Monitoring of pathogen-specific T-cell immune reconstitution after allogeneic hematopoietic stem cell transplantation

被引:11
作者
Fuji, Shigeo [1 ,2 ]
Kapp, Markus [1 ]
Einsele, Hermann [1 ]
机构
[1] Univ Hosp Wurzburg, Dept Internal Med 2, Div Hematol, D-97080 Wurzburg, Germany
[2] Natl Canc Ctr, Div Hematopoiet Stem Cell Transplantat, Tokyo, Japan
关键词
virus; fungi; T cell; immune reconstitution; allogeneic stem cell transplantation; CYTOMEGALOVIRUS-SPECIFIC CD4(+); CLINICAL-SCALE GENERATION; INVASIVE ASPERGILLOSIS; ADOPTIVE TRANSFER; ADENOVIRUS INFECTION; IDENTIFY PATIENTS; EBV REACTIVATION; ELISPOT ASSAY; LOW-FREQUENCY; CD8(+);
D O I
10.3389/fimmu.2013.00276
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The clinical outcome after allogeneic hematopoietic stem cell transplantation (HSCT) has been significantly improved during the last decades with regard to the reduction in organ failure, infection, and severe acute graft-versus-host disease. However, severe complications due to infectious diseases are still one of the major causes of morbidity and mortality after allogeneic HSCT, in particular in patients receiving haploidentical HSCT or cord blood transplant due to a slow and often incomplete immune reconstitution. In order to improve the immune control of pathogens without an increased risk of alloreactivity, adoptive immunotherapy using highly enriched pathogen-specific T cells offers a promising approach. In order to identify patients who are at high risk for infectious diseases, several monitoring assays have been developed with potential for the guidance of immunosuppressive drugs and adoptive immunotherapy in clinical practice. In this article, we aim to give a comprehensive overview regarding current developments of T-cell monitoring techniques focusing on T cells against viruses and fungi. In particular, we will focus on rather simple, fast, non-labor-intensive, cellular assays which could be integrated in routine clinical screening approaches.
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页数:6
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