- Open Access
Utilization of TREC and KREC quantification for the monitoring of early T- and B-cell neogenesis in adult patients after allogeneic hematopoietic stem cell transplantation
- Angela Mensen†1, 4,
- Christoph Ochs†1,
- Andrea Stroux2,
- Friedrich Wittenbecher3,
- Martin Szyska4,
- Luisa Imberti5,
- Simon Fillatreau6,
- Lutz Uharek3,
- Renate Arnold3,
- Bernd Dörken3,
- Andreas Thiel7,
- Carmen Scheibenbogen1, 8 and
- Il-Kang Na1, 3, 4Email author
© Mensen et al.; licensee BioMed Central Ltd. 2013
- Received: 10 May 2013
- Accepted: 7 August 2013
- Published: 14 August 2013
After hematopoietic stem cell transplantation (HSCT) T- and B-cell reconstitution from primary lymphoid organs are a prerequisite for an effective early lymphocyte reconstitution and a long-term survival for adult patients suffering from acute leukemia. Here, we asked whether quantification of T cell receptor excision circle, (TREC) and kappa-deleting recombination excision circle (KREC) before and within six month after allogeneic HSCT could be used to measure the thymic and bone marrow outputs in such patients.
We used a duplex real time PCR assay to quantify the absolute copy counts of TREC and KREC, and correlated the data with absolute cell counts of CD3+CD4+ T-cell and CD19+ B-cell subsets determined by flow cytometry, respectively.
By comparing two recently proposed naïve T cell subsets, CD31+ naive and CD31- naive T cells, we found a better correlation for the CD31+ subset with TREC level post alloHSCT, in line with the assumption that it contained T cells recently derived from the thymus, indicating that TREC levels reflected real thymic de novo production. Transitional as well as naïve B cells highly correlated with KREC levels, which suggested an association of KREC levels with ongoing bone marrow B cell output. CD45RO+ memory T cells and CD27+ memory B cells were significantly less correlated with TREC and KREC recovery, respectively.
We conclude that simultaneous TREC/ KREC quantification is as a suitable and practicable method to monitor thymic and bone marrow output post alloHSCT in adult patients diagnosed with acute leukemia.
- Allogeneic hematopoietic stem cell transplantation
- Acute leukemia
- Simultaneous TREC/KREC quantification assay
- Monitoring immune reconstitution
Allogeneic hematopoietic stem cell transplantation (alloHSCT) is a common treatment strategy to cure hematological malignancies and other hematological disorders . Pretransplant conditioning therapy providing space for stem cell engraftment as well as immune suppression therapy to prevent transplant rejection are usually associated with a profound long-term humoral and cellular immune deficiency [2, 3]. The development of graft-versus-host disease (GvHD) can further exacerbate lymphocytopenia thereby increasing the risk of life-threatening viral, bacterial and fungal infections [4, 5]. T- and B- cell reconstitution starts about 3–6 months after alloHSCT representing a mixture of peripheral naïve and memory cell expansion as well as de novo development from primary lymphoid organs [2, 6–9]. While expansion of mature T and B cells will only provide a transient immune protection and is likely to be repertoire restricted as well as potentially allo-reactive, the de novo production from hematopoietic stem cells is important for long-term immune protection and tolerance [2, 6, 7, 10, 11]. For individualized monitoring of immune reconstitution in the clinic, it is important to have validated methods to track T- and B-cell reconstitution after alloHSCT in the relevant patient groups.
A method to measure thymic output in the context of aging, immunodeficiency and HSCT is the quantification of T cell receptor excision circles (TRECs) [7, 12–19]. TRECs are stable episomal, non-replicative DNA circles generated during T cell receptor (TCR) alpha chain rearrangement when the excision of the D locus occurs . About 70% of all newly produced T cells are TREC positive. TREC level are elevated in T cell preparations of children and then decline with increasing age due to thymic involution . Nevertheless, TREC levels can still be detected in elderly people indicating that the thymus partly retains its function in old age [12, 21].
In the context of HSCT, the thymus was shown to substantially contribute to T-cell immune reconstitution after HSCT , and positive correlations between TREC and total naïve CD4+ T-cell counts were assessed in adult and pediatric alloHSCT patients [7, 15, 16]. Recently, CD31 was introduced as a marker to distinguish naïve T cells into recently thymic-derived CD4+CD31+ naïve T cells and more mature recirculating CD4+CD31- naïve T cells in the peripheral blood . CD4+CD31+ naïve T cells have a higher TREC content and broader TCR repertoire than CD4+CD31- naïve T cells. Clinical studies found a positive correlation between TREC content and frequency of CD4+CD31+ naïve T cells in adult autologous and pediatric allogeneic HSCT patients [17, 19]. However, these studies did not investigate CD4+CD31- naïve T cells, excluding the possibility of comparing the correlation of TRECs with these two subsets of naïve T cells in these patients. Since the regulation of CD31 expression on T cells is not known in this clinical context, the validity of this receptor as a marker of recent thymic emigrants after HSCT remains unresolved. Such comparison is also missing in adult alloHSCT patients, which present with different clinical features than the situations described above. Importantly, consideration of CD31 expression as a marker for recent thymic emigrants needs to take into account that “old” naïve T cells could maintain CD31 expression regardless of the time they egressed the thymus.
It recently became possible to simultaneously measure the thymic T- and bone marrow B-cell output using a duplex real-time PCR for quantification of TRECs and κ-deleting recombination excision circles (KRECs), which are generated during B cell development as a result of light chain rearrangements [13, 23]. Similarly to TRECs, KRECs are progressively diluted as B cells proliferate and mature in the periphery . KRECs are randomly found in about 50% of newly produced B cells. Studies in children post alloHSCT reported an increase in KREC level concomitant with B cell recovery [13, 18]. However, these studies investigated total blood B cells without considering their heterogeneity. In blood, B cells can be divided into immature transitional B cells, which recently emigrated from the bone marrow, naïve B cells, and memory B cells . In the context of HSCT, correlations between KREC levels and different B cell subsets remain to be compared.
The aim of our study was to evaluate the suitability of TREC and KREC quantification as a marker to monitor T and B cell reconstitution in adult alloHSCT patients. For this, we simultaneously correlated absolute TREC and KREC copy counts with different flow cytometric determined peripheral blood T- and B-cell subsets. Here, we focused on very early time points after transplantation as an effective lymphopoiesis during the first months after transplantation was shown to be associated with improved overall survival, thus emphasizing the importance of immune monitoring during that time period [16, 24].
Clinical characteristics of alloHSCT patients
Median age (range)
47 reduced intensity
GvHD (acute = + Chronic)
Flow cytometry analysis of lymphocyte subpopulations
Peripheral blood mononuclear cells (PBMCs) were isolated by density gradient centrifugation (Ficoll-Hypaque; GE Healthcare) from fresh heparinized patient blood samples. After washing with PBS the cells were stained in two staining panels for 20 min at 4°C with the following fluorochrome-conjugated anti-human monoclonal antibodies: T cell panel - CD3 APC/Cy7 (clone UCHT1), CD4 AlexaFluor 700 (clone RPA-T4), CD45RA PerCP-Cy5.5 (clone HI100), CD45RO Pacific Blue (clone UCHL1), CD62L APC (clone DREG-56), CD31 PE (clone WM59), CD197 (CCR7) Alexa Fluor 488 (clone TG8/CCR7) from Biolegend and CD27 PE-Cy7 (clone O323) from eBiosciences; B cell panel - CD19 Pacific Blue (clone HIB19), IgD-FITC (clone IA6-2), CD27 PerCP-Cy5.5 (clone O323), CD38 PE-Cy7 (clone HIT2) from Biolegend. PBMCs were washed and analyzed by flow cytometry using a BD™ LSRII flow cytometer (Becton Dickinson, Palo Alto, CA, USA) supported by FlowJo 9.3 software (TreeStar, Ashland, OR, USA).
Real-time PCR for TREC and KREC quantification
The mean of TRAC quantity was divided by two considering the presence of two TRAC gene copies per cell. True count beads (BD Biosciences) were added to whole blood samples of patients to determine the absolute lymphocyte and monocyte count per ml blood.
Clinical characteristics are presented as absolute and relative frequencies. In order to account for the intra-individual dependency over time of the TREC and KREC data and the corresponding T and B cell subsets data, GEE (generalized estimating equations) analyses  have been performed to calculate standardized regression coefficient betas (β) and p-values. The β coefficient measures the strength of the effect of the respective independent variable on the dependent variable that means the higher the β, the stronger the association between the two measurements. The standardized β values were used to achieve independency of the measure units. Additionally, logarithmic transformations have been performed to obtain normality. Two-sided p-values ≤ 0.05 are considered statistically significant. No Bonferroni correction has been performed. All statistical analyses were done using the commercially available software SPSS 20.
Molecular and flow cytometric assessment of T and B cell reconstitution in alloHSCT patients
Here, we simultaneously assessed the correlation between TREC/ KREC levels and different T-/ B-cell subsets in adult patients after alloHSCT (Table 1), with the aim to test whether this duplex real time PCR assay could be applied for monitoring of T- and B-cell neogenesis in this particular clinical context. This duplex PCR assay allows the quantification of TREC and KREC in the same PCR reaction. Thereby, naïve T and B cells emigrating from the thymus and bone marrow, respectively, can be monitored simultaneously without any additional expenses. Since T and B cell maturation/differentiation are organ-specific and exhibit individual kinetics, more information about the immune cell reconstitution can be achieved by using TREC and KREC.
To determine the specificity of the TREC/KREC quantification we performed the assay on genomic DNA from the human erythroleukemia cell line K562 and from the human T cell leukemia cell line Jurkat (Additional file 1: Table S1). Both cell lines are negative for TREC [27, 28] and KREC probably due to clonal proliferation, but positive for TRAC. Accordingly, we found an amplification of TRAC but no off-target amplification of TREC and KREC on these cell lines Genomic DNA from PBMCs of a healthy donor served as a positive control.
TREC and T cell subset recovery after alloHSCT
In parallel analyses, we determined absolute TREC counts from total peripheral blood mononuclear cells (PBMCs) as copies per ml blood. TRECs drastically declined after transplantation before recovering around day 180 (Figure 2A,C,E). At day 180, TRECs were still below the pretransplant level (mean 1285±634 copies/ml). TREC values of 2306 copies per ml were reported for healthy controls .
After having quantified amounts of distinct T cell subsets and TRECs at various time points after alloHSCT, we then tested the possible correlation between these parameters (Figure 2B,D,F). We determined standardized β-values by perfoming GEE analyses that account for longitudinal, i.e. intraindividually dependent data. Since in our study we consider the entire information of all measurement time points, the GEE analysis is most appropriate to model the longitudinal character of the data accurately. In contrast to these point estimates usual linear regression models would have been underestimated and thus been too optimistically. We observed that in line with previous publications, TREC recovery correlated with the numbers of both, CD4+CD45RA+CD31+ and CD4+CD45RA+CD31- naïve T cells [7, 15, 17, 19]. A better correlation was observed for CD4+CD45RA+CD31+ (Figure 2B) than for CD4+CD45RA+CD31- (Figure 2D) naïve T cells (ß = 0.518, p < 0.01 for CD4+CD45RA+CD31+ naïve; ß = 0.470, p < 0.05 for CD4+CD45RA+CD31- naïve). This is consistent with the notion that CD4+CD45RA+CD31+ naïve T cells are more likely recent thymic emigrants, while CD4+CD45RA+CD31- naïve T cells contain more mature cells that resided in the periphery for longer times and proliferated , even though this had not been tested so far in the context of alloHSCT. Lymphocytopenia after conditioning therapy and T cell-depletion drives cell proliferation in the “empty” host especially within the first weeks post transplantation when IL-7 serum levels are increased, leading to a subsequent loss of TRECs [15, 29]. However, the existence of “old” naïve T cells with maintained CD31 expression can not be excluded, so that CD31 expression does not necessarily represent an exclusive marker for T cells that recently emigrated from the thymus.  The poorest correlation was found for the CD4+CD45RO+ memory T cell subset (Figure 2F) (ß = 0.339, p < 0.05). This is in line with observations made in healthy individuals, whose memory T cells exhibited a ten-fold lower TREC content than naïve T cells .
Immune reconstitution differs in patients receiving full-conditioning and reduced-intensity conditioning therapy. For example, depending on the level of toxicity variable damage/ destruction of the bone marrow niche or thymus as well as of the host hematopoietic cell compartment occurs. Consequently, bone marrow and thymus output is more impaired after high-intensity conditioning therapy, whereas expansion of host T cells contributes more to the T cell repertoire after reduced-intensity conditioning therapy. We therefore separated patients receiving either full-conditioning or reduced-conditioning, and could still observe that TREC levels correlated with CD31+ naïve CD4 T cells (Additional file 2: Figure S1A).
More patients, preferably independent groups of patients, are required to estimate significant differences of β values between each of these T cell subsets and in dependency on different clinical parameters, which should definitely be analyzed in future studies in order to affirm this assay.
Recently, protein tyrosine kinase 7 (PTK7) as a novel marker for human CD4+ recent thymic emigrants and the assay to determine the sj-TREC / β-TREC ratio for thymic function assessment have been introduced [27, 32]. PTK7+ naïve CD4+ recent thymic emigrants contain a higher level of TRECs, are more responsive to interleukin 7 and rapidly decrease after thymectomy. Although promising, this marker has not been applied in the setting of HSCT. Interestingly, expression of PTK7 was also found on AML blasts , so value of PTK7 as a recent thymic emigrant marker post transplantation in AML patient should be evaluated . The sj-TREC / β-TREC ratio reflects the intensity of proliferation between DβJβ rearrangement and the VαJα rearrangement, which in turn is the major determinant of the number of recent thymic emigrants produced. The major advantages of this technology are independence of peripheral proliferation, measurement of thymic neogenesis of all αβ-T cells independent of their phenotype and gain of information about T cell receptor diversity . However, this powerful methodology is, in contrast to the duplex PCR assay presented here, labor intensive, even in the simplified approach presented by Ferrando-Martinez et al. .
KREC and B cell subset recovery after alloHSCT
Interestingly, already at the pretransplant period we observed a very low number of KRECs with 2331±1155 copies per ml of blood, while a KREC value of 14846 copies per ml was reported for healthy controls (Figure 3A,C,E) . In contrast to TRECs that dropped from higher pretransplant to low posttransplant levels, KRECs only slightly decreased upon transplantation. KRECs started to increase on day 60, and were fivefold higher on day 180 compared to pretransplant level, reaching values of 10809±4510 copies/ml. KREC recovery showed a good and statistically significant correlation with both transitional and naïve B-cell recovery, whereas memory B cells correlated less (Figure 3B,D,F) (ß = 0.585, p < 0.001 transitional; ß = 0.663, p < 0.001 naïve; ß = 0.383, p < 0.05 memory). B cells typically undergo several rounds of cell division during their differentiation into memory cells . Therefore, a low contribution to the KREC pool and consequently less correlation of memory B cells with KRECs was expected. When separating the patients into a full-conditioning and reduced-conditioning group again we still found that KREC levels correlated well with transitional B cells (Additional file 2: Figure S1B). Like for TREC, larger patients cohorts would allow to determine significant differences in ß values for different B cell subsets and different clinical settings.
We further compared the obtained TREC/ KREC values with patients total white blood cell count as measured at each time point in the hospital setting (Additional file 3: Figure S2). TREC as well as KREC kinetics clearly differed from the leukocyte kinetics showing no congruent course of TREC/KREC recovery with leukocyte recovery after alloHSCT. This suggests the TREC/KREC assay to provide useful additional information for monitoring the dynamics of immune system reconstitution after alloHSCT and therefore may have clinical utility. In particular, the duplex PCR presented here is a time- and laboratory costs-saving assay that allows simultaneous quantification of TREC and KREC in only one PCR reaction. TREC/KREC levels are normalized to the quantity of genomic DNA in the sample and variability related to direct DNA quantification is eliminated by using a unique standard curve and TREC/KREC quantification per ml of blood overcomes the issue of peripheral dilution. However, we are aware of the fact, that the measurements alone cannot be considered as direct markers for clinical episodes, because TREC/ KREC can persist in old emigrant cells and disappear after cell death. This easy performable assay rather represents a first-step screening that needs be tested in a larger patient cohort in correlation to clinical parameters, and also should be combined with other methods to help defining the reasons for low TREC/ KREC levels.
In summary, our study suggests that the combined quantification of absolute TREC and KREC counts is a suitable marker to monitor early T- and B-cell neogenesis in adult patients treated by alloHSCT for hematological malignancies. Both markers exhibited kinetics best comparable with the most primitive T/B cell phenotypes, CD4+CD45RA+CD31+ naïve T-cell as well as transitional (IgD+CD27-CD38hi) and naïve (IgD+CD27-CD38int) B-cell reconstitution, respectively, allowing an estimate of thymic and bone marrow output post alloHSCT. Having validated good correlations, relationship of TREC/ KREC levels and thereby thymic and bone marrow function should be tested next in correlation to clinical episodes such as GvHD, graft failure or Cytomegalovirus and Epstein-Barr virus reactivation in a considerably larger patient cohort allowing multivariate analyses and corrections for confounding effects due to clinical heterogeneity. In case of good correlations with these clinical parameters, TREC and KREC enumeration could be used in combination with T- and B-cell subset quantification in routine clinical monitoring to optimize personalized treatment strategies. For TREC and KREC quantification, low associated reagent costs, DNA stability as well as the need of only small blood volumes would be advantageous especially during lymphocytopenia during the first months after transplantation.
We thank Sandra Bauer for excellent technical assistance.
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