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Clinical-grade generation of peptide-stimulated CMV/EBV-specific T cells from G-CSF mobilized stem cell grafts

Journal of Translational Medicinevolume 16, Article number: 124 (2018) | Download Citation

Abstract

Background

A major complication after allogeneic hematopoietic stem cell transplantation (aSCT) is the reactivation of herpesviruses such as cytomegalovirus (CMV) and Epstein–Barr virus (EBV). Both viruses cause significant mortality and compromise quality of life after aSCT. Preventive transfer of virus-specific T cells can suppress reactivation by re-establishing functional antiviral immune responses in immunocompromised hosts.

Methods

We have developed a good manufacturing practice protocol to generate CMV/EBV-peptide-stimulated T cells from leukapheresis products of G-CSF mobilized and non-mobilized donors. Our procedure selectively expands virus-specific CD8+ und CD4+ T cells over 9 days using a generic pool of 34 CMV and EBV peptides that represent well-defined dominant T-cell epitopes with various HLA restrictions. For HLA class I, this set of peptides covers at least 80% of the European population.

Results

CMV/EBV-specific T cells were successfully expanded from leukapheresis material of both G-CSF mobilized and non-mobilized donors. The protocol allows administration shortly after stem cell transplantation (d30+), storage over liquid nitrogen for iterated applications, and protection of the stem cell donor by avoiding a second leukapheresis.

Conclusion

Our protocol allows for rapid and cost-efficient production of T cells for early transfusion after aSCT as a preventive approach. It is currently evaluated in a phase I/IIa clinical trial.

Background

Reactivation of cytomegalovirus (CMV) and Epstein–Barr virus (EBV) worsens outcomes of allogeneic stem cell transplantation (aSCT) and remains a major obstacle to its success [1]. Within the first 100 days after aSCT, 40–50% of patients reactivate CMV, and up to 40% of all patients reactivate EBV after aSCT as determined by virus-specific PCR of cells of the peripheral blood (PB). Approximately 95% of donors and patients are seropositive for EBV, and 40–70% for CMV [2]. Both CMV and EBV reactivation after aSCT are associated with increased mortality. Reactivation of EBV bears the risk of EBV-associated post-transplantation lymphoproliferative disease [3]. Reactivation of CMV can cause pneumonia with high mortality. Therefore both viruses require preemptive treatment upon reactivation in patients after aSCT [4].

Specific antiviral therapy is only available for the treatment of CMV. However, all drugs available (Ganciclovir, Foscarnet, Cidofovir, and others) display strong side effects including bone marrow and kidney failure. Furthermore, they frequently require inpatient treatment thereby compromising quality of life and most importantly do not solve the underlying problem of missing immunological control. For EBV, no approved specific therapeutic option exists. Off-label use of Rituximab, a B-cell depleting antibody, is increasing and seems to be effective [5,6,7]. However, Rituximab induces long lasting B-cell depletion resulting in frequent and obligatory transfusion of immunoglobulins. Similarly to the treatment of CMV, the fundamental problem of the lack of immunological control is not addressed with this therapy. As all antiviral therapies fail to boost the immune system, relapse of reactivation is frequent and repeated treatments are required, strongly contributing to the high costs of aSCT.

The rationale of strengthening specific T-cell immunity for both prevention and therapy of CMV and EBV reactivation therefore represents an intriguing therapeutic option. Several groups have shown that CMV- or EBV-specific T cells can be isolated or enriched from seropositive donors, and mediate viral control in aSCT patients after adoptive transfer [8,9,10,11,12,13,14]. Depending on the method of isolation, virus-specific T cells are only available in a minority of donor-patient pairs, their specificity is limited to single viral antigens or epitopes, or their preparation may be inconveniently long and laborious. Here, we describe a clinical grade protocol for manufacturing multi-epitope CMV/EBV-specific T cells suitable for application after aSCT. We use a generic set of peptides representing dominant CMV and EBV CD8+ and CD4+ T-cell epitopes from different viral antigens of each virus, presented by different HLA allotypes. Thus, this protocol is applicable in more than 80% of European donors, and has a high likelihood to enrich their dominant virus-specific T-cell populations. We applied this procedure to G-CSF mobilized stem cell grafts and non-mobilized apheresis products and show that it is equally effective in the relative expansion of CMV/EBV-specific T cells. As a result, CMV/EBV-specific T cells are available shortly after transplantation within 14 days (plus the time required for microbial safety monitoring) if G-CSF mobilized stem cells are used as a T-cell source, avoiding a second apheresis of the donor. The protocol is easily applicable within clean room facilities and can be modified according to preferences of the manufacturer. This manufacturing protocol is currently used in an ongoing phase I/IIa clinical trial for prevention of CMV/EBV-reactivation after aSCT (EudraCT 2012-004240-30).

Methods

Donor selection

Donor selection was based on a positive CMV and EBV serostatus and on at least one matching HLA class I allele for both peptide pools.

Cell culture

Collection of PBMC from G-CSF mobilized stem cell grafts were approved by the local ethics committee (Ref. No 4388). Only remaining cells from the tubing set and transfusion bag after transfusion of the stem cell graft were used. After transfusion of the stem cell graft, the line was disconnected from the patient and connection was sealed with a CombiStop tip. The transfusion bag and tubing set were flushed twice with 50 ml 0.9% NaCl solution through a three-way connection of the transfusion line. Leukapheresis products were obtained from non-mobilized volunteer donors and a small fraction was processed. On average, 1.3 × 109 ± 0.4 × 109 (Mean ± SD) CD45+ cells were cryopreserved as starting material for cell culture. For the clinical trial, autologous serum is obtained from the donors before apheresis using EVA bags (Maco Pharma International GmbH, Langen, Germany) for blood collection. For establishment, serum was collected by serum tubes with clotting activator (Sarstedt AG & Co GK, Nümbrecht, Germany). Serum was separated from clotted blood by centrifugation (three times 1800g, 10 min). PBMC from leukapheresis products were purified through Ficoll (GE Healthcare Europe GmbH, Freiburg, Germany) gradient centrifugation (800g, 20 °C, 20 min). Cells were washed twice with PBS, counted and cryopreserved at a concentration of 100 × 106/ml in a 20% HSA solution containing 10% DMSO.

For T-cell stimulation, cryopreserved cells were thawed and recovered overnight in serum-free CellGro DC Medium (CellGenix GmbH, Freiburg, Germany) at a concentration of 1–4 × 106/ml. After 18–24 h cells were harvested, counted and stimulated in two separate fractions with CMV and EBV peptide pools at a concentration of 1 µg/ml per peptide in standard Falcon tubes in 20 ml of prewarmed (37 °C) CellGro DC medium. After 2 h of incubation at 37 °C, remaining peptides were washed out. Peptides were purchased from JPT Peptides Technologies GmbH (Berlin, Germany) at a purity of ≥ 95% (see Table 3). Both cell fractions were united, washed with medium again, and transferred into a culture bag (MACS GMP Cell Differentiation Bag 500 ml, Miltenyi Biotec GmbH, Bergisch Gladbach, Germany) at a concentration of 2.5 × 106 cells/ml. Cells were cultured for 9 days at 37 °C in CellGro DC Medium with 50 IU/ml IL-2 (Aldesleukin, Novartis Pharma GmbH, Nürnberg, Germany), 1% (v/v) GlutaMAX™ (Gibco by Life Technologies GmbH, Darmstadt, Germany) and 1% (v/v) autologous serum (“complete medium”). On day 5 after peptide stimulation, complete medium (volume on day 0 multiplied by 1.5) was supplemented. On day 9, cells were harvested from the culture bag, analyzed and divided in appropriate doses. Cells were stored in the gas phase over liquid nitrogen until usage. The workflow is depicted in Fig. 1.

Fig. 1
figure1

Overview of the manufacturing process and quality controls

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Flow cytometric analysis

All antibodies were purchased from BD Biosciences (Heidelberg, Germany) unless otherwise specified.

For phenotypic analysis, cells were stained with anti-CD8 FITC (clone SK1), anti-CD25 PE (clone 2A3), anti-CD14 PerCP (clone MφP9), anti-CD56 APC (clone B159), anti-CD19 PE-Cy7 (clone SJ25C1), anti-CD4 APC-Cy7 (clone RPA-T4), anti-CD3 V450 (clone UCHT1), and anti-CD45 V500 (clone HI30). Gating included the exclusion of debris in a SSC vs FSC plot. Leukocytes were gated in a CD45 vs SSC dot plot as CD45+ cells. The CD45high/SSClow population was termed lymphocytes, and was clearly distinguished from monocytes and granulocytes. Within CD45high/SSClow cells, subsets were characterized by expression of CD3 (T cells), CD19 (B cells), and CD56 (negative for CD3) (NK cells). Monocytes were gated as CD14+ SSCintermediate cells. Cell number in whole blood was determined by FACS using fluorescent beads (Trucount™ Tubes, BD Biosciences, Heidelberg, Germany).

For analysis of CMV- and EBV-specific T cells, 1 × 106 PBMC were stained with peptide-loaded multimers (ProImmune Ltd., Oxford, United Kingdom) as indicated according to the manufacturer’s recommendation. Cells were stained in addition with anti-CCR7 FITC (clone 150503, R&D Systems), Fluorotag PE, anti-CD8 PerCP (clone SK1), anti-CD62L APC (clone DREG-56), anti-CD45RA PE-Cy7 (clone HI100), anti-CD4 APC-Cy7 (clone RPA-T4), and anti-CD3 V450 (clone UCHT1). Lymphocytes were gated in the SSC vs FSC dot plot. T cells were defined as CD3+/SSClow and further subdivided into CD4+ and CD8+ subsets. Pentamer-binding cells were determined as proportion of CD8+ T cells. Cells were analyzed subsequently after staining using a FACS Canto II (Becton–Dickinson, Heidelberg, Germany).

ELISpot assay

For ELISpot assays, cryopreserved T cells (day 9 of culture) and PBMC (day 0 of culture) were thawed for overnight recovery in RPMI1640 medium containing 10% human AB serum. At the same day, a Multiscreen plate (mixed cellulose ester membrane, MAHAS4510, Merck Millipore, Merck KGaA, Darmstadt, Germany) was coated with anti-IFN-γ antibody (clone NIB42, BD) in PBS (15 µg/ml, 50 µl/well). The plate was incubated for 12–18 h at 4 °C, then the antibody solution was removed, the plate was filled with medium containing 10% human AB serum, and kept for 2 h at 37 °C for blocking. PBMC served as APC and as background control. After blocking, PBMC alone, or PBMC and expanded T cells were plated in different T-cell concentrations and stimulated with CMV peptide pool, EBV peptide pool, or human gp100 control peptide at a concentration of 0.5 µg/ml. Plates were incubated for 19–24 h at 37 °C. After incubation, plates were washed six times with PBS + 0.05% Tween 20 (Sigma-Aldrich Chemie GmbH, Munich, Germany). Then, anti-IFN-γ-biotin antibody (clone 4S.B3, BD) in PBS (50 µl/well, c = 0.3 µg/ml) was added and plates were incubated overnight at 4 °C. Plates were washed four times with PBS, and streptavidin alkaline phosphatase (Bio-Rad Laboratories GmbH, Munich, Germany) was added in a dilution of 1:1600 in PBS. Plates were incubated for 2 h at room temperature and washed with PBS. Colorimetric AP substrate was added and incubated at room temperature in the dark for 10–30 min, depending on assay-specific spot development. Spots were quantified by a Bioreader 3000 System (Bio-Rad).

Cell counting

For microscopic cell counting, trypan blue-stained cells were counted in a Neubauer chamber. Cells were diluted in PBS depending on cell concentration to obtain a concentration of 0.5–1.0 × 106 cells/ml. Trypan blue was used in a concentration of 0.4%.

Storage in the gas phase over liquid nitrogen

Cells were cryopreserved in pre-cooled cryopreservation medium of 90% HSA-solution (Serum Albumin 20% Behring, CSL Behring GmbH, Hattersheim am Main, Germany) and 10% DMSO (100%, pharmacy of the University Hospital of Erlangen, Germany).

Analysis of data

Data were analyzed and graphically represented using GraphPad Prism V and Microsoft Excel 2010. Flow cytometry data were analyzed either by FACS Diva (BD), Kaluza (Beckman Coulter), or FlowJo (FlowJo LLC, Oregon, USA). For statistical analysis, the Mann–Whitney U test was used.

Sterility testing

Microbial contamination of products of mobilized donors was monitored by aerobic and anaerobic culture (BacTec sytem), and by eubacterial PCR. For the clinical trial, microbial control consists of monitoring of microbial growth according to Ph. Eur. 2.6.27, mycoplasma PCR according to Ph. Eur. 2.6.7, and endotoxin detection according to Ph. Eur. 2.6.14, performed by a subcontracted laboratory (Eurofins BioPharma Product Testing Munich GmbH, Planegg/Munich, Germany).

Results

We established a GMP-compliant process for manufacturing of CMV/EBV-specific T cells by peptide stimulation of leukapheresis products. The workflow is outlined in Fig. 1. Details of manufacturing are provided in Materials and Methods. We investigated this process with a particular focus on stimulation of T cells from leukapheresis products from G-CSF mobilized donors to ensure availability of the product as early as possible after transplant and, for donor safety, to avoid a second apheresis procedure.

Cellular composition of G-CSF mobilized and non-mobilized peripheral blood preparations

Standardized T-cell expansion protocols usually rely on leukapheresis products from untreated healthy volunteer donors. To be able to generate donor-derived virus-specific T cells for preventative use early after aSCT, we investigated the expansion of CMV- and EBV-specific T cells from aliquots of G-CSF mobilized hematopoietic stem cell grafts as a T-cell source. As shown in Fig. 2A and Table 1, analysis of absolute cell numbers in the peripheral blood before (b) and after (a) G-CSF mobilization revealed a strong increase of monocytes and granulocytes whereas absolute numbers of lymphocytes were moderately increased. Accordingly, the percentage of lymphocytes among leukocytes in the peripheral blood decreased after administration of G-CSF due to the massive increase in granulocytes (Fig. 2B, Table 1). Likewise, absolute numbers of T cells increased whereas their proportion decreased. In line with our findings, Rodriguez-Cortes et al. describe an extensive increase of leukocytes after G-CSF mobilization, including a moderate increase of lymphocytes [15]. Our observations are also consistent with data from Chevallier et al. [16] and Sica et al. [17].

Fig. 2
figure2

Influence of G-CSF mobilization on cell composition. Peripheral blood of donors before and after mobilization, and leukapheresis products from G-CSF mobilized donors after Ficoll and cryopreservation were analyzed. A Flow cytometry was used to determine absolute cell counts of monocytes (mono.), granulocytes (gran.), lymphocytes (lymph.), and T cells per µl of peripheral blood before (“b”) and after (“a”) G-CSF mobilization in stem-cell donors, n = 6. B Relative subset composition of leukocytes in donors before and after G-CSF mobilization (n = 6). C Absolute cell count of CD45+ and CD3+ cells in stem cell grafts. The mean value ± SD of 15 preparations from 15 donors is shown. D Cell composition of leukocytes before and after mobilization in peripheral blood and after cryopreservation at day 0 before peptide stimulation. The proportion of T cells, B cells, NK cells, monocytes, and remaining unassigned leukocytes is shown at the three different time points, n = 5. A, B Statistical analysis was performed using the Mann–Whitney U test

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Table 1 Cellular composition of peripheral blood before and after mobilization
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To obtain the desired number of 3.0–5.0 × 106 T cells per dose (5.0 × 104/kg body weight) and a sufficient number of cells for quality control after manufacturing, 1.3 × 109 ± 0.4 × 109 (mean ± SD) CD45+ cells were cryopreserved for the use as starting material for the T-cell stimulation process, both for mobilized and non-mobilized donors. On average, grafts from unrelated or related G-CSF mobilized donors in our institution contain 63.0 × 109 ± 20.7 × 109 CD45+ cells and 20.1 × 109 ± 7.8 × 109 CD3+ T cells (n = 15, Fig. 2C). Therefore, on average, 3.2% of the graft would be required to obtain 2 × 109 CD45+ cells as starting material. Our manufacturing process involves cryopreservation of the apheresis product after Ficoll density gradient centrifugation. This step was introduced to generate flexibility in manufacturing especially with regard to clean room availability but also includes the advantage of an additional strong reduction of the number of granulocytes, since these may have a negative impact on later T-cell expansion. When the relative cellular composition of peripheral blood cells before and after G-CSF mobilization was compared to the apheresis product after cryopreservation, thawing and overnight recovery (d0), the fraction of granulocytes (and their immature precursors) was strongly reduced in the day 0 product, monocytes were increased, and the proportions of T and B cells became comparable to peripheral blood before G-CSF mobilization. Cellular composition on day 0 displayed a preponderance of monocytes and T cells. The percentage of B cells and NK cells declined in the PB after mobilization (Fig. 2D). Cell recovery after thawing and recovery was 227 × 106 ± 160 × 106 cells for mobilized donors, 690 × 106  ± 221 × 106 for non-mobilized donors (Mean ± SD).

T-cell expansion after peptide stimulation and cultivation for 9 days

For expansion of CMV- and EBV-specific T cells we utilized G-CSF mobilized (n = 8) and, for comparison, non-mobilized (n = 8) apheresis products. Our primary intention was to establish the process for G-CSF mobilized stem cell products in order to avoid a second donation and to obtain T cells prior to transplantation. For stimulation of T cells, we used two peptide pools, one for each virus, with a total of 34 peptides which represent well-characterized CD8+ and CD4+ T-cell epitopes from various proteins (latent and lytic) of CMV and EBV (Table 3). HLA restrictions of the peptides cover approximately 80% of the Central European population with at least one HLA class I match [18]. For HLA class I, we only chose peptides that elicit responses in a majority of virus carriers with the relevant HLA allotype [19,20,21]. Loading of PBMC with peptides was performed separately for the EBV and the CMV pool; for cultivation after loading, the two portions were joined again. As shown in Fig. 3a, apheresis products from G-CSF mobilized donors (d0) contained more than twice as many monocytes and about half as many T cells compared to non-mobilized donors. This difference disappeared after peptide stimulation and 9 days of culture (d9). Peptide stimulation increased the proportion of CD3+ total T cells and CD8+ T cells in all cultures (Fig. 3b, c). In G-CSF mobilized apheresis products, mean relative T-cell enrichment was 2.5-fold (from 31.6 ± 10.5% at day 0 to 79.2 ± 12.2% at day 9, n = 8) compared to 1.5 fold (from 54.0 ± 13.6% at day 0 to 82.1 ± 12.8%, at day 9, n = 8) in non-mobilized donors (Fig. 3a, b). As shown in Fig. 3c, T-cell enrichment was mainly due to expansion of CD8+ T cells in both groups. The percentage of CD4+ T cells was variably altered in cultures from G-CSF mobilized products, and decreased in cultures from non-mobilized donors. Absolute numbers of CD3+ total T cells and CD8+ T cells increased or decreased during cultivation (Fig. 3d). Taken together, peptide stimulation of G-CSF mobilized and non-mobilized apheresis products resulted in relative T-cell expansion, dominated by CD8+ T cells. Other cell types such as monocytes, B cells, NK cells, and other cells decreased during the culture period.

Fig. 3
figure3

Comparison of cell composition on day 0 before peptide stimulation and day 9 at the end of expansion. a Relative composition of leukocytes at day 0 (d0) and day 9 (d9) after peptide stimulation from G-CSF mobilized (upper panel, n = 8) and non-mobilized donors (lower panel, n = 8). b Proportion of CD3+ T cells in total cells. c Proportion of CD8+ and CD4+ T cells within the CD3+ population. d Absolute counts of CD3+ T cells and of CD8+ CD3+ T cells. e Expression of T-cell differentiation markers on day 0 and day 9 of culture from one exemplary donor; cm, central memory; eff/em, effector and effector memory. f Cumulative analysis of T-cell differentiation in cultures from 7 donors of each type (G-CSF mobilized and non-mobilized donors)

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Approximately 94% of all cells collected by apheresis from G-CSF mobilized donors were lost during cryopreservation, peptide stimulation and culture until harvest of cells on day 9 (see Additional file 1: Figure S1). This loss of cells was mainly due to the depletion of granulocytes, but also of monocytes, B cells, NK cells, and T cells of supposedly irrelevant specificity.

Reduction of the naïve compartment after expansion of virus-specific T cells

After peptide stimulation and cultivation for 9 days, composition of T-cell subsets substantially changed with respect to their status of differentiation. As shown by flow cytometric analysis in Fig. 3e exemplarily for a representative donor, the percentage of CD3+ T cells increased to 95%. Further analysis of T-cell subsets revealed an increase of effector (eff) and effector memory (em) T cells (CD45RA±, CCR7−), whereas naïve T cells (CD45RA+, CCR7+) and central memory (cm) T cells (CD45RA−, CCR7+) were reduced. Figure 3f shows the compilation of data from different G-CSF mobilized and non-mobilized donors (n = 7 each group) on day 0 before peptide stimulation and on day 9 after expansion. On average, eff/em T cells increased from 53.1 ± 16.3% to 88.8 ± 11.3% in G-CSF mobilized donors and from 36.6 ± 9.4% to 75.3 ± 12.8% in non-mobilized donors. Of note, in the day 9 products from G-CSF mobilized donors we found fewer naïve T cells (7.2 ± 9.2%) compared to products derived from non-mobilized donors (14.8 ± 7.9%). In addition, whereas the central memory T-cell compartment was reduced on average from 12.8 ± 6.5 to 4.0 ± 4.0% in G-CSF mobilized PBMC, numbers of central memory T cells from non-mobilized donors were slightly higher before and after stimulation (22.4 ± 6.7% reduced to 10.0 ± 5.6%). Thus, T-cell cultures from both mobilized and non-mobilized donors were characterized by strong expansion of CD8+ T cells with effector or effector memory phenotype.

Specificity of the T-cell product

Expansion of virus-specific T cells after 9 days was determined by flow cytometry using HLA-peptide multimers appropriate for each donor’s HLA class I alleles and according to the peptide pool used for stimulation (Tables 2, 3). At the time of establishment of the protocol, not all HLA-peptide multimers were available. Table 2 shows which pentamers were used for analysis of virus-specific T cells for each donor. As shown in Fig. 4a, an increase in the relative number (cumulative percentage of multimer-binding cells) of virus-specific T cells could be observed in both G-CSF mobilized and non-mobilized donors (expansion of proportion varying from 0.6- to 94-fold for CMV and 0.4- to 496-fold for EBV, n = 16). Overall, both CMV-specific and EBV-specific CD8+ T cells were enriched in 15 of 16 cultures. Figure 4b illustrates the enrichment of antigen-specific CD8+ T cells of one representative G-CSF mobilized donor as measured by HLA-peptide multimer staining; the peptide-stimulated culture from this donor contained 20% of T cells specific for the VTE epitope from CMV pp50, and 43% of T cells specific for the RAK epitope of EBV BZLF1. Absolute expansion of virus-specific T cells was observed for each virus in each culture (Fig. 4c).

Table 2 HLA alleles of mobilized and non-mobilized donors
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Table 3 CMV- and EBV- derived peptides used for stimulation of T cells
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Fig. 4
figure4

Analysis of CMV- and EBV-specific T cells before and after peptide stimulation. a Proportion of CMV-specific (CMV epitopes, left row) and of EBV-specific T cells (EBV epitopes, right row) on day 9 compared to day 0 as determined by HLA/peptide multimer staining (left panel: mobilized donors, n = 8; right panel: non-mobilized donors, n = 8). The cumulative proportions of T cells obtained from stainings with each applicable (HLA-compatible) multimer is shown for each donor. b Flow cytometric analysis for HLA/peptide multimer binding cells (% of CD8+ T cells) of one representative donor. c Comparision of absolute cell count of CMV-specific (CMV epitopes, left row) and EBV-specific T cells (EBV epitopes, right row) on day 9 compared to day 0 as determined by HLA/peptide multimer staining (left panel: mobilized donors, n = 8; right panel: non-mobilized donors, n = 8). a, c D01 to D12 designate the donors, as listed in Table 2

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CMV/EBV peptide-specific activation and cytokine secretion

Activation of T cells was determined by flow cytometric analysis of the expression of the IL-2Rα chain (CD25). As shown in Fig. 5a, peptide stimulation resulted in activation and significant upregulation of CD25 expression on CD8+ T cells from G-CSF mobilized (n = 7, p = 0.0021) and non-mobilized donors (n = 7, p = 0.0006), which is in line with results showing T-cell expansion in Fig. 3c. Activation was consistent but less intense (up to 31.3%) on CD4+ T cells from G-CSF mobilized (p = 0.0105), but more variable on CD4+ T cells from non-mobilized donors (p = 0.2593). Of note, we observed a significantly higher CD25 expression on non-mobilized CD4+ T cells on day 0 as compared to CD4+ T cells of G-CSF mobilized donors (p = 0.0105). Restimulation of expanded T cells from day 9 with the same peptide pools used for initial stimulation resulted in specific secretion of IFN-γ as determined by ELISpot assay (Fig. 5b). This analysis showed that the proportions of CMV- and EBV-specific, cytokine-secreting T cells were, on average, elevated between one and two orders of magnitude during peptide-driven expansion, both in mobilized and non-mobilized donors. Of note, the cumulative proportion of spot-forming CMV- and EBV-specific T cells was, on average, stronger in mobilized (mean: 4380 SFC/50.000 PBMC) than in non-mobilized donors (mean: 801 SFC/50.000 PBMC).

Fig. 5
figure5

Activation and cytokine production of CMV- and EBV-specific T cells. a CD25 expression as activation marker is shown on day 0 and day 9 for CD4+ and CD8+ T cells of G-CSF mobilized (left panel) and non-mobilized (right panel) donors, analyzed by flow cytometry. b Secretion of the effector cytokine IFN-γ was analyzed by ELISpot assay after restimulation with CMV or EBV peptide pool. Shown is the number of spot-forming cells (SFC)/50,000 PBMC as mean ± SD from 5 independent donors. As a negative control, the irrelevant gp100 peptide ITDQVPFSV was used

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Cost of manufacturing

The overall cost of the therapeutic T-cell product is approximately €11,400.- per manufacturing process. Materials costs account for 30% of the overall cost (approximately €3400.-) and include peptides and cytokines used for stimulation. Critical components are listed in Table 4. Approximately 40% of the total costs are caused by quality assessment. This includes sterility testing of the final product and during manufacturing, testing for mycoplasma and endotoxin, as well as sterility testing of critical materials such as peptide batches. The microbiological testing is outsourced to a subcontracted laboratory. Quality control costs also include cytogenetic analysis of the product as recommended by the German authorities (Paul-Ehrlich-Institute, Langen). Other costs (20%, €2100.-) include certified shipping, microbial monitoring throughout the manufacturing process, and cleaning of the GMP clean room facilities. Costs for staff (qualified person, head of quality control, head of production, technicians) were calculated on an hourly basis and amount to 10% of the overall costs.

Table 4 Critical materials
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Discussion

In this study we demonstrate that CMV- and EBV-specific T cells can be successfully enriched from CMV- and EBV-seropositive G-CSF mobilized donors by peptide stimulation in a GMP-compliant process, and specific T cells can be quickly obtained to allow for preventive application in patients after aSCT. Donor lymphocytes are stimulated with pools of defined viral peptides that represent dominant T-cell epitopes from various viral antigens with a range of HLA restrictions. A small portion of the G-CSF mobilized stem cell graft is sufficient as a source of T cells, eliminating the need for a second apheresis of the donor. Peptide stimulation resulted in expansion of T cells and increase of specific T cells, while reducing the proportion of naive T cells.

Several strategies to generate or isolate CMV- and/or EBV- specific T cells for adoptive transfer are currently available. Direct isolation of specific T cells without any period of cultivation generally requires the use of recombinant HLA/peptide multimers and magnetic or flow-cytometric sorting [22, 23]. This method is elegant and allows for high cell purity, but its routine clinical application is challenging since it cannot be used for all HLAs and epitopes, and a continuous stock of various manufacturing-grade multimer reagents and a separation device are needed. Antigen stimulation and subsequent isolation based on T-cell reactivity, e.g. IFN-γ secretion or CD137 up-regulation [24,25,26,27,28] is more versatile in terms of the T-cell specificities that can be included and can be performed within one or 2 days, but T-cell yield may be low and thus characterization of the product is often limited. Therefore, simplified approaches that take advantage of antigen-specific expansion of T cells in vitro by peptide stimulation have again attracted interest and have been explored in the clinical setting with promising results [29, 30]. One protocol [31] uses a general procedure similar to ours, but employs overlapping peptide pools covering 12 antigens from five viruses including EBV and CMV, employing approximately 2000 peptides in total, which is certainly a strong advance toward optimizing the breadth of the achievable response. In designing the present protocol, in which we used a total of 34 well-characterized peptides, 10 HLA class-I-restricted and 7 class-II-restricted peptides from each of the two viruses, we have considered it advantageous to strike a middle ground between simplicity and complexity, based on the following considerations. Our exclusive use of defined peptides with known HLA class I and II restrictions will make it possible to use HLA class I multimers (and potentially class II multimers) for a comprehensive quantitative analysis of the specific T cells in the product, and to track them in patients. Since we avoid the use of thousands of potentially irrelevant peptides, we decrease the probability that T cells with unwanted specificities that accidentally cross-react with some of these peptides will be activated and expanded. Moreover, it is very likely that our specificities of choice will be more efficiently activated if the number of potentially competing peptides in the loading reaction is limited. Still, it is important to include peptides from a range of antigens from different phases of viral replication. For CMV, it is far from clear which T-cell antigens provide the best protection from viral reactivation [28, 32, 33], and the situation for EBV is complex as well. Our choice of a limited number of epitopes and HLA restrictions will nevertheless ensure that a majority of donor/patient pairs can be covered. The idea that the use of a full-length viral antigen (or antigen-covering peptide library) is HLA-independent may be illusory, since a given viral protein will contain only epitopes presented by a finite, sometimes rather limited, number of HLA allotypes.

The presence of some remaining naïve T cells of unknown specificity in our T-cell cultures may be a safety issue in patients after aSCT, since alloreactive T cells are mainly found in the naïve compartment [34]. However, adoptive transfer of peptide-stimulated virus-specific T cells with isolation [25, 28] or without isolation [29, 30] was proven safe so far. Immunodominant peptides with known allogeneic cross-reactivity such as the EBV-derived FLR [35] were deliberately excluded from the peptide mix to minimize the risk of acute GvHD after adoptive transfer.

Furthermore, we anticipate using our T-cell product for prevention of viral reactivation at an early stage after transplantation, when most patients are still receiving calcineurin inhibitors such as cyclosporine A for acute GvHD prophylaxis. There is evidence that activated T cells become cyclosporine A resistant and therefore can exert their function in vivo despite ongoing immunosuppression [36].

A recent study described that the functionality of antiviral T cells from G-CSF mobilized stem cell grafts or after G-CSF treatment in vitro is reduced [37]. This is consistent with our observation of reduced cytokine secretion in early stages of the T-cell culture (data not shown). Furthermore, Rutella et al. described that serum of G-CSF treated healthy donors reduced lymphocyte proliferation but this effect was overcome by addition of IL-2 [38]. However, after completion of our stimulation protocol, our data show no evidence for impairment of virus-specific T cells due to the use of material from G-CSF mobilized donors. Nawa et al. [39] described a reduced stimulatory potential of monocytes from G-CSF mobilized donors in mixed lymphocyte reactions, potentially indicating reduced potential of such monocytes to stimulate T-cell responses; however, they described that T-cell function was not directly altered by G-CSF mobilization. Others described that the cell count of dendritic cells per µl PB is increased after mobilization [15, 16] bearing the advantage that these dendritic cells as APCs may contribute to effective expansion of antigen-specific T cells in protocols such as ours. During our cultivation process, however, G-CSF is absent, and we observed that 9-day cultures from G-CSF mobilized donors resulted in equal relative expansion of virus-specific T cells in comparison to cultures from non-mobilized donors, and T-cell function, as measured in ELISpot, was even better for mobilized donors. In line with our results, Samuel et al. showed that a successful expansion of CMV-reactive T cells from G-CSF mobilized donors is possible [40]. In addition, Chevallier et al. reported no significant differences in the composition of T-cell subsets of peripheral blood of G-CSF mobilized and non-mobilized donors [16]. The reduction of naïve T cells in the products of both donor types is encouraging, as the naive T-cell compartment is considered the main source of alloreactive T cells [34].

Conclusions

One major advantage of this manufacturing protocol is its cost efficiency. First, in comparison to current standard therapies of CMV or EBV reactivation (ganciclovir, rituximab, etc.), specific T-cell therapy in general is a competitive option in terms of costs. Second, among possible protocols to prepare specific T cells, the present one is particularly economic, since it does not depend on expensive proprietary technology for specific cell cultivation or isolation, but uses only general-purpose machinery that has multiple uses in transfusion medicine departments. Multiple doses can be produced in one manufacturing run, and can be stored for repeated application if necessary. Our protocol is versatile, and will allow for including peptides from additional viral or other microbial pathogens without any changes in the workflow.

We are currently conducting a phase I/IIa clinical trial exploring a preventive strategy using this T-cell product in patients after aSCT (Eudract 2012-004240-30). Peptide-stimulated T cells are stored over liquid nitrogen and administered at a dose of 5 × 104/kg CD3+ cells/kg body weight on days 30, 60, and 90 after aSCT. Aside from safety we aim at demonstrating efficacy of this T-cell product. In a more long-term perspective, we are confident that simplified protocols to prepare CMV/EBV-specific T-cells for adoptive therapy after aSCT will help make this therapy more widely available, especially for prophylactic intervention to prevent reactivation and disease caused by these widespread viruses. We believe this may decrease virus reactivation rates, thereby reducing hospitalization time and need for medication prone to side effects, and improving quality of life for patients after aSCT.

Abbreviations

APC:

antigen-presenting cell

aSCT:

allogeneic stem cell transplantation

cm:

central memory

CMV:

cytomegalovirus

DLI:

donor lymphocyte infusion

DMSO:

dimethyl sulfoxide

EBV:

Epstein–Barr virus

G-CSF:

granulocyte colony-stimulating factor

GMP:

good manufacturing practice

GvHD:

graft-versus-host disease

HLA:

human leukocyte antigen

HSA:

human serum albumin

IFN:

interferon

IL:

interleukin

NK:

natural killer

PB:

peripheral blood

eff:

effector

em:

effector memory

PBMC:

peripheral blood mononuclear cells

PBS:

phosphate-buffered saline

SFC:

spot-forming cells

References

  1. 1.

    Ljungman P, Brand R, Einsele H, Frassoni F, Niederwieser D, Cordonnier C. Donor CMV serologic status and outcome of CMV-seropositive recipients after unrelated donor stem cell transplantation: an EBMT megafile analysis. Blood. 2003;102:4255–60.

  2. 2.

    Lamberson HV, Dock NL. Prevention of transfusion-transmitted cytomegalovirus infection. Transfusion. 1992;32:196–8.

  3. 3.

    Gottschalk S, Rooney CM, Heslop HE. Post-transplant lymphoproliferative disorders. Annu Rev Med. 2005;56:29–44.

  4. 4.

    Boeckh M, Leisenring W, Riddell SR, Bowden RA, Huang ML, Myerson D, Stevens-Ayers T, Flowers ME, Cunningham T, Corey L. Late cytomegalovirus disease and mortality in recipients of allogeneic hematopoietic stem cell transplants: importance of viral load and T-cell immunity. Blood. 2003;101:407–14.

  5. 5.

    Milpied N, Vasseur B, Parquet N, Garnier JL, Antoine C, Quartier P, Carret AS, Bouscary D, Faye A, Bourbigot B, et al. Humanized anti-CD20 monoclonal antibody (Rituximab) in post transplant B-lymphoproliferative disorder: a retrospective analysis on 32 patients. Ann Oncol. 2000;11(Suppl 1):113–6.

  6. 6.

    van Esser JW, Niesters HG, van der Holt B, Meijer E, Osterhaus AD, Gratama JW, Verdonck LF, Lowenberg B, Cornelissen JJ. Prevention of Epstein–Barr virus-lymphoproliferative disease by molecular monitoring and preemptive rituximab in high-risk patients after allogeneic stem cell transplantation. Blood. 2002;99:4364–9.

  7. 7.

    Svoboda J, Kotloff R, Tsai DE. Management of patients with post-transplant lymphoproliferative disorder: the role of rituximab. Transpl Int. 2006;19:259–69.

  8. 8.

    Riddell SR, Watanabe KS, Goodrich JM, Li CR, Agha ME, Greenberg PD. Restoration of viral immunity in immunodeficient humans by the adoptive transfer of T cell clones. Science. 1992;257:238–41.

  9. 9.

    Rooney CM, Smith CA, Ng CY, Loftin S, Li C, Krance RA, Brenner MK, Heslop HE. Use of gene-modified virus-specific T lymphocytes to control Epstein–Barr-virus-related lymphoproliferation. Lancet. 1995;345:9–13.

  10. 10.

    Leen AM, Christin A, Myers GD, Liu H, Cruz CR, Hanley PJ, Kennedy-Nasser AA, Leung KS, Gee AP, Krance RA, et al. Cytotoxic T lymphocyte therapy with donor T cells prevents and treats adenovirus and Epstein–Barr virus infections after haploidentical and matched unrelated stem cell transplantation. Blood. 2009;114:4283–92.

  11. 11.

    Heslop HE, Bollard CM, Gottschalk S, Kuehnle I, Huls MH, Gee AP, Brenner MK, Rooney CM. Immune therapy for EBV infections after hemopoietic stem-cell transplant. Cytotherapy. 2002;4:433–4.

  12. 12.

    Heslop HE, Slobod KS, Pule MA, Hale GA, Rousseau A, Smith CA, Bollard CM, Liu H, Wu MF, Rochester RJ, et al. Long-term outcome of EBV-specific T-cell infusions to prevent or treat EBV-related lymphoproliferative disease in transplant recipients. Blood. 2010;115:925–35.

  13. 13.

    Mackinnon S, Thomson K, Verfuerth S, Peggs K, Lowdell M. Adoptive cellular therapy for cytomegalovirus infection following allogeneic stem cell transplantation using virus-specific T cells. Blood Cells Mol Dis. 2008;40:63–7.

  14. 14.

    Peggs KS. Adoptive T cell immunotherapy for cytomegalovirus. Expert Opin Biol Ther. 2009;9:725–36.

  15. 15.

    Rodriguez-Cortes O, Vela-Ojeda J, Lopez-Santiago R, Montiel-Cervantes L, Reyes-Maldonado E, Estrada-Garcia I, Moreno-Lafont MC. Granulocyte colony-stimulating factor produces a decrease in IFNgamma and increase in IL-4 when administrated to healthy donors. J Clin Apher. 2010;25:181–7.

  16. 16.

    Chevallier P, Robillard N, Illiaquer M, Esbelin J, Mohty M, Bodin-Bressollette C, Guillaume T, Stocco V, Auffray F, Derenne S, et al. Characterization of various blood and graft sources: a prospective series. Transfusion. 2013;53:2020–6.

  17. 17.

    Sica S, Rutella S, Di Mario A, Salutari P, Rumi C, Ortu la Barbera E, Etuk B, Menichella G, D’Onofrio G, Leone G. rhG-CSF in healthy donors: mobilization of peripheral hemopoietic progenitors and effect on peripheral blood leukocytes. J Hematother. 1996;5:391–7.

  18. 18.

    Schmidt AH, Baier D, Solloch UV, Stahr A, Cereb N, Wassmuth R, Ehninger G, Rutt C. Estimation of high-resolution HLA-A, -B, -C, -DRB1 allele and haplotype frequencies based on 8862 German stem cell donors and implications for strategic donor registry planning. Hum Immunol. 2009;70:895–902.

  19. 19.

    Khan N. The immunological burden of human cytomegalovirus infection. Arch Immunol Ther Exp (Warsz). 2007;55:299–308.

  20. 20.

    Hislop AD, Taylor GS, Sauce D, Rickinson AB. Cellular responses to viral infection in humans: lessons from Epstein–Barr virus. Annu Rev Immunol. 2007;25:587–617.

  21. 21.

    Ameres S, Mautner J, Schlott F, Neuenhahn M, Busch DH, Plachter B, Moosmann A. Presentation of an immunodominant immediate-early CD8+ T cell epitope resists human cytomegalovirus immunoevasion. PLoS Pathog. 2013;9:e1003383.

  22. 22.

    Cobbold M, Khan N, Pourgheysari B, Tauro S, McDonald D, Osman H, Assenmacher M, Billingham L, Steward C, Crawley C, et al. Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA-peptide tetramers. J Exp Med. 2005;202:379–86.

  23. 23.

    Schmitt A, Tonn T, Busch DH, Grigoleit GU, Einsele H, Odendahl M, Germeroth L, Ringhoffer M, Ringhoffer S, Wiesneth M, et al. Adoptive transfer and selective reconstitution of streptamer-selected cytomegalovirus-specific CD8+ T cells leads to virus clearance in patients after allogeneic peripheral blood stem cell transplantation. Transfusion. 2011;51:591–9.

  24. 24.

    Zandvliet ML, van Liempt E, Jedema I, Kruithof S, Kester MG, Guchelaar HJ, Falkenburg JH, Meij P. Simultaneous isolation of CD8(+) and CD4(+) T cells specific for multiple viruses for broad antiviral immune reconstitution after allogeneic stem cell transplantation. J Immunother. 2011;34:307–19.

  25. 25.

    Moosmann A, Bigalke I, Tischer J, Schirrmann L, Kasten J, Tippmer S, Leeping M, Prevalsek D, Jaeger G, Ledderose G, et al. Effective and long-term control of EBV PTLD after transfer of peptide-selected T cells. Blood. 2010;115:2960–70.

  26. 26.

    Peggs KS, Thomson K, Samuel E, Dyer G, Armoogum J, Chakraverty R, Pang K, Mackinnon S, Lowdell MW. Directly selected cytomegalovirus-reactive donor T cells confer rapid and safe systemic reconstitution of virus-specific immunity following stem cell transplantation. Clin Infect Dis. 2011;52:49–57.

  27. 27.

    Icheva V, Kayser S, Wolff D, Tuve S, Kyzirakos C, Bethge W, Greil J, Albert MH, Schwinger W, Nathrath M, et al. Adoptive transfer of Epstein–Barr virus (EBV) nuclear antigen 1-specific t cells as treatment for EBV reactivation and lymphoproliferative disorders after allogeneic stem-cell transplantation. J Clin Oncol. 2013;31:39–48.

  28. 28.

    Feuchtinger T, Opherk K, Bethge WA, Topp MS, Schuster FR, Weissinger EM, Mohty M, Or R, Maschan M, Schumm M, et al. Adoptive transfer of pp65-specific T cells for the treatment of chemorefractory cytomegalovirus disease or reactivation after haploidentical and matched unrelated stem cell transplantation. Blood. 2010;116:4360–7.

  29. 29.

    Gerdemann U, Katari UL, Papadopoulou A, Keirnan JM, Craddock JA, Liu H, Martinez CA, Kennedy-Nasser A, Leung KS, Gottschalk SM, et al. Safety and clinical efficacy of rapidly-generated trivirus-directed T cells as treatment for adenovirus, EBV, and CMV infections after allogeneic hematopoietic stem cell transplant. Mol Ther. 2013;21:2113–21.

  30. 30.

    Papadopoulou A, Gerdemann U, Katari UL, Tzannou I, Liu H, Martinez C, Leung K, Carrum G, Gee AP, Vera JF, et al. Activity of broad-spectrum T cells as treatment for AdV, EBV, CMV, BKV, and HHV6 infections after HSCT. Sci Transl Med. 2014;6:242ra283.

  31. 31.

    Papadopoulou A, Krance RA, Allen CE, Lee D, Rooney CM, Brenner MK, Leen AM, Heslop HE. Systemic inflammatory response syndrome after administration of unmodified T lymphocytes. Mol Ther. 2014;22:1134–8.

  32. 32.

    Malouli D, Hansen SG, Nakayasu ES, Marshall EE, Hughes CM, Ventura AB, Gilbride RM, Lewis MS, Xu G, Kreklywich C, et al. Cytomegalovirus pp65 limits dissemination but is dispensable for persistence. J Clin Invest. 2014;124:1928–44.

  33. 33.

    Bunde T, Kirchner A, Hoffmeister B, Habedank D, Hetzer R, Cherepnev G, Proesch S, Reinke P, Volk HD, Lehmkuhl H, Kern F. Protection from cytomegalovirus after transplantation is correlated with immediate early 1-specific CD8 T cells. J Exp Med. 2005;201:1031–6.

  34. 34.

    Distler E, Bloetz A, Albrecht J, Asdufan S, Hohberger A, Frey M, Schnurer E, Thomas S, Theobald M, Hartwig UF, Herr W. Alloreactive and leukemia-reactive T cells are preferentially derived from naive precursors in healthy donors: implications for immunotherapy with memory T cells. Haematologica. 2011;96:1024–32.

  35. 35.

    Burrows SR, Khanna R, Burrows JM, Moss DJ. An alloresponse in humans is dominated by cytotoxic T lymphocytes (CTL) cross-reactive with a single Epstein–Barr virus CTL epitope: implications for graft-versus-host disease. J Exp Med. 1994;179:1155–61.

  36. 36.

    Geginat J, Clissi B, Moro M, Dellabona P, Bender JR, Pardi R. CD28 and LFA-1 contribute to cyclosporin A-resistant T cell growth by stabilizing the IL-2 mRNA through distinct signaling pathways. Eur J Immunol. 2000;30:1136–44.

  37. 37.

    Bunse CE, Borchers S, Varanasi PR, Tischer S, Figueiredo C, Immenschuh S, Kalinke U, Kohl U, Goudeva L, Maecker-Kolhoff B, et al. Impaired functionality of antiviral T cells in G-CSF mobilized stem cell donors: implications for the selection of CTL donor. PLoS ONE. 2013;8:e77925.

  38. 38.

    Rutella S, Rumi C, Lucia MB, Sica S, Cauda R, Leone G. Serum of healthy donors receiving granulocyte colony-stimulating factor induces T cell unresponsiveness. Exp Hematol. 1998;26:1024–33.

  39. 39.

    Nawa Y, Teshima T, Sunami K, Hiramatsu Y, Maeda Y, Yano T, Shinagawa K, Ishimaru F, Omoto E, Harada M. G-CSF reduces IFN-gamma and IL-4 production by T cells after allogeneic stimulation by indirectly modulating monocyte function. Bone Marrow Transplant. 2000;25:1035–40.

  40. 40.

    Samuel ER, Newton K, Mackinnon S, Lowdell MW. Successful isolation and expansion of CMV-reactive T cells from G-CSF mobilized donors that retain a strong cytotoxic effector function. Br J Haematol. 2013;160:87–100.

  41. 41.

    Elkington R, Walker S, Crough T, Menzies M, Tellam J, Bharadwaj M, Khanna R. Ex vivo profiling of CD8+-T-cell responses to human cytomegalovirus reveals broad and multispecific reactivities in healthy virus carriers. J Virol. 2003;77:5226–40.

  42. 42.

    Longmate J, York J, La Rosa C, Krishnan R, Zhang M, Senitzer D, Diamond DJ. Population coverage by HLA class-I restricted cytotoxic T-lymphocyte epitopes. Immunogenetics. 2001;52:165–73.

  43. 43.

    Diamond DJ, York J, Sun JY, Wright CL, Forman SJ. Development of a candidate HLA A*0201 restricted peptide-based vaccine against human cytomegalovirus infection. Blood. 1997;90:1751–67.

  44. 44.

    Khan N, Cobbold M, Keenan R, Moss PA. Comparative analysis of CD8+ T cell responses against human cytomegalovirus proteins pp65 and immediate early 1 shows similarities in precursor frequency, oligoclonality, and phenotype. J Infect Dis. 2002;185:1025–34.

  45. 45.

    Weekes MP, Wills MR, Mynard K, Carmichael AJ, Sissons JG. The memory cytotoxic T-lymphocyte (CTL) response to human cytomegalovirus infection contains individual peptide-specific CTL clones that have undergone extensive expansion in vivo. J Virol. 1999;73:2099–108.

  46. 46.

    Gavin MA, Gilbert MJ, Riddell SR, Greenberg PD, Bevan MJ. Alkali hydrolysis of recombinant proteins allows for the rapid identification of class I MHC-restricted CTL epitopes. J Immunol. 1993;151:3971–80.

  47. 47.

    Wiesner M, Zentz C, Hammer MH, Cobbold M, Kern F, Kolb HJ, Hammerschmidt W, Zeidler R, Moosmann A. Selection of CMV-specific CD8+ and CD4+ T cells by mini-EBV-transformed B cell lines. Eur J Immunol. 2005;35:2110–21.

  48. 48.

    Kern F, Bunde T, Faulhaber N, Kiecker F, Khatamzas E, Rudawski IM, Pruss A, Gratama JW, Volkmer-Engert R, Ewert R, et al. Cytomegalovirus (CMV) phosphoprotein 65 makes a large contribution to shaping the T cell repertoire in CMV-exposed individuals. J Infect Dis. 2002;185:1709–16.

  49. 49.

    Ameres S, Liang X, Wiesner M, Mautner J, Moosmann A. A diverse repertoire of CD4 T cells targets the immediate-early 1 protein of human cytomegalovirus. Front Immunol. 2015;6:598.

  50. 50.

    Lee SP, Thomas WA, Murray RJ, Khanim F, Kaur S, Young LS, Rowe M, Kurilla M, Rickinson AB. HLA A2.1-restricted cytotoxic T cells recognizing a range of Epstein–Barr virus isolates through a defined epitope in latent membrane protein LMP2. J Virol. 1993;67:7428–35.

  51. 51.

    Steven NM, Annels NE, Kumar A, Leese AM, Kurilla MG, Rickinson AB. Immediate early and early lytic cycle proteins are frequent targets of the Epstein–Barr virus-induced cytotoxic T cell response. J Exp Med. 1997;185:1605–17.

  52. 52.

    Saulquin X, Ibisch C, Peyrat MA, Scotet E, Hourmant M, Vie H, Bonneville M, Houssaint E. A global appraisal of immunodominant CD8 T cell responses to Epstein–Barr virus and cytomegalovirus by bulk screening. Eur J Immunol. 2000;30:2531–9.

  53. 53.

    Meij P, Leen A, Rickinson AB, Verkoeijen S, Vervoort MB, Bloemena E, Middeldorp JM. Identification and prevalence of CD8(+) T-cell responses directed against Epstein–Barr virus-encoded latent membrane protein 1 and latent membrane protein 2. Int J Cancer. 2002;99:93–9.

  54. 54.

    Hill AB, Lee SP, Haurum JS, Murray N, Yao QY, Rowe M, Signoret N, Rickinson AB, McMichael AJ. Class I major histocompatibility complex-restricted cytotoxic T lymphocytes specific for Epstein–Barr virus (EBV)-transformed B lymphoblastoid cell lines against which they were raised. J Exp Med. 1995;181:2221–8.

  55. 55.

    Burrows SR, Gardner J, Khanna R, Steward T, Moss DJ, Rodda S, Suhrbier A. Five new cytotoxic T cell epitopes identified within Epstein–Barr virus nuclear antigen 3. J Gen Virol. 1994;75(Pt 9):2489–93.

  56. 56.

    Bogedain C, Wolf H, Modrow S, Stuber G, Jilg W. Specific cytotoxic T lymphocytes recognize the immediate-early transactivator Zta of Epstein–Barr virus. J Virol. 1995;69:4872–9.

  57. 57.

    Rickinson AB, Moss DJ. Human cytotoxic T lymphocyte responses to Epstein–Barr virus infection. Annu Rev Immunol. 1997;15:405–31.

  58. 58.

    Landais E, Saulquin X, Scotet E, Trautmann L, Peyrat MA, Yates JL, Kwok WW, Bonneville M, Houssaint E. Direct killing of Epstein–Barr virus (EBV)-infected B cells by CD4 T cells directed against the EBV lytic protein BHRF1. Blood. 2004;103:1408–16.

  59. 59.

    Leen A, Meij P, Redchenko I, Middeldorp J, Bloemena E, Rickinson A, Blake N. Differential immunogenicity of Epstein–Barr virus latent-cycle proteins for human CD4(+) T-helper 1 responses. J Virol. 2001;75:8649–59.

  60. 60.

    Adhikary D, Behrends U, Moosmann A, Witter K, Bornkamm GW, Mautner J. Control of Epstein–Barr virus infection in vitro by T helper cells specific for virion glycoproteins. J Exp Med. 2006;203:995–1006.

  61. 61.

    Mautner J, Pich D, Nimmerjahn F, Milosevic S, Adhikary D, Christoph H, Witter K, Bornkamm GW, Hammerschmidt W, Behrends U. Epstein–Barr virus nuclear antigen 1 evades direct immune recognition by CD4+ T helper cells. Eur J Immunol. 2004;34:2500–9.

  62. 62.

    Milosevic S, Behrends U, Adhikary D, Mautner J. Identification of major histocompatibility complex class II-restricted antigens and epitopes of the Epstein–Barr virus by a novel bacterial expression cloning approach. J Virol. 2006;80:10357–64.

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Authors’ contributions

RG, MA and AGe established the protocol, discussed the data, and wrote documents for the local and federal authorities. RG analyzed the data and wrote the manuscript. SMo and SS carried out the experiments and helped establishing the protocol. AGo is responsible for the quality management of documents. SMa was responsible for the preparation, finalization and submission of all documents to the authorities. RZ, JZ and JS helped transferring the protocol to the cleanroom facility. AMa provided ideas and material for this study. AMo and JM discovered some of the viral epitopes and their restriction. AMo furthermore played a pivotal role in the composition of the peptide pools and the set-up of the protocol. AGe coordinated the study. All authors read and approved the final manuscript.

Acknowledgements

The authors would like to thank the staff of the BMT unit and BMT outpatient clinic in Erlangen for continuous support of research efforts as well as the staff of the Department of Transfusion Medicine.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Consent for publication

Not relevant.

Ethics approval and consent to participate

The use of remaining PBMCs recovered from stem cell graft transfusion bags was approved by the local ethics committee of the University of Erlangen (Ref No.: 4388).

Funding

This work was supported by funds of the BayImmuNet network of the Government of Bavaria, by grants from the German Research Foundation (DFG: SFB-643 project C8/SFB-TR36 project 4), and by the Helmholtz Alliance on Immunotherapy of Cancer.

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Author notes

  1. Regina Gary and Michael Aigner contributed equally to this work

  2. Andreas Moosmann and Armin Gerbitz contributed equally to this work

Affiliations

  1. Dept. of Hematology/Oncology, University Hospital of Erlangen, Ulmenweg 18, 91054, Erlangen, Germany

    • Regina Gary
    • , Michael Aigner
    • , Stephanie Moi
    • , Stefanie Schaffer
    • , Anja Gottmann
    •  & Andreas Mackensen

  2. DZIF Research Group Host Control of Viral Latency and Reactivation (HOCOVLAR), Helmholtz Zentrum München, Marchioninistr. 25, 81377, Munich, Germany

    • Andreas Moosmann

  3. Center for Clinical Studies CCS, University Hospital of Erlangen, Krankenhausstr. 12, 91054, Erlangen, Germany

    • Stefanie Maas

  4. Department of Transfusion Medicine and Hemostaseology, University Hospital of Erlangen, Krankenhausstr. 12, 91054, Erlangen, Germany

    • Robert Zimmermann
    • , Jürgen Zingsem
    •  & Julian Strobel

  5. Clinical Cooperation Group Pediatric Tumor Immunology, Helmholtz Zentrum München, and Technical University of Munich, Marchioninistr. 25, 81377, Munich, Germany

    • Josef Mautner

  6. Department of Hematology, Oncology and Tumorimmunology, Charité Berlin, Berlin, Germany

    • Armin Gerbitz

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Additional file

12967_2018_1498_MOESM1_ESM.tif

Additional file 1: Figure S1. Yield of cells during manufacturing process. Proportion of cell count on d-1, d0, and d9 of manufacturing process compared to cell count of starting material before cryopreservation of 5 independent manufacturing processes of material of mobilized donors.

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Keywords

  • Stem cell transplantation
  • Allogeneic
  • CMV
  • EBV
  • Reactivation
  • T cell
  • Adoptive transfer

Journal of Translational Medicine

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