Prospective analysis between the therapy of immunosuppressive medication and allogeneic microchimerism after liver transplantation

被引:5
作者
Araujo, M. B. [1 ]
Leonardi, L. S. [2 ]
Leonardi, M. I. [2 ]
Boin, I. F. S. F. [2 ]
Magna, L. A. [3 ]
Donadi, E. A. [4 ]
Kraemer, M. H. S. [1 ]
机构
[1] Univ Estadual Campinas, Fac Med Sci, Dept Clin Pathol, Immunogenet Transplant Lab, Campinas, SP, Brazil
[2] Univ Estadual Campinas, Fac Med Sci, Dept Surg, Campinas, SP, Brazil
[3] Univ Estadual Campinas, Fac Med Sci, Dept Med Genet, Campinas, SP, Brazil
[4] Univ Sao Paulo, Fac Med, Dept Internal Med, BR-14049 Ribeirao Preto, Brazil
基金
巴西圣保罗研究基金会;
关键词
Allogeneic microchimerism; Immunosuppressive medication; Liver transplantation; ORGAN-TRANSPLANTATION; PCR-AMPLIFICATION; GRAFT ACCEPTANCE; CELL-MIGRATION; CHIMERISM; TOLERANCE; REJECTION; PREVALENCE; BLOOD;
D O I
10.1016/j.trim.2008.08.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After liver transplantation, migration of donor-derived hematopoietic cells to recipient can be detected in pheripheral blood. This state is termed microchimerism. The aim of this study was to investigate prospectively the presence of allogeneic microchimerism, the occurrence of acute cellular rejection and the level of immunosuppression in transplanted patients. Microchimerism occurrence between 10 days and 12 months after liver transplantation was analyzed in 47 patients aged between 15 and 65 by a two-stage nested PCR/SSP technique to detect donor MHC HLA-DR gene specifically. A pre-transplant blood sample was colleted from each patient to serve as individual negative control. Microchimerism was demonstrated in 32 (68%) of the 47 patients; of these, only 10 patients (31.2%) presented rejection. Early microchimerism was observed in 25 patients (78.12%) and late microchimerism in 7 patients (21.8%). Among the patients with microchimerism, 14 were given CyA and 18 were given FK506. In the group without microchimerism, 12 patients were given CyA and 03 were given FK506. There was a significant association between the presence of microchimerism and the absence of rejection (p=0.02) and also between microchimerism and the type of immunosuppression used. Our data indicate that microchimerism and probably differentiation of donor-derived leukocytes can have relevant immunologic effects both in terms of sensitization of recipient and in terms of immunomodulation toward tolerance induction. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 198
页数:4
相关论文
共 28 条
[1]   Molecular mechanisms associated with donor-specific microchimerism in peripheral blood of Brazilian patients after liver transplantation [J].
Araujo, M. B. ;
Leonardi, L. S. ;
Boin, I. F. S. F. ;
Leonardi, M. I. ;
Meirelles, L. ;
Magna, L. A. ;
Donadi, E. A. ;
Kraemer, M. H. S. .
TRANSPLANTATION PROCEEDINGS, 2006, 38 (05) :1411-1417
[2]   Development of donor-specific microchimerism in liver transplant recipient with HLA-DRB1 and-DQB1 mismatch related to rejection episodes [J].
Arújo, MB ;
Leonardi, LS ;
Boin, IFSF ;
Leonardi, MI ;
Magna, LA ;
Donadi, EA ;
Kraemer, MHS .
TRANSPLANTATION PROCEEDINGS, 2004, 36 (04) :953-955
[3]   RAPID HLA-DRB1 GENOTYPING BY NESTED PCR-AMPLIFICATION [J].
BEIN, G ;
GLASER, R ;
KIRCHNER, H .
TISSUE ANTIGENS, 1992, 39 (02) :68-73
[4]   The liver: A special case in transplantation tolerance [J].
Benseler, Volker ;
McCaughan, Geoffrey W. ;
Schlitt, Hans J. ;
Bishop, G. Alex ;
Bowen, David G. ;
Bertolino, Patrick .
SEMINARS IN LIVER DISEASE, 2007, 27 (02) :194-213
[5]   Microchimerism after liver transplantation: Absence of rejection without abrogation of anti-donor cytotoxic T-lymphocyte-mediated alloreactivity [J].
Bettens, F ;
Tiercy, JM ;
Campanile, N ;
Giostra, E ;
Majno, P ;
Rubbia, L ;
Roosnek, E ;
Mentha, G ;
Villard, J .
LIVER TRANSPLANTATION, 2005, 11 (03) :290-297
[6]   Frequency of recipient-derived chimerism and relationship with acute rejection and HLA tissue typing in transplanted livers [J].
Bilezikçi, B ;
Sahin, F ;
Uyar, P ;
Yilmaz, Z ;
Demirhan, B ;
Turan, M ;
Arat, Z ;
Haberal, M .
TRANSPLANTATION PROCEEDINGS, 2006, 38 (02) :598-601
[7]   Microchimerism after heart transplantation:: Prevalence, predisposing factors, natural history, and prognosis [J].
Crespo-Leiro, MG ;
Hermida-Prieto, M ;
Rodriguez, JA ;
Muñiz, J ;
Barral, S ;
Paniagua, MJ ;
Hermida, LF ;
Juffé, A ;
Castro-Beiras, A .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (01) :161-163
[8]   Microchimerism and rejection in clinical transplantation [J].
Elwood, ET ;
Larsen, CP ;
Maurer, MH ;
Routenberg, KL ;
Neylan, NF ;
Whelchel, JD ;
OBrien, DP ;
Pearson, TC .
LANCET, 1997, 349 (9062) :1358-1360
[9]   How should chimerism be decoded? [J].
Ferrand, C ;
Perruche, S ;
Robinet, E ;
Martens, A ;
Tiberghien, P ;
Saas, P .
TRANSPLANTATION, 2003, 75 (09) :50S-54S
[10]   The complementary roles of deletion and regulation in transplantation tolerance [J].
Lechler, RI ;
Garden, OA ;
Turka, LA .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (02) :147-158