Langerhans-type and monocyte-derived human dendritic cells have different susceptibilities to mRNA electroporation with distinct effects on maturation and activation: implications for immunogenicity in dendritic cell-based immunotherapy

mRNA electroporation of dendritic cells (DCs) facilitates processing and presentation of multiple peptides derived from whole antigen, tailored to different HLA molecules. Clinical responses to electroporated moDC vaccines, however, have been suboptimal. Human Langerhans-type DCs (LCs) are the most potent conventional DC subtype for inducing CD8+ cytotoxic T lymphocytes (CTLs) in vitro. We recently demonstrated that Wilms’ tumor 1 (WT1) mRNA-electroporated LCs are superior to moDCs as stimulators of tumor antigen-specific CD8+ CTLs, even though they are comparable stimulators of allogeneic T cell proliferative responses. A detailed comparative evaluation of the effects of mRNA electroporation on LCs versus moDCs, however, is needed. Immature and partially-matured human moDCs and LCs electroporated with mRNA were compared for transfection efficiency, phenotypic changes, viability, retention of transgene expression after cryopreservation, and immunogenicity. Student t test was used for each pairwise comparison. One-way analysis of variance was used for multiple group comparisons. Transfection efficiency after electroporation with enhanced green fluorescent protein (eGFP) mRNA was higher for immature than for partially-matured moDCs. In contrast, transfection efficiency was higher for partially-matured than for immature LCs, with the additional benefit that electroporation itself increased maturation and activation of CD83+HLA-DRbright LCs but not moDCs. Electroporation did not impair final maturation and activation of either DC subtype, after which both mRNA-electroporated LCs and moDCs were functionally similar in stimulating allogeneic T cell proliferation, a standard assay of DC immunogenicity. These findings support mRNA electroporation of DCs, and in particular LCs, as an effective non-viral method to stimulate specific, potent CD8+ CTL responses. The differences between LCs and moDCs regarding this form of antigen-loading have important implications for DC-based immunotherapies.


Introduction
Effective therapeutic cancer vaccination requires the optimization of tumor antigen presentation by antigenpresenting cells (APCs) to induce strong antigen-specific T cell responses, especially CD8 + cytolytic T lymphocytes (CTLs) with a sufficiently broad repertoire and immunologic memory [1]. Human conventional dendritic cells (DCs) are the most potent APCs and are critical to the onset of immunity. DCs prime T cell responses by coupling antigen to all the requisite co-stimulatory, cytokine, and chemokine signals required for the activation of naive and resting T cells [2]. Numerous studies have demonstrated the feasibility of DC-based immunization to induce host responses against tumors [3].
Electroporation of DCs with mRNA encoding specific tumor-associated antigens is an effective non-viral method to stimulate T cell responses in vitro and in vivo [4][5][6][7][8][9][10][11]. This method of antigen loading, which facilitates processing and presentation of multiple class I and II MHC-restricted epitopes from the translated protein [12], is more efficient than peptide pulsing and less problematic than retroviral transgenes, which carry the risk of genome integration [13]. mRNA electroporation also allows individuals of any HLA type to process and present peptides tailored to their own MHC molecules.
Human Langerhans-type DCs (LCs) derived from CD34 + hematopoietic progenitor cells are the most potent conventional DC subtype for stimulating CD8 + CTLs in vitro [14][15][16][17]. We recently showed that WT1 mRNA-electroporated LCs are superior to moDCs as stimulators of antigen-specific CTLs in vitro, using an IL15R-α/IL15/pSTAT5-dependent mechanism [16]. LCs synthesize abundant IL15 mRNA and protein, whereas moDCs are dependent on exogenous IL15 for stimulating comparably potent WT1-specific CTLs [16]. The effects of mRNA electroporation on moDCs have been described [18]. A detailed comparative evaluation of the effects of mRNA electroporation on LCs versus moDCs is still needed, however.
In this study, we compared moDCs and LCs after mRNA electroporation for transfection efficiency, phenotypic changes, viability, retention of transgene expression after cryopreservation, and allo-stimulatory capacity. Our findings clearly demonstrate that the maturation state of moDCs and LCs differentially affects their susceptibility to electroporation, and electroporation itself has a useful maturational effect on LCs but not moDCs. These findings underscore the importance of tailoring electroporation conditions to specific DC subtypes when designing DC-based immunotherapies.

Blood samples
Peripheral blood mononuclear cells (PBMC) or granulocyte colony stimulating factor (G-CSF)-elicited CD34 + hematopoietic progenitor cells (HPC) were obtained from healthy volunteers or allogeneic hematopoietic stem cell transplant donors. Buffy coats purchased from the Greater New York Blood Center, American Red Cross, were also used as a source of cells from healthy donors. Biospecimen sample collection and use adhered to protocols approved by the Institutional Review and Privacy Board of Memorial Hospital, Memorial Sloan-Kettering Cancer Center (MSKCC).

Generation of moDCs and LCs with recombinant human cytokines
MoDCs were generated from PBMCs, and LCs were generated from G-CSF-elicited CD34 + HPCs. Media, media supplements, and cytokines were exactly as published [14]. In brief, for immature moDC generation, tissue culture plastic adherent CD14 + monocytes were cultured in complete RPMI-1% normal human serum (NHS) with GM-CSF and IL-4 for 5 to 6 days. For immature LC generation, CD34 + HPCs were cultured in serum-free X-VIVO 15, supplemented with GM-CSF, TGF-β, and TNF-α, to which c-kit-ligand and FLT-3-ligand were added for only the first 5 to 6 days of a 10-to 12-day culture. Terminal maturation of moDCs and LCs was induced with a combination of TNF-α, IL-1β, IL-6, and prostaglandin E 2 .
T lymphocytes T cells were obtained from tissue culture plasticnonadherent PBMCs, further purified by nonadherence and elution from nylon wool columns (Polysciences). This achieved >95% purity without bystander activation of T cells.

Production of in vitro-transcribed mRNA
For eGFP mRNA transcription, the pGEM4Z/eGFP/A64 plasmid was linearized with SpeI (New England Biolabs) before mRNA transcription in vitro, which was performed with T7 RNA polymerase (mMessage mMachine T7 kit; Ambion). For WT1 mRNA transcription, the pGEM-4Z/WT1 plasmid was linearized with HindIII (New England Biolabs) before mRNA transcription in vitro, which was performed with SP6 RNA polymerase (mMessage mMachine SP6 kit; Ambion). For both eGFP and WT1 mRNA, agarose gel electrophoresis confirmed production of full-length capped mRNA, and spectrophotometry measured mRNA concentration.

Electroporation of cells
Immature moDCs were electroporated on day 5-6 and immature LCs on day 10-11. Partially-matured moDCs were electroporated on day 7-8 and partially-matured LCs on day 12-13, reflecting the different times required to generate these two DC subtypes in vitro [14,15]. After harvesting, cells were washed twice and resuspended in OptiMEM (Gibco, Invitrogen) at 15×10 6 cells/ml. 200 μL of cell suspension were then mixed with 20-40 μg mRNA and electroporated in a 2 mm gap cuvette at 650-900 V for 1-3 pulses at 0.5 msec/pulse, using a BTX ECM 830 square-wave electroporator (BTX Harvard). After electroporation, cells were immediately transferred to culture to minimize cell death. While in culture, immature cells were partially or terminally matured by exposure to inflammatory cytokines for 24 or 48 hours, respectively.

Statistics
Student t test was used for each pairwise comparison. One-way analysis of variance was used for multiple group comparisons. A P value less than .05 was considered statistically significant.

Results
The transfection efficiency of mRNA electroporation varies with the maturation status of moDCs and LCs Immature and 24-hour, partially-matured moDCs and LCs were electroporated with eGFP mRNA. After electroporation, cells were immediately returned to culture for at least 24 hours of maturation before being assessed for eGFP expression as an index of transfection efficiency. As shown in Figure 1A, transfection efficiency was higher for immature than for partially-matured moDCs (peak value at 24 hours: 77.9 ± 12.4% for immature cells and 59.4 ± 15.4% for partially-matured cells). In contrast, transfection efficiency was higher for partially-matured than for immature LCs ( Figure 1B; peak value at 48 hours: 67 ± 6.9% for partially-matured cells and 55.2 ± 2.9% for immature cells). Thus, both the type and maturation status of DCs influence mRNA transfection efficiency.
Optimal electroporation parameters for immature moDCs and partially-matured LCs were determined by varying set voltage, number of electroporation pulses, and amount of mRNA to maximize transfection efficiency while minimizing cell loss. For immature moDCs, best results were achieved with 700 V, 1 pulse, and 40 μg mRNA. For partially-matured LCs, best results were achieved with 700 V, 2 pulses, and 30 μg mRNA. Results are summarized in Figure 2.

Cell loss and viability of moDCs and LCs after electroporation and cryopreservation
Electroporation of cells can induce cell death due to the deleterious effects of direct electrical current and disruption of the cell membrane. Electroporation of immature and partially-matured moDCs and LCs resulted in up to approximately 40% initial cell death, as determined by trypan blue exclusion on direct hemacytometer counts ( Figure 4A). After electroporation, DCs were returned to culture for 24 hours, and cell viability was reassessed. Immature and mature moDCs and LCs demonstrated >85% viability ( Figure 4B; 94.2 ± 3.0% for immature moDCs and 88.7 ± 6.3% for immature LCs; 87.1 ± 7.1% for partiallymatured moDCs and 92.9 ± 3.8% for partially-matured LCs).
MoDCs and LCs electroporated with mRNA retain transgene expression after cryopreservation Immature and mature moDCs and LCs were electroporated with eGFP mRNA, and post-electroporation eGFP expression was determined by flow cytometry. Cells were then cryopreserved, and post-thaw eGFP expression was compared with expression prior to cryopreservation. Retention of protein expression was similar between immature and mature moDCs and LCs ( Figure 5).

mRNA-electroporated moDCs and LCs remain potent stimulators of allogeneic T cells in mixed leukocyte reactions
Having shown that mRNA-electroporated moDCs and LCs possess the ability to respond normally to inflammatory cytokines by upregulating phenotypic markers of maturation and activation, we further assessed their functional capacity to stimulate resting allogeneic T cell proliferation. While distinct DC subtypes have different capacities to stimulate CD8 + CTLs [14,15], their comparable stimulation of bulk allogeneic T cell proliferation in MLRs remains a standard assay of overall DC immunogenicity [14]. MoDCs and LCs were therefore electroporated with eGFP or WT1 mRNA, or were mock electroporated with no mRNA and then matured with inflammatory cytokines for 24 hours. The resulting mature moDCs ( Figure 6A Figure 6A). DCs also retained their allo-stimulatory capacity after cryopreservation and thawing, as measured by a colorimetric proliferation assay ( Figure 6B). Thus, both moDCs and LCs remain functionally potent stimulators of allogeneic T cell proliferation, unaffected by prior mRNA electroporation or cryopreservation and despite their differences in CTL stimulation.  for stimulating allogeneic T cell proliferation in MLRs, despite their inherent differences in capacity for CD8 + CTL stimulation [14][15][16][17].

Discussion
For moDCs, our observation of greater transfection efficiency of immature cells than for mature cells differs from another study in which the transfection efficiency of immature and mature moDCs was roughly equivalent [18]. Various electroporation conditions with disparate degrees of transfection efficiency, however, have been reported for moDCs [8,[19][20][21]. These discrepancies underscore the importance of revalidating electroporation parameters for any differences in electroporation machine, voltage, number of pulses, cell concentration, or amount of mRNA, as depicted in Figure 2.
Peak transfection efficiency is lower for LCs than for moDCs. Likely contributing to this difference is that moDCs are derived from a more differentiated and committed starting population than are LCs, resulting in greater cell population purity. Thus the difference in absolute transfection values would have favored moDCs, as the LCs would have had other contaminating, non-LCs competing for mRNA uptake during electroporation. Purification of LCs by HLA-DR selection on magnetic beads is one potential solution to increase transfection efficiency, but this should not be necessary to the extent that one can quantify the proportion of electroporated LCs by flow cytometry in the final antigen-presenting cell population.
Consistent with previous studies [22][23][24], the immediate post-electroporation viability of mRNA-electroporated DCs is less than the initial starting population. Subsequent survival of viable cells is minimally affected, however. Cryopreservation can further decrease cell recovery, so an appropriate excess of electroporated DCs should be aliquoted for cryopreservation. This will ensure sufficient DC yields, irrespective of moDC or LC subtype, from thawed aliquots for vaccination.
We previously reported the results of a clinical trial in AJCC stage III/IV melanoma patients, comparing vaccination with peptide-loaded LCs versus peptide-loaded moDCs [12]. The rationale for this trial was based on our established findings in vitro that human LCs are consistently superior to moDCs on a cell-for-cell basis in eliciting MHC-restricted, antigen-specific CTLs [14,16], which has been corroborated by other investigators [15,17]. A clinical trial conducted by Banchereau and colleagues for similarly advanced-stage melanoma patients using bulk CD34 + HPC-derived DCs, which included LCs, pulsed with a mixture of melanoma-derived peptides, resulted in durable immune responses associated with long-term survival [25]. Although patients treated on the LC arm of our trial generated significantly greater reactivity against tyrosinase than those treated with moDCs, significant differences were not observed for gp100 or the control fluMP antigen [12]. This begged the obvious question as to whether loading class I MHC-restricted single peptides onto any defined DC subtype would ever be sufficient to stimulate durable immunity against tumor antigens.
Our group has since discovered that LCs from healthy volunteers, electroporated with Wilms' tumor 1 (WT1) mRNA, promote sustained presentation of antigenic peptides, which in conjunction with IL15R-α/IL15, induce robust autologous, WT1-specific CTLs [16]. The CTLs develop after just 7 days' stimulation without exogenous cytokine supplementation and lyse MHCrestricted targets, including primary WT1-expressing blasts from leukemia patients. MoDCs, in contrast, require exogenous IL15 to promote immune responses comparable to LCs. Thus LCs provide a more favorable cytokine milieu for the activation of T cells than do moDCs, thereby explaining their superior induction of antigen-specific CTLs in the absence of exogenous cytokines. These data support the use of mRNA-electroporated LCs, or IL15-supplemented moDCs, as cancer vaccines to overcome tolerance against self-differentiation tumor antigens. The pivotal role of IL15 in LCmediated stimulation of CTLs has also been confirmed using individual peptides rather than mRNA encoding full-length protein [17,25].
Given the importance of LCs and their provision of IL15, as well as the possible application of IL15supplemented moDCs in DC-based vaccines, we thought it essential to ascertain the optimal conditions for their respective electroporation with mRNA to express fulllength protein. Such expression enables cells to process and present antigenic peptides tailored to their own MHCs, allowing clinical investigators to move beyond single defined peptides for a given tumor, if they are even known, and circumvent the limitations of specific HLA types in patients. There may be additional, as yet undiscovered reasons for LCs' potency over moDCs, which may nonetheless prove sufficiently compelling to favor LCs in vaccine trials. MoDCs offer the potential benefit of activating NK cells via IL12p70 [26]. LCs do not secrete IL12p70 but maintain NK cell viability via IL15 [14,26]. It will be important to determine whether moDCs supplemented with IL15 are an adequate substitute for LCs, or whether the two DC subtypes should be used in combination to capitalize on the efficacy of moDCs in activating NK cells and the potency of LCs in inducing CD8 + CTLs.

Conclusions
Enhanced antigen presentation by DCs can be achieved with mRNA electroporation but requires modifying conditions to the specific DC subtype. Our findings with LCs and moDCs provide key parameters on the optimal timing of mRNA electroporation, effects on cell maturation, and anticipated cell losses and yields. Investigators should now have the tools in hand to address key questions about DC-based cancer immunotherapy in vivo in humans, with reasonable maintenance of LC or moDC viability and preservation of the activated phenotype and baseline immunostimulatory capacity.

Competing interests
The authors have no competing interests to declare.
Authors' contributions DJC designed and performed experiments, analyzed and interpreted data, and wrote the manuscript. ER designed and performed experiments, analyzed and interpreted data, and made comments on the manuscript. ER and MM designed the WT1-encoding plasmid. KBP, JAS, and ETSA performed experiments. JWY designed the overall study, supervised performance of experiments, analyzed and interpreted data, and wrote the manuscript. All authors read and approved the final manuscript.