Down-Regulating Humoral Immune Responses: Implications for Organ Transplantation

被引:15
|
作者
Stegall, Mark D. [1 ,3 ]
Moore, Natalie [1 ]
Taner, Timucin [2 ]
Li, Han [2 ]
Dean, Patrick G. [2 ]
机构
[1] Mayo Clin, Dept Surg, Div Transplant Surg, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Immunol, Rochester, MN USA
[3] Mayo Clin, Div Transplant Surg, Rochester, MN USA
关键词
Humoral immunity; Alloantibody; Plasma cells; Complement; Memory B cells; Immunoregulation; Tolerance; Kidney transplantation; Antibody-mediated rejection; ANTIBODY-MEDIATED REJECTION; POSITIVE CROSS-MATCH; MEMORY B-CELLS; PLASMA-CELLS; HLA ANTIBODIES; KIDNEY-TRANSPLANTATION; RENAL-TRANSPLANTATION; SECRETING CELLS; DENDRITIC CELLS; BORTEZOMIB;
D O I
10.1097/TP.0b013e3182a72115
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alloantibody can be a major barrier to successful organ transplantation; however, therapy to control antibody production or to alter its impact on the allograft remains limited. The goal of this review is to examine the regulatory steps that are involved in the generation of alloreactive B cells, with a specific emphasis on how known mechanisms relate to clinical situations in transplant recipients. Thus, we will examine the process of activation of mature, naive B cells and how this relates to de novo antibody production. The role of long-lived plasma cells in persistent antibody production and the factors regulating their longevity will be explored. The regulation of memory B cells and their possible roles in alloimmunity also will be assessed. Finally, we will review current therapeutic approaches aimed at controlling alloantibody and assess their efficacy. By examining the pathways to antibody production mechanistically, we hope to identify important gaps in our current knowledge and gain insight into possible new therapeutic approaches to overcoming antibody in transplant patients.
引用
收藏
页码:247 / 257
页数:11
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