Background
Interleukin-7 (IL-7) is a key cytokine in allogeneic stem cell transplantation (aHSCT) and drives homeostatic, extrathymic T-cell expansion in lymphopenic hosts [
1]. IL-7 may also promote expansion of alloreactive T-cells that mediate graft-versus-host disease (GVHD) [
2]. Elevated IL-7 levels in serum have been shown to be associated with acute GVHD [
3,
4]. Several cell types have been described to contribute to IL-7 production, e.g. stromal cells [
5], macrophages [
6], B-cells [
7] and thymic epithelial cells. Several conditions may impair IL-7 production, including infections associated with tissue damage of stromal cells, the fibroblastic reticular network (FRC) [
8] and cytotoxic therapies in the course of anti-cancer treatment or in conditioning regimens for HSCT. Murine studies have shown that radiation, provided in the course of HSCT, can result in reduced thymic stromal IL-7 production [
9]. However, it has not been unequivocally proven that thymus-derived IL-7 contributes substantially to systemic IL-7 levels. IL-7 is consumed by the pool of available immune cells expressing the heterodimeric IL-7 receptor (IL-7R, CD127) along with the common gamma chain (CD132) [
1,
3]. Expression of the IL-7R on T-cells is associated with T-cell differentiation and maturation, based on CD45RA and CCR7 expression [
10]. Precursor T-cells exhibited the highest numbers of IL-7R molecules per cell and terminally differentiated T-cells were found to express the lowest number of IL-7R molecules per cell.
The role of IL-7 in immune reconstitution after HSCT is multifaceted: it promotes thymopoiesis by driving development of immature thymocytes [
11,
12]. Some reports have suggested that IL-7 treatment leads to improved—but transient—immune reconstitution [
11] without increased alloreactivity [
13,
14]. In contrast, other studies have shown that IL-7 aggravates GVHD [
2] and that subsequent blockade of the alpha chain of the IL-7R may prevent GVHD [
15]. The situation is even more complex, since the IL-7R is not only available in the cell-membrane-bound format, but also as a soluble form (sIL-7R). The soluble IL-7R binds IL-7 with an affinity similar to that of the membrane bound IL-7R [
16], leading to sIL-7R-mediated inhibition of IL-7 signaling in T-cells [
17]. sIL-7R is not only generated by shedding of membrane-bound receptors, it is also associated with polymorphism in the IL-7R gene (rs6897932), which leads to increased splicing in the transmembrane domain of exon 6 in the 8-exon Il-7R gene [
18‐
20] resulting in increased sIL-7R generation. This SNP has been associated with autoimmune diseases, i.e. type-I diabetes mellitus [
21] and rheumatoid arthritis [
22]. IL-7R polymorphism has also been studied in adults after HSCT with inconclusive results concerning SNP analysis of donors [
23] and recipients [
24]. Up to now, the protein concentrations of IL-7 combined with its receptor IL-7R have not been measured in plasma from children and adults during 12 months after HSCT. We therefore designed a longitudinal study to determine IL-7/IL-7R plasma levels in 61 individuals after HSCT and we investigated associations between IL-7/IL-7R and clinical events after HSCT.
Methods
Patients and controls
The study involved 29 children and 32 adults (Table
1). Forty-eight patients underwent HSCT for malignant disorders, 16 patients were in first complete remission. 21 patients received grafts from HLA-identical sibling donors and the remaining patients received grafts from matched unrelated donors (n = 33), or HLA-mismatched unrelated donors (n = 8). The sources of stem cells were bone marrow, peripheral blood stem cells, or in a few individuals, cord blood transplants. Genomic HLA typing (MHC class I and class II four-digit typing) was performed as described previously [
25]. IRB approval (Stockholm Ethical Committee South 2010/760-31/1) was in place. Peripheral blood mononuclear cells (PBMCs) were from adult participants (n = 32) and in the case of children (n = 29), consent was obtained from their parents or legal guardians (on file at CAST; Center for allogeneic stem cell transplantation). Samples were obtained from 61 patients at 1, 2, 3, 6, and 12 months after HSCT and 26 controls (15 adults and 11 children). Plasma was obtained after centrifugation and stored at -20°C; PBMCs were isolated from heparinized blood over a ficoll hypaque gradient. The cells were preserved in liquid nitrogen using fetal bovine serum (FBS) containing 10% DMSO.
Table 1
Summary of patient characteristics
Age
| 18 (<1–65)* |
Children
(
<18 y
)
| 29 |
Sex (
M/F
)
| 38/23 |
Diagnosis:
| |
Non-malignant | 13 |
Acute myeloid leukemia/Acute lymphoid leukemia | 12/13 |
Chronic lymphoid leukemia | 4 |
Myelodysplastic syndrome | 11 |
Other malignancies | 8 |
Stage (
early/late
)
| 16/32 |
Donor age
| 26 (0–62) |
Donor sex (
M/F
)
| 38/23 |
Donor
| |
Sibling/HLA-identical, related | 21 |
MUD | 32 |
HLA-mismatched, unrelated | 8 |
Conditioning
| |
MAC/RIC | 34/27 |
Chemo-based | 38 |
TBI-based | 23 |
ATG
| 47 (77%) |
GVHD prophylaxis
| |
CsA ± MTX | 41 |
CsA + Prednisolon | 3 |
Tacrolimus + Sirolimus | 16 |
CsA + MTX + Cy | 1 |
Stem cell source:
| |
BM/PBSCs/CB | 25/31/5 |
HSCT regimen
Conditioning
Conventional myeloablative conditioning was given to 34 patients and consisted of cyclophosphamide (Cy) at 60 mg/kg for two days in combination with fractionated TBI (FTBI) at 3 Gy/day for four days (n = 15), or busulphan (Bu) at 4 mg/kg/day for four days (n = 17) [
26]. Two patients received other protocols. Reduced-intensity conditioning (RIC) was given to 27 patients and consisted of fludarabine (Flu) at 30 mg/m
2 for 3–6 days in combination with either Bu at 4 mg/kg/day for two days (n = 7), FTBI at 3 Gy/day for two days and Cy at 60 mg/kg/day for two days (n = 7), Cy at 30 mg/kg/day for two days (n = 7), treosulphan at 12–14 g/m
2/day for 3 days (n = 5), or TBI (2 Gy) (n = 1).
GVHD prophylaxis and CMV PCR
Immunosuppressive treatment mainly consisted of cyclosporine (CsA) in combination with a short course of methotrexate (MTX) (n = 41), or tacrolimus and sirolimus (n = 16) [
27]. All patients with an unrelated donor or a non-malignant disease received anti-thymocyte globulin (ATG) (Thymoglobulin, Genzyme, Cambridge, MA) (n = 45) or alemzumab (Genzyme) (n = 2) for 2–4 days during conditioning [
28]. During the first month, blood CsA levels were kept at 100 ng/mL in patients with malignancies when a sibling donor was used and at 200–300 ng/mL when an unrelated donor was used and also in patients with non-malignant disorders regardless of the donor. In the absence of GVHD, CsA was discontinued after three to six months for patients with malignancies and after 12–24 months for patients with non-malignant disorders. Patients were monitored for CMV viral load with a quantitative PCR on whole blood from the time of engraftment weekly until day 100 after HSCT as published previously. Later than three months after HSCT, weekly monitoring was continued only in those patients who had experienced CMV reactivation or had severe GVHD, while the other patients were monitored at each visit to the transplant center occurring every 2-3 weeks until 6 months after HSCT. Pre-emptive antiviral treatment with either i.v. ganciclovir 5 mg/kg BID or oral valganciclovir 900 mg BID was given at the center’s chosen intervention limit > 1000 copies/mL blood. The duration of therapy was a minimum of two weeks and was discontinued when the CMV viral load was < 500 copies/mL [
29,
30].
Supportive care
All patients were kept in reversed isolation or they were treated at home, as described in detail previously [
31].
Statistical analysis
Differences between patient groups (i.e. children versus adults) or within each group (i.e. comparing different time points) were analyzed using Mann-Whitney U-test or the Wilcoxon test using the Statistical software program (version 10) and GraphPad Prism 4 software. In the multivariate analysis of factors affecting the levels of sIL-7R at different time points, multiple regression were used. To determine whether there was any correlation between CD127 (IL-7R) positive immune cells and soluble IL-7R levels, we used linear regression analysis with the GraphPad software.
Quantification of plasma IL-7 and IL-7R
IL-7 quantification was performed using the ELISA IL-7 Eli-pair (Cat. 851.680.010; Cell Sciences, Inc., Canton, MA) according to the manufacturer’s protocol (standard range between 200 and 3,125 pg/mL). Soluble CD127 was measured using an IL-7R ELISA; the anti-IL-7R alpha chain-directed antibody R34.34 (anti-CD127 purified Ab, 1 μg/ml; Beckman Coulter Inc., Brea CA) served as the capture antibody (50 μL/well) by incubation overnight with plasma at 4°C. The recombinant human IL-7 R alpha/CD127 Fc Chimera (306-IR; R&D Systems, Minneapolis, MN) served as the standard (ranging between 0.78125 and 100 ng/mL). Standard and samples were incubated for 4 h, followed by washing steps (PBS, 0.05% Tween) as described earlier [
16]. sIL-7R was detected with a biotinylated anti-CD127 antibody (BAF306; R&D Systems). Incubation was for 1 h at RT, followed by washing as described above. Streptavidin-HRP was applied (554066: BD Biosciences, Frankin Lakes, NJ) for 30 min, with subsequent development using Tetramethylbenzidine (TMB). The absorbance was read at 450 nm.
Flow cytometry
PBMCs (0.5 × 10
6 cells) were first stained with anti-CCR7 for 15 min at 4°C, followed by addition of the 10-color antibody mix as described in detail previously [
10]. The PBMC-antibody mixture was incubated for 15 min at 4°C. The anti-CD27 antibody was then added to the cells, which were incubated at 4°C for 15 min, followed by washing with 1 mL of PBS containing 0.1% BSA. The cell pellet was resuspended in 200 μL of PBS (with 0.1% BSA) and the cells were analyzed as described previously [
10].
For analysis of PBMCs from children, frozen PBMCs were thawed and 1 × 106 cells were incubated at 4°C for 15 min with the following antibodies: peridinin-chlorophyll-protein complex- (PerCP-) conjugated anti-CD3 (SK7), allophycocyanine 7- (APC-Cy7-) conjugated anti-CD8α chain (SK1), phycoerythrincyanin 7- (PE-Cy7-) conjugated anti-CCR7 (3D12) purchased from BD Biosciences (Stockholm, Sweden), Krome Orange-conjugated anti-CD4 (13B8.2), fluorescein isothiocyanate- (FiTC-) conjugated anti-CD8β chain (2ST8.5H7), APC-Alexa Fluor 700-conjugated anti-CD107a (H4A3), PE-Texas Red-conjugated anti-CD45RA (2H4), APC-conjugated anti-CD127 (R34.34) purchased from Beckman Coulter (Marseille, France), and Brilliant Violet-conjugated anti-CD117 (104D2) purchased from BioLegend (London, UK). After washing, flow cytometric analysis was performed using a Navios flow cytometer (Beckman Coulter, Miami, FL, USA) and data were analyzed by using FlowJo software (Tree Star Inc., Ashland, OR; USA).
Discussion
The motivation for examining soluble IL-7R after HSCT was threefold. First, increased sIL-7R levels have been shown to be associated with an increased risk of developing autoimmune responses [
18] and we hypothesized that altered levels of sIL7R may drive GVHD. Secondly, increased soluble IL-7R has been shown to bind free IL-7 and to inhibit IL-7 signaling (and therefore immune effector functions) in CD8
+ T-cells from patients with infections [
33]; inhibition of IL-7, via binding to soluble IL-7R, could potentially impact on GVHD development. Thirdly, increased sIL-7R has been associated with improved immune reconstitution and immune competence in patients with HIV infection [
34]. All three biological scenarios, i.e. immune reconstitution, resistance to infection, and higher risk of developing autoimmune responses are clinically relevant after HSCT. Up to now, it has not yet been well defined which cell type or tissue is responsible for generating sIL-7R. The soluble IL-7R could be generated by shedding from cells or by splicing of the IL-7r associated with a polymorphism in the IL-7R gene (rs6897932) [
18‐
20].
Recipients of grafts from HLA-identical siblings showed higher sIL-7R levels than recipients of grafts from URD (unrelated donors) (Figure
4). This difference was not only significant in the univariate analysis but also in the multivariate analysis at 2, 3, and 6 months and with a trend at 12 months after HSCT (Table
2). It is possible that minor histocompatibility antigens (mHags) contributed to immune reconstitution and increased sIL-7R levels after HSCT. Poor immune reconstitution, including low sIL-7R plasma levels, may be associated with increased risks for infection in recipients of grafts from URD as compared to recipients of HLA-identical sibling grafts [
35].
Earlier studies showed a close correlation between CMV infection and GVHD [
36,
37]. A significant finding in the univariate and the multivariate analysis in the current study was the decreased level of plasma sIL-7R in patients with any grade of acute GVHD (Figure
5, Table
2). Acute GVHD and also chronic GVHD have a profound effect on immune functions after HSCT [
38,
39] including increased risk of CMV infection: In the univariate analysis, patients with CMV infection exhibited lower levels of sIL-7R at 2 months after HSCT as compared to patients without CMV infection. This is the timeframe when most patients experience CMV reactivation after HSCT. Immune responses to herpesviruses in general, and CMV infection in particular may trigger acute GVHD. Not mutually exclusive, GVHD, may also pave the way for CMV infection, which delays immune recovery and increases risk of infections [
40,
41] after HSCT. sIL-7R and CMV infection was not significant in the multivariate analysis, which may suggest that GVHD is more important than CMV infection leading to decreased sIL-7R plasma levels.
We also found a tendency of lower sIL-7R levels in plasma from patients treated with ATG (Table
2). We treat all recipients of unrelated bone marrow grafts with ATG to prevent GVHD [
42] at our center. In addition, patients with non-malignant disorders are also treated with ATG, since they do not benefit from GVHD. ATG has a prolonged effect on T-cell immune reconstitution and may therefore interfere with the generation of (soluble) IL-7R. The use of ATG also affects the rate of infections after HSCT in a dose-dependent fashion [
28]. The data from the present study suggest that circulating T-cells (the numbers of which are reduced upon ATG treatment) contribute substantially to generation of soluble IL-7R generation, particularly since IL-7R expression is associated with T-cell maturation and differentiation [
10].
Reduced levels of IL-7 protein were also identified in plasma from recipients of bone marrow as compared to patients who received peripheral blood stem cell transplants (Table
3). These two transplant types have different composite of the graft, which may be biologically relevant for IL-7 and soluble IL-7R production as well as IL-7 consumption. Blood cell grafts contain ten times more T-cells and NK-cells than bone marrow grafts [
43,
44], supporting the notion that sIL-7R is produced from circulating immune cells. Decreased sIL-7R levels were also identified in plasma from recipients of grafts from unrelated donors as compared to recipients of grafts from HLA-identical siblings. Furthermore, there was a correlation between acute graft-versus-host disease—and to some extent also CMV infection after HSCT—and lower sIL-7R levels.
Three independent studies showed that elevated sIL-7R is associated with an increased risk of to develop autoimmunity, a situation which maybe at first glance counter-intuitive: since soluble IL-7R may bind free IL-7 and neutralizes its effects [
16]. Two alternative mechanism, not mutally exlusive, could explain the increased risk of developing autoimmunity due to elevated sIL-7R. The sIL-7R/IL-7 complex may serve as a buffer system and will first neutralize free IL-7. Serum IL-7 levels (which are one tenth of sIl-7R levels) are tightly controlled [
45]. Firstly, IL-7, complexed to the sIL-7R, could be released later from its (soluble) receptor and drive autoimmune responses. Secondly, sIL-7R/IL-7 complexes may be more potent in driving expansion of CD8
+ T-cell subsets (in murine experiments) [
46]. It could very well be that IL-7, complexed to sIL-7R, delivers a more potent signal to the cell-bound IL-7R, an event which would be even more accentuated in ‘hypersensitive’ autoreactive T-cells [
33]. To summarize, the IL-7/sIL-7R complex represents a double-edged sword: free IL-7 supports immune reconstitution and promotes increased immune reactivity in infections [
47,
48]; yet free IL-7 may also drive GHVD [
3]. ‘Neutralized’ IL-7, by binding to the sIL-7R may not accessible to IL-7R-positive immune cells; this situation may be associated with increased risk of infections. Subsequently, IL-7, released from the sIL-7R, may be available to antigen-specific T-cells and ensure T-cell survival, which may also include immune cells mediating GVHD. Until now, the detailed dynamic of sIL-7R and IL-7 interaction in
ex vivo collected clinical material has not been determined, yet a biologically and clinically relevant time frame to test for sIL-7R would be monthly within the first three month after HSCT; a time frame with a high risk to develop CMV infection and/or GVHD.
Competing interests
The authors declare that there have no competing interests.
Authors’ contributions
TP carried out analyses and performed statistics, processed patient samples and wrote the manuscript, LR carried out analyses and established the sIL-7R ELISA, MR performed statistical analyses, BO was involved in patient recruitment, clinical management and data interpretation; NKV was involved in sample procurement and analyses, RA performed flow cytometric analyses, IE was involved in study design, data analyses and writing the manuscript, JW and AGJ were responsible for children’s care management, sample procurement, data analyses and interpretation, IM was responsible for flow cytometry, OR was involved in patient care and management, data analysis, study design and writing the manuscript, MM was responsible for the study design, data analyis and wrote the final version of the manuscript. All authors read and approved the final manuscript.