A novel polymer-conjugated human IL-15 improves efficacy of CD19-targeted CAR T-cell immunotherapy

Chimeric antigen receptor (CAR)–modified T-cell therapy represents a new paradigm for the treatment of relapsed/refractory (R/R) B-lineage malignancies and shows promise for the treatment of other tumors. As of June 2022, there are 6 Food and Drug Administration–approved CAR T-cell products.^1-8 Although the outcomes in many studies of CAR T-cell therapy are encouraging, there remains a significant fraction of patients in whom CAR T-cell therapy fails to elicit a durable response.

Limited in vivo proliferation and survival of infused CAR T cells are key causes of failure in CAR T-cell therapy.^9-16 Lymphodepleting chemotherapy is typically administered before adoptively transferring T cells to reduce the levels of endogenous lymphocytes that compete with infused T cells for homeostatic cytokines that maintain T-cell survival.¹⁷ Interleukin 15 (IL-15) is one such homeostatic cytokine that promotes proliferation and survival of T cells.¹⁸ In patients with R/R B-cell malignancies treated with CD19 CAR T cells, high peak serum IL-15 concentration was associated with response.^10,19 These results suggest that IL-15 supplementation could augment CAR T-cell proliferation and/or survival and improve outcomes.

Treatment with native IL-15 is problematic owing to its short half-life (t_1/2), resulting in the need to administer high and frequent doses or give continuous infusions.^20,21 PEGylation, which involves covalently attaching a polyethylene glycol (PEG) moiety to a molecule, has successfully improved the pharmacokinetics (PK) and pharmacodynamics (PD) of various drugs that are currently used in clinical settings.^22,23 NKTR-255 is a novel clinical grade PEG-conjugated IL-15 agonist that engages the entire IL-15 receptor complex (IL-15Rα/IL-2Rβγ), resulting in downstream signaling effects similar to native IL-15 in human mononuclear cells.²⁴ Compared with recombinant human IL-15 (rhIL-15) and precomplexed rhIL-15/IL-15Rα, single-agent NKTR-255 treatment of mice demonstrated enhanced activation of natural killer (NK) and CD8⁺ T cells and tumor eradication,²⁴ supporting investigation of NKTR-255 for augmenting the antitumor efficacy of CAR T cell in humans. Here, we report our preclinical findings on the PK and immune cell PD of NKTR-255 in nonhuman primates (NHPs) and demonstrate the enhanced in vitro function and in vivo efficacy of human CD19 CAR T cells combined with NKTR-255 than CD19 CAR T cells alone.

Serum IL-15 concentrations (Luminex Corporation) and CAR T-cell persistence (quantitative reverse transcription polymerase chain reaction; FlapEF1α copies per μg DNA) were analyzed in 190 patients with R/R B-cell malignancies treated in a phase 1/2 clinical trial of CD19 CAR T cells (#NCT01865617), as previously described.^{9,15,16,25-27} The study was conducted according to the principles of the Declaration of Helsinki with approval by the Fred Hutchinson Cancer Center Institutional Review Board.

rhIL-15 and NKTR-255 were manufactured by Nektar Therapeutics (San Francisco, CA) and formulated in aqueous buffer at near-neutral pH. For in vivo experiments, NKTR-255 was administered in IL-15 protein equivalents, excluding the mass of PEG. Injection volumes were ∼2 mL/kg for cynomolgus monkeys or 5 mL/kg for mice. K562 cells stably expressing CD19 (K562-CD19⁺) and Raji cells stably expressing firefly luciferase and enhanced green fluorescent protein (eGFP) (Raji-ffluc-eGFP) were generated as previously described.^28,29 The cell lines were cultured in RPMI 1640 with 10% fetal bovine serum, 0.71 mM L-glutamine, and 100 U/mL penicillin-streptomycin, and maintained at 37°C and 5% CO₂.

NHP studies were conducted under accreditation by the Association for Assessment and Accreditation of Laboratory Animal Care or the Canadian Council on Animal Care. All studies met the ethical and humane criteria for transportation, housing, and care established by the US National Institutes of Health guidelines or Canadian animal care regulators. Young adult male and female cynomolgus monkeys weighing 2.0 to 3.5 kg and 2.2 to 2.5 kg, respectively, at treatment initiation were obtained from the spare colony at the International Toxicology Research Laboratories Canada Inc (Baie d’Urfe, Quebec, Canada). The animals were cohoused in pairs or groups, except during the initial dosing period. A standard diet and water were available ad libitum.

Cynomolgus monkeys received a single dose of NKTR-255 (0.1 mg/kg) either subcutaneous (SC) or IV (2 male animals per group) or a single IV dose of rhIL-15 (0.05 mg/kg) or NKTR-255 (0.1 mg/kg) (1 male and 1 female per group). Peripheral blood was collected at 0.033, 0.25, 1, 4, and 12 hours after rhIL-15 and NKTR-255 administration and at 1, 2, 3, 4, 5, 6, and 7 days after NKTR-255 infusion. Plasma IL-15 concentrations were measured using a qualified enzyme-linked immunosorbent assay method. PK parameters (t_1/2, volume of distribution, and clearance) were determined by noncompartmental analysis using Phoenix WinNonlin (version 6.4; Certara Inc, Princeton, NJ).

Male cynomolgus monkeys (3-4 per group) received a single IV dose of NKTR-255 (0.001, 0.01, or 0.1 mg/kg). Blood samples were collected before NKTR-255 infusion (days −5 and −2) and at multiple intervals following infusion to evaluate absolute cell counts and Ki-67 (BD Biosciences) and pSTAT5 (BD Biosciences) expression in NK cells and CD8⁺ and CD4⁺ T cells by flow cytometry. To evaluate IL-15 signaling, fresh whole blood samples from 3 animals were stimulated ex vivo for 20 minutes at 37°C with rhIL-15 or NKTR-255. pSTAT5 was assessed in CD3⁻CD56⁺ NK cells, CD3⁺CD8⁺ T cells, and CD3⁺CD4⁺ T cells by flow cytometry. Data were acquired using an LSRFortessa X-20 or FACSCanto II (BD Biosciences) and analyzed using the FlowJo software (BD Life Sciences).

CD8⁺ and CD4⁺ T cells were isolated from healthy donor leukaphereses using the EasySep Human T Cell Isolation Kit (STEMCELL Technologies). Isolated CD8⁺ or CD4⁺ T cells were activated using Dynabeads Human T-Activator CD3/CD28 (Thermo Fisher Scientific) and cultured in RPMI 1640 with 10% human serum, 3.51 mM L-glutamine, 0.05 mM β-mercaptoethanol, 100 U/mL penicillin-streptomycin, and 50 IU/mL IL-2 (PeproTech). After 24 hours, activated T cells were spinoculated at 800g and 32°C for 90 minutes with a lentivirus encoding a CAR comprising an FMC63-derived CD19-specific single-chain variable fragment (scFv), 4-1BB costimulatory domain, and CD3ζ signaling domain. A truncated cell-surface human epidermal growth factor receptor (EGFRt) was separated from the CAR using a ribosomal skip sequence to enable the detection of transgene expressing cells by flow cytometry. Dynabeads were removed on day 5. Transduced EGFRt⁺CD8⁺ and EGFRt⁺CD4⁺ T cells were flow-sorted (BD FACSAria or Sony MA900) on day 7 and expanded by coculture with irradiated allogeneic CD19⁺ lymphoblastoid cell line for 8 days. Media were changed every 2 days. CAR T cells were used for further experiments on days 14 to 16.

CAR T-cells or single-cell suspension of mouse bone marrow were stained with live dead fixable AmCyan or Violet (Life Technologies) in phosphate-buffed saline (PBS) at 4°C. Cells were washed with staining buffer (PBS/2% fetal bovine serum) and blocked with human FcR (Miltenyi Biotec) and/or mouse FcR (BioLegend). Surface staining (CD45, CD3, CD8, CD4, anti-EGFR, PD-1, and TIM-3) was performed using a Brilliant Stain Buffer (BD Biosciences). For intracellular staining, the cells were fixed and permeabilized using a BD Cytofix/Cytoperm Solution Kit (BD Biosciences) and stained with BCL-2 and Ki-67 antibodies (BD Biosciences). Cells were washed and resuspended in Perm/Wash Buffer containing Liquid Counting Beads (BD Biosciences). Data were acquired using LSR II, FACSymphony A5, or LSRFortessa X-50 (BD Biosciences) and analyzed using FlowJo software.

To assess STAT5 phosphorylation, CAR T cells were washed twice with PBS, resuspended in IL-2–free media at 2 × 10⁶ cells per mL, and incubated overnight (humidified incubator, 37°C, and 5% CO₂). Dead cells were removed by density gradient centrifugation using a Histopaque-1077 (Sigma-Aldrich). CAR T cells were cultured (20 minutes at 37°C) with rhIL-15 or NKTR-255, fixed with BD Cytofix Fixation Buffer (BD Biosciences) for 20 minutes at 37°C, washed with staining buffer, and permeabilized at −20 °C with 100% methanol before incubation (30 minutes at 4°C) with pSTAT5 antibody (BD Biosciences). Data were acquired using a FACSCelesta (BD Biosciences) and analyzed using FlowJo software.

CAR T cells were labeled with 0.5 μM carboxyfluorescein succinimidyl ester (CellTrace, Thermo Fisher Scientific) and cocultured with irradiated (15 000 cGy) K562-CD19⁺ cells at different effector to target (E:T) ratios and concentrations of NKTR-255. Proliferation was assessed using carboxyfluorescein succinimidyl ester dilution after 96 hours. Liquid counting beads were used to determine the absolute cell counts. Flow cytometry data were acquired using FACSCelesta and analyzed using FlowJo software.

Mouse experiments were approved by the Fred Hutchinson Cancer Center Institutional Animal Care and Use Committee. Six- to 8-week-old NOD.Cg-Prkdc^scidIl2rg^tm1Wjl/SzJ (NOD/ severe combined immunodeficiency/γc^−/−) (NSG) mice were bred in house. The mice were engrafted with 5 × 10⁵ Raji-fflu-eGFP cells via tail vein injection. Six to 7 days later, tumor-bearing mice received 0.8 × 10⁶ CD8⁺ and CD4⁺ CD19 CAR T cells at a 1:1 ratio. NKTR-255 or buffer was injected via the tail vein at the designated time points. Bioluminescence imaging was performed using a Xenogen IVIS imaging system and luciferase activity was analyzed using Living Image software.³⁰ The dosing and frequency of NKTR-255 infusions were selected based on PK data in mice.²⁴ Blood was collected via retro-orbital bleeding. Single-cell bone marrow suspensions were obtained by flushing bilateral femurs and tibias. Red blood cells were lysed with ACK Lysing Buffer (Thermo Fisher Scientific) and washed with PBS before immunophenotyping.

A proportional odds logistic regression was used for multivariable modeling of CAR T-cell kinetics according to peak serum IL-15 concentrations in patients treated with CD19 CAR T cells using RStudio software (RStudio, Boston, MA). Other statistical analyses were performed using Prism software (GraphPad, San Diego, CA). Half maximal effective concentration (EC₅₀) values were calculated using 4-parameter nonlinear regression curves. The area under the curve (AUC) was calculated using the trapezoidal rule. Two-tailed Mann-Whitney, unpaired 2-tailed t test, or log-rank tests were used for comparisons. P < .05 was considered statistically significant.

We and others have previously reported that a higher peak serum IL-15 concentration after CD19 CAR T-cell infusion was associated with better clinical outcomes in patients with R/R B-cell lymphomas in univariate analysis.^10,16 Using multivariable modeling, adjusting for disease type, prelymphodepletion serum lactate dehydrogenase, and type of lymphodepletion, we found that a higher peak serum IL-15 concentration after CAR T-cell infusion correlated with a higher CAR transgene AUC from days 0 to 90 (AUC_0-90; odds ratio, 4.88; P = .002) (Figure 1). The median time to peak serum IL-15 levels was 1 day after CAR T-cell infusion (range, 0-3 days). These data demonstrate an association between endogenous IL-15 concentration and in vivo CAR T-cell counts, providing a rationale for IL-15 supplementation to augment CD19 CAR T-cell efficacy.

The short t_1/2 of native IL-15 complicates its systemic administration.²¹ We investigated the PK and PD of NKTR-255 in NHPs, given that simian and human IL-15 share 97% sequence identity.³¹ We compared SC and IV administration of NKTR-255 in preclinical studies and observed injection site reactions with SC infusion. Furthermore, SC administration of NKTR-255 in cynomolgus monkeys was not associated with a clear PK benefit. Therefore, the IV administration route was selected for further studies. We treated cynomolgus monkeys (1 male and 1 female per group) with a single IV dose of rhIL-15 (0.05 mg/kg) or NKTR-255 (0.1 mg/kg) and evaluated plasma IL-15 concentrations at intervals after infusion. These dose levels were used because previous studies showed lower binding affinity for IL-15Rα of NKTR-255 relative to rhIL-15.²⁴ In animals that received rhIL-15, we observed a transient increase in IL-15 concentration with rapid decline to undetectable levels 12 hours after infusion. In contrast, in animals that received NKTR-255, the levels of IL-15 were maintained in the first 12 hours after infusion and declined more slowly than rhIL-15 (Figure 2A). There was a longer IL-15 t_1/2 (30.5 vs 1.2 hours), lower volume of distribution (72.8 vs 112.0 mL/kg), and slower clearance (4.3 vs 161.4 mL/h per kg) in NKTR-255–treated monkeys compared with those treated with rhIL-15. These data demonstrate the favorable PK of NKTR-255 compared with native IL-15 in cynomolgus NHPs.

To determine whether NKTR-255 induces signaling in NHP immune cells, fresh whole blood from 3 animals was incubated with rhIL-15 or NKTR-255, and phosphorylation of STAT5 was evaluated in NK cells and CD8⁺ and CD4⁺ T cells. We observed dose-dependent STAT5 phosphorylation in each NHP cell subset (Figure 2B). The EC₅₀ of STAT5 phosphorylation in NK cells and CD8⁺ and CD4⁺ T cells incubated with NKTR-255 was higher than that observed with rhIL-15, owing to the lower binding affinity of NKTR-255 for IL-15 receptor.²⁴ To determine if systemic administration of NKTR-255 changes immune cell subset composition, we treated cynomolgus monkeys (n = 3-4 per group) with a single IV dose of NKTR-255 (0.001, 0.01, or 0.1 mg/kg) or vehicle. NKTR-255 induced a dose-dependent increase in the absolute numbers of NK cells and CD8⁺ and CD4⁺ T cells in the blood (Figure 2C) but did not significantly affect B-cell and monocyte counts (supplemental Figure 1). At the highest dose level (0.1 mg/kg), NK cells and T cells began to increase in the blood between 2 and 3 days after infusion, peaked around days 4 to 5, and then declined to baseline by day 10. Similar patterns were observed after NKTR-255 0.01 mg/kg dose, albeit with lower peak counts. The lowest dose (0.001 mg/kg) did not result in significant increases in NK cells and CD8⁺ or CD4⁺ T cells. We observed dose-dependent increases in the fraction of immune cells expressing pSTAT5 (Figure 2C), with the most significant changes observed in NK cells and CD8⁺ T cells. Dose-dependent increases in Ki-67 expression peaked 3 to 7 days after infusion, predominantly in NK cells and CD8⁺ T cells, consistent with in vivo proliferation (Figure 2C). Ki-67⁺ cells were found in the naïve and memory T-cell subsets (supplemental Figure 2). The fractions of NK cells and CD8⁺ and CD4⁺ T cells expressing Ki-67 returned to baseline ∼10 days after NKTR-255 infusion (0.1 mg/kg). These data indicate that NKTR-255 IV is associated with increased proliferation and absolute NK cell and CD8⁺ and CD4⁺ T-cell counts in cynomolgus NHP blood.

The favorable PK and immune cell PD observed after NKTR-255 treatment of NHPs suggests that NKTR-255 administration might enhance the efficacy of CD19 CAR T-cell therapy in humans. We first demonstrated IL-15Rα expression in human CD8⁺ and CD4⁺ CD19 CAR T cells (Figure 3A) and found a dose-dependent increase in STAT5 phosphorylation following incubation with NKTR-255 (Figure 3B). The EC₅₀ of STAT5 phosphorylation in CAR T cells incubated with NKTR-255 was higher than that observed with rhIL-15, as seen in NHP T cells. NKTR-255 and rhIL-15 also induced the dose-dependent proliferation of human CD8⁺ and CD4⁺ CAR T cells (Figure 3C). Consistent with the lower affinity for IL-15Rα and pSTAT5 EC₅₀ data, higher concentrations of NKTR-255 were required to achieve the same proliferation of CD8⁺ and CD4⁺ CAR T cells as seen with rhIL-15. NKTR-255 induced a dose-dependent increase in the expression of the prosurvival protein, BCL-2, in both CD8⁺ and CD4⁺ CAR T cells (Figure 3D). Consistent with the increased proliferation and expression of BCL-2, we observed a dose-dependent increase in the accumulation of CD8⁺ and CD4⁺ CAR T cells during in vitro culture (Figure 3E). These data indicate that in the absence of antigen, NKTR-255 induces a dose-dependent increase in proliferation, BCL-2 expression, and accumulation of CD8⁺ and CD4⁺ CAR T cells.

The extent of NKTR-255-induced augmentation of T-cell proliferation and accumulation may differ in the absence or presence of antigen. To address this, we cocultured CAR T cells with CD19-expressing K562 cells at different E:T ratios in the presence of increasing NKTR-255 concentrations. As expected, both CD8⁺ and CD4⁺ CAR T cells proliferated in response to the antigen, and the addition of NKTR-255 further enhanced the proliferation of CAR T cells in a dose-dependent manner (Figure 4A-B). This finding was more pronounced in the setting of lower target cell abundance, especially for CD4⁺ CAR T cells, in which the effect of NKTR-255 supplementation was more pronounced at high E:T ratios (Figure 4B). The increase in BCL-2 expression induced by increasing concentrations of NKTR-255 in the absence of antigen (Figure 3E) was also observed in the presence of antigen (Figure 4C). Consistent with the increased proliferation and BCL-2 expression (Figure 4A-C), we found a dose-dependent increase in the accumulation of CAR T cells with increasing NKTR-255 concentrations (Figure 4D), with the most marked increases observed with lower target cell abundance (high E:T ratio) and in the CD8⁺ CAR T cells. At a given E:T ratio, coculture of CD8⁺ and CD4⁺ CAR T cells with NKTR-255 in the presence of antigen did not significantly increase interferon gamma or tumor necrosis factor α (supplemental Figure 3A-B). The cytolytic activity of CD8⁺ CAR T cells cocultured with or without NKTR-255 against ⁵¹Cr-labeled CD19-expressing K562 cells analyzed by a standard 4-hour chromium release assay³² was also comparable (supplemental Figure 3C). These data indicate that NKTR-255 enhances the proliferation of CD8⁺ CAR T cells at high and low target cell burden and CD4⁺ CAR T cells mainly at low target cell burden, with limited effects on cytokine secretion and cytotoxicity.

We next examined the effects of systemic administration of NKTR-255 on the in vivo efficacy of human CD19 CAR T cells in NSG mice with Raji lymphoma. Mice treated with PBS, NKTR-255 buffer, or NKTR-255 IV weekly starting 6 days after Raji inoculation showed similar tumor growth and short survival, indicating that neither NKTR-255 buffer nor NKTR-255 had a direct effect on tumor growth (supplemental Figure 4). In our phase 1/2 clinical trial of CD19 CAR T cells (#NCT01865617), the serum IL-15 concentration was elevated in the first week after CAR T-cell infusion owing to lymphodepletion chemotherapy, suggesting that early IL-15 supplementation might increase the risk of CAR T-cell–associated toxicities. Therefore, we decided to designate an initial NKTR-255 starting time of ∼1 week after CAR T-cell infusion. We first treated Raji tumor-bearing mice with a subtherapeutic dose of CD19 CAR T cells alone or supplemented with NKTR-255 (0.03 mg/kg or 0.3 mg/kg IV), starting on day 6 after CAR T-cell infusion and then weekly from day 14 (Figure 5A). One group of mice received PBS alone, without CAR T cells. Treatment with a subtherapeutic dose of CAR T cells alone increased survival compared with PBS alone, however, disease control was transient. In contrast, mice who received CAR T cells and NKTR-255 exhibited prolonged survival, with optimal tumor clearance observed in those that received NKTR-255 at 0.3 mg/kg compared with 0.03 mg/kg (Figure 5B-D).

We then examined whether efficacy was affected by different NKTR-255 starting days beyond the first week after CAR T-cell infusion. We evaluated NKTR-255 at 0.3 mg/kg IV weekly starting on days 7, 14, or 21 after CAR T-cell infusion (Figure 6A). Days 14 and 21 were chosen to examine NKTR-255 supplementation starting at the CAR T-cell peak of expansion and contraction, respectively. Optimal tumor control was observed in mice receiving NKTR-255 starting on day 7 after CAR T-cell infusion (day 7 compared with day 21) (Figure 6B-C); and mice that received CAR T cells and NKTR-255 had longer survival compared with mice that received CAR T cells alone (day 7 vs CAR T cells only, P = .002; day 14 vs CAR T cells only, P = .007; and day 21 vs CAR T cells only, P = .04) (Figure 6D). Mice that received CAR T cells and NKTR-255 starting on day 7 had higher AUC_0-28 of CD8⁺ and CD4⁺ CAR T-cell counts in blood compared with mice that received CAR T cells alone (P = .008 for both) (Figure 6E). The AUC_0-28 of CD4⁺ CAR T cells was also higher in mice starting NKTR-255 on day 14 compared with CAR T cells alone (P = .008) (Figure 6E). These data indicate higher CAR T-cell counts in the blood and better tumor control in mice receiving CAR T cells followed by NKTR-255 starting on day 7 after CAR T-cell infusion.

To determine whether NKTR-255 affected the accumulation of CAR T cells in bone marrow, cohorts of mice receiving CAR T cells and NKTR-255 at 0.3 mg/kg IV weekly starting on day 7 after CAR T-cell infusion were euthanized and CAR T cells were assessed in the bone marrow. Administration of NKTR-255 was associated with a higher percentage of Ki-67⁺ CD8⁺ and CD4⁺ CAR T cells in the first 8 to 11 days after CAR T-cell infusion (Figure 7A). By day 14, the fraction of Ki-67⁺ CAR T cells declined in the CAR T cells/NKTR-255 cohort, consistent with the rapid tumor elimination in this cohort (supplemental Figure 5; Figure 7A). Importantly, BCL-2 expression was higher in CD8⁺ and CD4⁺ CAR T cells in the CAR T cells/NKTR-255 cohort at all time points (Figure 7B), even after tumor clearance, resulting in persistently higher numbers of CD8⁺ and CD4⁺ CAR T cells in the bone marrow through day 28 after CAR T-cell infusion (Figure 7C-D). Despite profoundly higher numbers of CD8⁺ and CD4⁺ CAR T cells in the bone marrow on day 28 of mice in the CAR T cells/NKTR-255 cohort than in the CAR T cells alone cohort (CD8⁺ CAR T cells, 5.6-fold; CD4⁺ CAR T cells, 54.1-fold), evidence of ongoing activation/exhaustion by PD-1 and TIM-3 inhibitory receptor coexpression was not identified in CAR T cells from the CAR T cells/NKTR-255 cohort compared with the CAR T cell alone cohort (supplemental Figure 6A). CAR T cell samples from both cohorts showed similar fractions of interferon gamma and tumor necrosis factor α coexpression (supplemental Figure 6B).

To investigate whether persistent CAR T cells after NKTR-255 administration could protect mice from tumor rechallenge, mice that cleared the tumor after receiving CAR T cells and NKTR-255 at 0.3 mg/kg IV weekly starting on day 7 after CAR T-cell infusion were rechallenged with Raji tumor cells on day 36 after CAR T-cell infusion (rechallenged mice) (Figure 8A). A separate cohort of mice with no prior CAR T cells or NKTR-255 treatment (naïve mice) was inoculated with Raji tumor cells alone. All rechallenged mice rejected the tumor 6 days after the rechallenge and remained tumor free (Figure 8B). Two rechallenged mice died of probable xenogeneic graft-versus-host disease without any evidence of tumor. In contrast, all naïve mice developed marked early tumor progression by day 13 and died. Together, these data show that NKTR-255 administration resulted in enhanced and early antitumor efficacy of human CD19 CAR T cells in lymphoma-bearing NSG mice and robust and sustained persistence of functional CAR T cells after tumor clearance.

Peak serum IL-15 was associated with a higher probability of response in previous CD19 CAR T-cell studies^10,19,33 and we demonstrated that peak serum IL-15 after CAR T-cell infusion was independently associated with CAR T-cell counts in the blood. In conjunction with the previously described effects of IL-15 on T-cell proliferation and survival,¹⁸ these data suggest that IL-15 supplementation may improve the efficacy of CAR T-cell therapy.

To enable clinical IL-15 supplementation, engineered IL-15–based molecules have recently been developed.^24,34-36 We found that, compared with the administration of native IL-15, NKTR-255, a novel PEGylated form of IL-15, resulted in an extended IL-15 t_1/2 (30.5 vs 1.2 hours) and increased NK cells and CD8⁺ T cells in NHP blood. NKTR-255 also increased the proliferation, accumulation, and antitumor efficacy of human CD19 CAR T cells. A first-in-human phase 1 clinical trial of single-agent NKTR-255 in patients with R/R hematologic malignancies (#NCT04136756) is currently enrolling,^37,38 and preliminary results show a promising toxicity profile with no dose limiting toxicities and only transient elevations of cytokine release syndrome (CRS)–related cytokines.³⁹ In this study, an increase in CAR T cells after NKTR-255 treatment was observed in all patients who had received and progressed after prior CAR T-cell therapy and had detectable CAR T cells in blood at the time of the first NKTR-255 infusion.⁴⁰ These data provide strong support to test the combination of NKTR-255 and CAR T cells in human clinical trials.

The time to start IL-15 supplementation in relation to CAR T-cell infusion may affect efficacy and toxicity. Our previous clinical trial data suggested that adequate IL-15 concentration shortly after CAR T-cell infusion is associated with robust CAR T-cell accumulation. The concentrations of cytokines increase in response to lymphodepletion administered before CAR T-cell infusion,^10,16 and adequate IL-15 concentrations at or shortly (within a week) after CAR T-cell infusion can be achieved following the administration of appropriate lymphodepletion chemotherapy. However, early exogenous IL-15 supplementation might improve CAR T-cell counts and/or function, especially in patients with preexisting T-cell dysfunction owing to disease or previous therapies or an inadequate response to lymphodepletion. The possibility that early NKTR-255 supplementation could enable a decreased lymphodepletion intensity is intriguing and needs to be further tested in suitable models.

Particularly in patients with normal T-cell function and/or high tumor burden, early IL-15 supplementation may increase the risk of toxicities such as CRS and/or immune effector cell–associated neurotoxicity syndrome (ICANS) owing to rapid and enhanced CAR T-cell proliferation. Approaches are still in development to consistently and prospectively characterize CAR T-cell potency to identify patients who could benefit from early IL-15 supplementation and those in whom early supplementation may increase the risk of CRS and/or ICANS. Patients who ultimately develop severe CRS/ICANS usually present within the first week after CAR T-cell infusion.⁴¹ Therefore, we considered that the earliest suitable time after CAR T-cell infusion to start IL-15 supplementation in initial clinical trials would be from around days 7 to 14, to allow deferral of patients with severe CRS/ICANS early after CAR T-cell infusion and decrease potential toxicities from IL-15 supplementation.

In our preclinical in vivo studies, we studied the starting days from 7 to 21 after CAR T-cell administration and found that the timing of NKTR-255 after CAR T-cell infusion was an important determinant of efficacy. NKTR-255 starting 7 days after CAR T-cell infusion was associated with increased CAR T-cell survival and accumulation (AUC_0-28) in the blood and tissue and better disease control. The effects of NKTR-255 on human T cells and CAR T-cell efficacy were dose dependent. However, the enhanced proliferation of CAR T cells was mainly evident under conditions of low target cell abundance. At a high target cell burden, proliferation and cytokine secretion were mainly antigen dependent. The dichotomy of NKTR-255–mediated enhanced CAR T-cell proliferation with limited effects on effector functions is intriguing and requires further investigation. The limited augmentation of effector functions by increasing doses of NKTR-255 under conditions of high antigen burden might limit toxicity, providing additional support for starting NKTR-255 7 to 14 days after CAR T-cell infusion, when the tumor burden is lower. Importantly, tumor control was rapid and high CAR T-cell counts were sustained after tumor elimination in NKTR-255–treated mice. Although additional studies are required to definitively exclude exhaustion and demonstrate functional quiescence in CAR T cells in NKTR-255–treated mice, we did not observe evidence of ongoing activation/exhaustion by increased inhibitory receptor expression in persistent CAR T cells in these mice, in contrast to mice that did not receive NKTR-255. Our data does not demonstrate that NKTR-255 prevents exhaustion; however, NKTR-255–treated mice were protected against tumor rechallenge, indicating that persistent CAR T cells retained their functional capacity.

Our results show that NKTR-255 enhances endogenous T cells and NK cells in NHP and improves the efficacy of human CD19 CAR T cells in a xenogeneic lymphoma model. A phase 1 clinical trial of NKTR-255 and CD19 CAR T-cell combination therapy in patients with R/R large B-cell lymphoma (#NCT05359211) is ongoing.

The authors acknowledge the Fred Hutchinson Cancer Center Shared Resources, including the Comparative Medicine, Preclinical Imaging, and Flow Cytometry Cores.

This work was supported by grants from the National Institutes of Health, National Cancer Institute (T32CA009351 and 5K12CA076930-20) (C.K.C.), and in part by research funding from Nektar Therapeutics (C.J.T.).

Some figures were created with BioRender.com.

Contribution: A.V.H., C.K.C., T.K., and J.G. collected the research data; C.K.C., R.N.S., H.A.D., S.P.F., and R.M.H. performed the experiments; A.V.H., C.K.C., and S.F. analyzed and interpreted the data; S.R.R., M.Q.M., and C.J.T. designed the experiments; A.V.H., C.K.C., and C.J.T. wrote and edited the manuscript; and all authors reviewed and edited the final version of the manuscript.

Conflict-of-interest disclosure: A.V.H. reports honoraria from Bristol Myers Squibb (BMS) and Novartis and receives research funding from Juno Therapeutics (a BMS company) and Nektar Therapeutics. C.K.C. is an employee and stockholder of Genentech/Roche. T.M. is an employee and stockholder of Nektar Therapeutics. J.G. reports honoraria from EUSA Pharma, JMP, Larvol, and Multerra Bio; serves on scientific advisory boards for Legend Biotech, Janssen, Kite (a Gilead company), and MorphoSys; and receives research funding from Sobi, Juno Therapeutics, Celgene (a BMS company), and Angiocrine Bioscience. S.F. reports grants from BMS and other support in the form of pending equity from Link Immunotherapeutics outside of the submitted work; and has issued patents for PCT/US2021/025255 and PCT/US2021/025248d, and a patent for PCT/US2021/025260 issued, licensed, and with royalties paid from BMS. W.W.O. is an employee and stockholder of Nektar Therapeutics. S.R.R. is a cofounder and adviser to Lyell Immunopharma; has research funding from and intellectual property licensed to Lyell Immunopharma; was a cofounder of Juno Therapeutics; is an inventor of patents licensed to Juno Therapeutics; and served as an adviser to Juno Therapeutics and Adaptive Biotechnologies. M.Q.M. is an employee and stockholder of Nektar Therapeutics. C.J.T. has received research funding from Juno Therapeutics and Nektar Therapeutics; serves on scientific advisory boards for Precision BioSciences, Eureka Therapeutics, Caribou Biosciences, T-CURX, Myeloid Therapeutics, ArsenalBio, and Century Therapeutics; has stock/options in Precision BioSciences, Eureka Therapeutics, Caribou Biosciences, Myeloid Therapeutics, and ArsenalBio; serves on a data safety monitoring board for Kyverna; has the right to receive royalties from Fred Hutchinson Cancer Center as an inventor on patents related to chimeric antigen receptor T-cell therapy; and served on ad hoc advisory boards or as a consultant (last 12 months) for Allogene, Sobi, Decheng Capital, GlaxoSmithKline, and Nektar Therapeutics. The remaining authors declare no competing financial interests.

The current affiliation for C.J.T. is Faculty of Medicine and Health, The University of Sydney, Camperdown, NSW, Australia.

Correspondence: Alexandre V. Hirayama, Clinical Research Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave N, Seattle, WA 98109; e-mail: ahirayama@fredhutch.org.