Received Date: January 30, 2016; Accepted Date: February 16, 2016; Published Date:February 18, 2016
Citation: Shimodaira S, Koya T, Higuchi Y, Okamoto M, Koido S (2016) Quality Verification of Dendritic Cell-Based Cancer Vaccine. Pharm Anal Acta 7:465.doi: 10.4172/2153-2435.1000465
Copyright: © 2016 Shimodaira S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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In the era of personalized cancer therapy, immunotherapy is now emerging as a potential option. Therapeutic cancer vaccination has been developed for the induction of an efficient immune response targeting tumor-associated antigens. The efficacy of dendritic cell (DC)-based vaccines is attributed to their ability to induce immunity against cancers. Criteria for the approval of therapeutically active DCs, such as their viability and purity, are here verified based on phenotypic characteristics, linked to their antigen-presenting ability and functional analyses of phagocytosis and pinocytosis. A standardized phenotype of DCs harboring bioactive functions would be useful to provide personalized vaccines for cancer immunotherapy.
Dendritic cells, Cancer vaccination; Cytotoxic T cells; Phenotype; Antigen presentation; Phagocytosis; Pinocytosis
DCs: Dendritic Cells; GM-CSF: Granulocyte– Macrophage Colony-Stimulating Factor; IL: Interleukin; MDCs: Mature DCs; DCs: Immature; HLA: Human Leukocyte Antigen; WT1: Wilms’ Tumor 1; CTLs: Cytotoxic T Cells; OK-432: Streptococcal Preparation; FITC: Fluorescein Isothiocyanate; PE: Phycoerythrin; MART-1: Melanoma Antigen Recognized by T Cells 1; PBLs: Peripheral Blood Lymphocytes; FCS: Fetal Calf Serum; MFIs: Mean Fluorescence Intensities
Immunotherapy is now emerging as a potential option for personalized cancer therapy. Because of their specific bioactivity against tumor-associated antigens, vaccines using dendritic cells (DCs) may offer survival benefits in some patients with cancer by extending the number of quality-adjusted life years . DCs with potential bioactivity used in active cancer immunotherapies [2-4] have been conventionally generated using peripheral monocytes with granulocyte–macrophage colony stimulating factor (GM-CSF) and interleukin (IL)-4 [5,6].
Mature dendritic cells (mDCs) express cell surface molecules necessary for antigen presentation. CD83, CD86, and human leukocyte antigen (HLA)-DR were found to stimulate T cells in vitro in almost all mDCs . The expression of CD197 (C-C chemokine receptor type 7) was also shown to increase with maturation and induced chemotaxis associated with macrophage inflammatory protein 3β . It was also found that immature DCs (imDCs) have an endocytic pathway, such as antigen uptake through the mannose receptor and pinocytosis, which decreased after DC maturation .
DC vaccines primed with HLA class I/II-restricted Wilms’ tumor 1 (WT1) peptides have been identified as a feasible option for patients with advanced cancers [9,10]. Immune response monitoring using tetramer analysis and/or enzyme-linked immunosorbent spot assay has been applied to determine the efficacy of DC vaccines targeting WT1 [10,11]. Because the standardized detection of cancer-associated antigens would also be useful for personalized cancer immunotherapy , clinical efficacy is also confirmed based on good targets in tumors for cancer vaccines that are effectively recognized by antigen-specific cytotoxic T cells (CTLs) . These DC vaccines are required to meet the following criteria: purity defined as > 90% CD11c+ CD14− CD86+ HLA-DR+ cells, > 80% viability, mature DC phenotype, negative for bacterial and fungal infection after 14 days, presence of endotoxin ≤ 0.05 EU/ml, and negative for mycoplasma . In this article, we present our commentary on the findings obtained thus far and our insights regarding DC vaccines and vaccinations.
A conventional IL-4-DC vaccine
mDCs were generated under Good Gene, Cell & Tissue Manufacturing Practice conditions according to “The Act on the Safety of Regenerative Medicine” introduced in Japan on November 25, 2014 . imDCs were generated by culturing adherent cells in AIM-V medium (Gibco, Gaithersburg, MD, USA) containing GMCSF (50 ng/ml; GENTAUR Belgium BVBA, Brussels, Belgium) and IL-4 (50 ng/ml; R&D Systems Inc., Minneapolis, MN, USA) for 5 days using mononuclear cell-rich fractions isolated through apheresis, as previously described . mDCs were differentiated from imDCs by stimulation with OK-432 (10 μg/ml streptococcal preparation; Chugai Pharmaceutical Co., Ltd., Tokyo, Japan) and prostaglandin E2 (50 ng/ ml; Daiichi Fine Chemical Co., Ltd., Toyama, Japan) for 24 h. mDC products were cryopreserved at −152°C or in the gas layer of a liquid nitrogen tank until the day of administration.
Phenotype of imDCs and mDCs
The phenotype of mDCs was defined as CD11c+, CD14−, HLADR+, HLA-ABC+, CD80+, CD83+, CD86+, CD40+, and CD197+, as determined using flow cytometry . DCs were stained using monoclonal antibodies conjugated with FITC or PE, such as CD14, CD40, CD83 (eBioscience, Inc., San Diego, CA, USA), HLA-ABC, CD80, CD86, CD11c (BD Biosciences, San Jose, CA, USA), and CD197 (R&D Systems Inc.), for 30 min at 4°C. CD3 and CD19 (BD Biosciences) were used for the detection of lymphocytes to evaluate DC purity. The expression of each surface marker on DCs was analyzed in the viable cells by excluding dead cells by processing with propidium iodide (2 μg/ml; Sigma–Aldrich Co. LLC., Tokyo, Japan). The phenotype was determined using flow cytometry (BD FACSCanto™ II; BD Biosciences).
Functional analysis of DCs
The antigen-presenting ability of both imDCs and mDCs in patients with HLA-A *02:01 was studied using MART-1 [16-18]. In short, DCs were pulsed with 20 μg/ml melanoma antigen recognized by T cells 1 (MART-1)26–35 A27L (ELAGIGILTV) peptide at 37°C for 1 h, followed by processing with mitomycin C (MMC, 25 μg/ml; Kyowa Hakko Kogyo Co., Ltd., Tokyo, Japan) for 1 h. Peripheral blood lymphocytes (PBLs) as a responder were mixed with 1 × 106 of DCs as a stimulator at a ratio of 10:1, which were cultured in AIM-V medium containing IL-2 (Immunace, 2.5 U/ml; Shionogi Pharmaceutical Co., Ltd., Osaka, Japan), IL-7 (5 ng/ml; R&D Systems), and IL-15 (10 ng/ ml; PeproTech, Rocky Hill, NJ, USA) for 3–5 days. Depending on the increase in PBLs, mixed cells were supplemented in AIM-V medium with 10% fetal calf serum (FCS), and additionally cultured for 2–3 days. Harvested cells were stained using CD8-FITC (Beckman Coulter, Inc., Brea, CA, USA), CD3-APC (eBioscience, Inc.), and T-select HLA-A *02:01 MART-1 tetramer-ELAGIGILTV-PE (MBL; Medical & Biological Laboratories Co., Ltd., Nagoya, Japan) to detect MART-1- specific CTLs. A negative control was applied as PBLs cultured without mixing with DCs.
The ability of DCs to perform phagocytosis and pinocytosis was evaluated in accordance with previous reports [19-21]. Both imDCs and mDCs were incubated with 10 μg/ml DQ-ovalbumin (Molecular Probes, Thermo Fisher Scientific K.K., Yokohama, Japan) for the evaluation of phagocytosis in AIM-V with 10% FCS (Thermo Fisher Scientific K.K.) at 37°C for 30 min. DCs incubated at 4°C were used as a negative control. The type of DC was determined using flow cytometry (BD FACSCanto™ II).
A total of 1 × 106 cells/ml of imDCs and mDCs were incubated with 250 μg/ml FITC-conjugated dextran (molecular weight, 40,000 Molecular Probes, Thermo Fisher Scientific K.K.) in AIM-V containing 10% FCS (Thermo Fisher Scientific K.K.) at 37°C for 3 h to clarify pinocytosis using flow cytometer (BD FACSCanto II). DCs reacted at 4°C were also analyzed as a negative control.
Wilcoxon signed rank test was applied to assess the differences between imDCs and mDCs. Univariate analysis of variance using the Dunnett’s test was applied for multiple comparisons between PBLs cultured with imDCs or mDCs. A p value of <0.05 was set to indicate statistical significance using IBM SPSS Advanced Statistics ver. 23.0 (IBM Japan, Tokyo, Japan).
Phenotype of imDCs and mDCs
Manufactured DCs primed with OK-432 were compatible with the mDC phenotype, expressing HLA- ABC+ DR+ CD40+ CD80+ CD86+ CD197+ as shown in Figure 1. mDCs were revealed to be more prominently consisting of a CD11c+/CD14–HLA-class I+/II+ population compared with imDCs. HLA-related molecules, such as CD80, CD83, and CD86, as well as CD40 and CD197, were expressed at higher levels in mDCs than in imDCs.
Figure 1: Phenotype analysis of immature DCs (imDCs) and mature dendritic cells (mDCs). The phenotype panels from patients with pancreatic cancer indicate HLA-ABC+DR+CD40+CD80+CD86+CD197+, which should meet the criteria. Upper panels are for imDCs and lower ones for mDCs. The numbers in quadrants indicate the percentage of the panels.
Functional analysis of DCs
The numerical value in the panel shows the ratio of induced MART- 1-specific CTLs (Figure 2A). Antigen-presenting ability was detected for both imDCs and mDCs, but it was confirmed that this ability was increased in mDCs, concomitant with their mature phenotype of HLAABC, HLA-DR, CD80, CD83, and CD86. The estimated marginal means (N = 5) were 0.50, 1.22, and 4.32 in PBLs cultured without DCs, with imDCs, and mDCs, respectively. The mean different was significant between PBLs with mDCs and PBLs without DCs (p = 0.001), and PBLs with imDCs (p = 0.006), as shown in Figure 2B.
The ability of DCs to perform phagocytosis and pinocytosis was evaluated as shown in the left and right panels of Figure 2C, respectively. A solid line (blue, imDC; red, mDC) indicates the reaction at 37°C, and a dashed line indicates a negative control in Figure 2C. The median mean fluorescence intensities (MFIs) using DQ-ovalbumin to evaluate phagocytosis (N = 9) were 1,882 and 1,436 in imDCs and mDCs, respectively, as shown in Table 1. The median MFIs using FITC-dextran to evaluate pinocytosis (N = 9) were 462 and 239 in imDCs and mDCs, respectively. The manufactured mDCs shifted to lower intensities of phagocytosis (24% reduction in the median, p = 0.015) and pinocytosis (48% reduction in the median, p = 0.038) than the imDCs (Table 1).
Despite recent advances in encouraging clinical results, a lot of elements of DC-based vaccine and vaccination strategies need to be optimized for successful implication for the cancer therapy [22,23]. The use of murine models can provide direct efforts toward an effective vaccine, and contribute to the design of successful DC-based cancer immunotherapy . Anti-tumor immune response in the human setting was exploited with different DC-based vaccines to induce immune responses capable of controlling tumor growth and generating immune memory .
mDCs manufactured using GM-CSF and IL-4 primed with OK- 432 for clinical use expressed the HLA- ABC+ DR+ CD40+ CD80+ CD86+ CD197+ phenotype at a higher intensity that was sufficient for antigen presentation to detect MART-1-specific CTLs in in vitro model than imDCs, as shown in Figure 2. Authors conducted a phase I study to investigate the safety and immunogenicity using the DC vaccines targeting Wilms’ tumor 1 manufactured using GM-CSF and IL-4 primed with OK-432 for patients with pancreatic cancer  and colorectal cancer . The preclinical analyses on DC vaccines in vitro confirmed clinical efficacy to evaluate acquired cancer immunity based on immune monitoring using tetramer analyses and enzyme-linked immunosorbent spot assays.
On the other hand, mDCs shifted to lower levels of phagocytosis and pinocytosis than imDCs, as shown in Table 1. Efficacy of vaccines with mDCs for clinical use comprised activities of 76% phagocytosis and 52% pinocytosis. These profiles, other than antigen presentation, are labeled as functional tags in the preclinical and clinical development of DC-based anticancer therapeutics .
Qualification of the phenotype and functional analyses of the adapted DC vaccines would prove their efficacy for cancer immunotherapy.
Disclosure of Interests
All authors declare no conflicts of interest that could be perceived as prejudicing the impartiality of the reported research.
This study was supported by a Grant of Funding Programs: A-STEP (Adaptable and Seamless Technology Transfer Program through Target-driven R&D) from the Japan Society and Technology Agency. The authors would like to thank Enago (www.enago.jp) for the English language review.
The study was supported by a grant from the Japan Society and Technology Agency.