Clinical significance of T cell receptor excision circle (TREC) quantitation after allogenic HSCT

被引:9
作者
Mikhael, Neveen Lewis [1 ]
Elsorady, Manal [2 ]
机构
[1] Alexandria Fac Med, Clin Pathol Dept, Elkhartoum Sq, Alexandria, Egypt
[2] Alexandria Fac Med, Clin Hematol Dept, BMT Unit, Alexandria, Egypt
关键词
TRECs; Immune; Allogenic; HSCT; Outcomes; ACUTE MYELOID-LEUKEMIA; THYMIC FUNCTION; IMMUNE RECONSTITUTION; GRAFT SOURCE; TRANSPLANTATION; RECOVERY; PREDICTS; OUTPUT; ONSET;
D O I
10.5045/br.2019.54.4.274
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Hematopoietic stem cell transplantation (HSCT) is a well-established treatment modality for a variety of diseases. Immune reconstitution is an important event that determines outcomes. The immune recovery of T cells relies on peripheral expansion of mature graft cells, followed by differentiation of donor-derived hematopoietic stem cells. The formation of new T cells occurs in the thymus and as a byproduct, T cell receptor excision circles (TRECs) are released. Detection of TRECs by PCR is a reliable method for estimating the amount of newly formed T cells in the circulation and, indirectly, for estimating thymic function. The aim of this study was to determine the role of TREC quantitation in predicting outcomes of human leucocyte antigen (HLA) identical allogenic HSCT. Methods The study was conducted on 100 patients receiving allogenic HSCT from an HLA identical sibling. TREC quantification was done by real time PCR using a standard curve. Results TREC levels were inversely related to age (P =0.005) and were significantly lower in patients with malignant diseases than in those with benign diseases (P =0.038). TREC levels could predict relapse as an outcome but not graft versus host disease (GvHD) and infections. Conclusion Age and nature of disease determine the TREC levels, which are related to relapse.
引用
收藏
页码:274 / 281
页数:8
相关论文
共 36 条
[1]   Pretransplant thymic function predicts acute rejection in antithymocyte globulin-treated renal transplant recipients [J].
Bamoulid, Jamal ;
Courivaud, Cecile ;
Crepin, Thomas ;
Carron, Clemence ;
Gaiffe, Emilie ;
Roubiou, Caroline ;
Laheurte, Caroline ;
Moulin, Bruno ;
Frimat, Luc ;
Rieu, Philippe ;
Mousson, Christiane ;
Durrbach, Antoine ;
Heng, Anne-Elisabeth ;
Rebibou, Jean-Michel ;
Saas, Philippe ;
Ducloux, Didier .
KIDNEY INTERNATIONAL, 2016, 89 (05) :1136-1143
[2]   Immune Reconstitution after Allogeneic Hematopoietic Stem Cell Transplantation: Time To T Up the Thymus [J].
Chaudhry, Mohammed S. ;
Velardi, Enrico ;
Malard, Florent ;
van den Brink, Marcel R. M. .
JOURNAL OF IMMUNOLOGY, 2017, 198 (01) :40-46
[3]   Prognostic value of pretransplantation host thymic function in HLA-identical sibling hematopoietic stem cell transplantation [J].
Clave, E ;
Rocha, V ;
Talvensaari, K ;
Busson, M ;
Douay, C ;
Appert, ML ;
Rabian, C ;
Carmagnat, M ;
Garnier, F ;
Filion, A ;
Socié, G ;
Gluckman, E ;
Charron, D ;
Toubert, A .
BLOOD, 2005, 105 (06) :2608-2613
[4]   Thymopoiesis in Pre- and Post-Hematopoietic Stem Cell Transplantation [J].
da Rocha, Luis Klaus A. ;
de Barros, Samar Freschi ;
Bandeira, Francine ;
Bollini, Alexia ;
Testa, Lucia Helena de A. ;
Simione, Anderson Joao ;
Souza, Marina de O. e ;
Zanetti, Lilian P. ;
de Oliveira, Leila Cibele S. ;
dos Santos, Ana Claudia F. ;
de Souza, Mair Pedro ;
Colturado, Vergilio Antonio R. ;
Kalil, Jorge ;
Machado, Clarisse M. ;
Guilherme, Luiza .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[5]   Immune Reconstitution after Allogeneic Hematopoietic Cell Transplantation in Children [J].
de Koning, Coco ;
Plantinga, Maud ;
Besseling, Paul ;
Boelens, Jaap Jan ;
Nierkens, Stefan .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2016, 22 (02) :195-206
[6]   Reconciling Longitudinal Naive T-Cell and TREC Dynamics during HIV-1 Infection [J].
Drylewicz, Julia ;
Vrisekoop, Nienke ;
Mugwagwa, Tendai ;
de Boer, Anne Bregje ;
Otto, Sigrid A. ;
Hazenberg, Mette D. ;
Tesselaar, Kiki ;
de Boer, Rob J. ;
Borghans, Jose A. M. .
PLOS ONE, 2016, 11 (03)
[7]   Onset of thymic recovery and plateau of thymic output are differentially regulated after stem cell transplantation in children [J].
Eyrich, M ;
Wollny, G ;
Tzaribaschev, N ;
Dietz, M ;
Brügger, D ;
Bader, P ;
Lang, P ;
Schilbach, K ;
Winkler, B ;
Niethammer, D ;
Schlegel, PG .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2005, 11 (03) :194-205
[8]   Patterns of T-cell reconstitution by assessment of T-cell receptor excision circle and T-cell receptor clonal repertoire after allogeneic hematopoietic stem cell transplantation in leukemia patients - a study in Chinese patients [J].
Fu, Yue Wen ;
Wu, De Pei ;
Cen, Jian Nong ;
Feng, Yu Feng ;
Chang, Wei Rong ;
Zhu, Zi Ling ;
Qiu, Qiao Chen ;
Zhu, Ping .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2007, 79 (02) :138-145
[9]   Assessment of TREC, KREC and telomere length in long-term survivors after allogeneic HSCT: the role of GvHD and graft source and evidence for telomere homeostasis in young recipients [J].
Gaballa, A. ;
Norberg, A. ;
Stikvoort, A. ;
Mattsson, J. ;
Sundberg, B. ;
Uzunel, M. ;
Remberger, M. ;
Uhlin, M. .
BONE MARROW TRANSPLANTATION, 2018, 53 (01) :69-77
[10]   T Cell Receptor Excision Circle (TREC) Monitoring after Allogeneic Stem Cell Transplantation; a Predictive Marker for Complications and Clinical Outcome [J].
Gaballa, Ahmed ;
Sundin, Mikael ;
Stikvoort, Arwen ;
Abumaree, Muhamed ;
Uzunel, Mehmet ;
Sairafi, Darius ;
Uhlin, Michael .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (10)