Heat-shock protein 70-dependent dendritic cell activation by 5-aminolevulinic acid-mediated photodynamic treatment of human glioblastoma spheroids in vitro

Background: T-cell responses contribute to the anti-tumoural effect of photodynamic therapy (PDT). For such responses to occur, dendritic cells (DCs) have to migrate to the tumour, take up tumour antigens and respond to danger signals with maturation, before they engage in T-cell activation. Here, we have studied the effect of 5-aminolevulinic acid (ALA)-mediated PDT on DCs in vitro in a human spheroid model of glioblastoma (GB). Methods: Spheroids of the GB cell lines U87 and U251 were treated with ALA/PDT, and effects on attraction, uptake of tumour antigens and maturation of DCs were studied. To block heat-shock protein-70 (HSP-70) on the spheroids, neutralising antibodies were used. Results: 5-Aminolevulinic acid /PDT-treated GB spheroids attracted DCs that acquired tumour antigens from the spheroids effectively. Moreover, co-culture with ALA/PDT-treated spheroids induced DC maturation as indicated by the upregulation of CD83 and co-stimulatory molecules as well as increased T-cell stimulatory activity of the DCs. Heat-shock protein-70 was upregulated on the spheroids after ALA/PDT treatment. Uptake of tumour antigens and DC maturation induced by the ALA/PDT-treated spheroids were inhibited when HSP-70 was blocked. Conclusion: ALA/PDT treatment of glioma spheroids promotes the three initial steps of the afferent phase of adaptive immunity, which is at least partially mediated by HSP-70.

Photodynamic therapy (PDT) is a promising approach in the treatment of various tumours (Dolmans et al, 2003). It is based on the preferential accumulation of a photosensitiser in tumour cells and its excitation with light of a defined wavelength. This excitation initiates a photochemical reaction, resulting in the generation of reactive oxygen species within the tumour cells, for example, singlet oxygen, which cause secondary reactions leading to cell death. Photodynamic therapy results either in apoptosis or necrosis of the tumour cells, depending on the photosensitiser and its intracellular localisation, the cell type, oxygen concentration and PDT dose (Castano et al, 2006).
Although PDT-induced phototoxicity kills tumour cells directly, it is well established that there is also an immunological component to the anti-tumoural effect of PDT (Dolmans et al, 2003;Castano et al, 2006). Reduced efficacy of PDT in immunodeficient mice lacking T cells (Korbelik et al, 1996;Hendrzak-Henion et al, 1999;Preise et al, 2009) indicates a pivotal role of T cells. This is further supported by adoptive transfer experiments (Korbelik and Dougherty, 1999;Preise et al, 2009) and lymphocyte-depletion studies (Hendrzak-Henion et al, 1999;Korbelik and Cecic, 1999;Korbelik and Dougherty, 1999), identifying CD8 þ cytotoxic T cells as main effectors. However, for such T-cell responses to occur, tumour antigens have first to be taken up by immature dendritic cells (DCs), danger signals have to induce DC maturation, associated with migration of DCs to local lymph nodes and mature DCs in the lymph nodes have to present the tumour antigens to the specific T cells in the context of adhesion, co-stimulatory and other accessory molecules, either directly or after antigen transfer to other DCs (Ueno et al, 2010).
Photodynamic therapy generates an altered tumour microenvironment that appears to promote this afferent phase of adaptive immunity. Tumour cells undergoing necrosis or apoptosis release tumour antigens that can be taken up by DCs (Green et al, 2009). Moreover, immediately after PDT an inflammatory response develops providing danger signals such as pro-inflammatory cytokines. Together with stress proteins like heat-shock proteins (HSP) induced on the surface or released by the tumour cells after PDT and the dead tumour cells themselves, these cytokines may promote DC maturation (Gollnick et al, 1997;Dolmans et al, 2003;Jalili et al, 2004;Korbelik et al, 2005;Castano et al, 2006). In several mouse models for extracranial tumours, attraction of DCs towards PDT-generated vaccines (Korbelik and Sun, 2006), uptake of tumour antigens by DCs (Jalili et al, 2004) and PDT-induced DC maturation (Gollnick et al, 2002;Jalili et al, 2004) have been reported. No such studies have been performed on human cells or cranial tumours.
Glioblastoma (GB) is the most frequent and aggressive malignant primary brain tumour (Fisher et al, 2007). Despite a multimodal therapeutic approach combining maximal cytoreductive surgery with fractionated radiotherapy and alkylating temozolomide chemotherapy, prognosis remains dismal: median survival of patients is 14.6 months, with a 2-year survival rate of 27.2% (Stupp et al, 2009). After 3 years, most patients have relapsed and median survival after relapse is 6.2 months (Stupp et al, 2009). As a consequence, PDT in combination with highly selective photosensitisers, for example, 5-aminolevulinic acid (ALA), is gaining clinical interest for the treatment of patients with GB (Beck et al, 2007;Eljamel et al, 2008;Stummer et al, 2008). 5-Aminolevulinic acid is an intermediate of the haem biosynthesis pathway. In many tumour cells including GB, an excess of the exogenous pro-drug ALA results in the accumulation of protoporphyrin IX, probably mainly due to low ferrochelatase activity (Krammer and Plaetzer, 2008;Teng et al, 2011). If exposed to a wave length of 400 nm, this preferential accumulation of protoporphyrin IX in tumour cells allows their intraoperative identification during fluorescence-guided surgery. In GB, the extent of resection can thereby be increased significantly, leading to improved progression-free survival of patients (Stummer et al, 2006). When exposed to 635 nm, protoporphyrin IX acts as a potent photosensitiser, which can be exploited for intraoperative as well as stereotactic PDT of GB (Beck et al, 2007;Eljamel et al, 2008;Stummer et al, 2008). In a patient with non-resectable, recurrent GB, who had failed multimodal therapy, stereotactic ALA/PDT resulted in a long-sustaining response (Stummer et al, 2008). Moreover, in a recent phase III study combining ALA-and photofrin-mediated fluorescence-guided resection and PDT, a benefit in survival and time to progression was observed (Eljamel et al, 2008). The phototoxic damage caused by ALA/PDT, however, can extend only up to a depth of 4 mm in cerebral tissue (Olzowy et al, 2002), and therefore would not reach the glioma cells in the more distant infiltration zone of the tumour. Hence, even for cranial tumours like GB, an immunological effector mechanism may be part of the action of ALA/PDT. Glioblastoma can be a target of anti-tumoural immune responses (Van Gool et al, 2009), and PDT causes inflammatory conditions at extracranial sites like those that are needed to attract DCs to the brain (Zozulya et al, 2007). Moreover, despite a lack of typical lymph drainage, DCs from the brain appear to acquire antigens there and migrate to the cervical lymph nodes to initiate CD8 þ T-cell responses, which is well documented, for example, for neuroinflammatory conditions (Karman et al, 2004a, b;Hatterer et al, 2008;Steel et al, 2009). However, little is known about such mechanisms in GB and about the influence of ALA/PDT treatment of gliomas on the afferent phase of adaptive immunity. Therefore, we have studied in a human tumour spheroid model the effects of ALA/PDT on attraction, tumour antigen uptake and maturation of DCs, and provide evidence that ALA/PDT in vitro promotes all of these activities.

Generation of GB spheroids
The human GB cell lines U87 and U251 were maintained in DMEM medium (Lonza, Verviers, Belgium) supplemented with 10% foetal calf serum, 100 U ml À1 penicillin, 100 mg ml À1 streptomycin and 2 mM L-Gln (all from Lonza) at 37 1C and 5% CO 2 in tissue culture flasks (Greiner, Nürtingen, Germany). To induce glioma spheroid formation, cells were harvested, and 2 Â 10 6 cells were plated in 20 ml supplemented DMEM medium without phenol red in agarcoated T75 tissue culture flasks. After 3 to 4 days of culture, spheroids with a diameter of 200 mm had formed.

ALA/PDT treatment of GB spheroids
Spheroid cultures were incubated with 12.5 mg ml À1 ALA (Merck, Darmstadt, Germany) for 4 h at 37 1C and 5% CO 2 as described (Etminan et al, 2011). A measure of 10 ml of culture was transferred into 10-cm Petri dishes, spheroids collected under microscopic control and transferred (25 spheroids per well) into agar-coated flat-bottom 96-well plates (Greiner) containing 100 ml per well of DMEM medium without phenol red. For laser-lightonly controls, spheroids not treated with ALA were transferred into 96-well plates. Exposure of spheroids to laser light was performed for 625 s with 1 W (equivalent to 25 J s À1 ) using a Ceralas 633 nm PDT diode laser (Biolitec, Jena, Germany). For ALA-only controls, spheroids were treated with ALA, but not exposed to laser light. After laser light exposure, spheroids were used directly for the experiments. Under these conditions, viability of cells was 50% after 16 h of tissue culture as determined by WST-1 assay, and TUNEL staining indicated apoptosis in about 60% of cells (Etminan et al, 2011).

Generation of DCs
Buffy coats were obtained from healthy individuals after informed consent. CD14 þ monocytes were immunoselected from PBMCs using LS separation columns on a VarioMACS (Miltenyi Biotec, Bergisch Gladbach, Germany) as described (Rapp et al, 2006). Differentiation and maturation of DCs from monocytes was performed following a protocol adapted from Zhou and co-workers (Zhou and Tedder, 1996;Rapp et al, 2006). Briefly, CD14 þ monocytes were cultured in 24-well plates (Greiner) at 1 Â 10 6 cells per ml and 2 ml per well in serum-free CellGroDC medium (Cellgenix, Freiburg, Germany) supplemented with 1000 U ml À1 GM-CSF (Leukine, Berlex, Richmond, CA, USA) and 1000 U ml À1 IL-4 (Cellgenix). After 3 days, half of the medium was replaced by fresh medium containing cytokines. Immature CD14 À DCs were harvested after 6 days of culture. To induce DC maturation, 1000 U ml À1 TNFa (Cellgenix), GM-CSF and IL-4 were added to immature DCs on day 6, and cultures were continued for 3 days.
The influence of GB spheroids on DC maturation was studied in co-cultures. In all, 25 untreated spheroids or spheroids that had been treated with ALA (ALA-only) or exposure to laser light (laserlight-only) or both (ALA/PDT) were added to the DC cultures on day 6 and cultures continued for 3 days before analysis. To study the effect of blocking HSP-70 on glioma spheroids, the spheroids were pre-incubated with goat-anti-human HSP-70 polyclonal IgG antibody (1 :20 ; Santa Cruz, Heidelberg, Germany) before the co-cultures were initiated.

Flow cytometry and monoclonal antibodies
To assess uptake of tumour material, treated and untreated spheroids were labelled with CFSE (Molecular Probes/Invitrogen, Karlsruhe, Germany) and co-cultured with immature DCs. After 16 h of co-culture, DCs were labelled with anti-HLA-DR monoclonal antibody (mAb) and uptake of tumour material by HLA-DR þ DCs was determined by flow cytometry on an FACS Canto using the DIVA software (BD Biosciences, Heidelberg, Germany), identifying antigen uptake by the appearance of HLA-DR/CFSE double-positive DCs within living cells identified based on forward-vs side-scatter characteristics. At least 10 000 living cells were acquired in each experiment. To study the effect of blocking HSP-70 on antigen uptake, the spheroids were pre-incubated with goat-anti-human HSP-70 polyclonal IgG antibody before assessing antigen uptake by flow cytometry.

Migration assay
To assess migration of immature DCs towards spheroids, a transwell assay was used. Spheroids, CellGroDC medium (negative control) and medium containing 40 ng ml À1 CCL3 (positive control; R&D Systems, Wiesbaden, Germany) were transferred into a 24-well plate (500 ml per well). Transwell inserts (8 mm pore size; Greiner) were coated with 100 ml fibronectin (5 mg ml À1 ; Sigma/Aldrich, Seelze, Germany) for 1 h at room temperature, placed in the 24-well plate containing the migration targets and immature DCs in CellGroDC medium (50 000 DCs/200 ml per well) were added into the insert. After 16 h of incubation at 37 1C and 5% CO 2 , cells were fixed with methanol and migrated DCs stained with Fields solution (Alfa Aesar, Karlsruhe, Germany) before microscopically determining the number of migrating cells. Counting of cells was performed automatically using the ImageJ software (http://rsbweb.nih.gov/ij/).

Allogeneic mixed leukocyte reaction
Graded doses of immature DCs, TNFa-matured DCs or immature DCs, which had been co-cultured for 3 days with ALA/PDT-treated or untreated spheroids, were co-cultured with 10 5 allogeneic T cells, which were obtained by negative selection from buffy coats as described (Sorg et al, 2001). After 5 days of co-culture, cells were pulsed with bromodeoxyuridine for 16 h, and bromodeoxyuridine uptake was determined using the bromodeoxyuridine enzymelinked immunosorbent assay kit as recommended by the manufacturer (Roche Diagnostics, Mannheim, Germany).

Statistics
If not stated otherwise, all data are presented as mean ± s.e.m. Statistical analysis was performed with the Graph Pad Prism Software Version 5.01 (GraphPad, San Diego, CA, USA). Statistical significance was evaluated with the Student's t-test or the two-way ANOVA test.
Enhanced uptake of tumour material by immature DCs after ALA/PDT treatment of spheroids To determine uptake of tumour material from glioma spheroids, CFSE-labelled ALA/PDT-treated spheroids or control spheroids were co-cultured with immature DCs for 16 h, and antigen uptake by the DCs was subsequently quantified by flow cytometry. Pretreatment of spheroids with ALA/PDT resulted in a significant uptake of tumour material by the DCs from U251 (Figures 2A -C; 1324.0 ± 297.6 vs 349.3 ± 108.0 mean fluorescence intensity (MFI) FITC; n ¼ 4, P ¼ 0.0217) as well as from U87 spheroids ( Figure 2D; 794.3±172.1 vs 164.3±33.1 MFI FITC; n ¼ 4, P ¼ 0.0114) compared to untreated control spheroids. Spheroids that had been treated with ALA-only or laser-light-only showed no such activity. Fluorescence microscopy of DCs revealed perinuclear localisation of the fluorescent tumour material ( Figure 2B).

ALA/PDT-treated spheroids induce maturation of DCs
To study the influence of glioma spheroids on DC maturation, immature DCs were co-cultured for 3 days in the presence or absence of ALA/PDT-treated or control spheroids. Subsequently, the expression of the maturation marker CD83 and the co-stimulatory molecules CD40, CD80 and CD86 was analysed. Chemoattractive activity of glioma spheroids for immature DCs. Immature DCs were assessed for migration towards ALA/PDTtreated, ALA-only-treated, laser-light-only exposed and untreated U251 (A) and U87 spheroids (B). Culture medium served as negative control and medium supplemented with CCL3 as positive control. Data are presented as mean ± s.e.m for n ¼ 4. Statistically significant differences compared to negative control cultures in the absence of spheroids are indicated; **Pp0.01, *Pp0.05.
Cultures with TNFa for 3 days served as positive controls for DC maturation. In the presence of ALA/PDT-treated spheroids, a significant proportion of DCs had matured as evident by an increased frequency of CD83 þ cells compared to control cultures in the absence of maturation stimuli (U251, 43.5 ± 12.6 vs 4.5 ± 1.9% CD83 þ ; n ¼ 4, P ¼ 0.0223; U87, 46.1 ± 10.4 vs 3.1 ± 1.4% CD83 þ ; n ¼ 5, P ¼ 0.0034). In contrast, co-culture of immature DCs with control spheroids (untreated, ALA-only-or laser-lightonly-treated) did not induce DC maturation ( Figure 3A). Similar results were obtained when the expression of the co-stimulatory molecules was analysed. Only after co-culture with ALA/PDTtreated spheroids, but not with the control spheroids, a significant upregulation of CD40, CD80 and CD86 on the DCs compared to control cultures without maturation stimuli was observed ( Figure 3B). Functional activity of DCs matured in the presence or absence of ALA/PDT-treated or untreated spheroids of the cell lines U251 ( Figure 4A) or U87 ( Figure 4B) was evaluated in an allogeneic mixed leukocyte reaction. Control immature DCs that were neither exposed to spheroids nor to the maturation-inducing TNFa revealed allostimulatory activity, which was comparable to that of DCs co-cultured with untreated spheroids (P40.05 (ANOVA); n ¼ 3), with a trend towards reduced allostimulatory activity of the DCs after co-culture with untreated U251 spheroids (P ¼ 0.0644).
When maturation of DCs was induced with TNFa, allostimulatory activity increased significantly compared to the immature DCs (P ¼ 0.0094 for Figure 4A and P ¼ 0.0004 for Figure 4B (ANOVA); n ¼ 3). Increased allostimulatory activity of DCs was also observed after co-culture with ALA/PDT-treated U251 (P ¼ 0.0014 (ANOVA); n ¼ 3) or U87 spheroids (Po0.0001 (ANOVA); n ¼ 3) compared to co-cultures with untreated spheroids. Co-cultures of DCs with ALA/PDT-treated U87 spheroids reached allostimulatory activity levels similar to TNFa-matured DCs (P40.05 (ANOVA); n ¼ 3). For U251 spheroids, ALA/PDT treatment could compensate the reduction of allostimulatory activity observed after co-culture of immature DCs with untreated spheroids and activity increased to levels comparable to the immature DCs (P40.05 (ANOVA); n ¼ 3). Thus, for both cell lines an increased functional activity of DCs after co-culture with ALA/PDT-treated spheroids was observed, which is consistent with the induction of DC maturation.

ALA/PDT treatment of glioma spheroids induces HSP-70, which mediates uptake of tumour antigens and maturation of DCs
Heat-shock protein-70 has been shown to be upregulated on the surface of mouse squamous cell carcinoma cells after photofrinmediated PDT and to contribute to immune activation (Korbelik When HSP-70 surface expression was compared for untreated and ALA/PDT-treated U251 and U87 spheroids, a clear upregulation of surface HSP-70 was evident for the treated spheroids. Heat-shock protein-70 was absent or expressed at only very low levels on the untreated spheroids ( Figure 5A, representative results of three independent experiments).

DISCUSSION
There is clear evidence for an immunological component in the anti-tumoural effect of PDT from extracranial tumours (Castano et al, 2006). Immediately after PDT, there is immigration of neutrophils into the tumour (Krosl et al, 1995), and depletion of neutrophils before treatment abrogates the curative effect (de Vree et al, 1996;Korbelik and Cecic, 1999), suggesting an important contribution of innate immunity to the efficacy of PDT. However, results from immunodeficient NOD/SCID mice, lacking B and T cells, and nude mice, lacking T cells only (Canti et al, 1994;Korbelik et al, 1996;Hendrzak-Henion et al, 1999;Preise et al, 2009), indicate an essential role of adaptive T-cell immunity as well, with CD8 þ cytotoxic T cells as main effectors and a supportive role for CD4 þ T-helper cells (Hendrzak-Henion et al, 1999;Korbelik and Cecic, 1999;Korbelik and Dougherty, 1999;Preise et al, 2009). Moreover, Mroz et al (2010) identified antigen-specific cytotoxic T cells after benzoporphyrin-derivative/PDT treatment in a CT26.CL25 colon carcinoma model. Furthermore, a recent case report suggests that an immune response contributes to tumour eradication also in humans: CD4 þ and CD8 þ T-cell infiltrates have been observed in lesions after Fotolon-mediated PDT of recurrent angiosarcoma, which underwent remission after therapy (Thong et al, 2007).
For such effector T-cell responses to occur, immature DCs have to migrate to the tumour, take-up tumour antigens and respond to local danger signals with maturation, before they will engage in T-cell activation in the draining lymph nodes in the afferent phase of cellular adaptive immunity (Ueno et al, 2010). Consistent with this view, Preise et al (2009) reported higher recurrence rates of CT26 colon carcinomas treated with WST11-mediated PDT after DC depletion. When the migration of human immature DCs to glioma spheroids was analysed here, ALA/PDT treatment resulted in significantly increased attraction of the DCs towards the tumour cells. Moreover, the immature DCs took up tumour material from the ALA/ PDT-treated spheroids efficiently, whereas they did not from untreated tumour spheroids or spheroids that had only been treated with ALA or laser light alone. Thus, two of the initial steps of the afferent phase of adaptive tumour immunity are promoted by ALA/PDT. The efficiency of PDT-treated tumour cells as vaccines for induction of anti-tumoural immunity has been shown for SCVII squamous cell carcinoma, Lewis lung carcinoma, EMT6 mammary sarcoma, P815 mastocytoma and C6 rat glioma models using photofrin, benzoporphyrin derivative or haematoporphyrin as photosensitisers (Gollnick et al, 2002;Korbelik and Sun, 2006;Shixiang et al, 2010). This implies that the PDT-treated cancer cell vaccines are recognised and taken up by the DCs. Indeed, Korbelik and Sun (2006) reported that the vaccine cells were intermixed with DC 1 h after injection, suggesting active migration of DC towards the tumour vaccines in vivo. Evidence for uptake of tumour antigens after PDT also comes from the intratumoural injection of DCs following PDT treatment: improved survival of animals and induction of tumour-specific immunity indicate that the DCs have taken up tumour antigens (Jalili et al, 2004;Saji et al, 2006;Sur et al, 2008). Furthermore, when immature DCs were co-cultured in vitro with CT-26 colon carcinoma cells subjected to photofrin/PDT, enhanced uptake of tumour material by the DCs was detected (Jalili et al, 2004).
Attraction of DCs and uptake of tumour antigens alone, however, are not sufficient for the initiation of an immune response, but may result in immunological tolerance (Green et al, 2009;Tisch, 2010;Ueno et al, 2010). An activating danger signal inducing DC maturation is required. Here, ALA/PDT-treated spheroids provided such a maturation-inducing stimulus. When immature DCs were co-cultured with ALA/PDT-treated spheroids, maturation of DCs was induced as indicated by the induction of the marker for mature DCs, CD83 and upregulation of the co-stimulatory molecules CD40, CD80 (B7.1) and CD86 (B7.2). Importantly, these changes in the expression of immunorelevant molecules were associated with an increased T-cell stimulatory activity of the DCs. From the efficacy of PDT-generated vaccines, which was superior compared to vaccines generated using UV or ionising irradiation (Gollnick et al, 2002;Korbelik and Sun, 2006), and from the efficacy of intratumourally injected DCs following PDT (Jalili et al, 2004;Saji et al, 2006;Sur et al, 2008) as well as from increased frequencies in IFNg-secreting cells and the generation of tumour-specific CTL in the treated animals reported by others, it can be concluded that DCs have undergone maturation owing to PDT treatment of the tumour cells in these studies as well. This has been confirmed by in vitro analyses showing induction of MHC class II molecules, CD80, CD86 and IL-12 in co-culture experiments of DCs and PDT-treated mouse tumour cells (Gollnick et al, 2002;Jalili et al, 2004) or DCs and acid-eluted material from PDT-treated C6 rat glioma cells (Shixiang et al, 2010).
The factors and mechanisms involved in promoting attraction, antigen uptake and maturation of DCs following PDT are not well understood. Depending on the photosensitiser, its location within the cell and dose, the cell type and oxygen concentration, PDT results in apoptotic or necrotic cell death (Castano et al, 2006). The protocol used in this study mainly induced apoptosis as determined by TUNEL staining (Etminan et al, 2011). Induction of apoptosis after ALA/PDT treatment of GB cells has also been reported by Inoue et al (2007). Apoptotic cells release several chemoattractive factors, including nucleotides, lipids and chemokines, which may attract DCs. Changes in surface molecules on apoptotic cells, for example, expression of calreticulin or HSP-70 and -90, allow recognition and engulfment of apoptotic bodies (Green et al, 2009;Zitvogel et al, 2010). Although apoptotic cells have been suggested to fail to induce DC maturation and to be associated with induction of immunological tolerance, this also appears to depend on the pre-apoptotic conditioning, for example, stress, of the cells together with the sequence of the events rather than solely on apoptotic vs necrotic cell death. The release of inflammatory mediators, damage-associated molecular patterns and alarmins like the pro-inflammatory cytokines HMGB1 and IL-1a during apoptosis may contribute to DC maturation (Green et al, 2009;Zitvogel et al, 2010). It is well established that PDT results in the upregulation of inflammatory mediators, including IL-1b, IL-6, TNFa, prostaglandins and various HSPs, and glucoseregulated proteins (Gollnick et al, 1997;Dolmans et al, 2003;Jalili et al, 2004;Korbelik et al, 2005;Castano et al, 2006). For the glioma spheroids, we observed upregulation of HSP-70 surface expression, and when HSP-70 was blocked by antibodies, uptake of tumour antigens as well as DC maturation induced by the ALA/PDTtreated spheroids was almost completely inhibited. Korbelik et al (2005) and Korbelik and Sun (2006) also suggested a pivotal role of surface HSP-70 in PDT-induced immune activation: inhibitors to HSP-70, Toll-like receptors 2 and 4 or specific inhibition of NF-kB blocked macrophage activation and TNFa release induced by photofrin-mediated PDT of SCCVII mouse squamous cell carcinoma cells. Thus, surface expression of HSP-70 appears to be a major DC maturation-inducing stimulus after PDT in mice as well as in humans. Whether other factors, including pro-inflammatory cytokines and HSP or glucose-regulated proteins, which have been reported to be upregulated on tumour cells in response to PDT (Gollnick et al, 1997;Dolmans et al, 2003;Jalili et al, 2004;Korbelik et al, 2005;Castano et al, 2006), are also upregulated and contribute to attraction, antigen uptake and maturation of DCs by ALA/PDT-treated GB cells is currently unknown.
For human GB, the immunological consequences of ALA/PDT have not been analysed so far. In this study, we could show that ALA/PDT treatment of GB spheroids attracts DCs and promotes uptake of tumour antigens as well as DC maturation in vitro. However, our study holds limitations: although the spheroid model may mimic microtumours more closely than monolayer cultures (Sutherland, 1988;Hirschhaeuser et al, 2010), differences between the established cell lines used here and primary tumour cells in vitro or the tumour, including its vasculature and stroma in vivo, may result in a different effect of ALA/PDT. In addition, it remains to be elucidated whether the above-described effects on DCs result in cross-presentation of tumour antigens and induction of cytotoxic T-cell-mediated anti-tumoural immunity in vivo. Therefore, further studies evaluating the effect of ALA/PDT on primary tumour cells as well as in vivo studies are needed to document efficacy of PDT in GB and the contribution of an anti-tumoural immune response to it.
In summary, like in extracerebral tissues, ALA/PDT may not only kill GB cells directly due to its phototoxic effect, but may also result in the induction of anti-tumoural immunity, mediated by the induction of HSP-70 surface expression. This immunological effect may contribute to long-sustaining responses and the potential clinical benefit of ALA/PDT for GB (Eljamel et al, 2008;Stummer et al, 2008).