High Levels of B-Cell Activating Factor During the Peri-Transplant Period Are Associated with the Reduced Incidence of Acute Graft-Versus-Host Disease Following the Myeloablative Allogeneic Stem Cell Transplantation.

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 2229-2229
Author(s):  
Byung Sik Cho ◽  
Chang Ki Min ◽  
Hee Je Kim ◽  
Seok Lee ◽  
Yoo Jin Kim ◽  
...  

Abstract Abstract 2229 Poster Board II-206 To determine whether serum B-cell activating factor (BAFF) levels that were previously found to be elevated in patients with chronic graft-versus-host disease (GVHD), and C-reactive protein (CRP) levels known as a predictor for aGVHD as well as a marker for systemic inflammation during the peri-allogeneic stem cell transplantation (SCT) period, could be used to predict the occurrence of acute GVHD (aGVHD), 45 consecutive patients who had undergone myeloablative allogeneic SCT for hematologic malignancies were assessed. Serum BAFF and CRP levels were measured using ELISA (R&D Systems, Minneapolis, MN, USA) before conditioning and on day 0, day +7, and day +14 after transplant. Thirty-three of 45 patients (cumulative incidence, 73=) developed aGVHD between 16 days and 98 days after transplant. Analyses using repeated measures of ANOVA revealed that the serum BAFF levels were significantly lower in patients with aGVHD than in those without aGVHD (P=0.001), whereas no association was detected between CRP levels and aGVHD (P=0.508). Receiver operating characteristic curve (ROC) analysis showed that serum BAFF levels at every time point were available for the prediction of development of aGVHD (pre-conditioning; P=0.005, day 0; P=0.002, day +7; P=0.004, and day +14; P=0.005). Using ROC curve analysis, the identical cutoff value of 43 pg/ml at every time point that divides patients into two groups, high (> 43 pg/ml) or low (≤ 43 pg/ml) BAFF group, was determined, which could assure 75= sensitivity and 73-82= specificity for the prediction of aGVHD at every time point. The analyses of the cumulative incidence of aGVHD at each time point by BAFF groups (high vs. low) showed that serum BAFF level at every time point plays a significant predictive role for the occurrence of aGVHD (pre-conditioning; P=0.040, day 0; P=0.023, day +7; P=0.003, and day +14; P=0.026). This study is, to the best of our knowledge, the first to show that high serum BAFF levels during the peri-transplant period may play a protective role against aGVHD in humans. The results of this study also show that the BAFF levels during peri-transplant period may be considered to be a predictor for aGVHD. Further trials with a larger cohort will be necessary to determine a definite cutoff value of high BAFF level as well as to construct an index with previously known factors for the prediction of aGVHD. Disclosures: No relevant conflicts of interest to declare.

Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 3036-3036
Author(s):  
Caron A. Jacobson ◽  
Haesook T Kim ◽  
Stefanie Sarantopoulos ◽  
Lixian Sun ◽  
Sean McDonough ◽  
...  

Abstract Abstract 3036 There is evidence that B cells play a role in the development of chronic graft-versus-host disease (cGVHD), a major cause of non-relapse morbidity and mortality following hematopoeitic stem cell transplantation (HSCT). Elevated levels of B cell activating factor (BAFF) relative to the number of circulating B cells have been associated with the development of cGVHD as well as its response to treatment. To better define the relationship between BAFF levels, the recovery of CD19 B cells, and BAFF/CD19 B cell ratios and cGVHD following HSCT, we prospectively analyzed 440 hematologic malignancy patients who underwent HSCT. Two hundred and fifty four patients (58%) underwent a reduced intensity HSCT; 375 (85%) received filgrastim-mobilized peripheral blood stem cells. Sixty-one percent developed cGVHD, with a median time to development of cGVHD of 221.5 days. Whole blood and plasma samples were collected at 1, 3, 6, and 12 months after HSCT and analyzed by flow cytometry and enzyme linked immunosorbent assay for CD19 B cells and BAFF levels respectively. Results in patients who developed cGVHD were compared to patients who did not develop cGVHD. At 1 month after HSCT, BAFF levels were significantly higher in the no cGVHD cohort compared to the cGVHD cohort (14.78 versus 11.31ng/ml, p=0.003)(see figure below). BAFF levels gradually fell in the no cGVHD cohort while remaining stable in the cGVHD cohort such that they were significantly lower in the no cGVHD cohort by 12 months after HSCT (5.63 versus 9.11ng/ml, p=0.018). In contrast, CD19 B cell count was similar between the two cohorts through 6 months after which point it was higher in the no cGVHD cohort (279.0 versus 119.0 cells/μL at 12 months, p=0.062). This correlated to a significantly decreased BAFF/CD19 B cell ratio in this cohort at 12 months after HSCT (0.03 versus 0.15, p=0.01). Prednisone is known to lower BAFF levels so each cohort was further analyzed based on the concurrent use of prednisone at the time of sample collection. BAFF levels were lower in patients who received prednisone at the time of analysis. BAFF levels fell sharply in both the cGVHD and no cGVHD cohorts on prednisone between 1 and 3 months after HSCT such that there was no significant difference between the two groups. However, within the group of patients who received prednisone at 3 months, patients who did not develop cGVHD had a significantly higher CD19 B cell count at this time than those who subsequently developed cGVHD (88.0 versus 20.5 cells/μL, p=0.037). These results suggest that patients who do not develop cGVHD achieve higher BAFF levels early after HSCT followed by more rapid B cell recovery, which in turn results in the normalization of BAFF levels and BAFF/CD19 B cell ratios. In contrast, B cell recovery is delayed and high BAFF/CD19 B cell ratios persist in patients who develop cGVHD. Disclosures: No relevant conflicts of interest to declare.


Blood ◽  
2013 ◽  
Vol 121 (18) ◽  
pp. 3745-3758 ◽  
Author(s):  
Emily Blyth ◽  
Leighton Clancy ◽  
Renee Simms ◽  
Chun K. K. Ma ◽  
Jane Burgess ◽  
...  

Key Points Infusion of CMV-specific T cells early posttransplant does not increase acute or chronic graft-versus-host disease. CMV-specific T cells early posttransplant reduce the need for pharmacotherapy without increased rates of CMV-related organ damage.


2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Isabella de Vere Hunt ◽  
James M. Kilgour ◽  
Robert Danby ◽  
Andy Peniket ◽  
Rubeta N. Matin

Abstract Background Graft-versus-host disease (GVHD) is a significant cause of morbidity and mortality following allogeneic stem cell transplantation. These patients face unique challenges due to the complexity of GVHD which can affect multiple organ systems, and the toxicity of treatments. Despite the known impact on quality of life (QOL), qualitative data within the bone marrow transplantation (BMT) literature is rare, and there has been no qualitative work exploring patient experience of specialist healthcare provision for GVHD in the United Kingdom. Methods We conducted a primary explorative qualitative study of the experience of QOL issues and multidisciplinary care in patients with chronic GVHD following allogeneic stem cell transplantation. Eight patients were identified using convenience sampling from specialist BMT outpatient clinics. Following consent, patients were interviewed individually via telephone. Transcripts of interviews were analyzed using an inductive thematic approach. Results Mean participant age was 61-years-old (range 45–68), with a mean time post-transplant of 3 years at time of interview (range 3 months–15 years). Five key QOL themes were identified: (1) ‘Restricted as to what I can do’; (2) Troubling symptoms—‘you can sort of get GVHD anywhere’; (3) Confusion/uncertainty over GVHD symptoms—‘Is this the GVHD?’; (4) Unpredictable course and uncertainty about the future; and (5) Adapting to the sick role. In addition, four themes related to experience of service provision were identified: (1) personal care and close relationship with BMT nurses; (2) efficiency versus long waits—‘On the case straight away’; (3) information provision—‘went into it with a bit of a rosy view’; and (4) the role of support groups. Conclusions These qualitative data reflect the heterogeneity of experiences of the GVHD patient population, reflecting the need for a flexible and nuanced approach to patient care with emphasis on comprehensive information provision. We have identified the key role that BMT specialist nurses within the multidisciplinary team play in supporting patients. We advocate future research should focus on ways to meet the complex needs of this patient group and ensure that the personal care and close relationships are not lost in service redesigns embracing remote consultations.


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