PD-1 expression contributes to functional impairment of NK cells in patients with B-CLL (2024)

B cell chronic lymphocytic leukemia (B-CLL) is a common leukemia subtype [1] and compromised immune function is a major clinical problem leading to increased mortality among patients [2].

Natural killer (NK) cells recognize and kill transformed or virally infected cells through mechanisms including granule-mediated cell lysis, cytokine release, and antibody-dependent cell-mediated cytotoxicity (ADCC) [3, 4]. However, NK cells are frequently dysfunctional in patients with cancer, and this profile is also seen in patients with CLL. An imbalance in the relative expression of activating and inhibitory receptors is an important mechanism of immune evasion, with decreased expression of the dominant activatory receptors NKG2D, DNAM-1 and NCRs as a common feature. This phenotype is associated with reduced degranulation and impaired lysis of target cells [5,6,7].

Recent studies have shown that NK cells can express a range of inhibitory checkpoint proteins that may also negatively regulate the activity of NK cells. In particular, PD-1 expression has been demonstrated in patients with several cancer subtypes, including hematological malignancies [8, 9], and is associated with functional impairment which can be reversed by PD-1 blockade [10, 11].

It is well established that engagement of PD-1 on T cells with its PD-L1 ligand can inhibit T cell functional responses to CLL tumor cells and mediate an exhausted T cell phenotype [12, 13]. Indeed, PD-1 blockade in patients with B-CLL, either as a single agent therapy or in combination with ibrutinib, has elicited clinical responses [14], although the role of PD-1 on NK cells in patients with B-CLL has not been explored.

Here we investigated the expression of a range of checkpoint receptors, including PD-1, on NK cells from B-CLL patients. We characterized the phenotype and functional capacity of PD-1^pos NK cells compared to their PD-1^neg counterparts and evaluated the impact of PD-1:PD-L1 blockade on the tumor-specific activity of NK cells against both primary NK cells and NK lines.

The immune checkpoint co-expression pattern of PD-1, CTLA-4, LAG-3, TIGIT and TIM-3 was further examined using Boolean gating. The expression of a range of checkpoint combinations was increased in the patient group (Fig.1B). In particular, the proportions of PD-1/TIGIT; CTLA4/LAG3; PD-1/CTLA4; PD-1/LAG3; PD-1/TIGIT/LAG3; PD-1/CTLA4/TIGIT; and PD-1/CTLA4/TIGIT/LAG3 co-expressing NK cells were all increased in the patient group. Co-expression of the strong inhibitory checkpoints PD-1 and TIGIT was noteworthy as a phenotype not observed in healthy donors but comprising over 2% of the NK cell pool in many patients. Furthermore, it is notable that PD-1 expression is a component in 6 of the 7 checkpoint combinations that are increased on NK cells in patients, implying a potentially important central role for PD-1 in the checkpoint regulation of NK cells in CLL.

The expression of differentiation and activating receptors was next determined on PD-1^pos and PD-1^neg NK cells. PD-1^pos populations expressed high levels of the late differentiation marker CD57 (85 ± 3.5%) but less expression of NKG2A, a protein typically found on less mature NK subsets (22 ± 9.4%). Comparable values were 78 ± 2.4% and 35 ± 9.1% for PD-1^neg NK cells respectively (p = 0.0078 for both) (Fig.2B). Importantly, the expression of the NK-activating receptors NKG2D, NCRs and DNAM-1 was substantially downregulated on PD-1^pos NK cells compared to PD-1^neg populations (Fig.2C). In particular, NKG2D was expressed on 66% ±9.3% of PD-1^pos NK cells compared to 84 ± 4.3% of PD-1^neg NK cells (p = 0.0137). Downregulation of NKp30 and NKp46 was even more dramatic, with expression values of 36 ± 12% vs. 63 ± 8% (p = 0.049), and 8.5 ± 3.5% vs. 31 ± 6%, respectively (p = 0.001). DNAM-1 expression was reduced by 62% on PD-1^pos populations, present on 33 ± 11% of cells compared to 87 ± 3% of PD-1 ^neg cells (p = 0.023).

scRNA-Seq was used to compare the transcriptome of FACS-sorted PD-1^pos and PD-1^neg NK cells but revealed relatively subtle differences between populations (Supplementary Fig.3). Transcription of PDCD1, the gene encoding PD-1, was observed in the PD-1^pos subset, indicating that trogocytosis is not the sole determinant of protein expression [15]. Of note, the transcriptomes of PD-1^pos and PD-1^neg NK cells did not separate into two distinct clusters, implying that PD-1 expression is not a dominant transcriptional NK lineage marker. Enrichment for genes associated with cytotoxicity and immune synapse formation may reflect high levels of ongoing activation.

The functional relevance of PD-1 expression on NK cells in patients with B-CLL was next explored. NK cells were stimulated with PD-L1-positive 721.221 target cell lines that express both PD-L1 and PD-L2 (Supplementary Fig.4) and cytokine production was measured using intracellular flow cytometry. IFN-γ and TNF-α production was 10-12-fold lower from PD-1^pos cells compared to PD-1^neg subsets (IFN-γː 0.2 ± 0.08% vs. 2.6 ± 0.4% (p = 0.002); TNF-αː 0.2 ± 0.07% vs. 2.4 ± 0.4% (p = 0.002)) (Fig.2D). To assess whether impairment of cytokine production could be reversed by blockade of PD-1 with its ligand, NK cells were stimulated in the presence of antibodies against PD-L1 and PD-L2. Indeed, PD-1:PD-L blockade doubled the proportion of IFN-γ+ PD-1^pos NK cells (3.1 ± 0.4% vs. 1.5 ± 0.5%; p = 0.0313) (Fig.2E). Of interest, PD-L blockade had no impact on the relative proportion of TNF-α + NK cells following activation (data not shown), potentially reflecting the impact of additional checkpoint receptors on PD-1^pos cells.

We next assessed CD107a expression as a marker of stimulation-induced NK cell degranulation. CD107a expression was observed on only 9.9 ± 1.6% of PD-1^pos NK cells compared with 13.5 ± 1.9% of PD-1^neg NK cells (p = 0.001; Fig.2F). This value increased to 11.6 ± 2.2% after PD-L blockade (p = 0.027) (Fig.2F) whilst no increase was observed with PD-1^neg NK cells.

As the number of PD-1^pos NK cells was too low to undertake a direct cytotoxicity assay, the functional impact of PD-1 expression was determined by transduction of the NK-92 cell line using a retroviral vector (Supplementary Fig.3). Flow cytometry was then used to determine the relative degranulation and cytotoxic ability against the 721.221 cell line. In line with observations from primary cells, PD-1^pos NK-92 cells expressed markedly lower CD107a levels than control NK-92 cells following stimulation with 721.221 (1.6 ± 0.2% vs. 8.8% ± 1.5% (p = 0.0079)) (Fig.2G). Cytotoxicity against PD-L1/2-expressing 721.221 cells was also substantially reduced (7.4 ± 1.7% vs. 33 ± 3.4% (p < 0.001)) (Fig.2H). Importantly, antibody blockade against PD-L1 and PD-L2 increased CD107a expression to 3.3 ± 0.4% (p = 0.016) (Fig.2G) whilst cytotoxicity increased to 16 ± 2.4% (p = 0.024) (Fig.2H).

In conclusion, the expression of a range of inhibitory checkpoint proteins is increased on NK cells in patients with CLL and PD-1 is a common shared factor in many cases. PD-1^pos cells have impaired functional activity but this may be partially improved by inhibition of ligand engagement. Enhancement of NK cell function may therefore contribute to the clinical utility of antibody mediated PD-1 checkpoint blockade in patients with B-CLL.