Contribution of diminished kidney transplant GFR to increased circulating chemokine ligand 27 level

Chemokines and their ligands (CCLs) are a family of chemotactic cytokines that have ability to induce migration of different cell types especially those of lymphoid origin [1]. They coordinate leucocyte trafficking [2]. CCLs are expressed in tissues in response to injury or infection [3]. There are four families of chemokines; CCL, CXCL, CX3CL, and CL. Many chemokines can bind to multiple receptors and most receptors bind many chemokines [4].

The role of inflammatory CCLs in kidney dysfunction [5], including transplant injury [6], is widely recognized. These mediators play a pivotal role in acute allograft insult [7, 8] as well as chronic allograft injury and tissue fibrosis [9‐11]. Plasma CCLs levels have been postulated to be biomarkers, which may assist in predicting transplant outcomes [12‐17] as well as a therapeutic potential in kidney disease acute and chronic allograft nephropathy [18‐20].

Chemokines were found to be associated with kidney function in diabetic kidney disease [21, 22]. Previously, we reported on the elevated plasma levels of CCLs in stable RTR [23].

The debate of the relative contribution of diminished eGFR to heightened inflammation in the renal patient remains unsettled.

We propose that the study of stable renal transplant patients with varying eGFR constitute a reasonable cohort to determine the contribution of diminished GFR to elevated plasma levels of CCLs, independent of other known factors. As such, the aim of this work was to characterize which circulating plasma chemokines ligands associated with diminished eGFR.

This study included 101 stable renal transplant recipients and 20 healthy persons as a control group. The protocol for this study was approved by ethical committee of this institution. Informed consent was obtained from all participants. All RTR were older than 18 years with stable kidney function defined by no previous hospital admission and no change of serum creatinine more than 10% for the last 3 months. Patients with acute rejection, CMV disease or BK virus kidney disease diagnosed by a biopsy were excluded. All patients were followed at the Saskatchewan transplant program. Blood samples were collected for detection of CCLs. Multiplexed fluorescent bead-based immunoassay for detection of CCLs was described previously [24].

Nineteen CCLs (1, 2, 3, 4, 5, 8, 11, 13, 15, 17, 21, 24, 26, 27, CXCL5, 8, 10, 12 and 13) were measured.

RTR were divided arbitrary into three groups according eGFR, group 1: eGFR ≥ 60 ml/min, group 2: eGFR 30–59.9 ml/min and group 3: eGFR ≤ 29.9 ml/min.

The eGFR was calculated from the following equation:

GFR (CKD-EPI) =141X min(Scr/k,1)^α X max(Scr/k,1)^-1.209 X.993^Age X1.018 [if female] X (1.159 [if black] where k = 0.7 if female, k = 0.9 if male, α = − 0.329 if female, α = − 0.411 if male, min = minimum of Scr/k or 1 and max = maximum Scr/k or 1, Scr = serum creatinine (mg/dL).

This study included 101 stable RTR and 20 healthy persons as control group.. Nineteen CCLs were measured. Table 1 showed demographics and laboratory data of the stable RTR. Among the three patient groups, levels of hemoglobin, serum phosphorus, Parathyroid hormone, and urinary albumin creatinine ratio were significantly different. The rest of the twenty one demographic variables tested were similar including age and duration of transplantation.

Table 2 shows comparison between the nineteen CCLs levels. All levels were presented as median and CI because of the wide variation in their respective levels and thus were non-normalized values. Comparison of studied groups showed that CCL1, CCL4, CCL15, CCL27, CXCL8 and CXCL10 were significantly different among the tested groups. Control CCL4, CCL15, CCL27, CXCL8 and CXCL10 levels were significantly lower than that in the three patient’s groups. Comparison between each two groups is further illustrated in Table 2. CCL27 was significantly elevated in group 3 compared to groups 1, 2 while there was no significant difference among groups 1 and 2 as seen in Fig. 1. Spearman correlation between eGFR and CCL27 showed significant negative correlation (Fig. 2).

Table 3 shows the univariate (UVA) and multivariate (MVA) analyses between the tested CCLs and eGFR. The UVA showed that CCL15 and CCL27 was independent associate with eGFR. While in the MVA, CCL27 was the only independent associate with reduced eGFR.

Chemokines are small hormone- like polypeptides which regulate cell trafficking and tissue homing [2]. Structure and biology of Chemokines and their ligands are well covered by extensive reviews [4].

The role of chemokines and cytokines in renal injury is well recognized [5] and others have investigated their roles in RTR [6‐11].

Therefore we will limit our discussion to our positive results on the increased CCL 27 levels in the context of diminished GFR. First, our assay measures the human mature total CCL 27 and not any of its fragments as per the supplier communication.

Secondly, the increased sensitivity limits of the luminex immunoassay have made it possible to quantify extreme levels of circulating chemokines. The validity of these assay have been confirmed by other researchers [25, 26]. In our previous work we demonstrated elevated levels of most of the studied chemokines in stable RTR compared to control group [23] which may emphasize a state of generalized subclinical inflammation in apparently clinically stable patients. In our study we investigated the role of chemokines in context to eGFR in stable RTR.

It is recognized that CCL27 chemokine is a chemoattractant for cells bearing the CCR 10 receptor and which is found on keratinocytes [27], normal mucosa associated colon epithelium, trachea, mammary glands, retina and cells in the central nervous system [28].

It appears that T cell helper type 2 cytokines stimulate CCL27 secretion and CCL27 promote T helper type 1- activating antigen presenting cells’ It is suggested that CCL27 main function is to recruit lymphocytes to inflammatory tissues particularly the skin [29, 30].

CCL27 is also known as cutaneous T cell- attracting chemokine (CTACK) the only known receptor for CCL27 is CCR 10, which is expressed in normal skin and help to retain memory T cells homing during inflammatory skin conditions as well as immune surveillance [31].

In the skin, CCL27 is produced by keratinocytes and binds to CCR 10 receptor, characteristic of the majority of T lymphocytes infiltrating the skin. Specifically, CCL27 helps in lymphocyte adhesion in the skin, leading to pathological inflammatory skin diseases such as psoriasis, atopic dermatitis, mastocytosis [32] and drug induced cutaneous reactions [33]. It has been shown that CCL27 triggers resistance in myeloma cells [34]. Likewise, CCL27 is found in normal nasopharyngeal tissue samples particularly those individuals with seropositive Epstein- Bar virus capsid antigen- specific IgA level (VCA-IgA- positive) and is suggested as a plasma novel biomarker for nasopharyngeal carcinoma [35]. More recently, elevated CCL27 levels in patients with multiple sclerosis was observed. These investigators went further to suggest the Skin- Brain connection hypothesis in which the skin is proposed to be involved in MS pathogenesis [30, 36].

On the other hand CCL27 has been suggested to show a better prognosis in patients with cutaneous malignant melanoma [37].

It is not known why CCL27 is elevated in transplant patients with diminished eGFR. It is unlikely to support diminished clearance as a main cause of elevated levels of CCL27 because other CCLs would have been also retained. It is possible that elevated blood CCL27 level is a response to other inflammatory molecules associated with diminished renal function. After all, renal insufficiency is an inflammatory state [38]. Psychophysical stress may enhance CCL27 production [39].

With that in mind we foresee clinical significance of our findings for future studies. For example, it is intriguing to postulate that Skin changes associated with reduced GFR [40] may be attributed to increased CCL27. There is a link between psoriasis and reduction in kidney function [41, 42] representing another skin kidney connection. Of further interest, CCL27 was found to be highly associated with cutaneous psoriasis [32, 43‐45]. Similarly, higher incidence of skin cancer seen in organ transplantation [46, 47] may be related to high levels of CCL27. In this context, it is intriguing to postulate the existence of a renal- skin axis similar to that between the skin- brain connections postulated by other researchers [30]. Of further interest, CCR 10, the receptor for CCL27 ligand, is expressed by the podocytes [48] and thus a role for CCL27 in podocytes function and injury in chronic allograft nephropathy is a potential hypothesis for future studies. As such, our finding raises more interesting possibilities such as a role of CCL27 in maintains alloreactive memory by supporting skin memory T cell population [49, 50]. If true the skin can be targeted for therapeutic manipulations of CCL27 to reduce inflammation in transplant and kidney diseases. Taken together we raise the intriguing potential of CCL27 as a potential putative marker of those patients who may have progressive decline in kidney function and that it may be a target to protect kidney function.

Elevated PTH is considered a putative uremic toxin in patients with chronic kidney disease. PTH is reported to associate with elevated inflammatory markers such as serum monocyte chemokine protein 1 [51]. Our literature review failed to find a relationship between CCL27 and PTH and thus we cannot speculate on the mechanism by which elevated PTH may enhance production of CCL27 at this stage.

There are limitations to our work. First the clinical relevance of elevated CCL27 needs confirmation by further studies including patients with native kidney diseases. We did not measure tissue levels of CCL27 or its receptor CCR 10. A prospective study of repeated measurement of chemokine and changes in GFR were not done. Finally the cause of decreased renal transplant function such as chronic allograft nephropathy versus other causes of reduced eGFR was not studied in detail. Of note, all our patients were at least stable at the time of study. In addition we stress the fact that there was no significant relationship between CCL27 levels and recipient age, or the duration of transplantation.

We report on the increased inflammatory chemokine ligands in transplant patients with reduced glomerular filtration rate. In particular, we found elevated blood levels of CCL27 in stable RTR with reduced GFR and raises the possibility of a skin- kidney connection to maintain alloreactivity. Our finding raises the intriguing possibility of targeting the skin as a mean to inhibit CCL27 and thereby decrease renal inflammation in transplant patients and even in native kidney diseases. Future work should test the likelihood that CCL27 can serve as a biological marker for patients who are at excessive risk for progressive decline in kidney function and whether blocking CCL27 may retard progression to kidney failure.