CD127 expression in peripheral T cells of pediatric kidney transplant recipients

Introduction

Although kidney transplantation (KT) is the preferred treatment for end-stage renal disease (ESRD) in children, the occurrence of rejection is a dominant risk factor for adverse graft outcome [1]. Understanding the mechanisms of rejection and tolerance can lead to the development of new non-invasive methods to monitor the immune response in children after KT. CD4+CD25+Foxp3+ T cells are now widely considered to be the classic Treg population. Foxp3 is an intracellular molecule, detection of which requires fixation and permeabilization of cells. The fixed cells cannot be used in studies of Treg function. So, finding a specific cell surface marker of Treg cells is mandatory for further study [2]. In many studies, CD127 (IL7 receptors) expression in CD4+CD25+ cells was correlated inversely with FoxP3 expression, and CD4+CD25+CD127 cells showed suppressive activity [3-5]. Previous data suggested that the CD127 biomarker can be used to more selectively enrich human Treg cells for further in vitro and in vivo studies [6]. However, the clinical significance of changes in percentages of circulating CD4+ regulatory T cells after transplantation is not yet clear and needs further studies. In the present work, we aimed to study the percentage of CD127 in peripheral T cells of pediatric kidney transplant recipients by flow cytometry and to detect the association between CD127 surface marker and the development of rejection among this group of patients.

MATERIAL AND METHODS

The study included fifty pediatric kidney transplant recipients recruited from the Kidney Transplantation Outpatient Clinic, Cairo University Children’s Hospital (CUCH). Twelve healthy children who attended the Pediatric Clinic of the Medical Research Centre of Excellence (MRCE), National Research Centre (NRC) with no clinical signs or family histories of renal disease were included for comparison of measured lymphocyte subset values. The study was conducted from 2014 to 2017. Kidney transplant recipients showing signs of ureteral obstruction and/or renal artery stenosis of the graft, arterial, venous thrombosis, and infection-induced fever were excluded from the study. The time elapsed from the time of transplantation to the point of the study was 2.54 ±1.35 years (range 0.5-6 years). Peripheral blood samples were obtained from KT recipients.

Ethical issues

All included patients’ guardians gave informed written consent before participating in the study, which was read and approved by the Ethics Committee of NRC in Egypt. Immunosuppressive (IS) regimens Antibody induction therapy was used in 46 patients, while 4 patients did not receive antibody induction immunosuppression. IL-2 receptor blocking antibody (basiliximab) was administrated in 12 patients while anti-thymocyte globulin (ATG) was administrated in 34 patients. All children received intravenous methylprednisolone perioperative as a part of induction immunosuppressive therapy. Steroids then gradually tapered to oral prednisolone after the first week that was tapered down to 2.5-7.5 mg/day by the first year of transplantation. In addition to steroids; immunosuppressive protocol included calcineurin inhibitor (CNI) and mycophenolate mofetil (MMF). Tacrolimus was the CNI used in 32 patients while cyclosporine (CsA) was given in 18 patients. Mycophenolate mofetil was administrated as an adjuvant therapy to all patients for at least one-month post-transplantation then continued in 46 patients afterward. Everolimus was administered in 4 patients (in combination with steroids and low dose CsA) after at least one-month post-transplantation.

Clinical and laboratory parameters

The donor relation (related vs. unrelated), acute rejection (AR) episodes, cytomegalovirus (CMV) infection, CsA/tacrolimus trough serum concentrations, and current graft function were reviewed. Cold ischemia time was defined as the Time elapsed between clamping of donor graft artery and de-clamping of the anastomosing vessel in the recipient (signifies the duration of ischemia/reperfusion injury). AR was defined as a rise in serum creatinine of 20-30% from baseline levels and accompanied by clinical symptoms and signs as fever (temperature of more than 37.5°C), graft tenderness, and oliguria [7]. Presumed acute rejection (PRAR) was defined as an episode of AR, which is clinically diagnosed and medically treated (by pulse methylprednisolone), but a biopsy sample was not taken or did not show signs of rejection according to the Banff criteria [8]. Biopsy proven acute rejection (BPAR) was defined as acute graft dysfunction associated with pathological evidence of rejection.
Chronic allograft dysfunction (CAD) was defined clinically as a progressive deterioration of graft function with ≥ 15% irreversible rise in creatinine within 1 to 3 months and proteinuria ≥1 g/24 h together with a histologic diagnosis of interstitial fibrosis and tubular atrophy (IFTA) [9]. Patients with chronic antibody-mediated rejection (cAMR) were defined as patients having progressive allograft dysfunction (rise of creatinine and/or proteinuria ≥ 0.5 g/d) over recent months, together with evidence of circulating donor-specific antibodies and a biopsy-proven diagnosis of cAMR (based on the Banff ’07 criteria [10] with detection of C4d in peritubular capillaries. From the 7 patients with CAD, one patient was diagnosed with cAMR and 6 patients were diagnosed with chronic allograft nephropathy.

Flow cytometric analysis

Fresh blood samples on EDTA (100 Ul) with monoclonal antibodies were incubated 20 min at room temperature in the dark. Samples were lysed with 0.5 ml lysing solution Optilyse C (Beck man Coulter, Brea, CA, USA) 10 min the room temperature in the dark. Lysing reaction was stopped with 1 ml Cell Wash (optimized PBS) (Beck ton Dickinson Bioscience, Benelux, Belgium), the pellet was suspended in PBS and kept in dark between 2 and 8°C. Samples were measured on an FC 500 flow cytometer (Beck man Coulter, Brea, CA, USA). Gating strategy: As described before [11, 12] cells were gated by side scatter and CD4 expression. Subsequently, CD127 was measured on the cell surfaces. A flow cytometry analysis was performed with at least 100 events in the gate. The frequency of CD127 is expressed as a percentage of peripheral blood mononuclear cells (PBMCs).

Statistical analysis

Data were tabulated and subjected to computer-assisted statistical analysis using SPSS version 16.0. Nominal data will be described as frequency and percentage and compared using χ2 tests. Numerical data were described as a mean and a standard deviation and compared using the Student t-test. Correlation between various variables was done using the Spearman rank correlation equation. Nonparametric data were compared using Mann-Whitney and Kruskal-Wallis Tests. ANOVA post hoc test was used for multiple comparisons. Accuracy was represented using the terms sensitivity and specificity. Receiver operator characteristic (ROC) analysis was used to determine the optimum cut-off value for the IL-7R level in predicting active rejection. Logistic regression was done to detect independent predictors of the CAD. A p-value less than 0.05 was considered significant.

RESULTS

Patient characteristics

The mean age of the study group was 10.36 ±3.84 years with the mean post-transplantation (post-Tx) duration of 30.9 ±16.5 months. The male/female ratio was 35/15. The original renal disease was obstructive uropathy in 18 patients (36%), inherited nephropathy in 14 patients (28%), unknown in 14 patients (28%), and chronic glomerulopathy in 4 patients (8%). All included patients received living donor kidney transplant [related (LRKT)/unrelated (LUKT) = 4/1]. All patients received their first renal transplant except 1 patient with a previously failed graft due to venous thrombosis. All included recipients were negative for HIV ab, HBV surface antigen before KT; eleven (22%) recipients were HCV ab positive after receiving antiviral treatment (interferon) with low-grade viremia as tested by RT-PCR study at the time of transplantation. CMV IgG was positive for donors and recipients in 44 patients, negative for both in 4 cases, and negative recipients received from positive donors in 2 patients.
Demographic, clinical characteristics, and laboratory data of transplanted patients are summarized in Table 1. The mean CD127 expression of transplanted patients was significantly elevated than that of controls (2.76 ±3.26% vs 0.95 ±0.94%, p = 0.042) (Figure 1). The associations between the percentage of CD127 and the clinical-laboratory parameters Significant positive correlation was found between CD127 expression and diastolic blood pressure (DBP) (p = 0.047, CI = 0.288). CD127% negatively correlated with hematocrit (p = 0.04, r = –0.359). In addition; no significant association was found between CD127 expression and any of demographic, other clinical, or laboratory data listed in Table 1. As illustrated by Table 2; donor relation, CMV status, immunosuppressive medications and AR episodes (either PRAR or BPAR) were not associated with significant differences in the frequency of CD127 expression. Only patients with CAD had significantly lower frequencies of CD127 compared with those with no CAD (0.61 ±0.549% vs. 3.08 ±3.375 %, p = 0.021) (Figure 2), signifying that these subgroups of T-cells may play regulatory rather than effector role in transplant recipients.

Predictors of CAD in transplanted patients

Clinical and laboratory parameters of recipients with CAD (n = 7) were analyzed in table 3. A significant association was found between the occurrence of CAD and the non-use of antibody induction therapy, CsA use, and occurrence of previous AR episodes with all their clinical subtypes (p = 0.015, 0.02, and < 0.05 respectively). As expected, serum creatinine was significantly elevated, and consequently, glomerular filtration rate (GFR) was significantly lower in the CAD group (p < 0.005). CAD was significantly associated with lower prednisolone doses at 1 month as well as increased recipient age (p = 0.04 and 0.08 respectively). Logistic regression analysis demonstrated that the factors affecting the occurrence of CAD in transplanted patients were CD127% (β = –0.371, p = 0.001), and serum creatinine level (β = 0.626, p = 0.000) after adjusting other confounding factors (age and gender) (Table 4).

Role of CD127 in the prediction of CAD

For comparison of the gross achievement of the CD127 biomarker in the prediction of CAD, distinctly of the pre-specified threshold levels, we tested the comprehensive degree of test performance using the AUROC. As shown in Figure 3, the Receiver Operating Characteristics (ROC) curve depicts the sensitivity (true positive fraction) and 1-specificity (false positive) for various levels of serum CD127. The statistically significant area under the curve (p = 0.021) was 0.794, with a 95% confidence interval of 0.633-0.954. The cutoff value of CD127% at which CAD can be predicted is 1.305 with a sensitivity of 100% and specificity of 43% (Table 5, Figure 3).

DISCUSSION

T-cells with a CD4-CD25 high FOXP3 phenotype (Treg) have been identified as biomarkers of tolerance in kidney transplant recipients [13]. In order to isolate Treg efficiently and to high purity, reliable markers of identification are required. Given the non-specificity of CD25 and FoxP3 expression, a number of other markers have been explored. Of these markers, CD127 is currently one of the most useful. The benefit of CD127 is that a population of Tregs can be isolated by negative selection alone without the need for CD25 positive selection [14]. The aim of this work was to study the expression of IL-7 receptor (CD127) in peripheral T cells of pediatric kidney transplant recipients & to detect the association between CD127 surface marker and the development of rejection among this group of patients.
We found that the absolute number of T cells with the surface marker of CD127 was significantly higher in the transplanted population than normal controls after a mean post Tx duration of 30.9 ±16.5 months. This finding is in agreement with previous data in the literature [15-17]. Pablo et al. studied circulating lymphocyte subsets after KT. They found that the percentage of CD127low T cells in patients with stable graft function was decreased at 0.5 and 2 years after KT in comparison to healthy individuals. However, they increased in the time approaching similar values to those in healthy individuals at 5 years post-Tx [18]. So, it seems that the T cell subset distribution in transplant recipients is a dynamic process and that it is not only differed by the different clinical situations but also by post-Tx duration. Seddiki et al. [19] and Liu et al. [4] demonstrated that CD127 is downregulated on all human T cells after activation and, in contrast with the reported re-expression of CD127 on the majority of peripheral memory and effector T cells, Treg CD4+CD25 Foxp3+ cells remain CD127 low. Constitutively reduced expression of CD127 in Tregs may result from the Foxp3 interaction with the CD127 promoter that reduces the expression of CD127 in this subset [4]. On the other hand, Foxp3 induced by activation in effector T cells is not sufficient to permanently suppress CD127 expression in these cells and after the initial, post-activation decline of CD127 expression in Teff cells CD127 is reconstituted [6, 20].
In the current study; the expression of CD127 in patients with AR was not significantly different from that in patients without AR. Furthermore, we found a higher percentage of CD127 cells in recipients without CAD than those with CAD signifying that these subgroups of T-cells (CD127 +) may play a regulatory rather than effector role in transplant recipients. Many previous reports did not support our finding [15, 16, 21, 18]. Codarri et al. [15] and Vallotton et al. [16] showed that T cells expressing interleukin-7 receptor α (IL-7Rα; CD127) contain allospecific cells that expand in the peripheral blood compartment of patients with chronic rejection more than in patients without chronic rejection. Furthermore, an increased number of CD127 cells and a decreased number of FoxP3+ regulatory T cells have been associated with CHR in renal transplant recipients [21]. Pablo et al. [18]; demonstrated that although CD127 expression is decreased after 5 years post-Tx in recipients with stable graft function, it increases again in children with CAD.
On the other hand, Klein et al. supported our finding by reporting that a high frequency of CD127low/cells did not express FOXP3 and, conversely, that there was a high proportion of FOXP3-expressing CD1271ow cells in healthy individuals [22], suggesting that these markers did not represent the same population of Tregs and need further studies. Indeed, in a murine kidney allograft model, a higher and sustained level of Foxp3+ regulatory T cells has been demonstrated in tolerated compared with rejecting allografts. However, the presence of Foxp3+ regulatory T cells in human renal allografts was less clearly associated with stable function [23, 24, 18]. Hence, the clinical significance of changes in percentages of circulating CD4+ regulatory T cells after transplantation is not yet clear. The discrepancy in the previous reports and our results might be explained by the fact that our included patients with CAD were few (only 7 recipients, 1 patient with cAMR and 6 patients with chronic allograft nephropathy). In addition; changes in these activated CD25+ CD4+ T-cell populations are caused by other factors as HCV infection. Finally, differences in the cumulative dosages of IS therapy may influence results from this type of studies [25].
cAMR gradually becomes the most important cause of dysfunction in the late period of renal graft, and there is no viable clinical prophylaxis or treatment [26]. The follicular helper T cell (Tfh cell) is important in the generation and the development of cAMR, as it aids B cell differentiation into plasma cells and the production of donor-specific antibody (DSA) through the secretion of IL-21 [27]. The number of Tfh cells in the patient is consistent before and after renal transplantation, but their ability for IL-21 secretion decreases dramatically after renal transplantation, suggesting that immunosuppressive therapy may affect Tfh cell function and phenotypic change [28].
Although we failed to find a significant association between CD127 expression and the types of IS drugs used; Mammalian target of rapamycin-inhibitors (m-TORI) are shown to selectively spare CD4+ regulatory T cells [29]. Also, CNIs (CsA and tacrolimus) may exert different effects on regulatory T-cell numbers [30]. It was reported previously that CNIs have a markedly negative impact on graft tolerance by affecting Treg function and survival, mainly by interfering with IL-2 production [31, 32]. Conversely, corticosteroids have been reported to increase Treg frequency and FOXP3 expression in patients with autoimmune diseases [33, 34]. In addition, renal transplant recipient received MMF showed significantly higher CD4+CD25hiFOXP3+ Tregs compared to patients on other treatments [32]. More recently it has been demonstrated that the treatment with MMF, Tacrolimus, and methyl-prednisolone, but not m-TORI, decreased Treg viability and proliferation [35]. Our study is limited by the fact that it was conducted in a single institution with small sample size. Also, the study lacks sequential analysis of CD127 lymphocyte expression at different time intervals post-Tx. Despite these limitations, our results nevertheless indicate that circulating CD4+CD127 T cells is a potential novel immune marker for CAD. External validation of circulating CD4+CD127 T cell as a predictor of CAD could eventually guide organ allocation and therapeutic interventions aimed at individual-specific targets of Treg cell.

CONCLUSIONS

The percentage of CD127+ T cell subset is highly expressed in pediatric renal transplant recipients than normal subjects. CD127+ cells expression significantly increased in transplanted children with stable graft function than those with CAD. CAD might be associated with a deficient percentage of CD127 and it could be helpful to monitor these cells in estimating the immune status of pediatric kidney transplant recipients to make convenient preventive strategies. The cause-effect mechanism between CD127+ cells low percentage and the CAD is a subject for further large cohort studies.

ACKNOWLEDGMENT

This work was supported by NRC, in Egypt, the grant number is 10010008.

DISCLOSURE

The authors declare no conflict of interest.

References