present embodiments.
Even though there are similarities in phenotype between DCs and traditionally matured DCs, the DCs of the present embodiments display many marked advantages.
Cryopreservation Mier culture initiation and activation, the cells ate harvested and the vaccine is cryopreserved. For example, peripheral blood monncytes are obtained by lenkapheresis. The cells ate cultured in seratt free Medium with:CiNKSF and IL-

4 for a period of time -followed by pulsing the cells with a desired.antigen.
Following pulsing the cells with a desired antigen, the antigen pulsed dendritic cells are incubated with ITN-7 followed by a TLR agonist (e.g., LPS). The activated antigen pulsed dendritic cell is harvested and cryopreserved in a freezing medium and. stored in liquid nitrogen. In one embodiment the freezing medium comprises 55% plasmalyte, 40% human serum albumin, and 5% DMSO.
The cryopreservation aspect of the embodiments allow for the generation of an FDA- approved injectable multi-dose antigen pulsed dendritic cell vaccine. An advantage of the embodiments is that the multi-dose antigen pulsed dendritic cells retain their ability to produce signals critical to T cell function after thawing. As contemplated herein, the present embodiments include a variety of cryopreservation techniques and cryomedia, as would be understood by those skilled in the art_ For example, in certain embodiments, the freezing medium comprises 55% plasmalyte, 40% human serum albumin, and 5% DMSO. Accordingly, the embodiments provide the ability to produce the multi-dose antigen pulsed dendritic cell vaccine of the embodiments at a centralized area comprising of an initial immunizing dose and multiple "booster" doses.
Therefore the multi-dose antigen pulsed dendritic cell vaccine can be shipped to remote medical centers for serial administration to the patient with no special FDA quality control/quality assurance requirements at the administration site.
In one embodiment, the dendritic cell vaccine of the embodiments is cryppreserved in aliquots for multiple doses. For example, the cells are cryopreserved at. a concentration of 30x1 06 cells/mL. For example, a bag of freezing medium containing a 20- volumecqual to the cell volume is Prepared. 'Working rapidly, the freezing medium is added to the cell bag and the cells are transferred to labeled cryovials. In one embodiment, the vials are frozen using a rate controlled freezer. For example, eryovials are frozen using an automated rate controlled freezer at PC/min and stored in vapor phase nitrogen.
In one embodiment, the vials are frozen using a rate controlled freezer.
The vials are placed in a freezing chamber and liquid nitrogen enters the chamber through an electronic solenoid valve. Since vaporization is almost instantaneous, controlling the rate at which liquid nitrogen enters the chamber directly controls the rate.at which heat is absorbed and removed from the freezing chamber and its Contents.
As contemplated herein, the present embodiments include a variety of cryopreservation techniques and freezing medium, as would be understood by those skilled Mahe- art For example, in certain enibodiments, the freezing .medium -for cultured cells can include about 55% plasmalyte, about 40% human serum albumin, and about 5%
DMSO. In other embodiments, the cryomedia can be serum-free. In certain etribodiments, controlled rate freezing may be used, while other embodiments can include use of insulated containers in which vials of cells mixed with freezing medium are placed in the freezer, such as at temperatures ranging from about -70ri-C to -80"C, The present embodiments provide a method to preserve activated DCs in such a manner so as to further facilitate clinical application of such cells, and to reduce the need for extensive and repeated pherisis and elutriation steps. As contemplated herein, cryopreservation techniques may be used for both small-scale and large-scale batches.
When considering the extensive utility for activated DC, the ability to provide a steady supply of cryopreserved activated DC represents a significant advantage that can facilitate various therapeutic uses of such cells. For example, a large-scale culture of activated DC may be cryopreserved in aliquots of the appropriate size comprising an initial immunizing, dose and multiple "booster" doses, according to the methods of the present embodiments, such that individual doses of cells can later be used in any particular immunotherapeutic protocol. In certain embodiments, activated DCs can be cryopreserved for 2-24 weeks at temperatures of approximately -70 C or tower. At lower temperatures, such as at about -120 C. or lower, activated 'Des can be 20- cryopreserved for at least a year or longer.
In one exemplary embodiment, the Des are suspended in human serum and approximately 5% DMSO (v/v), Alternatively, other serum types, such as fetal calf serum, may be used. The suspended cells can be all quoted into smaller samples, such as in 1.8 ml vials, and stored at approximately -70 C or lower. In other embodiments, the freezing medium may include about 20% serum and about 10% DMSO, and suspended cells can be stored at about -180 C. Still further embodiments may include medium containing about 55% plasmalyte, and about 5% DMSO. Other exemplary freezing media May it:a:Jude about 12%,DM50 and about 2:5-40% aernin.
While the present embodiments as described herein may include specific concentrations of serum, it should be understood by those skilled in the art that the exact amount of serum in the freezing medium may vary, and in some embodiments may be entirely absent but will generally be within the range.ofabout '1% to 30%. Of Mine, any concentration of serum that results in a cell viability of around 50% and/or a cell recovery of around 50% may be used in any DC composition of the present embodiments, as well as with any cryopreservation method as described herein. Preferably, cell viability and recovery of at least 60%, more preferably at: least about 70%, oreven 80% is desired when recovering cryopreserved cells in the selected freezing medium.
Similarly, while the present embodiments as described herein may include specific. concentrations of DMSO, those skilled in the art should recognize that DMSO
may be entirely absent in some embodiments, while in other embodiments, concentrations from about 5% to as high as about 20% may be used in the freezing medium and included within the cryopreservation methods described herein.
Generally, lower concentrations of DMSO are preferred, such as between about 5% to about 10%.
However, any concentration of DMSO that results after thawing. in cell viability of at least 50% and a cell recovery of at least 50%, and preferably a cell viability and recOyery of at least 60%, more preferably about 70%, more preferably about 80% and even more preferably about 90% and higher, may be used.
While the present embodiments as described herein may include reference to a rate controlled freezing, it should be understood by those skilled in the art that methods of freezing in a rate controlled or non-rate controlled manner can routinely be employed.
It should also be understood by those skilled in.the- art that. the various cryopreservation media as described herein may either include serum or may be serum free.
Examples of serum free media can include XVIVO 10, XVIVO 15, XVIVO 20, StemPro, as well as any commercially available serum free media. When utilizing a serum-free freezing medium, the cryopreservation methods of the present embodiments are generally free of infectious agents, antibodies and foreign proteins, which may be antigenic, and any other foreign molecule that may typically be found in serum-based freezing medium.
(r opt aptigto loaded, aCtive.DCs can Occur at any point after activation of cells with a TLR agonist: In one embodiment, the activated DCs =
are cryopreserved approximately 6-8 hr after exposure to the MR agonist.
Preferably, the time point chosen to ci-3,,opreserve the activated cells should be based on the maximization of signal production of the cells, partieularlylL-12 production.
The present embodiments provide compositions and methods for producing large scale dendritic cell vaccines. in one embodiment, the large scale production of dendritic cell vaccines allows for the production of an FDA-approved injectable multi-dose antigen pulsed dendritic cell vaccine for the personalized treatment and prevention of cancer or other disorders. in one embodiment, there are provided compositions and methods for producing large scale of antigen pulsed type. .1 polarized dendritic cell vaccine (DC1).
I0 In one embodiment, the embodiments provide a method to cryopreserve dendritic cells that are in an antigen-loaded, pre-activated state in a large scale that is "syringe-ready", i.e. suitable for immediate injection into the patient without the necessity of any fin-01er cell processing that would require (e.g., by FDA
mandate) additional facilities and quality control/assurance steps.
In one embodiment, the embodiments provide a method to efficiently produce in a large scale injectable multi-dose antigen pulsed dendritic cell vaccine, preferably injectable multi-dose antigen pulsed type I polarized dendritic cell vaccine that exhibit maximal efficacy.
Packaging Of Compositions or Kit Components Suitable containeis for compositions of the embodiments (or kit components) include vials, syringes (e.g. disposable syringes), etc. These containers should be sterile.
Where a composition component is located in a Vial, the vial is .preferably made of a glass or plastic material. The vial is preferably sterilized before the composition is added to it. To avoid problems with latex-sensitive patients, vials are preferably sealed with a latex-free stopper, and the absence of latex in all packaging Material is preferred. The Vial may *Jude a single dose of vactine, or it may include more than one dose (a "multidose" vial) e.g. 10 doses. Preferred vials are made of colorless glass.

A vial can have a cap (e.g, a Luet lock) adapted -sit& that a pre-filled-syringe can be inserted into the cap, the contents of the syringe can be expelled into the.
vial, and the contents of the vial can be removed back into the syringe. After removal of the syringe from the vial, a needle can then be attached and the composition can be administered to a patient. The cap is preferably located inside a seal or cover, such that the seal or cover has to be removed before the cap can be accessed. A vial may have a cap that permits aseptic removal of its contents, particularly for multidose vials.
Where a compositionicompOnent is packaged into a syringe, the syringe may have a needle attached to it. if a needle is not attached, a separate needle may be supplied with the syringe for assembly and use. Such a needle may be sheathed.
Safety needles are preferred. 1-inch 23-gauge, 1-inch 25-gauge and 5/8-inch 25-gauge needles are typical. Syringes may be provided with peel-off labels on which the lot number, influenza season and expiration date of the contents may be printed, to facilitate record keeping. The plunger in the ,s,,ringe preferably has a stopper to prevent the plunger from being accidentally removed during aspiration. The syringes may have a latex rubber cap and/or plunger. Disposable syringes contain a single dose of vaccine. The syringe will generally have a tip cap to seal the tip prior to attachment of a needle, and the tip cap is preferably made of a butyl rubber_ if the syringe and needle are packaged separately then the needle is preferably fitted with a butyl rubber shield.
Containers maybe marked to show a-half-dose volume. e.g. to -facilitate delivery to children. For instance .a syringe. containinga 0S ml dose may have a mark showing a 0.25 ml volume.
Where a glass container (e.g. a syringe or a vial) is used, then it is preferred to use a container made from a borosilicate glass rather than from a soda lime glass.
A kit or composition may be packaged (e.g. in the same box) With a leaflet including details of the vaccine e,a, instructions for administration, details of the antigens within the =vaecine, etc, The instructions may also contain at flings e g to keep a solution of adrenaline readily available in case of anaphylactic reaction fallowing vaccination, etc, Methods for Treating a Disease The present embodiments also encompass 'methods of treatment and/or prevention of a disease caused by pathogenic microorganisms, autoimmune disorder and/or a hyperproliferative disease_ Diseases that may be treated or prevented by use of the present embodiments include diseases caused by viruses, bacteria, yeast, parasites, protozoa, cancer cells and the like, The pharmaceutical composition of the present embodiments may be used as a generalized immune enhancer (DC activating composition or system) and as such has utility in treating diseases. Exemplary diseases that can be treated and/or prevented utilizing the pharmaceutical composition of the present embodiments include, but are not limited to infections of viral etiology such as HIV, influenza, Herpes, viral hepatitis, Epstein Bar, polio, viral encephalitis, measles, chicken pox, Papilloma virus etc.; or infections of bacterial etiology such as pneumonia, tuberculosis, syphilis, etc.; or infections of parasitic etiology such as malaria, ttypanosomiasis, leishmaniasis, trichomoniasis, amoebiasis, etc.
:Preneoplastic or hyperplastic states that may be treated or prevented using the pharmaceutical composition of the present embodiments (transduced DCs, expression vector, expression construct, etc.) of the present embodiments include but are not limited to preneoplastic or hyperplastic states such as colon polyps, Crohn's disease, ulcerative colitis, breast lesions and the like, Cancers that may be treated using the composition :of the present embochments include, but are not limited to primary or metastatic melanoma, adenocarcinoma, squamous cell carcinoma, adenosquamous cell carcinoma, thymoma, lymphoma, sarcoma, lung cancer, liver cancer, non-Hodgkin's lymphoma, Hodgkin's lymphoma, leukemias, uterine cancer, breast cancer, prostate cancer, ovarian cancer, pancreatic cancer, colon cancer, multiple myeloma, neurciblastoma, NPC, bladder cancer, cervical cancer and the like.
Other hyperproliferative diseases that may be treated using DC activation systernOf the pm esenternbodiments include, but ate not littited to rheumatoid arthritis, inflammatory bowel disease, osteoattritis,:leionryornas, adenomas, lipomas, hemangiomas, fibromas, vascular occlusion, restenosis, atherosclerosis, pre-neoplastic iesions.0116-as .adenomatons hyperplasia'and prostatic intraepithelial neoplasia), carcinoma in situ, oral hairy leukoplakia, or psoriasis. .
Autoimmune disorders that may be treated using the composition of the present embodiments include, but are not limited to, AIDS, Addison's disease, adult respiratory distress syndrome, allergies, anemia, asthma, atherosclerosis, bronchitis, cholec37stitis, Crohn's disease, ulcerative colitis, atopic dermatitis, dermatomyositis, diabetes mellitus, emphysema, erythema nodosum, atrophic gastritis, glomerulonephritis, gout, Graves disease, hypereosinophilia, irritable bowel syndrome, lupus erythematosus, multiple sclerosis, myasthenia gravis, myocardial or pericardial inflammation, osteoarthritis, osteoporosis, pancreatitis, Tpolymyositis, rheumatoid arthritis, scleroderma, *gives syndrome, and autoimmune thyroiditis; complications of cancer, hemodialysis, and extracorporeal circulation; viral, bacterial, fungal, parasitic, protozoal, and helminthic infections; and trauma.
in the method of treatment, the administration of the composition of the embodiments may be for either "prophylactic" or "therapeutic" purpose. When provided prophylactically, the composition of the present embodiments is provided in advance of any symptom, although in particular embodiments the vaccine is provided following the onset of one or more symptoms to prevent further symptoms from developing or to prevent present symptoms from becoming worse. The prophylactic administration of composition .serves .to prevent or ameliorate ow subsequent infection or disease. When provided therapeutically, the pharmaceutical composition is provided at or after the onset-of a symptom of infection or disease. Thus, the present 'embodiments may be provided either prior to the anticipated exposure to a disease-causing agent or disease state or after the initiation of the infection or disease.
An effective amount of the composition would be the amount that achieves this selected result of enhancing the immune response, and such an amount could be determined as a matter of routine by a person Skilled in the art. For example, an 'effective amount of for treating an immune system deficiency against .cancer 'or pathogen could be that amountmecessary to cause activation of the immune system, resulting in the development of an antigen specific immune response upon exposure to antigen.
The term is also synonymous with "sufficient amount."

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The effective :amount for any particular application can an depending on such factors as the disease or condition being treated, the particular composition being administered, the size of the subject, and/or the severity of the disease or condition. One of ordinary skill in the art can empirically determine the effective amount of a particular composition of the present embodiments without necessitating undue experimentation.
Therapeutic applications The present embodiments include the generation of an antigen loaded, activated APC that produces significant levels of cytokirtes and che.mokines when thawed from cryopresmation, where the antigen loaded and activated APC is used in immunotherapy for a mammal, preferably a human. The response to an antigen presented by an APC may be measured by monitoring the induction of a cytolytic T-cell response, a helper T-cell response, and/or antibody response to the antigen using methods well known in the art The present embodiments include a method of enhancing the immune response in a mammal comprising the steps of: generating immature Des from monocytes obtained from a mammal (e.g., a patient); pulsing the immature Des with a composition comprising an antigenic composition; activating the antigen loaded Des with at least one TLR agonist; cryopreserving the activated, antigen loaded Des; thawing the activated, antigen leaded Des and then administering the activated, antigen loaded Des to a mammal in need thereof The composition includes at least an antigen, and may further be a vaccine for ex viva immunization and/or in viva therapy in a mammal.
Preferably, the mammal is a human.
Ex vim procedures are well known in the -art and are discussed more fay below. Briefly, cells are isolated from a mammal (preferably a human), The cells can be administered to a mammalian recipient to provide a therapeutic benefit. The mammalian recipient may be a human and the cells can be autologous with respect to the recipient.
Alternatively, the cells an be allogeneic, syngentic otxenogeneic with.
respect to the recipient.
In one embodiment, peripheral blood monocytes are obtained from. a patient by combined leukapheresis and elutriation. The monocytes can be cultured in SFM with -GM-C SF and 1L-4 overnight. The next dayõ immature DCs can be pulsed with, antigen, followed by contacting the DCs with IFN-T and LP& The activatedDes can then be suspended in a freezing medium and frozen until ready for use in immunotherapy.
Cryopreserved DCs can be cultured ex Vii,o wide conditions! effective to =
generate the percent recovery and percent viability of the cells as compared freshly activated DCs. DCs generated from cryopreserved samples can show similar stability as compared to freshly prepared DCs. Furthermore, comparisons of cryopreserved mature DCs with those of freshly prepared DCs can show virtually identical phenotypes as well as signal secretion profiles. As contemplated herein, DCs can be preserved at both small and large scale for approximately 2 to 24 weeks, in the various freezing media described herein, at temperatures of approximately -70 C to -80 C. At temperatures below about -120 C, the duration of storage can be extended. indefinitely or at least beyond 24 weeks without impacting cell recovery, viability, and functionality of the DCs. For example, in certain embodiments, the activated cells can be preserved for at least one year and still retain their ability to produce signal after thawing. The present embodiments provide for effective recovery and viability profiles upon thawing the cells, and furthermore the cryopreservation conditions described herein do not affect the ability of DCs to retain their signal profiles as explained herein throughout.
20. In an exemPlaty embodiment, ctyopreservation.may.be Performed after activation of DCs by re-suspending the cells in a freezing medium comprising about 55%
plasmalyte, about 40% human serum albumin, and about 5% DMSO. The mixture can then be aliquoted in 1.8 ml vials and frozen at about -80 C in a cryochamber overnight.
Vials can then be transferred to liquid nitrogen tanks the following day_ After about 2 to 24 weeks of ctyopreservation, the frozen DCs can be thawed and examined for their recovery and viability. Recovery of such DCs can be greater than or equal to about 70%
with a viability of greater than or equal to about 70%. In other embodiments, DCs or even inonocyieS can be cryopreserved prior to cell activation.
Alternatively, the procedure for a vivo expansion ofhematopoietic stem and progenitor cells is described in U.S. Pat. No. 5,199,942, which is incorporated herein by reference, can be applied to the cells of the present embodiments. In addition to the cellular growth factors 'described in U.S. PAt. No. 5,199,942, other factors such as flt3-Lõ
and c-kit ligand, can be used for culturing and expansion of the cells.
A variety of cell selection techniques are known for identiing and separating cells from a population of cells. For example, monoclonal antibodies (or other specific cell binding proteins) can be used to bind to a marker protein or surface antigen protein found on the cells. Several such markers or cell surface antigens are known in the art Vaccine Formulations The present embodiments further include vaccine formulations suitable for use in immtmotherapy. In certain embodiments, vaccine formulations are used for the prevention and/or treatment: of a disease, such as cancer and infectious diseases. In one embodiment, the administration to a patient of a vaccine in accordance with the present embodiments .for the prevention and for treatment of caneread take place before otafter a surgical procedure to remove the cancer, before or after: a chemotherapeutic. procedure for the treatment of cancer, and before or after radiation therapy for the treatment of cancer and any combination thereof. In other embodiments, the vaccine formulations may be administrated to a patient in conjunction or combination with another composition or pharmaceutical product. It should be appreciated that the present embodiments can also be used to prevent cancer in individual without cancer, but who might be at risk of developing cancer.
The administration of a cancer vaccine prepared in accordance with the present embodiments, is broadly applicable to the prevention or treatment of cancer, =
determined in part by the selection of antigens forming part of the cancer vaccine.
Cancers that can be suitably treated in accordance with the practices of the present embodiments include, without limitation, cancers of the lung, breast, ovary, cervix, colon, head and neck, pancreas, prostate, stomach, bladder, kidney, bone, liver, esophagus, gastroesophageal, brain, testicle, uterus and the Variousleukernias and lymphomas:
in oneembodiment, vaccines can be derived front the tumor or cancer cells to be treated. For example, in the treatment of I nag cancer, the lung cancer cells would be. treated as described hereinabove to produce a lung cancer vaccine.
Similarly, breast cancer vaccine, colon 'cancer vaccine, pancreas = Cancer vaccine, stomach canter.
vaccine, bladder cancer vaccine, kidney cancer vaccine and the like, would be produced and employed as immunotherapeutc agents in accordance with the practices for the prevention and/or treatment of the tumor or cancer cell from which the vaccine was produced_ In another embodiment, vaccines could, is stated, also be prepared to treat various infectious diseases which affect mammals, by collecting the relevant antigens shed into a culture medium by the pathogen. As there is heterogenecity in the type of immunogenic and protective antigens expressed by different varieties of organisms causing the same disease, polyvalent vaccines can be prepared by preparing the vaccine from a pool of organisms expressing the different antigens of importance.
In another embodiment, the vaccine can be administered by intranodal injection into groin nodes, Alternatively, and. depending on the vaccine target, the vaccine can be intradertnally of subcutaneously administered to the extreinities, arms and legs, of the patients being treated. Although this approach is generally satisfactory for melanoma and other cancers, including the prevention or treatment of infectious diseases, other routes of administration, such as intramuscularly or into the blood stream may also be used.
Additionally, the vaccine can be given together with adjuvants andlor immuno-modulators to boost the activity of the vaccine and the patierit'S.
response. Such adjuvants andlor iminuno-modulators are understood by those skilled in the am:and are readily described in available published literature.
As contemplated herein, and depending on the type of vaccine being generated, the production of vaccine can, if desired, be Scaled up by culturing cells in bioreactors or fermentors or other such vessels or devices suitable for the growing of cells in bulk. In such apparatus, the culture medium would be collected regularly, frequently or continuously to recover therefrom any materials or antigens before such materials or antigens. are degraded in the culture Medinnt.
If desired, devices or compositions containing the vaccine or antigens produced and recovered, in accordance with the present embodiments, and suitable for sustained or intermittent release could be, in effect, implanted in the body or topically applied thereto for a relatively slow or timed release of such materials into the body.
Other steps in vaccine preparation can be individualized to satisfy the requirements of particular vaccines. Such additional steps will be understood by those skilled in the art. For example, certain collected antigenic materials may be concentrated and in some cases treated with detergent and ultracentrifuged to remove transplantation alloantigens.
Combination Therapy The present embodiments provide an effective therapy to treat cancer Wherein the therapy includes changing the immune response in the tumor so that the immune cells in the tumor site are more effective in attacking the tumor cells In some instances.. the effective therapy includes improving the migration and activity of immune cells- in the tumor site. In one embodiment, there are provided compositions and methods of using a dendritic cell vaccine in combination with an inhibitor of one or more of HER2 and HER3 as a treatment regimen to treat cancer. In another embodiment., the treatment regimen comprises the use of a dendritic cell vaccine, an inhibitor of one or more of HER2 and HER3, and a chemokine modulator. In one embodiment, the chemokine modulator is a chemokine-activating agent. An example of a chemokine-activating agent is a .MR8. agonist.
In one embodiment, there amprovided.compositions and methods of using a dendritic cell vaccine in combination with blockage of HER-2 arid HER-3 as a treatment regimen to treat cancer. In another embodiment, there are provided compositions and methods of using a dendritic cell vaccine in combination with blockage of HER-2 and HER-3 with NF-a and IFN-y_ In another embodiment, there are provided compositions and methods of blocking both of HER-2 and HER-3 with the addition.
TNF-u. and IFN-7 as a treatment regimen to treat cancer.
In one embodiment, a treatment regimen can be used to treat cancer and therefore can be considered as a type of anti-cancer therapy. In another embodiment, a treatment regimen can be used in the context of a combination therapy with another anti-cancer or anti-tumor therapy including but not limited to surgety, chemotherapy, radiation therapy (e4 X lay)õ gene therapy,.immunotherapy, hormone .therapy, viral therapy, DNA therapy, RNA therapy, protein therapy, cellular therapy, and nanotherapy.
In one embodiment, there is provided a treatment regimen in combination with another cancer medicament for the treatment or prevention of cancer in subjects.
The other canter medicament is administered in synergistic amounts or in various dosages or at various time schedules with the treatment regimen of the embodiments. The embodiments also relate to kits and compositions concerning the combination of treatment regimens of the embodiments alone or in combination with a desired cancer medicament.
In one embodiment, a treatment regimen is used prior to receiving another anti-cancer therapy. In another embodiment, a treatment regimen is used concurrently with receiving another anti-cancer therapy. In another embodiment, a treatment regimen is used after receiving another anti-cancer therapy.
In some embodiments, the present embodiments provide a method of treating breast cancer that is negative fbr ER in a subject. in some embodiments, there is a method of treating breast cancer that is negative for ER and positive for HER2 in a subject. hi some embodiments, the breast cancer is a metastatic breast cancer.
In some embodiments, the breast cancer is at stage I, stage II, or stage M.
En another embodiment, the treatment regimen may be used in combination with existing therapeutic agents used totreat -cancer, in order to evaluate potential therapeutic efficacy of the trea.tmentregimen of the embodiments in combination with the antitumor therapeutics described elsewhere herein, these combinations may be tested for antitumor activity according to methods known in the art.
in one aspect, the present embodiments contemplate that a treatment regimen may be used in combination with a therapeutic agent such as an anti-tumor anent including but is not limited to a chemotherapeutic agent, an anti-cell proliferation agent or any combination thereof.
The embodiments - Should not limited to any particular chemotherapeutic agent, Rather, any chemotherapeutic agent can be used with the treatment regimen of the embodiments. For example, any conventional chemotherapeutic agents of the following exemplaty classes are included in the embodiments: alkylating agents;

nitrosoureas; antimetabolites; antitumor antibioties; plant alkyloids; taxanes ; hormonal agents; and Miscellaneous agents.
Alkylating agents are so named betatise of their ability to add- alkyl groups to many electronegative groups under conditions present in cells, thereby interfering with DNA replication to prevent cancer cells from reproducing. Most alkylating agents are cell cycle non-specific. In specific aspects, they stop tumor growth by cross -linking guanine bases in DNA double-helix strands. Non-limiting examples include busulfan, carboplatin, chlorambucil, cisplafin, cyclophosphamide, dacarbazine, ifosfamide, mechlorethamine hydrochloride, melphalan, procarbazine, thiotepa, and uracil mustard.
Anti-metabolites prevent incorporation of bases into DNA during the synthesis (S) phase oldie cell cycle, prohibiting normal development and division. Non limiting examples of antimetabolites include drugs such as 54luorouracil, 6-mercaptopurine, capecitabine, cytosine arabinoside, floxuridine, fiudarabine, gemcitabine, methotrexate, and thioguanine.
There are a variety of antitumor antibiotics that generally prevent cell division by interfering with enzymes needed for cell division or by altering the membranes that surround cells. Included in this class ate the anthracyclines, such as doxorubicin, which act to prevent cell division by disrupting the structure of the DNA
and terminate its function. These agents are cell cycle non-specific. Non-limiting examples of antitumor antibiotics include. dactinomycin, datutortibicirt, doxorubicin, idartibicin, mitomycin,C, and mitoxantrone.
Plant alkaloids inhibit or stop mitosis or inhibit enzymes that prevent cells from making proteins needed for cell growth. Frequently used plant alkaloids include vinblastine, vincristine, vindesine, and vinorelbine. However, the embodiments should not be construed as being limited solely to these plant alkaloids.
The taxanes affect cell structures called microttibules that are important in cellular functions. In normal cell growih, microtubules are formed when a cell starts dividing, but once the cell stops dividing, the tilicrottibulea'are disassetribled or destroyed. Taxanes prohibit the microtubules from breakMg down such that the cancer cells become so clogged with microtubnles that they cannot grow and divide.
Non-Limiting exemplary taxanes include paclitaxel and docetaxel.

Hormonal 'agents and hormone-like drugs are utilized for 4,-ertain types of cancer, including, for example, leukemia, lymphoma, and multiple myeloma. They are often employed with other types of chemotherapy drugs to enhance their effectiveness_ Sex hormones are used to alter the action or production of female or male hormones and are used tosloW the growth 'of breast,' Prostate, and endometrial cancers.
Inhibiting the production (aromatase inhibitors) or action (tarnoxifen) of these hormones can often be used as an adjunct to therapy. Some other tumors are also hormone dependent.
Tamoxifen is a non-limiting example of a hormonal agent that interferes with the activity of estrogen, which promotes the growth of breast cancer cells.
Miscellaneous agents include chemotherapeutics such as bleomycin, hydroxyurea, L-asparaginase, and procarbazine that are also useful in the embodiments.
An anti-cell proliferation agent can fluffier be defined as an apoptosis-inducing agent or a cytotoxic agent. The apoptosis-inducing agent may be a granzyme, Bc1-2 family member, cytochrome C, a caspase, or a combination thereof Exemplary granzymes include granzyme A, granzyme 13, granzyme C, granzyme D, granzyme E, granzyme F, granzyme G. granzyme H, granzyme I, granzyme J, granzyme K, granzyme L. gratrzyme M, granzyme N, or a combination thereof. In other specific aspects, the Bel-2 family member is, for example, Bax, Bak, r3c1-Xs, Bad, Bid, Bik, Hrk, Bok, or a combination thereof In additional asPects, the caspase is caspase-1,. easPase2, caspase-3 caspase4, caspase;-5, caspase-0.õ caspase-7, caspase-8. Caspaserg, caspase-IA
caspase-11, caspase-12, caspase-13, caspase-14, or a combination thereof. In specific aspects, the cytotoxie agent is TNF-a, gelonin, Prodigiosin, a ribosome-inhibiting protein (RIP), Pseudomonas exotoxin, Clostridium difficile Toxin B, Helicobacter pylori VacA, Yersinia enterocolitica YopT, .Violacein, diethylenetriaminepentaacetic acid, imfulwn, Diptheria. Toxin, mitogillin, ricin, boutlinum toxin, cholera toxin, saporin 6, or a combination thereof.
In one embodiment -a treatment regimen is used in combination with an anti-tumor agent wherein the anti-tumor agent is an antitutnotalky'lating agent, antitumor antimetabolite, antitumor antibiotics, plant-derived antitumor agent, antitumor platinum complex, antitumor campthotecin derivative, antitumor tyrosine kinase inhibitor, monoclonal antibody, intert7eron, biological response modifier, hormonal .anti-tumor agent, anti-tamor viral agent, angiogenesis inhibitor, differentiating agent, :PI3KirriT0RJAKT inhibitor, cell cycle inhibitor, apoptosis inhibitor, lisp 90 inhibitor, tubulin inhibitor, DNA repair inhibitor, anti-angiogenic agent, receptor tyrosine kinase inhibitor, topoisomerase inhibitor, taxane, agent targeting Her-2, hormone antagonist, agent targeting a growth factor receptor, or a pharmaceutically acceptable salt thereof. In some embodiments, the anti-tumor agent is citabine, capecitabine, valopicitabine or gemcitabine. In some embodiments, the anti-tumor agent is selected from the group consisting of Avastin, Sutent, Nexavar, Recentin, ABT-869, Axitinib, Irinotecan, topotecan, paclitaxel, docetaxel, lapatinib, Herceptin, lapatinib, tamoxifen, a steroidal aromatase inhibitor, a non-steroidal aromatase inhibitor, Fulvestrant, an inhibitor of epidetmal growth factor receptor (EGFR), Cetuximab, Panitumimab, an inhibitor of insulin-like growth factor 1 receptor (IGFI R), and CP-751871, In one embodiment, the anti-tumor agent is a chemotherapeutic agent.. A
chemotherapeutic agent as used herein is a chemical compound useful in the treatment of cancer. Examples of chemotherapeutic agents include alkylating agents such as thiotepa and cyclosphosphamide (CYTOXAN); alkyl sulfonates such as busulfan, improsullan and piposulfan; aziridines such as benzodopa, carboqu one, meturedopa, and uredopa;
ethylenimines and methylamelamines including altretamine, tfiethylenemelamine, trietylenephosphoramide, ti iethiylenethiophosphoramitkand tritnethylolotnelamMe;
acelogenins (especially bullatacin and bullatacinone); delta-9-tetrahydrocannabinol (dronabinol, MARINOL); beta,lapachone; lapkhol; colchicines; betulinic acid; a camptotbecin (including the synthetic analogue topotecan (HYCANITIN), CPT-11 (irinotecan, CAMPTOSAR), acetylcamptothecin, scopolecti.n, and 9-aminocamptothecin); bryostatin; callystatin; CC-1065 (including its adozelesin, carzelesin and bizelesin synthetic analogues); podophyllotoxin; podophyllinic acid;
teniposide; cr.,,ptophycins (particularly ctyptophycin 1 and cryptophycin 8);
dolastatin;
dtiocarinycin (including the synthetie analogues, KW.-21S9 andCB1-TM
eleutherobin;
pancratistatin; a sarcodictOrt; spongistatin; nitrogen mustards such as chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, mad mustard; ilitMSEtteas such as carmustine, chlorozotocin, fotemustine, lomustine, nimustine, and ranimnustine;
antibiotics such as the enediyne antibiotics (e. g., calicheamicin, especially calicheamicin gamma ii and calkheamicin omegall (see, e.g., Agnew, Chem Irttl. Ed. Engl., 33:183-186 (1994));
4/let/licit), including d3rnemicin A; an esperamicin; as well as neocarzinostatin chromophore and related chromoprotein enediyne antiobiotic chromophores), aelacinomysins, actinomycin, authramycin, azaserine, bleomycins, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycinis, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L-norlevcine, doxorubicin (including ADRIAMYCIN, morpholino-doxonthicin, cyanomorpholino-doxorubicin, 2-pyrrolino-doxorubicin, doxorubicin HCI liposome injection (DOX1L)õ liposomal doxorubicin TLC D-99 (MYOCET), peglylated liposomal doxorubicin (CAELYX), and deoxydoxorubicin), epirubicin, esorubiein, idaruhicin, marcellomycin, mitomycins such as mitomycin C, mycophenolic acid, nogalatnycin, olivomycins, peplomycin, potfiromycin, puromycin, quelamyein, rodorubicin, streptonigrin, streptozociuõ tubercidin, ubenimex, zinostatin, zorubicin; anti-metabolites such as methotrexate, gemcitabine (GEMZAR), tegafur (UFTORAL), capecitabine (XELODA), an epothilone, and 5-fluorouracil (5-FU);
folic acid analogues such as denopterin, methotrexate, pteropterin, trimenexate;
purine analogs such as fiudarabine, 6-mercaptopurine, thiamiprine, thioguanine; pyrimidine analogs such as ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxtuidine; anti-adrenals such as aminoglutethimide, mitotane, trilostane; folic acid replenisber such as frolinic acid;
aceglatone;
aldophospharnide glycoside; aminolevolinic acid; eniluracil; antsactine;
bestrabucil;
bisantrene; edatraxate; defofamine; demecolcine; diaziquone; elfomithine;
elliptinium acetate; etoglucid; gallium nitrate; hydroxyurea; leminan; lonidainine;
maytansinoids such as maytansine and ansamitocins; rnitoguazone; mitoxantrone; mopidanmol;
nitraerine; pentostatin; pheriamet; pirarubicin; losoxantrone; 2-ethylhydrazide;
procarbazine; PSK polysaccharide complex (11 l' Products, Eugene, Oreg.);
razoxane; rhizoxin; sizotimn; spirogermanium; tenuazonic acid; triaziquone;
trichlorotriethylamine; trichothecenes (especially T-2 toxin, verracurin A, roridin A and anguidine); urethan; dacarbazine; mannomustine; mitobronitol; mitolactol;
pipobroman;

=

.gaCytoSin; .arabinoside ("ArarC''); thiotepa; taxoid,e g paclitaxel(TAXOL) albumin-engineered nanoparticle formulation of paclitaxel (ABRAXANE), and docetaxel (TAXOTERE); chloranbucil; 6-thioguanine; mercaptopurine; methotrexate;
platinum agents such as cisplatin, oxaliplatin, and carboplatin; vincas, Which prevent tubulM
polymerization from forming microtubules, including vinblastine (VELBAN), vincristine (ONCOVIN), vindesine (ELDISINE, FILDESIN), and virtorelbine (NAVELBINE);
etoposide (VP-I6); itbsfamide; mitoxantrone; leticovovin; novantrone;
edanexate, datinornycin; aminopterin; ibandronate; topoisomerase inhibitor RFS 2000;
difluorometlhylomithine (DMF0); retinoids such as retinoic acid, including bexarotene (TARGRETIN); bisphosphonates such as clodronate (for example, BONEFOSO or OSTAC), etidronate (D1DROCAL), NE-58095, zoledronic acidizoledronate (ZOMETA), alendronate (FOSAMAX), pamidronate (ARENA), tiludronate (SKELID), or risedronate (ACTONEL); troxacitabine (a 1,3-dioxolatte nucleoside cytosine analog);
antisense oligonucleotides, particularly those that inhibit expression of genes in signaling pathways implicated in aberrant cell proliferation, such as, for example, PKC-alpha, Rat*, and epidermal growth factor receptor (EGF-R); vaccines such as THERATOPE.RTM, vaccine and gene therapy vaccines, for example, ALLOVECTIN vaccine, LEUVECTIN
vaccine, and VAXID vaccine; topoisomerase 1 inhibitor (e.g., LURTOTECAN);
rniRH
(e.g., ABARELIX); 13AY439006 (sorafenib; Bayer); SU-11248 (Pfizer);
perifosine, COX-2. inhibitor (e.g., celeeoxib or etoricoXib), proteoSonte inhibitor:(e,g.,.PS341);-bortezotnib (VELCADE); CC l-779; tipifamib (R11577); orafenib, ABT510; BU-2 inhibitor such as oblimersen sodium (GENASENSE); pixantrone; EGER inhibitors;
tyrosine kinase inhibitors; and pharmaceutically acceptable salts, acids or derivatives of any of the above; as well as combinations of two or more of the above such as CHOP, an abbreviation for a combined therapy of cyclophosphamideõ doxorubicin, vincristine, and prednisolone, and FOLFOX, an abbreviation for a treatment regimen with oxaliplatin (ELOXATIN) combined with 5-FU and leticovovin.
In another embodiment combinatiOns of immunotherapieS :are used to treat estrogen receptor,positiveiRER2-positive:(ERP9'1HERP') DCIS: breast cancer patients.
Anti-estrogen therapy such as, for example, tamoxifen is combined with amti-dendritic cell vaccination to improve pathologic complete response.

CA 02986687 2017-11-21 =

These methods described herein are by no means all-inclusive, and further methods to suit the specific application will be apparent to the ordinary skilled artisan.
Moreover, the effective amount of the compositions can be farther approximated through analogy to compounds known to exert the desired effect.
EXPERIMENTAL EXAMPLES
The embodiments are further described in detail by reference to the following experimental examples. These examples are provided for purposes of illustration only, and are not intended to be limiting unless otherwise specified. Thus, the embodiments should in no way be construed as being limited, to the following examples, but rather, should be construed to encompass any and all variations which become evident as a result of the teaching provided. herein.
Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the present embodiments and practice the claimed methods. The following working examples therefore, specifically point out the preferred embodiments, and are not to be construed as limiting in any way the remainder of the disclosure.
20. Example :A:CropreServed, pre-activated, : multi-dose dendritie cell vaccine;
To be able to produce These large scale vaccines, a process was developed to produce fully activated DCI vaccines pulsed with tumor antigen whereby the fully activated TX.:1 vaccines are cryopreserved as multi-dose syringe ready 6 pack DC I
vaccines, The DC1 are cryopreserved activated as DC1 as described elsewhere herein.
For example, they are oyopreserved in 55% Plasmalyte medium with 40% Human serum albumin and 5% DMSO. These vaccines have been generated and extensively tested in the laboratory and consistently meet quality standards set by the FDA for administration tOipatients.
Thematerials.aud methods employed in the experiments and examples disclosed herein are now described, Preparation ofJul hin aid D(.7Jul enOprescowtioti Freshly elutriated myeloid monocytes were cultured in 6 well microplates (12x106cells/well). Culture medium consisted of Serum Free Medium ( SFM
invitrogen Carlsbad CA). The final concentration of added GMCSF was 5Ongtml and of IL4 is Wail. Cells were cultured overnight at 3T C in 5% CO2. In some batches, the cells were pulsed with the adequate peptides after 16-20 hr and cultured for additional 6-8 hr, after which 1000LI/m1IFN-T was added. Dendritic cells were matured with TLR agonist LPS
(TLR 4, lOnginil) or R848 (TLR.8, li.tgim1). The maturation time was at least about 6hr.
After that, the TLR agonist-activated DCs were ready for cryopreservation Or immediate use.
To induce the production of the Thl-polarizing cytokine IL-12, the -DCs are activated with combinations of the cytokine IFNI, or the. TLR agonists bacterial LPS
and/or R848. This should induced T cells that produce IFN-y. Alternatively, the DCs can be activated with combinations of ATP, bacterial LTA, LPS and prostaglandin E2 (PGE2).. This can cause ILL23., 1L-6 and IL ID to be amplified, leading an immune response dontinated by 11 -17 and II,-22-secreting Th17 cells%
Olvpreerivtion of DC
Des were harvested by gentle scraping. MI medium and the cells were kept at wet ice at all times_ Cells were gently washed by centrifugation at about 800RPM
for 10 min. Cells (e.g., 10 x106 cells) were cryopreserved in freezing medium of plasmalyte 55%, human serum albumin 40% with 5% :DMS0 and stored in liquid nitrogen, The results of the experiments presented herein are now described, Multi-dose DC1 vaccines Experiments Were performed .to assess the recovery, viability and sterility Of the cell's., Briefly, .peripheral blood monocytes were.- obtained by cOrnhined leukapheresis the counter current elutriation and were cultured in serum free medium with GM-CSF and 1L-4 overnight. The next day they were pulsed with HER-2 peptides then W.NPt tbiloWed by LPs. The DC.1 were harvested at 40 hours and eiyopreServed in.
freezing medium of pla,smalyte 55%, human serum albumin 40% with 5% DMSO and stored in liquid nitrogen. Following I week they were thawed and release criteria were obtained including viability, yield, endotoxin testing, and sterility cultures. All 12 cultures had no bacterial growth and <0.1 EU endotoxin, Figure I demonstrates the viability and yield of cryopreserved DC1. As can be seen in Figure 1, recovery of cells was OP average.9% and viability waS 95% When cells were direetly thawed and counted.
These data demonstratethe cryopreservation and viabilityof the Del vaccine is maintained in Medium containing below the FDA allowable 7.5% DIVISO, It was observed that cell function was maintained following crypreservation..1L-12 and Thl chemokines were produced for 36 hours post thaw from multi-dose DC1 vaccines. Thawed cells produced high levels of IL-12 from about 6 hours post thaw through 36 hours. These levels of 1L-12 are comparable to prepared DC.1 vaccines made from cryopreserved monocytes.
.15 The results presented herein demonstrate that cryopreserved, preactivated, multi-dose dendritic cell vaccine sensitized against the HER-2 tumor target antigen on breast cancer is therapeutic. However, the embodiments are applicable to a variety of additional pathophysiological conditions.
The multi-dose syringe ready pack DC I vaccines can be used in HER-2 non-expressing breast cancer. HER-2 is expressed on approximately 25% of all breast Cancers. Breast cancers that do not produce detectable levels of HER -2 may not be susceptible to vaccination. To address this limitation, additional. target proteins can be added to the vaccine. For example, many breast cancers that do not produce high levels of HER-2 instead produce other, related proteins including HER-I and HER,3.
Without wishing to be bound by any particular theory, it is believed that adding these other proteins to the vaccine would allow the targeting of these other breast cancer phenotypes.
The multi-dose syringe ready pack DC I vaccines can be used in other cancer types: besides breast cancer. Anticipated target proteins such as HER-4, HER,=2 and 1-1ER.-3 c,air also be present on other types Of cancer including ovarian, prostate, pancreatic, colorectal, gastric, head and neck and non-small cell lung carcinoma, as well as other common cancers.

The multi-dose syringe ready pack .DCI vaccines can be used to treat chronic infectious diseases, including but not limited to, chronic infections like HIV or hepatitis virus C. Here, proteins specific for these viruses would replace the HER-2 or other cancer proteins to mobilize the patient's immune response against these persistent infections. It is possible that the enhanced immunity would greatly reduce viral load and attendant disease symptoms and progression, or could possibly help clear the infection entirely.
The multi-dose syringe ready pack Del 'vaccines can-be used to treat = autoimmune diseases. Diseases like rheumatoid arthritis and Lupus 'occur when the immune system mistakenly attacks the body's own normal tissues. Whereas the current vaccinetimmunotherapy formulation is designed to initiate and strengthen immune responses, without wishing to be bound by any particular theory, it is believed that in vitro signals can be provided to the DCs during vaccine production that induce these cells to switch off pathological immune responses.
Example 2: Crvopreservation of Activated DC1 Makes Large Scale Dendritic Cell 'Vaccines Feasible in Cancer Therapy Dentiritic cell-based vaccine therapy is :a promising directed therapy against a variety of cancers. While a variety of strategies have been employed to mature DCs to a 20- phenotype that optimizes sensitization of CD,1-4- and CD8+ I cells turecognize tumor epitopes and elicit antitumor immunity, experiments were designed to utilize a:method that employs the rapid maturation of monocytes in serum free media (SFM) using Interferon gamma (IFN-7) and lipopolysaccharide (1,PS), a toil-like receptor (TI.,R) 4 agonist, resulting in mature DCs capable of polarizing the immune response to a Thl type response and eliciting sensitization via an IL-12 dependent mechanism.
Results demonstrate the potential for this vaccine strategy to be used as an adjunct therapy in early breast cancer. Cryopreservation of dendritic cells (DCs) in a matured state permits 'easier production of accessibility to personalized therapy.
Rapid maturation of dendritic cells Both freshly matured :DCs (DC .I s) and IX s ctyopreserved in a mature State (cryoDCS) and subsequently thawed were compared for viability and recover as well as far phenotypic maturity as determined by expression of cell surface markers by flow cytometry. Function of dendritic cells was determined by measuring production of various cytokines, in particular, interleukin 12p70 (IL-12p70). The ability of these cells to stimulate naïve CD4+ and CD8+ tells was also assessed.
There was no significant difference in the viability (p-.4807), and recovery (p=.1220) (Figure 2).
Both populations had similar initial (7 hours post LPS addition) IL-12 p70 secretion (p=.0768). The populations continued to exhibit comparable secretion levels of IL-12 p70 over a 30 hour Observation period with no significant differences between the populations. (Figure 3), There was no significant difference between populations and-production of IL-lbeta (p-0.7690), IL-1 alpha (p-0.0841), Ratites (r0,902), MDC (r0.1514) IL-10 (p---.1937), (p--,2673), IP-10 (p-0.7366), IL-6 (p----0.24), IL-5 (p-0.0735), INF-beta (p=0,9422), IL-15(p=0.8878), MIP- I beta (1)=0.9217), INF-alpha (p-0.8972), 111L-8(p=0,7844). (Figure 4).
Cell surface markers denoting DC maturity between Deis and cryoDcs exhibit no significant difference in expression. Both populations elicited nonspecific alloantigeri CD4 .T cell responses as well as antigcn-specific CD S+I cells recognition with a:Thl polarized response. CM, 83, and 86 demonstrate DC maturation, expression revealed no significant difference. Functional abilities were induced by CD4+
T cells from diff7erent donors co-cultured with each population.resulting in a nonspecific alloantigen response and CD4+ I cells secreting INF-gamma (DC1s 107.40 ne,/mL
and cryoDCis 129.23 ng/mL). Antigen specific sensitizations initiated by co-culturing the two populations with tumor antigen specific CDS+ I cells elicit comparable :I:FN.-7 secretions for both groups and result in a TI-I1 polarized response. (Figure

5).
The results: presented herein demonstrate that rapid maturation method Of DC1 can be mopreserved functionally matured and maintains, phenotype and function, thus can be used to manufacture syringe ready DC:1 for use world-wide in cancer therapy.

In conjunction ith maintaining the DC 1 phenotype:to-drive a 'fhl polarized immune response, the results presented. herein demonstrate that the cryoDCs maintained the ability to primarily sensitize T cells. This also likely relates to the maturation strategy, as the DCIs matured with [FM-gamma and LPS exhibit an enhanced ability to primarily sensitize Cl) 4+ T cells compared to cytokine matured Des.
The present protocol for cry,ropreserved mature DC preparations can be easily adapted to current good manufacturing practice guidelines thereby increasing the availability of emerging therapy.
Example 3: Cvtokines from CD4 T cells and Herceptin make hieh HER-2-expressine breast cells susceptible to killing by CD8 T cells It has been demonstrated that that high HER-2-expressing breast cancer cells down-regulate molecules on the cell surface that make these cancer cells visible to C1)8 T cells and allow them to be killed by these immune cells. It has been shown that the cytokines interferon-gamma (IFNI) and tumor necrosis factor-alpha (TNIz-a) produced by CD4 cells, when combined with Herceptin, cause the intermediate and high :HER-2-expressing breast cancer cells to increase their Class I molecule expression. As a result of this, the CDS T cells are able to better see the breast cancer cells and kill them or to produce cytokines to kill them.
20. Trials were designed to assess the therapeutic effects of using Herceptin in combination with dendritie cell vaccines (e.g.. DC1 vaccines).
A phase I DCIS vaccine trial combining Herceptin with DC1 vaccines was designed. For example, a Phase I trial was designed for patients with high expressing DCIS to receive a DCI vaccine combined with 2 doses of Herceptin at week 1 and week 4. Without wishing to be bound by any particular theory, it is believed that this combination will increase the complete response rate from 30% to greater than 50% in patients with HER-2-expressing DCIS.
In addition, a Phase Ill DcIS Vaccine trial was designed. FQ:e e*ainple, vaccine:trial was developed to prevent recurrence of breast cancer in patients with estrogen independent (ER"), DCIS. There are three treatment arms in the study: 1) a standard therapy (surgery and radiation), 2) receiving a DCI
vaccine =

before stirgety, and 3)=teceivina DC:',1 vaccine plus Herceptin before surgery, Without wishing to be bound by any particular theory, those patients who have complete responses to the treatment can avoid radiation after surgery. It is also believed that this trial serves demonstrate the prevention of recurrence in patients with DC1S
using a vaccine.
In addition, a phase I neoadjuvant DC1 vaccine in combination with Ilerceptin in patients with early invasive FIER-2-P"''' breast cancer was designed. For example, a Phase i trial was designed to test whether the combination of Herceptin and vaccines along with a chemokine modulator (e.g., a chemokine-activating agent) can eliminate small HER-2-expressing invasive breast cancers prior to surgery and avoid the need for chemotherapy. Without wishing to be bound by any particular theory., it is believed that this neoadjuv ant (before surgery) strategy, with the possibility of adding an immune antibody that takes the brakes off the immune response, may eliminate the need for toxic chemotherapies for the treatment of breast cancer and therefore make immune therapy the standard of care for this disease, That is, the treatment regimen disclosed herein provides a step forward in the quest to eradicate breast cancer using the natural immune response, which can be restored with vaccines regimens of the embodiments.
The regiments discussed herein can drive immune cells into the tumor by changing the immune response in the tumor and enable the immune cells to work longer by taking the brakes .off the Cells. It is believed that combining DCI Niaccines with Fiereeptin and also addingthe ehemokine modulator improves the migration and activity of the immune cells within the tumor in the breast.
Without wishing to be bound by any particular theory, it is believed that in many cancers, if there are large numbers of good immune-fighting cells present, those patients do better with any type of therapy_ This means that if one gets immune cells into the tumor to tight it before it is removed, the patient likely does better and responds better to other therapies, including surgery, chemotherapy, and radiation.
Without wishing to be bound by any partiettlat an effective therapy to treat cancer would include agents that rapidly change the immune response in the tumor prior to surgery to improve outcomes for patients with breast cancer and other types of cancet7rhiS strategy can be applied to a variety of cancer including but is not limited to colon cancer, melanoma, lung, brain, pancreas, prostate, esophagus, and the like.
Experiments were designed to develop immune fluorescence assays to measure and quantify the types of immune cells that migrate into the breast after vaccination, the types of chemokines that are made to bring cells in, and the molecules they express to help eliminate cancer cells. These assays allow multiple cell types to be visualized at the same time and show where they are located in the tumor microenvironment. It has been observed that at least in some of the vaccinated patients, their tumors produced chemokines to recruit cells into the environment to kill the tumor cells, Example 4: Combination of Blockade of HER-2 and HER-3 The results presented herein demonstrate that the combination .of an effective anti-1-lER2 C1)4+ Th I response combined with HER2 and-IER3 blockade is extremely effective in causing tumor senescence and apoptosis in HER-2 expressing breast cancers.
It was observed that the combination of blockade of HER-2 and HER-3 together with the addition of combinations of Thl crokines TNE-tt and IFN-7 from CD4 Thl cells causes significant senescence and apoptosis of HER-2 expressing breast cancer, This has been verified in several different cells lines of both: high and intermediate HER2-expresSing breast cancer cells, The results demonstrate that this combination can be potent for prevention and prevention of recurrence.
METHODS-Cell culture and treatments Human breast. cancer cell lines SK-BR-3, 13T-474, T-47D, HCC-1419 and MDA-MB-231 were obtained from the American Type Culture Collection (Manassas, VA) and grown in RP1µ41 640 (Life technologies, Grand1Sland, NY) supplemented With 10% FRS ((ellgro. flerndon, VA). J1MT- I cells were a kind gift from Dr, Pravin Kaumaya (Ohio State University, Columbus, OH) and were grown in Dulbecco's modified Eagle's medium (MEM) (hvitrogen, Wallin), MA) supplemented ;with 10% PBS. Normal immortalized MCF,10 cells _N,i.ere:
obtained from the Karmanos Cancer Institute (Detroit, ME) and grown in DMEM/FI2 (Invitrogen) supplemented with 10 mM HEPES, 10 pginil insulin, 20 nginil EGF, 100 ngtml cholera toxin, 30 niM sodium bicarbonate, 0.5 gglml hydrocortisone, and 5% fetal horse serum.
All cells were grown at 37"C in a humidified 5% CO2 incubator.
Three hundred thousand of breast cancer cells were treated for 5 days with the indicated concentrations of human recombinant TNF-a (R&D Systems, Minneapolis, MN) and human recombinant IFN-y (R&D Systems) and then cultured for 2 more passages in absence of cytokines. Cells were subjected to senescence associated 0-.10 g,alactosidase enzyme (SA-fl-gal) detection or Ilysed and subjected to western blot analysis for pl5INK4b, pl6INK4a AND CLEAVED CASPACE-3.
In the some cases, the cells were treated with 10 Lig/nil trastuzumab (HERCEPTINTh) and pertuzumab (PERJETATm) (both, Genentech, San Francisco, CA) for the indicated times. This treatment was combined with cytokines or with human retombinant heregtilin (R&D Systems).
Fitly thousand cancer cells were also cultured in the lower chamber of a transwell system (BD Biosciences, San Jose, CA) with co-culture of I Ox j5 human CD4'.
T-cells and 105 mature (i.e. type 1 polarized) or immature human dendritic cells (DC's) in the upper chamber. DCs and CD4 T-cells were obtained from select trial subjects (Sharma et al., 2012 Cancer 118: 4354-4362). Mature and immature DC's were pulsed with Class II-derived HER2 or control irrelevant (BRAF and survivine) peptides (20 pg ml) for 5.days at 37"C, Control wells contained C04' T-cells only In additionõ
0,5x10' cells Were incubated in the presence of Dc/CD,V coeulture Supernatants for 5 days at 37 Cõ In both approaches, cells were then cultured for 2 more passages in absence of cytokines and subjected to senescence studies (SA-0-gal activity at pH 6 and p15INK4b and pl6INK4a western blot) or apoptosis studies (cleaved caspase-3 western blot). The following antibodies were added to cells 60 min before incubation with the co-caine of DC and CD4' T-cells to neutralize Thl-elaborated cytokines:
polyclimal goat IgG anti-human TNF-a. (0.06 jig/nil per 0.75 ngiml TNF-a) and liFN-y (0,3 uglml per 5 ngitril IFN-t), and. goat IgG isotype :as the corresponding negative control (all from R&D
Systems).

Plasmid transfections MDA-MB-231 cells were transiently transfected for 48 h with 2 pg of the wt HER2 expression vector (pcDNAHER2). As a control, cells were transfected with 2 pg of the empty vector (pcDNA3). Both vectors were kindly provided by Dr_ Mark Greene (University of Pennsylvania, Philadelphia, PA). The cells were transfected in complete medium without antibiotics with Ttubofect (Thermo Scientific, Waltham, MA), Transfection efficiency was evaluated by western blot 48 h after transfection.
Forty eight hours later, transfected cells were transferred to complete culture medium containing 0.4 mglinl G418 (Life Technologies). After 15 days of culture, colonies resistant to G418 were selected by limiting dilution. Transfection efficiency was evaluated by western blot.
RNA interference (RNAi) transfections Small interfering RNA (siRNA) SMART Pool: ON TARGET Plus HER2 siRNA, HER3 siRNA and SMART Pool: ON-TARGETplus Non-targeting Pool were purchased front GE Dharmacon-(Lafayette, CO). The following target sequences were used: HER2: UGGAAGAGAUCACAGGLIUA (SEQ ID NO: 9), GACIACCCGCLICiAACAAUAC (SEQ ID NO: 10), GGAGGAAUGCCGAGLIACUG
(SEQ ID NO: 11), GCUCAUCGCUCACAACCAA (SEQ ID NO: 12); HER3:
GCGAUGCLIGAGAACCAALIA (SEQ ID NO: 13), AGAIJUGUGCLICACGGGACA
(SEQ 1D NO: 14), GCAGUGGAUUCGAGAAGUG (SEQ ID NO: 15), UCCRICAUGULIGAACUAUA (SEQ ID NO: 16); Non-targeting:
LIGGULWACAUGLICGACUAA (SEQ ID NO: 17), UGGUULIACAUGULIGUGUGA
(SEQ ID NO: 18), UCKILTULJACAUGULTUUCUGA (SEQ ID NO: 19), UGGLIUUACAUGLIUIJUCCLIA (SEQ ID NO: 20). Three hundred thousand cells were transfected with siRNA sequences (25 nM) using RNA I Max Lipofectarnine (Life Technologies) in serum free medium, and afier 1 h the medium was supplemented with 10% FBS. Sixteen hours later, cells were subjected to 48 h of serum starvation followed by various designated treatments and western blot to check expression levels.

SA-0-nal activity at pH 6 Cells were washed twice in PBS, fixed in 3% formaldehyde, and washed again in PBS. The cells were incubated overnight at 37 C (without CO2) with freshly prepared senescence associated acidic 0-galactosidase (SA4I-gal) staining solution from Millipore (Billerica, MA) per manufacturer's instructions. The percentage of SA-0-gal-positive (blue) cells in each sample was determined after scoring 300 cells using a bright-field microscope (Evos Corer Bethel, WA/40X/ 2048 x 1536, 3.2 untlpixel; 3.1 MP
COLOR/ Captured images: Color TIFF, PNG, JPG or BMP-2048 x 1536 pixels) Western blot analysis Lysates were prepared from MCF-10Aõ SK-BR-3, and MCF-7, T-47 D or MDA-MB-231. cells. Cells were lysed in a buffer containing 50 mM Iris (pH
7.4), 150 mM NaC1, II mM EDTA, 1 mIVI ECM., 10% glycerol, 70% Tergitol, 0.1% SDS, 1 mM
Mg2C1 and protease inhibitor cocktail Sigma-Aldrich (St. Louis, MO); Lysates were centrifuged at 12,000xg for 15 min at 4 C. Proteins were solubitized in sample buffer (Life Technologies) and subjected to SDS-P,NGE. Proteins were electrohlotted onto PVDF. Membranes were imunmoblotted with the following antibodies: pl5INK4b (K-18), p16INK4a (50.1), IFN-yRa (C-20), HER3 (C-17) all from Santa Cruz Biotechnology (Santa Cmz, CA); Vinculin (V9131) from Sigma-Aldrich; HER2 (29D8), cleaved caspase-3 (Aspl 75) and TNF-R1 (C25C1) and phospho-Akt (Ser473) from Cell Signaling Technologies (Danvers, MA). After washing; membranes were incubated with I-MP-conjugated secondary antibody (Bio-16d, Hercules, CA). Bands were visualized and quantified by using the enhanced chemilumineseence (ECL) western blot detection system and the Image Reader LAS-1000 Lite version 1.0 software (Fuji).
Quantification of western blots was performed using Imagei software, Flow cytometrie analysis of cell death SK-BR-3 cells were untreated, treated with IFN-y (100 Ulm!) and TNF-a (lOnglin1), treated with trastuzumah (I Oug/m1) and pertuzumab (10ggim1), or treated with a combination of IFN-y, TNF-a, trastuzturiab, and pertuzumab, for 24 hours, After incubation, apoptosis induction was determined using F1TC-Annexin V apoptosis 'detection kit (BI) biostiences) according to manufactureeS instructions Briefly, untreated and treated SKBR3 cells were collected, washed with PBS and resuspended in Annexin V binding buffer at a concentration of 1x106 cellthnl. 100p1 of cell suspension was incubated with 5p1 P1 and 5p1FITC-annexin V for 15 min at room temperature in the dark. After incubation, 150platmexin V binding buffer was added and apoptosis induction was analyzed using a BD Accuri C6 flow cytometry (BD Biosciences) and data was analyzed with CFlow Plus software. UV-irradiated cells were used as positive controls.
Tumorigenesis studies For xenograft experiments, SK-BR-3 (2 x 106 cells mouse in 200 pi PBS) were injected into the flanks of six-week old female oathymic- (nude) Mice (Foxn0, Harlam Laboratories, 5 mice/group). When the tumors were palpable, the animals were treated s.c. with trastuzumab and pertuzumab (30 ugikg) and then injected s.c.
twice a week with brINF-a. and brfFN-y (10 ng/kg). Tumor formation was monitored by palpation and tumor volume in trim3 was determined with a. caliper twice a week: widtb2 x length/2. All animal experiments were carried out in compliance with the institutions guidelines.
Statistical analysis Unpaired Student's t-test (two-tailed) analysis was performed using .GraphPad Prism (GraphPad Software, La Jolla, CAõ USA). A P value of 0.05 or less was considered significant. ""P <0,05, **P <0.01, "V <0.001.
RESULTS.
Thl cytokines TNF-a and 1FN-y synergize to induce senescence in breast cancer cells SK-BR-3 cells were incubated with human recombinant tumor necrosis factor alpha (TNF-a) and interferon gamma (IFN-y) alone or combined for 5 days at 37 C to study if the elaborated crokines produced by the immune system cells could induce a specific senescence response in tumor cells. The cells were then cultured for 2 more paSS4OS and subjected to senescence studies.. The combination of both cytokines resulted in senescence induction of SK-8R-3 cells, evidenced by increased senescence associated acidic flialactosidase (SA-11-gal) staining (Figure 6A) and higher expression of the senescence-associated markers pl5INK4b and pl 6INK4a (Figure 68) compared to the control untreated cells or each cytokine alone detected by western blot.
Similar results were obtained in 8T-474, MCF-7 and T-471) breast cancer cell lines (data not shown).
Thus, T-47D cells were treated with several Concentrations of TINFet-, foarn 10 to 100 and IFNI, from 100 to 1000 or in combination. It was observed that the induction of the senescence phenotype was dose dependent (Figure 6C), Similar results were found in 5K-BR-3, 81-474 and MCF-7 cells.
Inverse correlation between the HER2 expression level in breast cancer cells and the Tit I
cytokines TINF-a and IFN-1 doses required to induce senescence Experiments were designed to determine whether the HER2 expression level plays a role in the senescence induced by the treatment with INF7a, and IFNI for 5 days at 37 C'followed by 2 more passages without thetytpkines.in SK BR-3 BT..474 MCF-7, 1-471) and MD.A-MB-231 breast cancer cells. In fact, the amount of SA43-gal positive cells was augmented in the high HER2 expressing cell lines (SK-13R-3, Figure 6D and BT-474, data not shown), with lower doses of TNF-a. and IFN-y compared to the intermediate HER2 expressing cell lines (T-47D, Figure 6D and MCF-7, data not shown) with higher cytokines concentrations. However even highest concentration of TNF-u. and IFN-1 could not induce senescence inthe low 1IER2-expressing cell line MDA-M13-(Figure 6D), These results clearly evidence a correlation between the TNT-a.
and IFN-y inducing senescence and the HER2 expression level..
1IER2 is .required for Thl cvtokines TNF-u. and IFN-'y tuediated_senescence and apoptosis in MDA-MB-231 breast cancer cells Only when MDA-MB-231 cells were stably transfected with a wild type HER2 plasmid (pcDNAHER2) and treated with high concentrations of TNF-a (200 ng/m1) and IFNI (2000 Li/m1.) for 5 days at 37C followed by 2 more passages in absence of cytokines, there was a strong increase in-SA43-0 positive cells (Figure 7A) and in p1SINK4b expression (Figure 713). 'Notably, since it was observed that not only there -was a relatively higher number of blue senescent cells when HER2-MDA-cells were cultured with highest concentrations of TNF-a and IFN-y, but also there was a significantly lower amount of cells, the experiment was repeated and the cells were subjected to western blot to detect active easpase-3 to study apoptosis (Figure 7B). The treatment of cellstranstected with .the control empty vector (pcDNA3) with increasing concentrations Of TNF-ct, front 75 to 200 nglinl, and IFNI, from 750 to 2000 in combination in the same conditions described above, had no effect on senescence induction assessed by SA-gal staining (Figure 7A) or p15INK4b and cleaved caspase 3 expressions (Figure 78). This finding reinforces that 'FIER2 is required in the mechanism of TNF-a and IFNI inducing senescence and apoptosis in breast cancer cells.
Cytokine receptors are expressed in similar levels in breast cell lines -15. The high HER2-expmssing cell lines SK-.13R4 and BT-474, the intermediate MCF-Tand T-47D. and the low -HER2-expressing.MDA-MB-231 breast.
cancer cell lines, like the low IHER2 normal immortalized MCF-10 breast cell line showed similar IFN-y and TNF-u receptor expression by western blot analysis (Figure 12). This result demonstrates that the expression level of these two cytokine receptors is independent of the HER2 expression level. It is in accordance with reports that describe the action of these cytokines in the different phases of the normal breast.
TNF-a has been 'invOlvedin pro1 iferation,. development and branching mot phogenesis of the normal mammary Wand (Lee et al., 2000 Endocrinology 141: 3764-3773). The receptor TNFRI.
expression mediates TNF-a-induced proliferation of mammary epithelial cells, and TNFR2 activation induces casein accumulation (Varela et al., 1996 Endocrinology 137:
4915-4924). Similarly, the active form of:117Ni, interacts with its receptor expressed on the surface of almost all normal cells (Ealick et al., 1991 Science 252: 698-702; Farrar et al., 199$ Annu. Rev. Immunol. 11:571-611).
=
30. Combined HER2 and HER3 blockage expression enhances Th I cytokines TNF-aand IFN-y senescence induction in breast cancer cells.

The previow results showing the enhancement of senescent and apoptosis phenotypes in high and intermediate HER2-expressing cell lines treated with the combination of cytokines led to studying the effect of knocking down HER2 and with siRNA. The therapeutic benefit of blocking HER2/HER3 signaling in breast cancer has been demonstrated by several studies (Lee-El oeftich et al., 2008 Cancer Res.
14:5878-87; Berghoff et al., 2014 Breast 14: S0960-9776). Although the combined treatment of TNF-a and IFN-7 in HER3-depleted cells did not significantly enhance the number of senescent or apoptosis cells, the double knock down with HER2 and siRNA strongly increased the SA4-gal staining (Figure 8A) and p15INK4b and active caspace-3 expression level (Figure 813) in SK-BR-3 cells. At the same time, it was observed that a higher apoptosis induction of the cells treated with the double knock down and the cytokines by western blot of active caspase-3 (Figure 8A).
Similar results were found in MCF-7 cells (Figure 13), BT-474 and T47D cells.
Combined HER2 inhibition and HER2-HER3 dimerization inhibition enhances Thi cytokines TNE-rx and IFN-7 senescenee induction and aptiptosis. in SK-BR,-3 breast cancer cells Trastuzumab and pertuzumab are antibodies that have been widely used in the clinic to treat HER2-positive breast cancer. To study the Th1 cytokines,-induced senescence and apoptosis in a translational approach, experiments were designed to pretreat SK-BR-3 cells with trastuzumab and pertuzumab and then, the cells were additionally treated with TNE-a.and IFN-y for 5 days at 37'C 'followed by 2 more passages withOut.the cytokines ,and antibodies. It Was observed that the amount of blue cells was highly increased in the cells that received the complete treatment compared to the cells treated with cytokines only, as measured by SA-11-gal staining (Figure 9A) and p15INK4b increased expression by western blot (Figure 913). interestingly, the double treatment also had a significant effect on the induction of apoptosis, both by increased active caspase 3 expression by western blot (Figure 9B) and by increased amount of anexin v and propidium iodide positive cells by flow cytometry analysis (Figure 9C), C1)4-' Thl-mediated senescence and apoptosis of HER2-ovexpressirig.human breast cancer cells Experiments were designed to co,culture HER2 Class H peptide-primed CD4 T-cells with SK-BR-3 breast cancer cellS;using a tranSwell culture System to Confirm that :the eywk*s produced by the immune system cells in vivo could also induce.aSpeeific senescence and apoptotic response in tumor cells. The cells were co-cultured for 5 days at 37"C and then cultured for 2 more passages in complete medium without immune system cells. The co-culture resulted in senescence and apoptosis of SK-BR-3 cells, evidenced by increased amount of SA-13-gal staining (Figure 10A) and increased expression of p 15INK4b and cleaved caspase 3 (Figure 108) detected by western blot CD4' T-cells primed either with immature dendritic cells (DCs) or mature DCs plus irrelevant Class H (BRAF or survivine) peptides were not able to induce either senescence, or apoptosis of SK-BR-3 cell (Figure 10).
The senescence and apoptosis observed was highly augmented in SK-BR-3 when the cells were co-cultured with HER2 Class H peptide-primed CD4' I-cells in presence of trastuzumab and pertuzumab in the transwell. This result was clearly evidenced by increase SA-Ii-gal staining (Figure 10A) and p15INK4b and cleaved caspase 3 expression levels (Figure 108).
As another approach, SK-BR-3 cells were co-cultured with the supernatant from CD4' T cell-mature DC co-culture and a similar specific senescence response was observed. The Thi -elaborated cytrikines fEN-y and TNF-a obtained from CD4.' T
cell-mature DC co-culture supernatants were previously confirmed using ELBA. By both experimental approaches, SK-BR,3 senescence and apoptosis..could be partially rescued by neutralizing IFN-y and TNF-a. blocking antibodies (Figure 14).
It was also observed that the effect was dose-dependent as increasing number of immune system cells induced higher SA-11-gal staining, pl 5INK4b and cleaved caspase 3 expression levels in SK-BR-3 cells by both approaches.
Thl cytokines TNF-ct and 1FN-y sensitize trastuzumab and pertuzumab resistant breast cancer cells to senescence and apeptosiS induction to continue unraveling the mechanism by which the I hi cytokines could induce senescence and apoptosis, it is believed that TNF-a and IFN-y could restore the sensitivity to trastuzumab and pertuzumab to breast cancer resistant cells. It was observed that the treatment with trastuzumab and pertuzumab could not prevent the activation of AKT in two resistant cell lines HCC-1419 (O'Brien et al., 2010 Mol Cancer Ther.

6:1489-502) and JIMT-I (O'Brien et al., 2010 !viol Cancer Ther. 6:1489-502;
Tanner et al, 2004 Mc! Cancer Ther. 12:1585-92) contrary to T-47D sensitive cells (Figure 16).
The treatment with INF-0. and IFN-y induced senescence and apoptosis in a dose dependent manner in HCC-1419 and JIMT-1 cells. When the cells were treated with trastuzumab and pertuzumab, senescence and apoptosis could not be evidenced even at higher doses (data not shown). However, the double treatment with cytokines and antibodies induced senescence by SA-11-gal assay (Figure 11A) and increase expression of pl5INK4b (Figure I 1B) in HCC-1419 and HMI- I cells. Moreover, the combination of cytokines and antibodies effectively induced cell death (Figure 11B) in HCC-I419 and JIMI-1 cells. This result demonstrates that the Thl cytokines IFN-y and INF-a could revert the resistance to the therapeutic agents that is affecting cancer patients widely.
DISCUSSION
Herein it has been demonstrated that INF-a and IFN-y induce senescence and apoptosis in breast cancer cells in a dose dependent manner. Also revealed is an inverse correlation between the HER2 expression level in breast cancer cells and the doses of TNF-a and IFN-y required to induce senescence in those cells. It has also been shown that cytokine receptors are expressed in similar levels M all the breast cell lines tested, implicating that this is not the cause of the differential response.
Furthermore, only when MDA-MB-231 cells (low HE-R2 level) were stably transfected with a wild type plasmid, high doses ant cytokines were able to induce senescence and apoptosis.
Thus, it seems that HER2 signaling is required to induce senescence and apoptosis by thl cytokines, because in cells that lack HER2 or express very low levels is not possible to induce senescence or apoptosis even with high doses of cytokines. However, in cells that express hid or intermediate levels of HER2, knocking down the gene induces senescence and apoptosis through a phenomenon called oncog,ene addiction. It has additionally been shown that combining 1{ER2 and HER3 siRNA enhances even more of CA 02986687 2017-11-21 =

,the senescence and apoptoSis induced by TNF-et and II N-I in breast cancer cells, taking a step ahead of HER3 over counting for the lack of HER2 signaling.
Example 5: Anti-Estrogen Therapy and Anti-HER2 Dendritic Cell Vaccination Improves Pathologic Complete Response in ER/HER2 P' DOS
The antigen-presenting capacity of dendritic cells ("DCs") has led to enthusiasm for their nse in anti-tumor vaCtination. The present group designed a HER2 peptide-pulsed autologous DC vaccine uniquely engineered to promote anti-HER2 Thl Sensitization and attraction. See United States Ser. No. 14/658,095, filed Match 13, 2015; United States Ser. No. 14/985,303, filed December 30, 2015, the disclosures of which are incorporated by reference herein in their entireties; Dana, i., et al., Oneohnmunology 4:8 e1022301 (2015) D01:10. 1080/2162402 X.2015. 1022301, and Dana, I., et al., Breast Cancer Res. 17(1):71 (2015). The feasibility, the safety, and the preliminary clinical results following the neoadjuvant use of the anti-HER2 vaccine in patients with HER2 f"-'s DCIS (1iIER2P ductal carcinoma in situ) has been reported.
Complete tumor regression (pathological complete response ("pCR")) was induced in 19% of patients; however, these results were concentrated in patients with hormone independent (ER) DOS, suggesting that patients with ERP'sDCIS were less responsive to the anti-HER2 DC vaccine than are those patients with hormone independent DCIS
(Sharma, Aõ et al., Cancer 118(17):4354-62 (2012)). The extensive bidirectional crosstalk between the HER2 and ER signaling pathways leads to enhanced cancettell proliferation and survival (Arnim. G., et al., Endocrine Reviews 29(2):217-233 (2008) and Prat, A., et al,, Nat. Qin. Proc. Oncol. 5(9):531-542 (2008)). Combined targeting of both of these two receptors may prevent them front continuing to activate each other. It is hypothesized that adding anti-estrogen ("AE") therapy to anti-HER2 DC
vaccination treatment would improve the response in patients with HER2P'-'/ERP"' Dos. In the studies reported herein comparisons were made between the clinical and the immune responses in anti-HER2 DC vaccinated patients with ER :nn DCIS ("ER), ER1" DOS

patients Who received the anti-HER2 DC- vaccine alone ("ERPN,ithotit At"), and ER.P"' DM patients who received both the anti-HER2 DC vaccine and concurrent anti-estrogen therapy ("ER P"' with AE").

T he results .presented. herein-demonstrate that COACUITtat Tie0adjUVant anti-estrogen therapy and anti-HER2 DC1 vaccination increases the immune response in the local sentinel lymph nodes and the rate of pathologic complete response in HER2106/ERN DC1S. These results further support individualized, targeted, combination therapy. -METHODS
Methods Summary: Eighty-one patients with HERn's DCIS received-a neoadjuvant anti-HER2 DC vaccine. Clinical response was measured in the resected surgical specimen. Immune response anti-HER2 CD4 Thl response - was measured in the peripheral blood pre- and post- vaccination and in the sentinel lymph nodes post-vaccination. Clinical and immune responses were compared between ER""e patients who underwent anti-HER2 vaccination alone, ER`" patients who underwent anti-HER2 vaccination alone, and ER"' patients that received anti-estrogen therapy concurrently with anti-HER2 vaccination.
The methods carried out are set forth below in detail, xperiMents Breast cancer cell.lines., SK13R3 (HER2P"' 3+1 ER"g) and ME. F7 (HERVg 2+1 ER), were treated with Th I cytokines (IFNy and TNFa)õ a tamoxifen metabolite (4-hydroxytamoxifen, -41-1r), or both for 72 hours. Metabolic activity was measured via Alamar Blue assay.
Trial Design After approval by the Institutional Review Board of the University of Pennsylvania, two neoadjuvant clinical trials of a HER2 peptide pulsed DC1 vaccine (NCT001 070211 and NCT02061332) were conducted. The primary objectives were to evaluate the feasibility, safety, and efficacy of DC1 vaccination. The secondary objective was to assess clinical and immune responses. .Preliminary results of these trials showed that the vaccine is safe, well tolerated, and induces decline or eradication of HER-2 exPression (Sharma ,.A., et al., Cancer I 18(l7):4354-62 (2012) ("Sharma, et al.")).
Further review of the preliminary results showed that vaccination was more effective in =

hormone independent (ER) patients [20, 21]. Based On the preclinical data and the preliminary results of the clinical trial, an addendum was approved to treat subsequent ERP 3 patients with hormone dependent ( ERP's) DCIS with concurrent AE
therapy.
Patient Selection Female patients older than 18 years of age with biopsy-proven HER2r"DOS and an ECOG Performance Status Score of 0 or I were eligible for the trial. Al!
tissue specimens were reviewed by a single pathologist for eligibility; HER-2 positivity was defined as >5% of cells expression 2+ or 3+ intensity of the 1-[ER-2 protein.
Women of childbearing age were required to have -a negative serum pregnancy test and were required to use a medically acceptable form of birth control. Women with cardiac dysfunction, HIV, HepC, coagulopathies, or a pre-existing medical illness or medications which might interfere with the study were excluded from the trial. Women who had received definitive treatment or whose DCIS was eliminated by excisional biopsy at diagnosis were not eligible for the trial. Eighty-one women were enrolled in the trial and completed the vaccination treatment. All 81 patients underwent surgical resection with pathologic examination of the resected specimen. The immune responses were measured in patients in the second trial (NCT02061332) - 53 of 54 patients had pre and post-vaccination CD4+ immune responseS measured in the peripheral blood; 40 patients had post vaccination CD4+ immune responses measured in the sentinel lymph nodes;
and 22 HLA-A21' patients had pre- and post-vaccination CD8+ immune responses measured in the peripheral blood.
Vaccination Procedure Vaccine preparation and delivery have been desctibed in detail previously.
See, for example, Sharma, et al., Czemiecki, BJ., et al., Cancer Res. 67(4):1842-52 (2007) (Czerniecki, et al.), and Koski, G.K., et al., i. .Thnnunother. 35(1) 54-56 (2012). The vaccination procedure is shown in Figure 16. Briefly, monocytic dendtitic cell precursors were obtained from patients via tandem leukapheresisicountercurrent centrifugal elutriation. Monocytes were cultured at 37 C in serum free medium (SFM) ativitrogen, CarlSbad, CA) with gralnliOtyle-maa0phage Coiony-stimulating factor (GM-CS 1) (Amgen, 'Newbury Park, CA) and IL-4. The following day, the cells were pulsed With six HER,2,derived majorhistocompatibility complex (MEW) class H binding peptides (American Peptide Corporation, Sunnyvale, CA) - three extracellular domain (ECD) peptides (peptide 42-56: FILDMLRFILYQGCQVV (SEQ ID NO: I); peptide 98-114:
RLRIVRGTQLFEDNYAL (SEQ ID NO: 2); and peptide 328-345:
TQRCEKCSKPCARVCYCIL (SEQ NO: 3)) and three intracellular domain (1CD) peptides (peptide 776-790: GVGSPYAISRLLGICL (SEQ ID NO: 4);. peptide 927-941:
PARE1PDLLEKGERL (SEQ ID NO: 5); and peptide 1166-1180 TILERPKTLSPGKNGV (SEQ ID NO: 6))_ After 8-12 hours, 10001,11mL of:MN-gamma (Inteimuneõ Brisbane, CA) was added, and 6 hours before harvest, 10mgina: of clinical grade LPS (gift from Dr Anthony Suffredini at the National Institute of Health (NM)) was added to complete the rapid maturation to a type-I dendritic cell (DC 1).
For H.LA-A2P patients, the monocyte pooi was pulsed with WIC class l. binding peptides and 689-697.
Four to six weekly injections of 10-20 million HER-2-peptide pulsed Del s were administered into the breast, the groin lymph nodes, or both the breast and the groin lymph nodes.
Patients were monitored for adverse effects for a minimum of 1-2 hours following each weekly vaccination. All adverse events were classified by National Cancer Institute Common Toxicity Criteria (NCI-CTC version 3.0), were assessed at least weekly during vaccination, and were Monitored until their resolution.
Clinical Monitoring Pathologic response was examined at the time of surgical resection -lumpectomy (n 48) or mastectomy (n 33). A pathologic complete response to immunization was defined as no residual DCIS or invasive breast cancer at the time of surgical resection.
Patients were monitored after surgical .resection for the des elOpment Of subsequent breast events A subsequent breast event was defined as a lesion ¨ DCIS or invasive breast cancer, identified in either the ipsilateral or contra-lateral breast.
Anti-Estrogen Therapy ER positive patients were _treated with anti-estrogen therapy concurrent with four to six weekly anti-HER2 DC1 vaccinations. A physician investigator decided.
which of the following anti-estrogen therapies was best suited for each patient:
17amoxifen (4-hydroxytamoxifen ("4H1") (NOLVADEXTm)); LetrozOle (FEMARATm); Anastrozote (ARMIDEXTm); Exemestane (AROMASINTm); Raloxifene (EVISTATm); or any other suitable anti-estrogen agent that blocks or modifies the actions of estrogen.
Immune 'Monitoring (.7D44.
Systemic. anti-HER2 CD4+ 'f-cell responses were generated from autologous peripheral blood mononuclear cells (PBMC) pulsed with six HER2-derived major histocompatibility complex (MHC) class 11 binding peptides peptides. Localized anti-HER2 CD4+ T-cell responses were measured in the locoregional sentinel lymph nodes (SLN) in 40 patients who underwent SLN biopsy. 1FN-y production was quantified via enzyme-linked immunosorbent spot (ELISPOT) assays as previously described in detail.
(Fracol, M., et aL Aim. Sorg. Oncol. 20(10):3233-9 (2013)) Briefly, PVDF
membrane plates (Mabtech, Cincinnati, OH) were coated overnight with anti-[FN-y capture antibody (ID! K). The following day, after the plates were washed with PBS (Mediatech, Manassas, VA) and blocked with 10% human serum,I.DMEM, 2x IW PBMCs on SUN
cells. Were plated in each well either unSrimulated, pulsed with HER2-derived Class li peptides:(4gg) (42-56, 98-114,.328-345, 776-79k927-941 1166-1180), or pulsed With anti-human CD3 and CD28 antibodies (0.5gginiL) (positive control, BD
Pharmingenõ
San Diego, CA), and incubated at 370C+ 5%C.02 for 24-36 hours. After the plates were washed with PBS, 10Opt of detection antibody (imgimL; 7 B6-1-biotin) was added to each well and the plates were incubated tbr 2 !lours. After the plates were washed again with PBS, 100AL of 1:1000 diluted streptavidin-HRP was added to each well and the plates were incubated for another hour. TMB substrate solution was added to reveal spot fOrMation. Spot forming 'OM (SFC) .viere counted using an automated reader (ImmtmoSpot CTL).
A positive response to an individual HER2 Class II peptide was defined as a minimum of 20 SFC/2x105 cells after subtracting the unstimulated background and at least a two-fold increase over the.uristimulated baekground. Three metrics were used to quantify the CD4+ Th I response: (I) overall response rate (the proportion of patients responding to? 1 peptide), (2) response repertoire (the number of peptides to which a patient responds), and (3) cumulative response (the sum of the SFCs across all peptides).
CD84- T-celh Systemic anti-HER2 CD8+ T-celli responses were measured in twenty two HLA-.A2im(HLA.2.1) patients . Anti-HER.2 CDS+ T-cell responses were generated by in vitro sensitization assays as previously described in detail by Czerniecki, et al...
Briefly, CD8+
T-cells were selected from the cryopreserved 120-140 lymphocyte cell fractions via negative selection (StemCell Technologies, Vancouver, BC). Autologous dendritic cells were suspended in serum free medium (SFM) (invitrogen, Carlsbad, CA) with GM-CSF
(long/m1). pulsed with a class] 1-IER2 peptide (lOuglinl) (369-377), and co-cultured with the CD8+ T-cells at a ratio of 10:1. IL-2 (30 MIMI) was added on day 1 On day 10, 1-cells were harvested and were tested against T2 target cells pulsed with either the Class I
HER.2 peptide or irrelevant controls (p53 and colon cancer peptide). After 24 hours, the supernatant was harvested and analyzed by enzyme-linked ittuunnosorbent assay (El. ISA): A. positive response to the HER2 Class I peptide was defined as a two-fold increase in CDS+ T-cell IFNy production compared to the irrelevant peptide controls.
Statistical Methods Descriptive statistics and univatiate logistic regression was used to evaluate demographic. and clinical data. P-values <0.05 were considered statistically significant.
Development of subsequent breast events was compared using Kaplan Meier analysis.
All analyses were performed with STATA 12.0/IC statistical software (STATA
Corp, College Station, TX).
RESULTS
Results Summary: Patients with ER DCIS and patients with ER" DCIS who were treated with anti-estrogen therapy bad a similar rate of pathologic complete response.(31.4% vs-28.6%, p 1.00);.and both rates wete significantly higher than the rate of pathologic complete response found in patients with ER P's DCIS that did not receive anti-estrogen therapy (4,0%, p 0.035). The anti-HER2 Thl immune response measured in the peripheral blood increased significantly following vaccination, but was similar across all three groups. In the sentinel lymph nodes, however, the anti-HER2 TM
immune response was significantly higher in the patients with ERP' DOS Who were treated with combination anti4HER2 vaccination and anti-estrogen therapy compared with the patients with ERP' DCIS who were treated with anti-HER2 vaccination alone.
The results are set forth below in detail, Pre-Clinical Experiments =
The SKBR3 breast cancer cell line (ER) increased anti-tumor activity in response to Thl cytokine treatment, but not in response to anti-estrogen treatment.
Furthermore, adding anti-estrogen treatment to the Thl cytokine treatment had no effect on the metabolic activity as shown in Figure 17A, -Conversely, the MCP breast .cancer cell line (ER!") did nOt increase anti-tumor activity in response to either Thl cytokine treatment or .anti-estrogen treatment; however, the combination of Thl cytokine treatment and anti-estrogen treatment together resulted in an increase in metabolic activity as shown in Figure 17B.
Trial; Patient Selection and Demostraphio Oldie 81 patients who participated in .the clinical trial, the median age was 2$ (interquartile range (IQR) 47-60), median BMI was 25.9 (IQR 22.4-31.0), and a majority of patients were post-menopausal (n .r 68; 84,0%) and white (n.-- 65, 80.2%).
All eligible patients were diagnosed with DOS at the time of biopsy ; however, a.minority of patients were found to have early invasive breast cancer (Stage 1) at-the time of final surgical resection (n. ¨ 1(, 19.8%). All eligible patients were diagnosed with 2+ In ¨ 28, 34.6%) or 3+ (ll ¨ 53, 65,4%) HER2P" 'DOS. Vaccination was administered into groin lymph nodes in 47 patients (58%), into the breast in 18 patients (22.2%), and into both the groin lymph nodes and the breast in 16 patients (20%). Surgical resection was completed via lumpectomy in 48 patients (59.3µ,`,10) and via, mastectomy it 33 patients (40.7%). Of those patients who underwent lumpectomy, 37,5% received post-operative radiation therapy.
The vaccine was well tolerated with only grade 1-2 adverse events. The. most commonly reported adverse events associated with the vaccine were fatigue (n.
41, 50.6%), injection site reaction (n 34, 42.0%), and chills/rigors (n ¨ 26, 32A%). No patients were unable to complete the trial due to the side effects.
Figure 18 shows that in the overall cohort, 35 patients (43.2%) had ER neg disease and 46 patients (56.8%) had ER' " disease. Of those patients with ER1"
disease, 25 patients (543%) received the DC1 vaccine alone and 21 patients (45.7%) received the DC1 vaccine and concurrent AE therapy. Demographic and clinical characteristics of these treatment groups are summarized in Table 1 below, and did not show any significant difference between the groups.
Table 1; Demographic and clinical characteristics comparing patients by ER
status and AE treatment.
Characteristic ER mg ERP s wiOut ERtms wi AE
Univariate (%) AE (%) Clot p-valuel Number of patients $ 432 25 O 9 21(259) i Median AVeJ101,956 (48-61151145-50)_ _ _54150-57) _ rfiM.Bi*tilignlligilgaiStiVP)pNEVIIARU)MMMMggigagggiligniii.gdidRMIRI
27.1 (23.2- 25.9 (22_6- 23.4 (21.8- 0.19 Median EIMI (IQR) 30.1) .111100,1011,111.1.1411(131011.111111:40PRISINIORAMEMINSARISEI
tigiggililiiitlifilliellitiggCallag.i2ZIOMOIREE915.0101).E.REEREEntita=
Charison Comorbidity Score 27 (77.1) 21 (84.0) , 21 (100.0) 0.07 152 8(22.9) 4(16.0) 0(0.0) ?.3 !*iavr:.E:77:7.7.77.7.7.7.77.77.75717.7,7.!.77:77.77.7..7.7r.T.7.7.7.77.7..!,77 7777:!!.!,:,7R
1111011111:111111111.1111129M9)IIIII17(80)I11111003)1111111140111 2+ 14 (40.0) 3(12.0) 11 (52.4) (1..01 ,,,,,,,,,, 22 (88.0) 10 (47.6) 9.11100*Sgeiggiggiaggallillagiogiggiggingligliigiglingnilignigigiggag Sg Res 111000411111111211410011=111100410111111111#10101111111=1111=111 MildtWAIIII11111110406411111111044411NRAMMENEMIRMEM
DIONEMENEMIEMASEIMEIRd011111101001111111111.11.111111011 , Lumpectomy 19 (54.3) 13 (52.0) 16 (76.2) 0.18 Mastectomy_ ,16 j45.7)_ 12148.0) 5 (23.81 illtiaattOWNEERNMeggreggiONFINFORROlgireggiORM
EgilliiitOgNESE.:iliiiiingNEERTMESPREM61461Pani.di:41;i4301i4danigg040iNWE':gli IttntingaiDeangiAMONEEINEMPIENNVIAIRMIERIEMEMEMENN
ER (estrogen receptor), AE (anti-estrogen), IQR (interquartile range), HER2 (human epidermal growth factor receptor 2).
bold indicates statistical shmificance 'following lumpectomy Clinical Response Rates to HER2 Vaccination The clinical response was available for all 81 patients_ Overall, 18 of the 81 immunized patients (22.2%) were found to have no residual disease identified in the resected surgical specimen; these patients were considered to have a pathologic complete response (pCR). As shown in Figure 19, pathologic, complete response in the ERneg group was higher than in the ER I" group. More specifically, pCR in the ER 'e group (II
= 11, 31_4%) and the ERI" group that received AE therapy (n = 6, 28.6%) were similar (p 1.001); however, the rate of pCR. in the ER" group that did not.
receive AE therapy (ti = 1, 4.0%) was significantly lower than the rate of pCR in the ER"g group (P =
0.01) and the ER " group that received .AE therapy (p 0.04) (Figure 19).
Pathologic coMplete.responsecorrelates with a decreased 1.7i* of recurrence See, for example, Tanioka,. M., et al, . Br. .1. -(7(1/leer 103(30:297.302 (2010) Subsequent breast lesions, defined as either DCIS or invasive breast cancer identified in either breast-, occurred in 6 vaccinated patients (7.4%). All of the patients who experienced subsequent breast events had residual disease identified at the time of surgical.
resection, < pCR
(Figure 20A). Two of the patients had ER' DCIS and four of the patients had ERP1' DCIS but did not receive AE therapy. None of the patients who had ER' DCIS and received: AE therapy have experienced a subsequenthreast..eVent (Figure 20B).
.25 patients enrolled later in the trial were treated with concurrent vaccination and AE =

therapy, and, therefore, median follow up was shorter for these patients. Of course, these patient S will continue to be monitored.
As shown in Table 1, the rate of lumpectomy was similar across all three groups;
however, the rate of radiation following lumpectomy was lower in the group of patients with ERP" DOS who received AE therapy (18.75%) than in the group of patients with ER' "' DOS who did not receive AE therapy (53.8%, p = 0.06). Patients with ER!' DOS
who received AE therapy have a decreased rate of subsequent breast events despite the lower rate of radiation.
Immune Response Rates to HER2 Vaccination CD4 4- T7I1 Response: Spiemic - Peripheral Blood The pre-vaccination and post-vaccination immune responses were measured in 53 patients. Overall, responsivity increased significantly from 36.25% pre-vaccination to 56.25% post-vaccination (p ¨ <0,001), Median response repertoire also increased significantly from 1(IQR 0-2) pre-vaccination to 2.9 (IQR 2-4) post-vaccination (p ¨
<0.001). Finally, median cumulative response increased significantly from 56A
(IQR
23,3-111.7) pm-vaccination to 133.1 (IQR 75.6-240.3) post-vaccination (p 0,002).
Responsivitv: Following vaccination, responsivity increased significantly in each group (ER 'eg 58,3% to 87.5%, p < 0,01; ER P"s without AE treatment 50.0% to 75.0%, p <
0.01; ERP' with AE treatment 57.1% to 90.5%, p < 0.01), Pre-vaccination responsivity rates were similar across all three groups 58.3%. Eltr"'s without AE
treatment 2$ 50.0%, ER" with AE treatment 57.1%; p = 0,9). Post-vaccination responsivity rates were also similar across all three groups (ElVeg 87.5%, ERP' without AB
treatment 75,0%. ER P" with AE treatment 90.5%; p 0.5, Figure 21A).
Response Repertoire: Following vaccination, response repertoire increased in each. group (ER .1. to 3, p 0.05; ER! " without AE treatment 0 t01.5, p 0.1;
ERP"
with AE treatment 1 to 3, p = 0.01). Pre-vaccination median response repertoire was similar across all three groups (EIVeg 1 (1QR 0-2), ERP' without AB treatment 0 (IQR 0-1.5), ER P"' with AE treatment 1 (IQR 0-2); p 0.5). Post-vaccination median response repertoire :was also. similar across all three groups (ER- 3 (IQR. 2-4.5)õ.ERP" without AE
treatinent 1.5 (IQR 0.5-3.5), ER P" with AE treatment 3 (IQR 2-5); p = 0.4.
Figure 21B).
Cumulative Response: Following vaccination cumulative response increased in each group (ER "g 56.3 to 149.7, p <0.01; ER P" without. AE treatment 41.1 to 178.7, p <
0.01; ERP" with AE treatment 58.6 to 100.9, p <0.01). Pre-vaccination median cumulative response was similar across all three groups (ER" 56.3 (IQR. 26.1-116.2), ERP' without AE treatment 41.1 (IQR 9.6-168.6), ER's with AE treatment 58.6 (IQR
24.2-87.9); p = 0.886). Post-vaccination median cumulative response was also similar across all three groups (ER's .1493 (IC* 977-246,7), .ER without AEtreatment 178.7 (IQR 64.7-278.3), ER"' with AE treatment 100.9 (T.QR 67,5-174A); p ¨ 0.5, Figure 21C).
CD4-i- Thi Response: Local Sentinel Lymph Node The post-vaccination immune responses were measured in 40 patients. Overall, responsiviti was 80%, median response repertoire was 2 (IQR 1-5), and median cumulative response was 76.5 (19R 23-197).
Responsivity: Responsivity rates were significantly higher in patients with HER2P"/MRP"' DOS who received with AE treatment compared to patients with IIER2P09/ERP"' DCIS who did not receive AE treatment (92.3% vs 43%; p 0.03.
Figure 22A).
Response Repertoire: Median response repertoire was also significantly higher in patients with HER2posiERpos DCES who received with AE treatment compared to patients with HER2pos/ERpos DOS who did not receive AE treatment (4 (IQR 2-6) vs 0 (IQR. 0-5); p 0.05. Figure 228), Cumulative Response: Median cumulative response was also significantly higher in patients with HER2P"./ERP" DCIS who received with AE treatment compared to patients with FIER2P"8/ERP" DCIS who did not receive AE treatment (102 (IQR 69-354) vs 23 (IQR 1-100); p 0.05. Figure 22C).

CD84. Response: Systemic - Peripheral Blood The pre-vac.cinationandpost-yaccination CDS+ tmtnune responseS were measured in 22 IILA-A2+ patients. Overall, tesponsivity increased significantly from 113% pre-vaccination to 723% post-vaccination (p = <0.0002).
Responsivitv: Following vaccination, responsivity increased in each group (ER"g 12.5% to 75%, p = 0.04; ER"' without AE treatment 0% to 100%, p < 0.03, ER!' with AE treatment 20% to 60%, p =0.1 7. Pre-vaccination responsivity rates were similar across all three groups (ER 'g 12.5%, ER'" 'without AE treatment 0%, ER ' with AE
treatment 20%; p = ). Post-vaccination responsivity rates were also similar across all three groups (EIV'eg- 75%, ERix's without AE treatment 100%. ER P"' with AE
treatment 60%; p =. Figure 23).
CONCLUSIONS: The study described herein clearly shows anti-HER2 DC.1 vaccines are clinically effective in ElltnIFIEVb: DCIS.patie.nts. DC1 , vaccines are also shown to be safe when combined with anti-estrogen therapy.
It was shown that concurrent neoadjuvant anti-estrogen therapy and anti-HER2 DC1 vaccination increases the immune response in the local sentinel lymph nodes and the rate of pathologic co Piet response in FIER21"/ERPY4DCIS patients The combination therapy with anti-estrogen may also reduce subsequent Breast Events_ These results may offer a personalized approach in DCISItherapy: These results further support individualized* targeted, combination anti-HER2 DC1 vaccine and anti-estrogen treatment. One skilled in the art can appreciate that other anti-proliferative combinations of anti-HER2 treatments such as Trastuzumab and Pertuzumab, and others, are possible.
These approaches may limit the need to extensive surgery, eliminate radiatition therapy, and reduce long term hormonal treatment.
Example 6:A Novel Dendritic Cell Vaccine Targeting Mutated BEM Overcomes Vemurafenib Resist= and Synergistically Improves Survival in BRA.F-Mutant Marine Melatioina BRAF inhibitor vemurafenib (PLX) improves survival in :MAP-mutant (BRAFv6m3-) melanoma, but resistance is common. A BRA.Fv"IE-puised typel-polarized dendritic cell vaccine (BRAF"."-DC1) induces antigen-specific CDr T-cells that impact murine BRAI"" melanoma. We investigated if combinations of BRAP"'-DC:1 and PLX elicit a synergistic clinical response.
METHODS
A transplantable BRAFv6mr=PTEN melanoma model was de eloped in the C57I31/6 background, DC1 were generated from bone marrow precursors using F1t3, IL-6, GM-CSF, 1L-4, CpG and LPS, and pulsed with class 1 BRAFw" peptide. In addition to untreated and ovalburnin-DC1 controls, BRAF'-DC1 (2x weekly injections) and PLX were administered alone or in designated combinations to tumor-bearing mice (n-10 each). Tumor growth and survival were determined, Induction of BRAF''-specific CDS T-cell responses from splenocytes were assessed by IFN-y ELISA.
Cytokine mRNA quantification in tumor microenvironments (TME) was performed by RTAPCR.
RESULTS
Figure 24 shows mice receiving BRAF'"E-DCI+PLX mithinations, either initiated concurrently or after BRAP"tx/13-DC I induction, demonstrated dramatically delayed tumor growth (P<0.001) and iMpiOVed median survival (86d and 73.5d, respectively) vs .BRAF'-DC1 (42d), PLX (43.5d), ovalbumin-DC I (28d)õ or untreated (24d) cohorts (P<0.00I); 35% were rendered disease-free following BRAF'b-DCI+PLX therapy, and remained immune to BRAFv6'a tumor rechallenge. BRAFv6"*-DCI+PLX, compared with individual, treatments induced synergistically improved systemic CDS' T-cell recognition of BRAFv6("-pulsed antigen-presenting cells and BRAFv uE tumor cells (p<0.001) measured by IFN-y release in vitro. In TME., 13RAF-DC1+FLX generated higher mRNA levels of Thl (IFN-T/TNF-a) and T-cell homing (CXCL9/CCL5) cytokines, while attenuating PD-L1 expression; CD8' TIL
trafficking was augmented by BRAFv'/".-DC1+PLX.
In conclusion BRAFvml"-DC1 vaccines overcome vernurafenib resistance in BRAFN.'")E melanoma, and synergistically improve immune and clinical responses. Such combinations will find use by those of skill in the art.

The disclosures of each and every patent, patent application, and publication cited herein are hereby incorporated herein by reference in their entirety.
While these embodiments has been disclosed with reference to specific embodiments, it is apparent that other embodiments and variations of these embodiments may be devised by others skilled in the art without departing from the true spirit and scope of the embodiments. The appended claims are intended to be construed to include all such embodiments and equivalent variations.

Claims (65)

What is claimed is.

1 A method of generating an injectable multi-dose antigen pulsed dendritic cell vaccine, comprising:
contacting at least one antigen to a dendritic cell (DC), activating said DC with at least one TLR agonist;
cryopreserving said DC in multiple doses wherein the multiple doses comprise an initial immunizing dose and multiple booster doses, wherein when said DC is thawed, and said DC produces an effective amount of at least one cytokine to generate a T cell response.

2. The method of claim 1, further comprising thawing said DC, wherein said DC
produces an effective amount of at least one cytokine to generate a T cell response

3 The method of claim 1, wherein said antigen is a tumor antigen

4 The method of claim 1, wherein said antigen is a viral antigen

The method of claim 1, wherein said TLR agonist is LPS.

6. The method of claim 1, comprising activating said DC with IFN-.gamma..

7. The method of claim 1, wherein said cryopreserving comprises freezing said DC
in a freezing medium comprising about 55% plasmalyte, about 40% human serum albumin, and about 5% DMSO

8. The method of claim 7, wherein said cryopreserving comprises freezing said DC
at a temperature of about -70°C or lower.

9. The method of claim 1, wherein the recovery and viability of the DC
after thawing is greater than or equal to about 70%.

10. The method of claim 1, wherein the recovery and viability of the DC
after thawing is greater than or equal to about 80%

11. The method of claim 1, wherein said DC are cryopreserved for at least about one week

12. The method of claim 1, wherein said cytokine is IL-12

13 The method of claim 1, wherein said DC exhibits a killer function whereby said DC are capable of lysing targeted cells.

14. A cryopreserved injectable multi-dose antigen pulsed dendritic cell vaccine for eliciting an immune response in a mammal, wherein the injectable multi-dose antigen pulsed dendritic cell vaccine comprises:
a DC loaded with at least one antigen;
wherein said DC has been activated by exposure to at least one TLR agonist;
and wherein said DC produces an effective amount of at least one cytokine to generate a T cell response

15. The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein said antigen is a tumor antigen.

16 The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein said antigen is a viral antigen

17. The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein said TLR agonist is LPS.

18. The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein said DC has been activated by exposure to IFN-.gamma..

19. The injectable multi-dose antigen pulsed dendritic cell vaccine claim 14, wherein said vaccine has been cryopreserved at a temperature of about -70°C or lower in a freezing medium comprising about 55% plasmalyte, about 40% human serum albumin, and 5% DMSO

20. The injectable multi-dose antigen pulsed dendritic cell vaccine claim 14, wherein the recovery and viability of the DC after thawing is greater than or equal to about 70%

21. The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein the recovery and viability of the DC after thawing is greater than or equal to about 80%.

22 The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein the composition is cryopreserved for at least about one week.

23. The injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14, wherein said cytokine is IL-12

24. A method of eliciting an immune response in a mammal, comprising administering a dose of said cryopreserved injectable multi-dose antigen pulsed dendritic cell vaccine of claim 14 to a mammal in need thereof.

25 A method for treating a subject having, or at risk of developing, a cancer, comprising administering to a subject in need of such treatment a dendritic cell vaccine and an inhibitor of HER-2 in an effective amount to treat the cancer or to reduce the risk of developing the cancer

26 The method of claim 25, further comprising administering a chemokine modulator to said subject

27. The method of claim 26, wherein said chemokine modulator is a TLR
agonist

28. The method of claim 26, wherein said chemokine modulator is a TLR8 agonist

29 The method of claim 25, further comprising administering a cancer medicament in an effective amount to treat said cancer or to reduce the risk of developing said cancer.

30. The method of claim 29, wherein said cancer medicament is selected from the group consisting of surgery, an anti-cancer agent, a chemotherapeutic agent, an immunotherapeutic agent, and a hormone therapy.

31. The method of claim 25, wherein said cancer is selected from the group consisting of breast cancer, ovarian cancer, lung cancer, prostate cancer, colon cancer, melanoma, pancreatic cancer, gastrointestinal cancer, brain cancer, and any combination thereof.

32. The method of claim 25, wherein said dendritic cell vaccine comprises an activated dendritic cell that has been contacted with at least one antigen and at least one TLR agonist.

33 The method of claim 25, wherein said dendritic cell vaccine comprises an activated dendritic cell that has been contacted with an agent that elevates the intracellular calcium concentration in said dendritic cell and an activating agent

34. The method of claim 33, wherein said agent elevates the intracellular calcium level by blocking the export of calcium out of the cytoplasm.

35. The method of claim 34, wherein said agent comprises a calcium ionophore

36. The method of claim 35, wherein said calcium ionophore is selected from the group consisting of A23187 and ionomycin

37. The method of claim 25, wherein said dendritic cell vaccine is in the form of an injectable multi-dose antigen pulsed dendritic cell vaccine

38. A method of improving the migration and activity of immune cells in a tumor site of a subject, comprising administering to said subject a dendritic cell vaccine and an inhibitor of HER-2 in an effective amount to change the immune response in said tumor so that the immune cells in the tumor site are more effective in attacking tumor cells

39. The method of claim 38, further comprising administering a chemokine modulator to said subject

40. The method of claim 39, wherein said chemokine modulator is a TLR
agonist

41. The method of claim 40, wherein said chemokine modulator is a TLR8 agonist

42. The method of claim 38, further comprising administering to said subject a cancer medicament in an effective amount to treat said cancer or to reduce the risk of developing said cancer.

43 The method of claim 42, wherein said cancer medicament is selected from the group consisting of surgery, an anti-cancer agent, a chemotherapeutic agent, an immunotherapeutic agent, and a hormone therapy

44. The method of claim 42, wherein said cancer is selected from the group consisting of breast cancer, ovarian cancer, lung cancer, prostate cancer, colon cancer, melanoma, pancreatic cancer, gastrointestinal cancer, brain cancer, and any combination thereof

45. The method of claim 38, wherein said dendritic cell vaccine comprises an activated dendritic cell that has been contacted with at least one antigen and at least one TLR agonist.

46. The method of claim 38, wherein said dendritic cell vaccine comprises an activated dendritic cell that has been contacted with an agent that elevates the intracellular calcium concentration in said dendritic cell and an activating agent

47. The method of claim 46, wherein the agent elevates the intracellular calcium level by blocking the export of calcium out of the cytoplasm.

48. The method of claim 47, wherein said agent comprises a calcium ionophore

49. The method of claim 48, wherein said calcium ionophore is selected from the group consisting of A23187 and ionomycin

50. The method of claim 38, wherein said dendritic cell vaccine is in the form of an injectable multi-dose antigen pulsed dendritic cell vaccine

51. The method of claim 38, wherein said dendritic cell vaccine and the inhibitor of HER-2 is administered to said tumor site

52. The method of claim 39, wherein said dendritic cell vaccine, said inhibitor of HER-2, and said chemokine modulator is administered to said tumor site

53. A method for treating a subject having, or at risk of developing, a cancer, comprising inhibiting one of more of HER-2 and HER-3 in said subject thereby causing tumor senescence in HER-2 expressing breast cancers

54. The method of claim 53, wherein inhibiting one or more of HER-2 and HER-comprises administering an inhibitor to said subject, wherein said inhibitor is an inhibitor of both HER-2 and HER-3 or a combination of a HER-2 inhibitor and a HIER-3 inhibitor

55. The method of claim 54, wherein said inhibitor is selected from the group consisting of a small interfering RNA (siRNA), a microRNA, an antisense nucleic acid, a ribozyme, an expression vector encoding a transdominant negative mutant, an antibody, a peptide, a chemical compound and a small molecule

56 The method of claim 53, further comprising administering a dendritic cell vaccine to said subject

57. The method of claim 53, further comprising administering TNF-.alpha., and INF-.gamma. to said subject

58. The method of claim 56, further comprising administering TNF-.alpha.
and INF-.gamma. to said subject.

59. A neoadjuvant treatment for a subject having estrogen receptor-positive/HER2-positive ductal carcinoma in situ breast cancer ("ER pos/HER2pos DCIS") comprising, administering at least one dose of an antigen-pulsed DC1 vaccine derived from said subject's monocytic dendritic cell (DC) precursors which are pulsed with six HER2-derived MHC class II binding peptides and said HER2-pulsed DC precursors are matured to type-1 dendritic cells (DC1s) in combination with anti-estrogen therapy

60. The treatment of claim 59, wherein said six HER2-derived MHC class II
binding peptides comprise peptide 42-56. HLDMLRHLYQGCQVV (SEQ ID NO: 1), peptide 98-114. RLRIVRGTQLFEDNYAL (SEQ ID NO 2), peptide 328-345:
TQRCEKCSKPCARVCYGL (SEQ ID NO 3), peptide 776-790: GVGSPYVSRLLGICL
(SEQ ID NO 4); peptide 927-941 PAREIPDLLEKGERL (SEQ ID NO 5), and peptide 1166-1180: TLERPKTLSPGKNGV (SEQ ID NO: 6).

61 The treatment of claim 59 wherein said anti-estrogen therapy comprises administration of an anti-estrogen agent selected from the group consisting of tamoxifen, letrozole, anastrozole, exemestane, raloxifene, and any combination thereof

62. The treatment of claim 59, wherein if said patient is HLA-A2 positive the monocytic DC precursors of said patient are pulsed with MHC class I binding peptides comprising peptide 369-377:KIFGSLAFL (SEQ ID NO.7), and peptide 689-697RLLQETELV (SEQ ID NO 8)

63 The treatment of claim 59, wherein systemic anti-HER2 CD4+ T-cell responses are generated pre- and post-vaccination from said subject's peripheral blood mononuclear cells (PBMC) pulsed with said six HER2-derived MHC class II
binding peptides which are then plated and treated to reveal spot formation of spot forming cells (SFCs) and to cause IFN-.gamma. production which is measured

64. The treatment of claim 62, wherein systemic anti-HER2 CD8+ T-cell responses are generated pre- and post-vaccination from said subject's peripheral blood mononuclear cells (PBMC) pulsed with HER2-derived MHC class II binding peptide 367-377 which are then plated and treated to reveal spot formation of spot forming cells (SFCs) and IFN-.gamma. production which is subsequently measured

65. The treatment of claim 59, wherein anti-HER2 CD4+ T-cell local regional immune response is measured in the sentinel lymph nodes of said subject post-vaccination.