Potential role of the soluble form of CD40 in deficient immunological function of dialysis patients: new findings of its amelioration using polymethylmethacrylate (PMMA) membrane

被引:32
作者
Contin-Bordes, Cecile [1 ,2 ]
Lacraz, Adeline [3 ]
de Precigout, Valerie [3 ]
机构
[1] Univ Victor Segalen, CNRS, UMR 5164, CIRID, Bordeaux, France
[2] Pellegrin Hosp, Dept Immunol, Bordeaux, France
[3] Pellegrin Hosp, Dept Nephrol, Bordeaux, France
关键词
haemodialysis; immune dysfunctions; polymethylmethacrylate (PMMA) membrane; hepatitis B vaccination; soluble CD40;
D O I
10.1093/ndtplus/sfq033
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Even though numerous studies have helped to better delineate abnormalities of either innate or adaptive immune system in end-stage renal disease (ESRD) patients, understanding immune dysfunctions in ESRD patients remains a very complex puzzle with missing pieces. In this context, we showed that the soluble form of CD40 (sCD40) is elevated in ESRD patients and is associated with a lack of response to hepatitis B vaccination. Interestingly, although most dialysis membranes are unable to clear sCD40, we demonstrated that polymethylmethacrylate (PMMA) BK-F membranes (Toray Medical Company, Japan) allow a dramatic diminution of the molecule. We took advantage of this observation to address the question of the potential usefulness of PMMA membrane (BK-F series) in the improvement of humoral immune response of ESRD patients. We, thus, present our recent data highlighting the potential role of BK-F membrane in the improvement of hepatitis B vaccination of ESRD patients who failed to mount a protective immune response despite one or more well-conducted anterior vaccination. Taken as a whole, our findings reinforced the concept of seeing dialysis membranes not just as a simple diffusive device but as a tool to tailor dialysis procedure to improve the global quality of life of ESRD patients. This opens a wide area of investigation, notably for the management of immunological dysfunction of ESRD patients.
引用
收藏
页码:I20 / I27
页数:8
相关论文
共 42 条
[41]   Serological evidence for reactivation of EBV infection due to uraemic immunodeficiency [J].
Winkelspecht, B ;
MuellerLantzsch, N ;
Kohler, H .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1997, 12 (10) :2099-2104
[42]  
Yamda S, 1999, CONTRIB NEPHROL, V125, P159