ALBERT

Description: Introduction: Methylation of CpG dinucleotides is a fundamental mechanism of epigenetic regulation in eukaryotic genomes that controls the expression of certain genes. FOX-P3 is a member of the forkhead/winged-helix family of transcriptional regulators which expression is constitutive in regulatory T lymphocytes CD4/CD25 (Treg). Recent evidence suggests that human effector T cells express FOX-P3, albeit transiently and with significantly lower levels. Therefore, FOX-P3 mehtylation within the promoter region and gene expression could play a role in allogeneic stem cell transplantation (alloSCT). Objective: To analyze the association between the mehtylation status and the levels of expression of FOX-P3 with the dynamics of chimerism and the development of complications after alloSCT. Patients and methods: The degree of methylation was quantified in a 600 pb CpG island within the regulatory sequence of FOX-P3 by quantitative methylation-specific real time-PCR from 32 peripheral blood (PB) samples obtained within the first month post-alloSCT. Moreover, the expression level of FOX-P3 mRNA was analyzed by real-time quantitative PCR in 18 patients from which RNA samples were available. Results were analyzed using Fisher’s exact test due to the reduced sample size. Results: A statistically significant association (Table 1) was observed between a higher degree of methylation in the FOX-P3 promoter and a lower incidence of acute graft versus host disease (GVHD) grades II-IV (35.3% vs a 88.9% in low methylation patients; p=0.014). Moreover, patients with higher degree of methylation showed significantly higher incidence of disease relapse (41.2% vs a 0% in low methylation patients; p=0.05). The observation of a high degree of methylation would reflect a lower amount of FOX-P3 expressing cells, both Treg and effector cells. Since Treg comprises a minority population, such observation would result from relative low levels of effector T cells, which would explain the lower graft-versus-host and graft-versus-leukemia effect observed in high mehtylation group. Surprisingly, when FOX-P3 mRNA levels were analyzed, an association with statistical significance between a higher methylation status and a higher expression of FOX-P3 (90% vs 55.8%; p=0.047) was observed. It has been shown that FOX-P3 is mainly produced by Treg while effector T cells produce very low amounts of FOX-P3 mRNA. In this sense, a higher amount of Treg cells produces high FOX-P3 mRNA levels and reduces the number of effector T cells, resulting in a higher methylation status in PB samples, in which most cells would have methylated FOX-P3. Low FOX-P3 expression would, in turn, indicate a lower amount of Treg to suppress the immune activation, resulting in higher amount of effector T cells and therefore would be associated with a lower methylation. Additionally, a significant association between higher FOX-P3 expression and lower incidence of death (7.7% vs 80%; p=0.007) was observed. Moreover, the main cause of death (3/4) in the group with lower expression of FOX-P3 was acute GVHD. The lower amount of effector T cells in PB samples with high FOX-P3 expression would protect from the development of GVHD. Conclusions: Both FOX-P3 mRNA expression and promoter methylation are of prognostic value for the development of complications post-SCT. These determinations would favor an early establishment of the immunotherapeutic options for an improved management of transplanted patients. Table 1. Association between FOX-P3 promoter methylation and mRNA expression with chimerism and complications post-SCT. MC, mixed chimerism; PB, peripheral blood; Fail/Reject., graft failure/rejection. p, Fisher`s Test. Methylation MC (PB) Fail/Reject. aGVHD (II-IV) cGVHD Relapse Exitus High 6/19 (31.6%) 4/19 (21.01%) 6/17 (35.3%) 10/13 (76.9%) 7/17 (41.2%) 5/19 (26.3%) Low 2/9 (22.2%) 0/9 (0%) 8/9 (88.9%) 3/8 (37.5%) 0/9 (0%) 4/9 (44.4%) p NS NS 0.014 NS 0.05 NS Expression MC (PB) Fail/Reject. aGVHD (II-IV) cGVHD Relapse Exitus High 4/13 (30.8%) 2/13 (15.4%) 6/12 (50%) 10/11 (90.9%) 3/12 (25%) 1/13 (7.7%) Low 0/5 (0%) 0/5 (0%) 4/5 (80%) 3/4 (75%) 1/5 (20%) 4/5 (80%) p NS NS NS NS NS 0,007

Description: Abstract 1329 Poster Board I-351 The detection of minimal residual disease (MRD) in AML patients after allogeneic stem cell transplantation (SCT) is important for the early detection of relapse and the selection of patients who can benefit from immunomodulation. Up to 65% of patients with AML lack of molecular markers useful for follow-up. The Wims tumor gene (WT1) is overexpressed in more than 80% of AML patients at diagnosis, hence its utility as MRD marker in these patients. The objective of this study is to analyze the usefulness of WT1 expression for MRD study and relapse prediction in patients with AML after allogeneic SCT and to compare the results with those from flow cytometry and chimerism. Methods 149 samples were studied (63 BM and 86 PB) from 11 patients with AML (table 1) lacking of other molecular markers at diagnosis, who underwent allogeneic SCT in a single center from 2003 and 2008. Quantification of WT1 expression was performed by quantitative RT-PCR (LightCycler 1.2) using cDNA obtained from 1 ug of RNA (Trizol®, Invitrogen). K562 cell line was used as calibrator and ABL as reference genes (relative quantification). Cut-off values were defined at 0.5% in BM samples and 0.01% in PB. Results were correlated with those from flow cytometry and chimerism from the same samples. Results WT1 overexpression correlated with the presence of disease before transplantation (table 1). Post-transplantation, 5 of the 11 patients showed low and stable WT1 levels in BM and PB in the follow-up, remaining in CR (median follow-up 48 months, range 8-61). These 5 patients showed complete chimerism (CC) and negative MRD by flow cytomety (figure A). On the other hand, 6 from the 11 patients showed WT1 overexpression after SCT: 4 of them showed after initial low values, a significant increase in WT1 expression up to reaching positive levels in a median of 139 days (50-167), while 2 patients showed positive values continuously. Two patients showed positive levels only in PB samples, one only in BM and 3 both in BM and PB. From these 6 patients, 5 relapsed (1 with extramedullar disease who showed WT1 overexpression only in PB) in a median of 9 months after SCT (2.4-11). In one case, WT1 overexpression occured at the same time as relapse, while in the other 4 cases, relapse occured in a median of 137 days (134-170) after a significant increase in WT1 levels was seen in two consecutive samples. In these 5 relapsed patients, neither flow cytometry nor chimerism predicted relapse (figure B). Conclusions WT1 overexpression correlated with disease burden in AML patients after allogeneic SCT. In realapsed patients, relapse both medullar and extramedullar was anticipated sinificantly by WT1 overexpression compared to flow cytometry and chimerism. Quantification of WT1 overexpression by RT-PCR should be used for MRD detection in the follow-up after SCT in AML patients (not only in BM but also in PB for extramedullar disease detection) in order to facilitate immunossupresive therapy management and to select early DLI candidates. Disclosures No relevant conflicts of interest to declare.