Donor Vδ1+ γδ T cells expand after allogeneic hematopoietic stem cell transplantation and show reactivity against CMV-infected cells but not against progressing B-CLL

γδ T lymphocytes play an important role in immune reactions towards infections and malignancies. In particular, Vγ9–Vδ1+ T lymphocytes are thought to play protective antiviral roles in human CMV infection. Recently, Vδ1+ T lymphocytes were proposed to also have anti- B-CLL reactivity. Here we report a case of 48-year-old man who received allogeneic stem cell transplantation for progressive B-CLL. Within one year after transplantation, lymphoma relapsed despite a dramatic increase of Vδ1+ T cells in the patient’s blood. In vitro killing assays revealed activity of patient’s γδ cells against CMV target cells, but not against the relapsing lymphoma-cells. This argues for a contribution of Vδ1+ cells in the immune reaction against CMV reactivation, but does not support a strong correlation of expanded Vδ1+ T cells and favorable disease outcome in B-CLL patients.


Background
Several types of T lymphocytes bearing γδ T cell receptors (TCR) are currently investigated as potential anticancer agents in cell-based immunotherapy. Recently, Vδ1 + T lymphocytes were shown to be cytotoxic to B-CLL-derived cell lines [1] and it was proposed that Vδ1 + T lymphocytes may contribute to limiting disease progression in B-CLL patients [2]. Activated Vδ1 + T lymphocytes can produce inflammatory cytokines such as TNF-α and IFN-γ and can be cytotoxic. Both cytokine release and cytotoxicity of Vδ1 + T lymphocytes are at least in part mediated through NKG2D receptor, which recognizes the stress-induced ligands MIC-A, MIC-B, and ULBP3 on target cells. At the same time, Vδ1 + T lymphocytes are implicated in the human immune response to cytomegalovirus infection [3][4][5][6][7]. Patients receiving allogeneic stem cell transplantation as treatment for CLL often encounter life-threatening viral infections in the posttransplant period due to strong immunosuppression. Thereby, Vδ1 + T lymphocytes expand during posttransplant CMV reactivation and likely participate in the immune response to CMV [3]. It has been suggested that during immune response to CMV both γδ TCR crossreactivity and NKG2D ligands confer cross-protection against tumor cells [8][9][10]. Here we report a case of fulminant CMV reactivation after second allogeneic stem cell transplantation as treatment for CLL. Despite expansion of donor Vδ1 + T lymphocytes up to 25% of all circulating peripheral blood lymphocytes, no reactivity against relapsing B-CLL could be observed.

Case presentation
A 48-year-old patient was diagnosed with stage I (Rai classification) CLL in 2002 with unmutated heavy chain immunoglobulin. After 4 months of observation, he required conservative immunochemotherapy for progressive leukocytosis and lymphadenopathy (six cycles Fludarabine). In 2006, he underwent allogeneic hematopoietic stem cell transplantation from his HLA-identical brother. This led to normalization of blood counts, regression of adenopathy, and a 6-months progression-free interval. Donor and recipient were CMV + , however, reactivation was not observed. In March 2007, due to declining donor chimerism, he was given donor lymphocyte infusions which, however, could not prevent clinical relapse of CLL four months later. Several cycles of immunochemotherapy (Rituximab alone or in combination with Fludarabine or Bendamustine) and donor lymphocyte infusions led to stabilization for about one year, when a second relapse of B-CLL occurred. In October 2011, after successful re-induction, the patient again underwent additional allogeneic hematopoietic stem cell transplantation, now from an unrelated donor. Main complications after this second allogeneic transplantation were repetitive CMV reactivations, which were treated with four cycles of antiviral therapies including 2x Ganciclovir, Foscarnet, and Cidofovir for CMV treatment. CMV reactivation resolved in March 2012. No CMV specific CD8 + donor T cells could be observed by tetramer staining (data not shown), but frequencies of donor γδ T lymphocytes rose up to 25% of all circulating peripheral lymphocytes ( Figure 1A). It is likely that T lymphocytes expanded during post-transplant CMV reactivation and participated in the immune response to CMV [3]. Of note, the patient showed no CMV reactivation after the first allogeneic transplantation, and frequencies of γδ T lymphocytes had not increased (3% and 4% of peripheral lymphocytes measured at 11 months and 1 month before second transplantation, respectively). Despite expanded donor γδ T cell counts, we observed a concomitant decline of donor chimerism and progressive lymphadenopathy ( Figure 1B).
Next, we sought to investigate the source, phenotype and reactivity of the expanded γδ T lymphocytes in more detail. First, we compared γδ T lymphocytes among donor and recipient lymphocytes. While almost all γδ T cells in peripheral blood of the stem cell donor were Vδ9 + , the vast majority (88%) of donor γδ T cells  recovered from the patient at 8.5 months after second transplantation were Vδ9 - (Figure 2). We suspected that the expanded T lymphocytes were Vδ1 + cells, which are known for CMV-reactivity [6]. Specific flow cytometric analysis confirmed that indeed 24% of all CD3 + lymphocytes expressed the Vδ1 + chain on their cell surface (Figure 3). Since donor chimerism had declined in spite of expanded donor γδ T cell counts, we tested the reactivity of FACSsorted γδ T lymphocytes from the patient against relapsing B-CLL. At the same time, in vitro killing of CMV-infected human foreskin fibroblasts (HFF) was assessed ( Figure 4). Interestingly, freshly ex vivo isolated γδ T lymphocytes from the patient, of which > 80% were Vδ1 + Vδ9cells, showed a titratable specific lysis of CMV infected human fibroblasts, but not against his own freshly sorted leukemia cells. It is tempting to speculate that the patient's B-CLL was not recognized because it expressed too low levels of NKG2D ligands such as MIC-A, MIC-B, or ULBP-proteins on its cell surface. Indeed, flow cytometric revealed lacking expression of these proteins on the cell surface of the patient's B-CLL cells (data not shown).

Conclusions
Our observations support the view that reactivity against CMV-infected cells was the driving force for Vδ1 + γδ T cell expansion in this patient. Previously, such expansion Total γδ T cells were sorted from patient's blood samples using PE-conjugated anti pan γδ TCR (clone 11 F2) after Ficoll separation using a FACS Aria cell sorter 9 months after transplantation. At the same time, B-CLL cells were sorted according to size and for positive signals using PerCPCy5.5-conjugated CD19 (clone 5J25C1) and PE-Cy7-conjugated CD20 (clone L27). Cytotoxicity assay: 51 chromium ( 51 Cr) release cytotoxicity assay was performed by using sorted γδ T cells as effectors and either (A) CMV-infected primary human foreskin fibroblasts or (B) autologous tumor cells as targets. After 51 Cr-labeling, target cells were washed and resuspended in medium (RPMI1640 supplemented with 10% foetal calf serum, 100 U/ml penicillin/streptomycin, 1 mM sodium pyruvate, and 2 mM glutamine). 100 μl of effector cells (1×10 6 /ml -1.25×10 5 /ml) were pipetted in triplicates at three effector to target (E/T) ratios (20:1, 10:1, and 2.5:1) in V-bottom microtiter plates containing 50 μl of target cell solution (1×10 5 /ml). The assay was incubated for 20 hours. The plates were centrifuged and 25 μl of cell-free supernatants were harvested. Specific cytotoxicity was measured by determining released 51 Cr. Background values were determined by incubating target cells without effector cells. Maximal values were obtained by lysing target cells with Triton X-100. Specific lysis was calculated by: experimental releasespontaneous release / maximum release -spontaneous release x 100. Generation of positive control target cells by HFF infection: HFF were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal calf serum (FCS) and antibiotics. Cells were infected with HCMV TB40/E UL11-V5 mutant [12] at an m.o.i. of 1 for 120 h prior to in vitro killing assay.
was neither observed in the stem cell donor's peripheral blood nor in the patient's blood before second transplantation. This argues for a contribution of Vδ1 + cells against CMV reactivation after transplantation, which is in line with recent literature [3]. However, the expanded Vδ1 + cells were unable to kill autologous tumor cells in vitro and likely also in vivo as the lymphoma was progressing. Taken together, our findings do not match the suggested strong correlation of expanded Vδ1 + T cells and favorable disease outcome in untreated B-CLL patients [2].

Consent
Written informed consent was obtained from the patient for publication of this case report.