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In vitro studies have demonstrated that cancer-specific T cell cytotoxicity can be induced both ex vivo and in vivo, but this therapeutic strategy should probably be used as an integrated part of a cancer treatment regimen. Initial chemotherapy should be administered to reduce the cancer cell burden and disease-induced immune defects. This could be followed by autologous stem cell transplantation that is a safe procedure including both high-dose disease-directed chemotherapy and the possibility for ex vivo enrichment of the immunocompetent graft cells. The most intensive conventional chemotherapy and stem cell transplantation are used especially in the treatment of aggressive hematologic malignancies; both strategies induce T cell defects that may last for several months but cancer-specific T cell reactivity is maintained after both procedures. Enhancement of anticancer T cell cytotoxicity is possible but posttransplant vaccination therapy should probably be combined with optimalisation of immunoregulatory networks. Such combinatory regimens should be suitable for patients with aggressive hematological malignancies and probably also for other cancer patients.
During the last two decades, effects of immunotherapy and autologous stem cell transplantation have been extensively studied in the treatment of human cancer. Immunotherapy often includes cancer vaccines, but vaccine-induced anticancer reactivity is often not associated with significant clinical responses [1–3]. Similarly, high-dose chemotherapy combined with autotransplantation has become a part of routine clinical practice only for a minority of cancer patients due to limited clinical benefits [4, 5].
Anticancer immune reactivity is probably important in autotransplantation, because early lymphoid reconstitution is associated with prolonged progression- or disease-free survival in many malignancies [6, 7]. This has been described in patients with B-cell malignancies, acute myeloid leukemia (AML), and solid tumors, suggesting that early reconstitution represents a general anticancer effect [7–10]. Even though cancer patients often have both disease-associated and treatment-induced immune defects that may persist for several months , the combined use of autotransplantation and anticancer vaccines should be considered to try to increase anticancer effects.
In the present paper we review the experience with intensive chemotherapy and immunotherapy for patients receiving intensive chemotherapy for aggressive hematological malignancies. We focus on acute myeloid leukemia (AML), one of the most aggressive human malignancies that is usually treated with very intensive therapy eventually in combination with stem cell transplantation. The experience from these patients is that anticancer immune reactivity is maintained and can be induced after the intensive treatment. It seems likely that similar therapeutic strategies should be possible also in other patients receiving less intensive chemotherapy for less aggressive malignancies.
Patients with acute myeloid leukemia receive intensive chemotherapy followed by a period of severe leukopenia, but even these patients have a functional T cell system, and rapid lymphoid reconstitution is associated with a decreased risk of AML relapse [11, 12]. T cell functions during cytopenia are characterised by the following.
Altogether, these observations clearly demonstrate that a functional T cell system remains during the severe posttreatment leukopenia even for patients receiving the most intensive conventional chemotherapy, and T cell targeting therapy may be possible even during this period.
Studies of immunological reconstitution after conventional intensive chemotherapy has been carried out for patients with nonHodgkin's lymphoma, sarcomas and brain tumors, but these patients generally received less intensive chemotherapy than patients with AML [19–23]. These studies have described a decrease in circulating CD4+ cells that may last for several months, and there seems to be a predominance of memory-type (CD4+CD45RO+CD45RA+/-) cells. This defect seems to be at least partly age-dependent and is less pronounced in children . The number of CD3−CD16+CD56+ NK lymphocytes is usually normalised within 6 weeks . It seems likely that similar defects are also seen after conventional chemotherapy for other malignancies, including the most intensive AML therapy. Certain drugs seem to cause more severe CD4+ T cell defects; this is especially true for fludarabine that can be used as a part of conventional chemotherapy and in the reduced intensity conditioning before allogeneic stem cell transplantation . Finally, the effect of chemotherapy on Treg cells seem to differ between cytotoxic drugs as reviewed recently , myeloid suppressor cells can be transiently increased early after recovery from chemotherapy and the heterogeneity within the dendritic cell population varies during the recovery phase after chemotherapy . The status of all these three cell types may influence the response to anticancer vaccines.
Hematopoietic stem cells (HSC) are now preferably harvested from peripheral blood after growth factor mobilisation [28, 29], and this method is associated with earlier engraftment than HSC aspired from bone marrow . Neutrophil engraftment with peripheral blood neutrophils >0.1 × 109/L is usually seen within 10–12 days and platelet engraftment with thrombocytes >20 × 109/L within 12–14 days [30, 31]. The conclusion from the overall results is therefore very clear: (i) mobilisation of peripheral blood stem cells is safe and effective; and (ii) the short time until hematopoietic reconstitution when using mobilised cells has increased the safety of the procedure .
G-CSF is the most widely used drug for stem cell mobilisation  and is thought to stimulate immature stem cells to produce progenitors of all classes . In addition G-CSF indirectly stimulates the production of progenitor cells by increasing the production of hematopoietic growth factors  and it promotes the release of progenitors into the general circulation . When administered early after chemotherapy, G-CSF acts synergistically with the natural increase in HSC that is seen during the recovery phase . The morbidity during and after G-CSF mobilisation is very low , and the most frequent side effects are bone pain, fever, and nausea. Successful mobilisation can also be achieved with longer-acting G-CSF (pegylated G-CSF)  its main advantage is less frequent administration .
Several strategies have been tried to increase the mobilisation of CD34+ cells. A combination of G-CSF plus stem cell factor (SCF) will often more than double the yield of CD34+ cells compared to G-CSF alone [39, 40]. The CXCR4 antagonist AMD3100 can also be combined with G-CSF to improve HSC mobilisation [41–43]. Finally, even though mobilisation regimens that include chemotherapy have more side effects than G-CSF alone , the use of chemotherapy is appealing because insufficient mobilisation of CD34+ cells is more common in cancer patients with G-CSF alone , and the disease-specific chemotherapy in such regimens can have additional anticancer effects.
Autologous stem cell grafts are usually cryopreserved, and the protocols are generally based on the use of the cryoprotectant dimethyl sulphoxide (DMSO) in the freezing medium [45–47]. After harvesting, the final product is often diluted with autologous plasma if the nucleated cell concentration is higher than 200 × 106 cells/mL to improve cell viability . Most centers will use a controlled programmed freezer and storage in nitrogen at −160°C.
The grafts are usually prepared by apheresis procedures alone without further enrichment of CD34+ stem cells, and large numbers of immunocompetent cells are therefore reinfused together with the stem cells. Early posttransplant lymphocyte reconstitution after both auto- and allotransplantation is associated with prolonged relapse-free survival in several malignancies [7–10]. For allotransplanted patients reconstitution of CD4+ T cells seems particularly important, and infusion of a high number of CD4+ T cells and NKT cells seems to be associated with a better prognosis . This may also be true for autografted patients, and these observations suggest that immunological events early after reinfusion are important for the risk of later relapse/progression. The amount and quality of reinfused lymphocytes may therefore be essential.
We investigated the viability of total lymphocytes and the distribution of various T cell subsets in peripheral blood stem cell autografts after long-term storage with 2%, 4%, 5% and 10% DMSO . The viability of the total lymphocyte population was significantly higher for cells preserved in 4% and 5% DMSO, but the DMSO effect differed between T cell subsets (Table 1). First, NKT cell viability was dependent on the DMSO concentration used. Second, naive and central memory T cells usually express CD62L, late effector T cells show intermediate/low expression, while effector memory T cells do not express CD62L . The effect of DMSO differed between these CD62L-defined T cell subsets. Third, the CCR7 chemokine receptor is expressed by naive and central memory T cells and directs migration to lymph nodes; this homing process is important for initiation of immune responses . Again the DMSO effect differed between CCR7-defined subsets and also between CCR2/CCR4 defined subsets. Finally, Foxp3 positive T cells are referred to as thymus-derived natural T regulatory (Treg) cells . The percentage of CD4+CD25+Foxp3+ cells among CD4+ T cells was significantly lower after cryopreservation with 10% DMSO.
Several NK cell subsets have now been characterised, including immunoregulatory (CD3−CD56brightCD16low/neg) and cytotoxic cells (CD3−CD56dimCD16bright) [54–56]. Cryopreservation with various DMSO concentrations did not alter the percentages among viable graft lymphocytes of total NK cells (CD3−CD56+) or the various NK cell subsets .
Taken together these results suggest that the procedures used for cryopreservation affect lymphocyte viability; this is not a nonspecific effect but rather an effect that differs between various T cell subsets and it may thereby affect posttransplant T cell reconstitution and immunocompetence. The mobilisation and harvesting procedures would also be expected to influence the graft lymphocyte content but to the best of our knowledge this has not been investigated in clinical studies.
The studies described above demonstrate that cytotoxic T cells are preserved and reinfused in autologous stem cell grafts. Furthermore, recent studies have demonstrated that T cells specific for leukemia-associated antigens remain in the circulation after intensive AML chemotherapy (see Section 5), and for this reason one would expect such cells also to be present in the autografts. At present it is not known whether reinfusion of such cells as a part of the transplantation procedure will have any clinical impact, or whether the immunocompetent cells in the graft will differ between various mobilisation procedures.
It is possible to separate graft cells into CD34+ and CD34− cells before freezing , and the CD34− subset could then be used for ex vivo enrichment of cancer-reactive T cells before reinfusion together with the CD34+ cells. Although techniques for enrichment of leukemia-reactive T cells are available, they have not been used in a large-scale clinical setting in combination with stem cell transplantation.
As stated above, in vitro expanded autologous T cells can be used in the treatment of cancer. This strategy has not been widely used in the aggressive hematological malignancies, but the experiences from solid tumors (e.g., malignant melanoma) suggest that such cells can induce clinically relevant antitumor activity [27, 58]. In a recent study a comparable strategy was also used as a posttransplant treatment in allotransplanted patient; donor-derived leukemia-reactive T cells were then reinfused in patients with leukemia relapse after allotransplantation . Taken together these studies suggest that infusion of ex vivo generated cancer-reactive T cells can be combined with high-dose chemotherapy and possible also with vaccination strategies.
T cell functions during the early posttransplant period with severe treatment-induced leukopenia seem to be very similar to AML patients receiving intensive conventional chemotherapy, and the later reconstitution also shows many similarities  (Table 2). Time until complete immunological reconstitution in adults may take years [61–63]. However, after transplantation the absolute number of circulating CD3+ cells usually remains decreased for three to five months . Low levels of circulating CD4+ cells have been reported for 12–18 months , whereas CD8+ T cells usually recover within 3–12 months . Defective proliferation of both CD4+ and CD8+ T cells in response to antiCD3 and antiCD2 persists for at least for 2–4 months, and this seems to be caused by defective IL-2 responsiveness [64, 66]. Furthermore, the specific cytotoxic T cell response against Epstein-Barr virus is significantly impaired for 2–5 months , whereas the frequency of circulating cytokine-secreting T helper cells and IL-2 responding T cells can be decreased for up to 5 years posttransplant .
Peripheral blood mobilized stem cells (PBMSC) are now used for most cancer patients treated with autologous stem cell transplantation. The immunological reconstitution differs between patients receiving peripheral blood and bone marrow autografts , and the following data on T cell subset reconstitution refers to patients transplanted with mobilized stem cells. PBMSC autografted patients show early recovery of CD14+ monocytes and CD56+ NK cells during the first month after autotransplantation [64, 69, 70]. The homeostasis of total circulating dendritic cells is usually achieved relatively early after transplantation, although differences in dendritic cell subset composition may be detected for several months . However, as pointed out by these authors the kinetics of dendritic cell reconstitution may differ between patients and also depend on the chemotherapy regimen . In contrast, a long-lasting T cell defect similar to chemotherapy-treated patients is also observed after autotransplantation [69, 70]. This defect is detected after 6 months for most patients, and for a minority the defect will last for more than a year . The total levels of CD8+ T cells seem to normalize within a few months, whereas total CD4+ T cell counts remain decreased for several months. The CD4 defect is mainly due to a reduction of naive CD3+CD4+CD45RA+ T cells, and there seems to be a reduction even of CD8+ naive T cells [69, 70].
As discussed by Dreger age may influence the T cell reconstitution after autotransplantation . Immunogenetic factors may also be important for posttransplant T cell functions; single nucleotide polimorphisms in immunoregulatory chemokine/cytokine genes seem to influence the risk of infections, graft versus host disease and leukemia relapse after allogeneic stem cell transplantation. (for a detailed discussion and additional references see Loeffler ). Such immunogenetic influences may also be important for the response to posttransplant vaccination therapy after conventional chemotherapy or stem cell transplantation.
The number of mature B cells is markedly decreased during the first 3 months posttransplant, but will thereafter gradually increase although complete normalisation may take up to 18 months . Both T cell-dependent and independent B cell response are decreased for 12–18 months , and the IgM production will normalise earlier (often within 6 months) than the corresponding IgG response .
NK cells usually recover within 1 month after transplantation . The NK cell number is often increased on day 15 posttransplant compared with normal individuals, but by day 75NK cell activity has usually returned to a normal level. NK cells are important for rejection of malignant cells , and pharmacological agents that increase cancer cell susceptibility to NK cell mediated lysis are now being developed .
As described in a recent review the immunological reconstitution after allogeneic stem cell transplantation differ between patients receiving myeloablative and reduced intensity conditioning therapy . Briefly, allotransplantation is also associated with a similar quantitative defect in CD4+ T cells, this defect may last for several months but early normalization seems to be more common for patients receiving reduced intensity conditioning (for detailed discussion and additional references see .
A major question is whether it is possible to induce anticancer T cell reactivity and especially cytotoxicity in patients who have recently received intensive chemotherapy. T cells specific for cancer-associated antigens can be detected in healthy individuals and also in untreated cancer patients despite their disease-induced immunosuppression, and many of these cells seem to be CD8+ cytotoxic effector memory cells . Many cancer patients develop additional therapy-induced immune defects. However, if it is possible to induce anticancer T cell reactivity by vaccination in AML patients who have a very aggressive disease and receive the most intensive chemotherapy, one would expect immunotherapy to be effective also in other cancer patients. Several strategies for immunotherapy in AML have been tried (Table 3). In this paper we will review the results from vaccination studies.
AML patients are very heterogeneous with regard to genetic abnormalities encoding leukemia-specific antigens . To find a common vaccination strategy the available studies have therefore focused on the use of either whole AML cells (cell lysates or modulated AML cells) or peptides derived from AML-associated proteins.
WT1 is a zinc finger transcription factor that is expressed in normal CD34+ hematopoietic cells, myoepithelal progenitors, renal podocytes, and some cells in testis and ovary . This protein is overexpressed in several hematological malignancies and solid tumors . Antibodies against this molecule have been detected in cancer patients and several immunogenic peptides have been identified . Briefly, both CD4 and CD8 T cell epitopes have been identified, and HLA-A0201 and HLA-A24-restricted CD8+ T cell cytotoxicity against WT1 expressing cancer cells have been detected. The CD4 peptides bind to different HLA-class II molecules and induce CD4+ T cell responses that enhance cytotoxic T cell reactivity either through induction of CD4+ cytotoxic T cells or through induction of CD4+ Th1 helper cells. Some peptides include epitopes recognised both by CD4+ and CD8+ T cells. Finally, a recent study demonstrated that WT1-specific cytotoxic T cells remain even after remission-inducing intensive AML chemotherapy .
Proteinase 3 is a differentiation antigen that is also overexpressed in leukemic blasts . A proteinase 3-derived peptide named PR1 has been identified by screening for binding avidity to HLA-A0201 . In vitro studies suggest that PR1-specific T cells can kill leukemic cells, including the more immature clonogenic subsets, but not normal hematopoietic stem cells [78, 80, 81]. However, it should be emphasized that these data are mainly based on studies of healthy individuals and cancer patients receiving low-toxicity chemotherapy. Untreated AML patients have also been investigated and circulating PR1 specific T cells could not be detected then . This may be due to apoptosis of high-avidity T cells induced by exposure to high peptide concentrations or leukemic cells overexpressing the proteinase 3 . However, PR1 specific T cells can be detected later after remission-inducing AML chemotherapy .
The receptor for hyaluronic-acid-mediated motility (RHAMM) is overexpressed in leukemic blasts from AML and CML patients but not in normal CD34+ hematopoietic cells . Greiner et al. identified a RHAMM-derived peptide (referred to as the RHAMM-R3 peptide) that could be presented by HLA-A2 and recognised by CD8+ T cells [78, 83]. This peptide was a naturally processed T cell epitope, specific T cells were detected in AML patients even following intensive chemotherapy, and in vitro primed T cells could lyse human AML blasts.
Taken together these studies clearly demonstrate that cancer-specific, HLA-restricted T cell reactivity, including specific cytotoxicity, is maintained even after the most intensive chemotherapy.
Oka et al. investigated the effect of WT1 peptide vaccination in 26 cancer patients, including 13 patients with de novo AML . They used intradermal injection of a modified 9-mer WT1 peptide emulsified in Montanide ISA51 adjuvant; 18 of the 26 patients completed the vaccination protocol with 3 or more injections every second week and most patients were vaccinated with a modified peptide that gave stronger cytotoxic T cell responses than the natural peptide. All patients were HLA-A2402 positive and their malignant cells showed high WT1 expression. Tetramer flow cytometry of circulating cells showed an increase in specific T cells during vaccination for 9 of the 13 AML patients. An increase in antigen-specific induction of IFNγ expression was also observed for 6 of the patients. Only 10 of these patients could be evaluated with regard to clinical responses: (i) 2 patients showed decreased residual AML; (ii) stable disease was seen for 2 patients; (iii) bone marrow expression of WT1 was used as a surrogate marker of residual disease for those patients without detectable AML blasts, and for 5 of these patients decreased expression was detected following vaccination; (iv) 1 patient showed progressive disease. There was a statically significant correlation between clinical and immunological responsiveness. These observations suggest that WT1 vaccination can induce a specific T cell response; these T cells can locate to the bone marrow compartment and they mediate WT1-specific antileukemic effects.
Another study examined a regimen with GM-CSF therapy on days 1–4 and vaccination with antigenic peptide + keyhole limpet hemocyanine on day 3 . All patients were HLA-A2 positive and had high expression of WT1 in their leukemia cells, 17 out of the 19 included patients had received previous chemotherapy and all patients had detectable AML with increased bone marrow blasts. The vaccines induced immunological responses judged from tetramer analyses of peripheral blood, and a significant increase of these cells was also seen in the bone marrow. Importantly, responses were recorded especially in patients that had received previous chemotherapy and showed relatively low levels of bone marrow blasts (<50%). Reduction of bone marrow WT1 levels was observed for a subset of patients following vaccination. Thus, previous intensive chemotherapy does not eradicate leukemia-reactive T cells; the chemotherapy-induced reduction of the AML cell burden rather seems to reduce disease-induced immune defects and thereby increase the efficiency of the vaccination.
PR1 responses have been investigated in a study that combined vaccination with WT1 and PR1 peptides . This vaccine was also based on concomitant GM-CSF administration and subcutaneous administration of peptides in Montanide adjuvant. Five AML patients in complete remission after previous intensive chemotherapy were included. Responses were evaluated by tetramer staining, and immunological responses were detected for one or both peptides in most patients. Increased T cell responses were also detected by IFNγ expression after specific stimulation. Bone marrow expression of WT1 was used as a surrogate marker for residual disease, and these levels decreased when immunological responses became detectable. Thus, even though in vitro exposure of PR1-specific T cells to AML cells with high antigen levels causes apoptosis of these cells (see Section 5.1), detectable PR1 T cell responses could be induced early after induction chemotherapy.
The RHAMM-R3 peptide identified in previous in vitro studies has been tried for vaccination in HLA-A2+ patients with hematological malignancies . This study included only 10 patients with AML, MDS, or multiple myeloma; all 3 AML patients had received intensive chemotherapy before vaccination and the 4 myeloma patients had received autologous stem cell transplantation. The vaccine consisted of injection of 300μg peptide in incomplete Freund adjuvant subcutaneously on day 3, GM-CSF was administered on days 1 and 5, and this cycle was repeated 4 times with 2-weeks intervals. Immunological responses were evaluated by tetramer flowcytometry and ELISpot analysis for IFNγ and Granzyme B. An immunological response was detected by at least one of these methods for 9 patients, only 1 AML patient in relapse did not respond. Vaccination-induced T cell cytotoxicity towards autologous AML cells or HLA-A2+RHAMM+ target cells could also be detected. A clinical response with further reduction of bone marrow blasts was observed for 1 AML and 2 MDS patients. This study illustrates that T cell reactivity against leukemia-associated antigenic epitopes is maintained after intensive conventional chemotherapy as well as autologous stem cell transplantation, and this reactivity can be enhanced by peptide vaccination.
The clinical toxicity of vaccination was generally low, the most common side effect being grade 1-2 reactions with pain and erythema at the injection site. One study observed progressing leukopenia in two patients with MDS and MDS-AML, respectively; this may be caused by immunological reactivity against normal stem cells in patients with disease-induced reduction of normal hematopoiesis . Oka et al. also described a patient with a febrile reaction during the first injection .
A recent article described two patients vaccinated with ex vivo generated monocytic dendritic cells that had been incubated with leukemic cell lysates and keyhole limpet hemocyanine . Subcutaneous injection of the pulsed dendritic cells was well tolerated. Another study also investigated preparation of monocyte-derived dendritic cells in AML; these authors combined ex vivo generation of the cells followed by cryopreservation before transfection of WT1 mRNA by electroporation . The procedure was successful for all patients and injections were well tolerated. It is difficult to see from these articles whether immunological responses were induced by the vaccination. An additional advantage with this approach could also be activation of NK cells and not only specific T cells and thereby induction of an additional anticancer effect .
Primary human AML cells can be induced to differentiate in the direction of a dendritic cell phenotype by exposure to various cytokines or cytokine combinations. These cells show dendritic morphology, increased expression of T cell costimulatory molecule, increased antigen-presenting capacity and a constitutive chemokine release profile consistent with a dendritic cell phenotype [89, 90]. One study has reported the efficiency and toxicity when using a vaccine based on subcutaneous injection of dendritic AML cells . Five patients treated in a palliative setting were included, and the authors observed increased immune responses towards a peptide derived from the leukemia-associated antigen PRAME. Thus, this methodological approach also seems to be effective and feasible. However, care should be taken when injecting ex vivo expanded cells, and possibly the cells should be irradiated before injection .
Even though the experience with dendritic cell vaccines in aggressive hematological malignancies is limited, the experience from other malignancies is promising . The dendritic cells orchestrate a repertoire of immune responses, but various dendritic cell subsets differ in their immunoregulatory characteristics . Dendritic cell vaccines can thereby be used for cross-presentation of cancer-associated antigens; a possible approach then being to load the cells with autologous cancer cell lysates . This therapeutic strategy seems safe and effective. As an example, a recent study in patients with lung cell cancer showed no serious side effects and increased T cell responsiveness to cancer-associated antigens for more than half of the patients vaccinated with antigen-loaded autologous dendritic cells . Another strategy is viral transfection of cancer-associated antigens alone or antigens together with various immunostimulatory molecules [95, 96]. The experiences from other cancers suggest that such therapeutic strategies should be further investigated also in hematological malignancies, and combination of chemotherapy and dendritic cell vaccination should then be possible. However, the optimal procedures for antigenic loading and dendritic cell preparation remain to be established.
The general intensity of the chemotherapy has to be decided based on a clinical evaluation of the patients, and one has to take into consideration that there is evidence from clinical studies that a low cancer cell burden is associated with increased anticancer T cell reactivity [1, 97]. Several additional points also have to be considered. Firstly, if possible one should use a regimen that induces immunogenic cancer cell apoptosis that will enhance anticancer immune reactivity; this has been described especially for the anthracyclines  (Figure 1). Second, if possible the chemotherapy should reduce the levels of regulatory T cells  (see Section 6.3). Finally, the vaccine studies described above started at least 4 weeks after chemotherapy, but even patients with severe chemotherapy-induced cytopenia have an operative T cell system and immunotherapy can probably start even earlier after chemotherapy .
There are several possible advantages if autotransplantation is combined with vaccination therapy. Firstly, additional disease-directed chemotherapy can be administered both for mobilisation and as high-dose intensive chemotherapy before transplantation; this is safe and may further reduce the cancer cell burden . Secondly, graft preparation offers the possibility to manipulate the immunocompetent graft cells and thereby combine chemotherapy and immunotherapy. CD34 enrichment is now possible as a part of routine therapy before cryopreservation , and by using similar methodological approaches as previously used in experimental studies, one could enrich anticancer cytotoxic T cells and reinfuse them as a part of the transplantation procedure. Finally, even though both chemotherapy and autotransplantation seem to induce a general quantitative CD4+ T cell defect, intensive chemotherapy does not eradicate cancer-specific T cells and enhancement of this reactivity in graft immunocompetent cells or posttransplant cells should therefore be possible.
The administration route of vaccines will probably be important. For example, animal experiments have shown that dendritic cells administered subcutaneously will localise to the draining lymph nodes, whereas intravenous administration will cause localisation to the spleen . Several techniques are now available for preparation of the vaccines; these strategies have been reviewed recently and are exemplified by the results summarized in Figure 2 and Tables Tables3 and3 and and4 4 [82, 104].
Manipulation of immunocompetent cells through stimulation of Toll-like receptors (TLR) seems to be of particular interest [108, 109]. TLR9 is expressed by dendritic cells and B cells, and CpG oligonucleotides can be used as TLR9 agonists. These oligonucleotides will increase anticancer immune reactivity through several mechanisms, including increased presentation of cancer-associated antigens by dendritic cells [105–107, 110] (Figure 2). These agents have been used alone, but they can also be used as adjuvants in cancer vaccines and be combined with the Montanide adjuvant used in the peptide vaccines (see Section 5.2). However, the overall results from experimental and clinical studies with regard to effects of adjuvants on T regulator cells (Treg) are conflicting and require further studies.
Other adjuvants should also be tried in vaccination therapy, especially chemokines that are now considered as possible therapeutic targets in proinflammatory conditions . These mediators can be released by malignant cells and have several biological effects including chemotactic, growth-stimulatory, immunomodulatory, and angioregulatory effects [26, 43, 112]. Other cytokines than GM-CSF are now investigated as vaccine adjuvants, including Flts-ligand as well as the chemokine CCL5 and CXCL9 [113–115]. These experiences from animal cancer models suggest that such approaches should be tried also in the treatment of human cancers, although the possible roles of chemokine decoy receptors have to be explored .
An alternative to in vivo expansion of antigen-specific T cells through vaccination would be ex vivo enrichment of specific cells followed by infusion of these cells. Based on experimental observations various strategies may be possible, including (i) stimulation and thereby in vitro prokiferation/expansion of antigen-specific T cells; or (ii) ex vivo generation of antigen-specific T cell reactivity through viral transduction of specific T cell receptor genes. First, antigen-loaded dendritic cells can be used to stimulate proliferation of cancer-specific cells, and this expansion can be increased by subsequent costimulation through CD28 [117, 118]. Costimulation through the CD40/CD40-ligand system may also be possible . Second, T cell receptor gene-modified lymphocytes can be generated, such cells persist in patients after infusion and reduction of tumor cell burden has been described [120, 121]. Whether in vivo (vaccination) and ex vivo expansion (in vitro culture) of cancer-reactive T cells can be combined in cancer patients has not been clarified, and future studies also have to clarify whether these therapeutic strategies will be effective in hematologic malignancies.
IL-17 is a family of T cell derived cytokines that triggers the production of proinflammatory cytokines and chemokines by a wide range of cells, including epithelial cells, endothelial cells and macrophages [122, 123]. In healthy individuals circulating Th17 cells constitute less than 1.0–1.5% of total circulating T cells , increased levels are observed in patients with advanced cancers, and tumor infiltrating Th17 cells have been detected in ovarian, pancreatic and renal cell cancer . Several experimental observations suggest that Th17 cells can increase specific antitumor immune activity  as well as anticancer NK cell reactivity . These animal studies suggest that the role of Th17 cells in human cancer should be further investigated, including the cryopreservation of Th17 cells in autologous stem cell grafts and the possibility to enhance anticancer reactivity through ex vivo enrichment of Th17 cells in the autografts before reinfusion.
Immunosuppressive Treg cells comprise 5–15% of peripheral CD4+ T cells [128, 129]. In animal models these cells prevent autoimmune diseases, graft rejection and anticancer reactivity [128, 130]. Several studies suggest that cytotoxic agents can alter the levels of Treg cells. Fludarabine therapy in patients with chronic lymphocytic leukemia often causes a decrease or abrogation of the activity of Treg cells . Suppression of Treg cells by cyclophosphamide may allow immunotherapy of established tumors to be curative in animal models , but no effect is observed after a single cyclophosphamide infusion combined with nonspecific immunotherapy in patients with metastatic carcinoma . The mTOR antagonist rapamycin that is used in anticancer therapy, increases the number of Treg cells , whereas docetaxel does not seem to have any effect . Thus, the effects of anticancer therapy on Treg levels seem to differ between therapeutic agents.
Previous studies in AML have demonstrated that increased Treg cells are detected in patients with newly diagnosed AML, and these high levels persist even after intensive chemotherapy and induction of disease control with hematological remission . Thus, the overall intensity of the chemotherapy is not decisive for elimination of these cells; rather the design and use of specific drugs seem to be essential. Experimental studies have demonstrated that suppressive Treg cells can be stimulated to develop into proinflammatory Th17 cells . The possibility to use this approach instead of chemotherapy for elimination of Treg cells and enhancement of immunoreactivity should be explored both with regard to ex vivo manipulation of stem cell grafts and in vivo immunomodulation.
Many of the vaccination studies reviewed above included only patients with certain HLA-types known to bind and present the vaccine peptides. Future studies have to consider how vaccination strategies should be designed to include all patients and not only selected subsets. Other immunogenetic factors also need to be considered then, for example, genetic polymorphisms in the chemokine system  or in T cell regulatory molecules .
Available studies have demonstrated that cancer cell vaccines can induce anticancer immune reactivity. This is possible even for patients with the most aggressive hematological malignancies that are treated with very intensive chemotherapy, and it should therefore be possible also in other malignancies. The future challenge will now be to design optimal combinations of conventional disease-reducing therapy (chemotherapy, surgery, and irradiation), induction of antigen-specific immunity through vaccination and antigen-nonspecific immunomodulation (e.g., targeting of Treg and Th17 cells as well as NK cells) to enhance anticancer reactivity.