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Artificial APCs (aAPCs) genetically modified to express selective costimulatory molecules provide a reproducible, cost-effective, and convenient method for polyclonal and Ag-specific expansion of human T cells for adoptive immunotherapy. Among the variety of aAPCs that have been studied, acellular beads expressing anti-CD3/anti-CD28 efficiently expand CD4+ cells, but not CD8+ T cells. Cell-based aAPCs can effectively expand cytolytic CD8+ cells, but optimal costimulatory signals have not been defined. 4-1BB, a costimulatory molecule expressed by a minority of resting CD8+ T cells, is transiently up-regulated by all CD8+ T cells following activation. We compared expansion of human cytolytic CD8+ T cells using cell-based aAPCs providing costimulation via 4-1BB vs CD28. Whereas anti-CD3/anti-CD28 aAPCs mostly expand naive cells, anti-CD3/4-1BBL aAPCs preferentially expand memory cells, resulting in superior enrichment of Ag-reactive T cells which recognize previously primed Ags and efficient expansion of electronically sorted CD8+ populations reactive toward viral or self-Ags. Using HLA-A2-Fc fusion proteins linked to 4-1BBL aAPCs, 3-log expansion of Ag-specific CD8+ CTL was induced over 14 days, whereas similar Ag-specific CD8+ T cell expansion did not occur using HLA-A2-Fc/anti-CD28 aAPCs. Furthermore, when compared with cytolytic T cells expanded using CD28 costimulation, CTL expanded using 4-1BB costimulation mediate enhanced cytolytic capacity due, in part, to NKG2D up-regulation. These results demonstrate that 4-1BB costimulation is essential for expanding memory CD8+ T cells ex vivo and is superior to CD28 costimulation for generating Ag-specific products for adoptive cell therapy.
Clinical trials have demonstrated beneficial effects of adoptive immunotherapy in viral infection (1, 2), HIV infection (3), EBV-associated lymphoproliferative disorder (4), EBV-associated nasopharyngeal carcinoma (5), Hodgkin's disease (6), and malignant melanoma (7, 8). In murine melanoma, combining adoptive T cell therapy with vaccination and cytokine therapy can induce durable regression of sizable tumors whereas similar results cannot be achieved with vaccination and/or cytokine administration alone (9). Thus, adoptive immunotherapy holds promise for the treatment of viral and neoplastic disease. Currently, most investigators generate cell products for clinical trials of adoptive immunotherapy by repetitive TCR-based stimulation of PBLs using one of a variety of APCs. No consensus exists regarding the optimal cell type or costimulatory signals needed to generate these products, therefore a variety of APCs have been used including EBV-immortalized lymphoblast cell lines (LBL)3 (2, 10), CD40-activated B cells (11), autologous monocytes (12), autologous PBMCs (13), and autologous dendritic cells (14, 15). Although each of these approaches has been demonstrated capable of expanding Ag-specific T cells, careful studies to identify the optimal costimulatory signals for generating CTL products have not been undertaken. Thus, it remains unclear which, if any, APC is superior to the others.
The CD28:B7 pathway is widely considered the most important costimulatory pathway for TCR activation (16) and, as a result, most approaches used to expand T cells have emphasized a critical role for CD28 costimulation. However, bead-based anti-CD3/CD28 artificial APCs (aAPCs) induce brisk expansion of CD4+ populations but not CD8+ T cells (17–19), demonstrating that the CD28 costimulation is not sufficient for expansion of CD8+ CTL. Using genetically modified autologous monocytes, Bukczynski et al. (12) identified a critical role for 4-1BBL in expanding Ag-specific CTL, and Maus et al. (19) demonstrated that the incorporation of 4-1BBL into an aAPC greatly augmented the capacity for Ag-specific expansion of CD8+ T cells ex vivo. Thus, these results provided evidence that 4-1BB signaling augmented ex vivo expansion of CD8+ CTL. However, the APCs used in both of these studies also provided CD28 signaling, and therefore the studies did not clarify whether 4-1BB costimulation was sufficient to induce expansion in the absence of CD28 signaling.
In this study, we used genetically modified aAPCs to directly compare CD28 vs 4-1BB costimulation for expanding cytolytic CD8+ cells. Surprisingly, we observed efficient expansion of CD8+ CTL using 4-1BB costimulation in the absence of CD28 signaling, thus demonstrating that CD28 costimulation is not necessary for efficient expansion of memory CD8+ CTL. Furthermore, we demonstrate that 4-1BB costimulation preferentially expands memory CD8+ T cells, and that 4-1BB signaling augments cytolytic function both directly, and indirectly, via up-regulation of NKG2D. Thus, 4-1BB is an essential costimulatory molecule for efficient ex vivo expansion of Ag-specific CD8+ CTL.
HLA-A0201+ PBLs were obtained from healthy donors by leukapheresis following informed consent according to National Institutes of Health Clinical Center and/or the University of Pennsylvania Institutional Review Board approved protocols. CD8 + T cells were isolated by negative selection according to the manufacturer's instructions via a MACS CD8 T cell isolation kit (Miltenyi Biotec). Resulting populations consisted of >90% CD8+ T cells. P815 and T2 (American Type Culture Collection (ATCC)) cell lines were cultured and maintained in RPMI 1640 containing 10% FCS (Harlan), 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin, and 50 μg/ml 2-ME at 37°C, 5% CO2.
K32 (20) and K32/4-1BBL (19) aAPCs were generated and maintained as described previously. Briefly, the parent K562 cell line (ATCC) was transfected with CD32 to generate the K32 aAPC, which is maintained in culture under G418 selection. The K32/4-1BBL aAPC was generated by transfecting the K32 line with 4-1BBL, and this line is maintained in culture under G418 and hygromycin selection. The procedures used to generate the KT series of cell lines have been detailed elsewhere (21). Briefly, K562 cells (ATCC) were transduced with lentiviral vectors to introduce genes for CD32, CD80, 4-1BBL, IL-15, and sorted into single-cell clones using high-speed MoFlo sorting (Cytomation) to generate KT-4-1BBL that express CD32 and 4-1BBL, KT80-4-1BBL that expresses CD32, CD80, and 4-1BBL, KTIL-15-4-1BBL-CD80 that secretes IL-15 and expresses CD32, 4-1BBL, and CD80, and KT80 that expresses CD32 and CD80. All aAPCs were irradiated (10,000 rad) and cryopreserved in 10% DMSO and 90% FCS then thawed before initiation of aAPC:T cell coculture.
Upon thawing, the aAPCs were suspended at a concentration of 107 cells/ml and coincubated with the designated mAbs: anti-CD3 (OKT3; Ortho Biotech), and/or anti-CD28 (clone 9.3; kindly provided by Dr. R. Gress, Experimental Transplantation and Immunology Branch, National Cancer Institute, Bethesda, MD), at 1 μg/ml for 15 min at room temperature, then washed and resuspended before coincubation with the CD8+ cells undergoing expansion. For experiments using HLA-A2-Fc fusion proteins, thawed K32 and K32/4-1BBL were maintained at cell concentrations of <107/ml and incubated with the HLA-A2-Ig-Fc fusion protein (BD Biosciences) at 1 μg/ml for 5 min at room temperature. The designated HLA-A2-binding peptide was then added at a concentration of 10 μM for an additional 10 min. The peptide-loaded HLA-A2-Ig-aAPCs were then directly placed into coculture without washing. CD8+ T cells were incubated with the cell based aAPCs at a 2:1 CD8:aAPC ratio or with anti-CD3/anti-CD28 beads (Dynal Biotech) at a 1:3 CD8:bead ratio. All cell expansion cultures used 10% human AB serum in AIM-V (Invitrogen Life Technologies) medium containing 20 IU/ml IL-2 (Chiron) and 10 ng/ml IL-7 (Cytheris).
T cells (~106/tube) were removed from culture, washed with FACS medium (PBS containing 0.5% FCS and 2 mM EDTA), collected by centrifugation, and resuspended in 100 μl of FACS medium. Cells were stained with the Abs indicated (fluorochrome-labeled Abs were purchased from Caltag Laboratories, unless specified otherwise) for phenotypic analysis on ice for 30 min. Anti-4-1BB-FITC, anti-IL-15-FITC, anti-IL-15Rα, CD107a-PE, and NKG2D-PE were purchased from BD Pharmingen. For tetramer-binding assays, cells were stained with the designated HLA-A2+ tetramers (Beckman Coulter) for 30 min at room temperature. Apoptosis was assayed using Annexin VFITC (BD Pharmingen) surface staining according to the manufacturer's manual. Flow cytometry was performed using a FACSCalibur and CellQuest software (BD Biosciences) and analyzed using FlowJo 8.3 (Tree Star). FACS sorting for CMV+ and Flu+ cells was performed using a FACSVantage (BD Immunocytometry Systems).
CD8 T cells, isolated as described above, were separated into naive (CD45RO−) and memory (CD45RO+) subsets using CD45RO microbeads, according to the manufacturer's instructions (Miltenyi Biotec). The resulting population consisted of >90% CD45RO− (collected negatively) or CD45RO+ (collected positively) T cells. Subsequently, naive and memory CD8 T cells (105 each per well) were added to a 96-well flat-bottom plate (Nunc), which was previously coated with OKT3 at 1 μg/ml and variable doses of anti-4-1BB (R&D Systems) and anti-CD28 as indicated. Cells were incubated for 5 days at 37°C in a final volume of 200 μl/well with 10% human AB serum and AIM-V medium. Proliferation was measured by adding 1 μCi of [3H]thymidine/well (ICN Pharmaceuticals) 16 –18 h before the cells were harvested and thymidine incorporation (expressed as cpm) was measured using a gamma counter (Beckman Packwood).
Where designated, cultures were harvested, cells were counted, and lytic activities were measured using conventional 4-h 51Cr-release assays using T2 target cells that were first pulsed with either 10 μM Flu M1 peptide (GILGFVFTL), CMV pp65 peptide (NLVPMVATV), or the carcinoem-bryonic Ag-derived HLA-A2-binding peptide CAP1 (GVLVGVALI; New England Peptide), then labeled with 51Cr (PerkinElmer). Radioactivity in the supernatant was measured and the percentage-specific 51Cr lysis was calculated using the following equation: percent-specific lysis = (test release − spontaneous release)/(maximal release − spontaneous release) × 100. Cytolysis was also measured using CD107a expression as a marker of degranulation as previously described (22).
For the T cell-redirected cytolytic assay, P815 cells (1 × 106) were labeled with 51Cr as described above, then coupled with anti-CD3 (Ortho-clone), anti-4-1BB (R&D Systems), anti-CD28 (BD Biosciences), and/or anti-NKG2D (R&D Systems) where designated for 15 min at room temperature. Expanded T cells were assayed for their ability to lyse 51Cr-labeled Ab-bound P815 target cells in an Ag-independent manner using a conventional 4-h 51Cr-release assay as described above. One lytic unit was defined as 30% lysis of 5 × 103 target cells. Blockade of lysis following coincubation with the anti-MHC class I mAb W6/32 (Leinco Tech) was used to confirm MHC-restricted killing.
Differences between values were evaluated using a two-tailed unpaired Student's t test. Significance was determined as p < 0.05.
4-1BB is not expressed by resting naive or memory peripheral blood CD8+ T cells, but is up-regulated following activation (23). To assess 4-1BB expression on normal human CD8+ PBL following anti-CD3/anti-CD28 vs anti-CD3/anti-4-1BB-based stimulation, CD8+ T cells obtained from healthy donors were stimulated with plate-bound anti-CD3/anti-CD28 or anti-CD3/anti-4-1BB. In both cultures, 4-1BB was transiently up-regulated on essentially all CD8+ cells from normal donors with peak expression between 8 and 10 h following stimulation (Fig. 1A). A similar time course and degree of 4-1BB expression was also observed following anti-CD3 stimulation alone (data not shown). Therefore, although 4-1BB is expressed by only a minority of resting peripheral blood CD8+ T cells, T cell activation induces rapid, transient up-regulation of 4-1BB on all circulating CD8+ T cells, raising the possibility that 4-1BBL could serve as an effective costimulatory molecule for ex vivo expansion of CD8+ cells.
To determine the relative efficiency of 4-1BBL and CD28 costimulation for expanding human CD8+ T cells, enriched peripheral blood CD8+ T cells were enumerated following two consecutive stimulations (days 0 and 7) with aAPCs comprising K32 cell-based anti-CD3/4-1BBL, K32 cell-based anti-CD3/anti-CD28, and anti-CD3/anti-CD28-coated magnetic beads (Fig. 1B). Anti-CD3/4-1BBL and anti-CD3/anti-CD28 stimulation delivered via the K32 aAPCs induced rapid growth with a mean 7-fold expansion at 7 days, whereas anti-CD3/anti-CD28-coated beads induced only modest CD8+ T cell expansion during the same period. Similar relationships were observed on day 14 with K32-based expansion cultures generating a median of 50-fold expansion compared with ~10-fold expansion using bead-based aAPCs (data not shown). These results confirm previous data demonstrating that bead-based aAPCs do not efficiently expand CD8+ T cells (17–19). To determine whether the differences in CD8+ T cell expansion induced by cell- vs bead-based aAPCs resulted from different apoptotic rates, we measured the percentage of cells expressing annexin V throughout the first 7 days of culture under the various conditions. Bead-based anti-CD3/anti-CD28-stimulated CD8+ T cells demonstrated more apoptosis compared with cells expanded using K32-based aAPCs (Fig. 1C), indicating that programmed cell death limits expansion of CD8+ T cells when using anti-CD3/anti-CD28-coated beads. Because cell-based aAPCs outperform the bead-based aAPCs for CD8 expansion, we investigated whether the K32 cells might express IL-15 and/or IL-15Rα, which could exert an antiapoptotic effect on expanding CD8+ T cells (24). Indeed, both K32 and K32/4-1BBL aAPCs express IL-15Rα and produce IL-15 (Fig. 1D), a key survival factor for activated and memory CD8+ T cells. Furthermore, neutralization of IL-15 in the cell-based aAPC:CD8+ cocultures substantially diminished CD8+ T cell proliferation, providing evidence that the augmented effectiveness of the cell-based aAPCs in this system results, at least in part, from the production and presentation of IL-15 by the K32 cells (Fig. 1E).
Adoptive immunotherapy typically seeks to eradicate large antigenic burdens in viral reservoirs or tumor cells in hosts already primed toward the Ag to be targeted. Therefore, one goal of adoptive immunotherapy is to increase the number of primed, Ag-specific CTL beyond that generated naturally in vivo. To compare the capacity for 4-1BBL vs anti-CD28-based costimulation to expand memory CD8+ CTL, we compared the frequency of flu- and CMV-specific CTL in HLA-A0201+ peripheral blood CD8+ T cells following expansion using anti-CD3/anti-CD28 vs anti-CD3/4-1BBL K32 aAPCs. As shown in Fig. 2 A, baseline flu matrix protein (FluM1)- and CMV (pp65)-specific cell frequencies were 0.02 and 0.04%, respectively; following anti-CD3/4-1BBL-based expansion, flu- and CMV-specific cells increased in frequency to 0.4 and 0.6%, respectively, whereas anti-CD3/anti-CD28 expansion did not enrich viral-specific cells in the expanded populations (Fig. 2A). An HLA-A2-binding peptide derived from ERBB2 (Her2Neu), a self Ag which is not expected to induce immune priming in healthy donors, served as a control because the low frequency of ERBB2-specific cells did not change following either anti-CD3/anti-CD28 or anti-CD3/4-1BBL-based expansion. The enrichment observed using tetramer enumeration is functionally significant because anti-CD3/4-1BBL expanded CD8+ PBL demonstrated lytic activity against the FluM1- and pp65-pulsed targets whereas the anti-CD3/anti-CD28-expanded CD8+ PBL did not (Fig. 2B). Therefore, anti-CD3/4-1BBL expansion rapidly enriches peripheral blood CD8+ populations for memory CTL, which retain functional activity.
These results suggested that 4-1BBL costimulation preferentially expands memory CTL whereas anti-CD28 costimulation preferentially expands naive CD8+ T cells. To directly address this, CD8 PBL were immunomagnetically separated into CD45RO+ and RO− subsets (purity >90%) and then cultured on plates coated with a submitogenic dose of OKT3 (1 μg/ml) and titrated doses of anti-4-1BB or anti-CD28. Whereas the combination of anti-CD3/anti-CD28 preferentially expands naive CD8 subsets, anti-CD3/anti-4-1BB costimulation preferentially expanded memory CD8 subsets (Fig. 2C). These results confirm the 4-1BBL preferentially expands memory CTL and further demonstrate that the differential results shown in Fig. 2A are not due to a previously unrecognized difference between the K32 and the K32/4-1BBL cell lines, because this study used plate-bound Abs instead of K32-based cellular aAPCs. Rather, the results are consistent with the known physiologic role for 4-1BB costimulation in sustaining expansion of Ag-specific memory CD8+ T cells in vivo during the evolution of an immune response, as demonstrated previously in other model systems (24–27).
These results demonstrate that 4-1BBL costimulation can modestly enrich viral-specific CTL following polyclonal expansion, however, many clinical applications seek to use a product with much higher levels of antigenic specificity than achieved using the polyclonal expansion approach shown above. We therefore investigated whether the K32 aAPCs delivering signals via anti-CD3 and 4-1BBL could effectively expand highly enriched Ag-reactive enriched CD8+ T cells from T cell populations which were electronically sorted based upon tetramer binding (Fig. 3A). Peripheral blood CD8+ cells from donors immune to influenza were first expanded for 10 days using anti-CD3/4-1BBL aAPCs to increase the frequency of flu-specific cells above that found at baseline. CD8 cells binding FluM1 tetramers were then electronically sorted and placed back into coculture with anti-CD3/4-1BBL aAPCs. Fourteen days following stimulation of the sorted populations, flu-specific CD8 cells comprised >85% of the culture and the cells had undergone 1 log expansion. The cells demonstrated robust IFN-γ production and degranulation following exposure to FluM1 peptide-pulsed targets but not targets pulsed with irrelevant peptide. In three similar experiments, a mean of 1 log expansion was observed in 14 days using electronically sorted populations. Therefore, anti-CD3/4-1BBL aAPCs can be used to generate sizable populations of highly enriched Ag-specific CTL from peripheral blood, which retain specificity and function. Furthermore, not only does this data demonstrate that CD28 costimulation is not necessary to expand memory CTL, but also CD28 costimulation was inferior to 4-1BBL in expanding these populations because K32 aAPCs delivering anti-CD3/anti-CD28 expanded the electronically sorted cultures but they did not retain Ag specificity or function (data not shown). These results suggest that either the small numbers of naive cells contaminating the sorted cell population were preferentially expanded via CD28 costimulation, resulting in a subsequent loss of Ag specificity and/or CD28 costimulation induced anergy in these populations as described previously (18).
Because T cells used in tumor-directed adoptive cell therapy often seek to target tumor-associated Ags which represent self Ags (28), we also sought to determine the relative efficiency of expanding self-reactive memory cells using this approach. For these experiments, the KT32 cells lines were used as these represent the product currently being developed for clinical application. A MART-1 reactive CTL line was generated from an HLA-A201+ donor by three cycles of stimulation with peptide-loaded autologous APC. After three cycles of stimulation, the culture comprised 10% MART-1-specific CD8+ T cells, as measured by tetramer flow cytometry. The cell line was then restimulated with the KT32 aAPC expressing anti-CD3 and 4-1BBL and/or CD80 as a source of costimulation (Fig. 3B). Whereas MART-1 cells expanded and maintained viability following stimulation with anti-CD3/4-1BBL and anti-CD3/4-1BBL/CD80 aAPCs, no viable MART-1-reactive CD8 T cells were recovered in the cells stimulated aCD3/CD80 aAPCs. Furthermore, the MART-1 cells recovered from the 4-1BBL-containing culture exhibited potent peptide-specific cytotoxicity (Fig. 3B, middle panel). In addition, three successive cycles of stimulation of the MART-1 cell line with an cell-based aAPC genetically manipulated to express IL-15, CD80, 4-1BBL, and CD32 (used to load anti-CD3) induced robust expansion of the MART-1-reactive CTL, to potentially therapeutic numbers (Fig. 3B, right panel).
Because electronic cell sorting is expensive, labor intensive, and requires large numbers of starting cells, we sought to determine whether the preferential expansion of memory cells induced by 4-1BBL costimulation could lead to selectively enriched Ag-specific memory CTL from polyclonal T cell populations without the requirement for electronic cell sorting. To that end, the CD32-expressing aAPCs described above were coupled to an HLA-A2 Ig-Fc fusion protein, which was subsequently pulsed with the CMV pp65 antigenic peptide to expand memory CD8 cells reactive toward CMV. Ag-specific T cell expansion was compared when the costimulatory signal was provided by anti-CD28 vs 4-1BBL. Fig. 4 shows the results of cell cultures stimulated in this manner weekly for 3 wk. On day 22 of culture, 4-1BBL expressing aAPC induced substantial enrichment of CMV-specific T cells (7% CMV positive) (Fig. 4A) which retained functionality and specificity, (Fig. 4B), whereas the K32 aAPC, bearing the same pp65 A2-Ig Fc but delivering anti-CD28 costimulation, did not expand CMV-specific T cells. Cytolytic activity quantitated based upon degranulation and measured using CD107a expression (22) suggest that the tetramer assay in Fig. 4A underestimated the true frequency of pp65-specific CTL. In a series of three consecutive experiments, 10- to 100-fold enrichment and >2 log expansion of viral Ag-specific CD8+ T cells was observed within 14 days using cells from three different normal donors stimulated with HLA-A2-Fc/4-1BBL aAPCs (Table I). Similar Ag-specific expansion was also accomplished using FluM1-pulsed HLA-A2-Fc molecules to expand flu-specific CTL (data not shown).
Ag-specific CD8+ T cells that persist in hosts with high viral or tumor burdens often lack effective cytolytic activity (29–32) and, in some models, this is associated with NKG2D down-regulation, which can limit the capacity for cytolytic T and NK cells to kill MIC-expressing tumor cells (33, 34). Therefore, adoptive immunotherapy also seeks to augment the functional capacity of cells generated ex vivo, in addition to increasing numbers of Ag-specific T cells available to the host. We previously reported that CD8+ T cells expanded polyclonally with aAPCs using anti-CD3/anti-CD28 and anti-CD3/4-1BBL could mediate MHC-unrestricted cytotoxicity (35). We therefore sought to determine whether NKG2D, a killer-activating receptor (KAR) which can mediate MHC-unrestricted killing (36–38), was expressed on anti-CD3/4-1BBL-activated CD8+ T cells. Resting CD8+ PBL express high levels of NKG2D, but CD8+ PBL maintained in culture for 7 days or expanded using anti-CD3/anti-CD28 aAPC-based costimulation showed minimal NKG2D expression. In contrast, CD8+ T cells expanded using 4-1BBL costimulation maintain substantial NKG2D expression (Fig. 5A). To determine whether the NKG2D expression induced by anti-CD3/4-BBL-based expansion conferred NKG2D-signaling capacity and augmented cytotoxic function, we used a T cell-redirected cytotoxicity assay. Although neither fresh resting CD8+ T cells nor anti-CD3/anti-CD28-expanded CD8+ T cells were cytolytic in this assay (data not shown), anti-CD3/4-1BBL-expanded CD8+ PBL showed baseline cytolytic function as evidenced by lytic activity following cross-linking with anti-MHC class I, used as a negative control in this assay. Furthermore, cytolytic activity was substantially increased when either anti-NKG2D (p = 0.02) or anti-CD3 was added to the culture (p = 0.03), demonstrating that both NKG2D and CD3 signaling mediated a cytolytic signal in the expanded populations. Although anti-4-1BB signaling alone did not induce augmented cytolytic activity (p = 0.13), the highest cytolytic activity was observed when CD3 signaling was combined with anti-4-1BB or anti-NKG2D (Fig. 5B). Therefore, 4-1BB costimulation not only facilitates survival of memory populations in vivo as reported previously (39–41), and expansion of memory cells ex vivo as shown in this report, but also augments cytolytic function directly and indirectly via up-regulation of NKG2D.
Ex vivo T cell expansion for adoptive immunotherapy seeks to rapidly generate large numbers of functional T cells to amplify Ag-specific effector function in vivo. Several groups have demonstrated that autologous APCs, generated from a variety of cell types, can effectively expand cytolytic T cells (2, 10, 14, 15, 42). Although autologous APCs are ideal in principle because they are natural APCs, they are difficult to standardize, expensive to generate, and are not optimal for identifying critical costimulatory pathways that are most effective in inducing CTL expansion. aAPCs (aAPC), off-the-shelf reagents that eliminate the requirement for generating patient-specific APCs to provide TCR stimulation and costimulation to induce ex vivo T cell expansion, represent a potentially cost-effective and less labor-intensive approach to developing cytolytic T cell products for adoptive immunotherapy. In general, the vast majority of aAPCs under study have incorporated CD28 ligands as the primary costimulatory signal (43–47). However, we and others have noted that anti-CD3/anti-CD28 mAbs conjugated to magnetic beads do not effectively expand CD8+ T cells (17, 19, 48), and it is well-known that CD8+ populations rapidly down-regulate CD28 upon acquisition of effector function (49). Alternatively, several studies have also demonstrated a role for 4-1BB costimulation in CD8+ T cell expansion, although each of these studies also delivered CD28 signals during the phase of CD8+ T cell expansion (12, 19, 20). 4-1BB, a member of TNFR family expressed primarily on activated lymphocytes (23), promotes CD8+ T cell proliferation, differentiation, and inhibits programmed cell death (50–53). The 4-1BB ligand is expressed by activated B cells, dendritic cells, and monocytes/macrophages and likely serves to augment survival of cytolytic CD8+ T cells during the evolution of an immune response (39–41).
In this report, we used a system of genetically modified aAPCs to directly compare the efficacy of CD28 vs 4-1BB signaling in the expansion of CD8+ CTL. Because K32 cells are not natural APCs, they do not endogenously express a host of stimulatory and inhibitory ligands, and thus allowed us to directly assess whether 4-1BB costimulation was sufficient to induce CD8+ CTL expansion. The data demonstrate K32 cell-based aAPCs, which deliver either anti-CD3/anti-CD28 signals or anti-CD3/4-1BBL signals, promote rapid expansion of peripheral blood CD8 T cells with a median 1.5 log expansion in 14 days. Such expansion was greater than that observed using bead-based APCs, in part, due to the production of IL-15 and expression of IL-15Rα expression on the K32-based aAPCs. Interestingly, the quantitative increases in CD8 expansion could not be reproduced by adding IL-15 to the bead-based cell cultures, perhaps due to inadequate presentation in the absence of IL-15Rα. CD8 expansion was numerically similar following 4-1BBL or CD28 stimulation despite vastly different levels of expression of CD28 and 4-1BB on resting T cells. However, our studies uncovered substantial qualitative differences in the CD8+ populations expanded using 4-1BB vs CD28 costimulation. Whereas anti-CD3/4-1BBL aAPCs preferentially expand memory CD8 T cells, resulting in an increased frequency of cells responding to viral recall Ags in the expanded cultures from healthy donors, anti-CD3/anti-CD28 aAPCs preferentially expand naive CD8+ cells and therefore do not enrich for viral-specific CTL. Interestingly, we did not detect any difference in the frequency or extent of 4-1BB expression following anti-CD3 signaling on naive vs memory CD8+ T cells (data not shown), therefore the basis for the selective expansion of memory cells via 4-1BB signaling cannot be ascribed to differential expression of 4-1BB on these two populations. Furthermore, while we observed increased short-term expansion of polyclonal memory populations compared with naive populations using 4-1BB costimulation as shown in Fig. 2C, it remains possible that there are also significant survival differences between naive and memory populations that contribute to the results reported here. Indeed, ample data in murine models demonstrate that 4-1BB signaling plays a critical role in survival of memory CD8+ T cells during the later stages of the immune response (24–27).
One theoretical advantage to the use of CD28-based costimulation might be a preferential expansion and/or retention of CD28-expressing CD8+ T cells, because multiple studies have demonstrated that CD28+ cells retain a greater proliferative potential and are more functional than the CD28− subset (49). We therefore analyzed the CD28+/CD28− ratio of CD8 T cells pre- vs post-expansion using either K32-based anti-CD3/anti-CD28 or anti-CD3/4-1BBL stimulation. Whereas normal human CD8+ PBL showed a CD28+/CD28− ratio of ~2:1, T cells expanded by K32-based anti-CD3/anti-CD28 and anti-CD3/4-1BBL aAPCs studied in this report resulted in a postexpansion ratio of 1:2 with no difference in the percent of cells expressing CD28 following anti-CD28 vs 4-1BBL costimulation (data not shown). Therefore, we found no evidence to suggest that CD28 costimulation was superior to 4-1BB costimulation in retaining or expanding CD28+ CTL.
In addition to demonstrating that 4-1BB costimulation preferentially expands memory CTL and the demonstration that 4-1BB costimulation alone is sufficient to induce dramatic expansions of CD8+ CTL, this report is also the first to demonstrate that 4-1BB signaling directly augments cytotoxic function in human CD8+ T cells. Furthermore, the up-regulation of NKG2D on 4-1BBL-co-stimulated cells potentially represents an important secondary mediator of cytolysis which may be particularly pertinent for adoptive immunotherapy, because NKG2D down-regulation contributes to immune escape in murine models of cancer and chronic infection (33, 34). The capacity for 4-1BBL-expressing aAPCs to generate a cell product with high levels of NKG2D that can augment cytolytic capacity is potentially favorable to avoid tumor immune escape by down-regulation of either MHC or shedding of NKG2D ligands. Indeed, consistent with this notion, we demonstrated previously that CD8+ T cells expanded with anti-CD3/4-1BBL-mediated non-MHC-restricted killing of tumor targets and mediated antitumor activity in vivo in a xenograft model whereas anti-CD3/anti-CD28-expanded CD8+ T cells did not mediate antitumor activity in vivo (35).
In conclusion, these results provide the first evidence that CD28 costimulation is not essential for generating CD8+ T cells for adoptive immunotherapy. Rather, TCR and/or CD3 signals combined with 4-1BB costimulation can generate large numbers of cytolytic CD8+ T cells with enhanced effector functions that are suitable for adoptive cellular immunotherapy. The expansion of electronically sorted populations or enrichment of large numbers of Ag-specific cells from polyclonal peripheral blood CD8+ T cells using K32/4-1BBL-HLA-A2-Fc APCs provides opportunities for expanding large numbers of Ag-specific T cells with MHC-restricted cytolytic activity. Furthermore, this approach yields CD8+ T cells with enhanced MHC-restricted cytolytic activity and the potential for non-MHC-restricted cytolysis as a result of NKG2D up-regulation, which is potentially important for the elimination of infected and/or transformed cells which can down-regulate MHC expression. Considering the wide range of diseases that are potentially amenable to treatment given a robust, reproducible approach for ex vivo expansion of Ag-specific CTLs, 4-1BBL-expressing cell-based aAPCs hold promise for improving the effectiveness of adoptive immunotherapy.
We thank Drs. Terry Fry and Ron Gress for their careful and critical reviews of this manuscript. H. Zhang performed most of the experiments shown, analyzed data, and partially wrote the manuscript. K. M. Snyder and M. M. Suhoski performed experiments demonstrating the capacity for aAPCs to expand purified populations of Ag-specific cells. M. M. Suhoski and M. V. Maus created the aAPCs, performed experiments, and analyzed data. C. H. June provided the intellectual insight to use 4-1BBL as a costimulatory molecule in aAPCs and provided the financial support for the creation of these cells. C. L. Mackall provided intellectual and financial support for the experiments shown, analyzed data, and partially wrote the manuscript.
1This work was supported, in part, by the Intramural Research Program of the National Cancer Institute.
3Abbreviations used in this paper: LBL, lymphoblast cell line; aAPC, artificial APC.
Disclosures: M. V. Maus and C. H. June have applied for a patent related to the work that is described in the present study.