Increased Serum B Cell-Activating Factor (BAFF) Level in Children with Atopic Dermatitis

2008 ◽  
Vol 121 (2) ◽  
pp. S120-S120
Author(s):  
H JEE ◽  
B CHOI ◽  
K KIM ◽  
M SOHN ◽  
G JANG ◽  
...  
Blood ◽  
2011 ◽  
Vol 118 (24) ◽  
pp. 6446-6449 ◽  
Author(s):  
Robert Whittle ◽  
Peter C. Taylor

Abstract Extracorporeal photopheresis (ECP) is an important therapeutic option in steroid-refractory chronic graft-versus-host disease (cGVHD). Few biomarkers predicting response exist. We measured serum B-cell activating factor (BAFF) in 46 cGVHD patients receiving ECP before and during treatment course. BAFF level at 1 month of ECP predicted 3- and 6-month skin disease response, with BAFF less than 4 ng/mL associated with significant skin improvement and complete resolution in 11 of 20 patients. High BAFF at 1-month ECP associated with a worsening median 6-month skin score and resolution in 1 of 10 patients. BAFF level at 3 months also predicted the likelihood of maintaining skin disease improvement at 6 months. BAFF level was not correlated directly with extracutaneous cGVHD response, although full cutaneous responders exhibited improved extracutaneous organ response rates compared with skin nonresponders (65% vs 35%). This study suggests that early BAFF measurement during ECP for cGVHD represents a potentially useful biomarker in prediction of treatment outcome.


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.


2009 ◽  
Vol 35 (6) ◽  
pp. 593-598 ◽  
Author(s):  
H. M. Jee ◽  
K. W. Kim ◽  
J. Y. Hong ◽  
M. H. Sohn ◽  
K. E. Kim

2010 ◽  
Vol 53 (8) ◽  
pp. 795 ◽  
Author(s):  
Hye Mi Jee ◽  
Bong Seok Choi ◽  
Kyung Won Kim ◽  
Myung Hyun Sohn ◽  
Man Yong Han ◽  
...  

2009 ◽  
Vol 123 (2) ◽  
pp. S73-S73 ◽  
Author(s):  
H. Jee ◽  
Y. Park ◽  
B. Choi ◽  
T. Song ◽  
H. Yum ◽  
...  

2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Tsutomu Hamada ◽  
Takuya Samukawa ◽  
Tomohiro Kumamoto ◽  
Kazuhito Hatanaka ◽  
Go Tsukuya ◽  
...  

2016 ◽  
Vol 16 (1) ◽  
Author(s):  
Tsutomu Hamada ◽  
Takuya Samukawa ◽  
Tomohiro Kumamoto ◽  
Kazuhito Hatanaka ◽  
Go Tsukuya ◽  
...  

Author(s):  
Antonia Margarete Schuster ◽  
N. Miesgang ◽  
L. Steines ◽  
C. Bach ◽  
B. Banas ◽  
...  

AbstractThe B cell activating factor BAFF has gained importance in the context of kidney transplantation due to its role in B cell survival. Studies have shown that BAFF correlates with an increased incidence of antibody-mediated rejection and the development of donor-specific antibodies. In this study, we analyzed a defined cohort of kidney transplant recipients who were treated with standardized immunosuppressive regimens according to their immunological risk profile. The aim was to add BAFF as an awareness marker in the course after transplantation to consider patient’s individual immunological risk profile. Included patients were transplanted between 2016 and 2018. Baseline data, graft function, the occurrence of rejection episodes, signs of microvascular infiltration, and DSA kinetics were recorded over 3 years. BAFF levels were determined 14 d, 3 and 12 months post transplantation. Although no difference in graft function could be observed, medium-risk patients showed a clear dynamic in their BAFF levels with low levels shortly after transplantation and an increase in values of 123% over the course of 1 year. Patients with high BAFF values were more susceptible to rejection, especially antibody-mediated rejection and displayed intensified microvascular inflammation; the combination of high BAFF + DSA puts patients at risk. The changing BAFF kinetics of the medium risk group as well as the increased occurrence of rejections at high BAFF values enables BAFF to be seen as an awareness factor. To compensate the changing immunological risk, a switch from a weaker induction therapy to an intensified maintenance therapy is required.


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