Evidence of indirect allorecognition in long-term human renal transplantation

被引:8
作者
Coelho, V [1 ]
Spadafora-Ferreira, M
Marrero, I
Fonseca, JA
Portugal, K
Kalil, J
机构
[1] Univ Sao Paulo, Inst Coracao, Lab Imunol Transplantes, BR-05403000 Sao Paulo, Brazil
[2] Univ Sao Paulo, Fac Med, Hosp Clin, Unidade Transplante Renal, BR-05403000 Sao Paulo, Brazil
关键词
indirect; alloreactivity; renal; transplantation;
D O I
10.1006/clim.1998.4626
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 purpose of this study was to investigate indirect alloreactivity in the peripheral blood of long-term renal transplanted patients. We evaluated the T cell proliferative response to a whole pool of donor cell-derived allopeptides, processed and presented by host antigen-presenting cells (APC), rather than to synthetic peptides. For the indirect pathway, proliferation assays were performed using APC-depleted donor cells. Indirect alloreactivity was detected in 57% (8/14) of the patients, 6 of whom presented no evidence of rejection, but 2 patients had a diagnosis of chronic rejection. In 4 of 8 positive cases (50%), proliferation was detected with 5 days of culture, and sometimes indirect alloresponse was the dominant route. We present evidence that the indirect alloproliferative response to a pool of naturally processed donor peptides is present in the peripheral blood of long-term renal transplanted patients irrespective of rejection. (C) 1999 Academic Press.
引用
收藏
页码:220 / 229
页数:10
相关论文
共 39 条
[1]  
ANSARI AA, 1992, J HEART LUNG TRANSPL, V11, P467
[2]   THE ROLE OF INDIRECT RECOGNITION IN INITIATING REJECTION OF SKIN-GRAFTS FROM MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II-DEFICIENT MICE [J].
AUCHINCLOSS, H ;
LEE, R ;
SHEA, S ;
MARKOWITZ, JS ;
GRUSBY, MJ ;
GLIMCHER, LH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3373-3377
[3]   INDIRECT T-CELL ALLORECOGNITION OF DONOR ANTIGENS CONTRIBUTES TO THE REJECTION OF VASCULARIZED KIDNEY ALLOGRAFTS [J].
BENHAM, AM ;
SAWYER, GJ ;
FABRE, JW .
TRANSPLANTATION, 1995, 59 (07) :1028-1032
[4]  
BENHAM AM, 1995, TRANSPLANT P, V27, P547
[5]  
BENICHOU G, 1994, J IMMUNOL, V153, P938
[6]   DONOR MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) PEPTIDES ARE PRESENTED BY RECIPIENT MHC MOLECULES DURING GRAFT-REJECTION [J].
BENICHOU, G ;
TAKIZAWA, PA ;
OLSON, CA ;
MCMILLAN, M ;
SERCARZ, EE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :305-308
[7]  
BESOUW NM, 1996, TRANSPLANTATION, V61, P165
[8]   PROCESSED MHC CLASS-I ALLOANTIGEN AS THE STIMULUS FOR CD4+ T-CELL DEPENDENT ANTIBODY-MEDIATED GRAFT-REJECTION [J].
BRADLEY, JA ;
MOWAT, AM ;
BOLTON, EM .
IMMUNOLOGY TODAY, 1992, 13 (11) :434-438
[9]   MEDIATION OF ACUTE BUT NOT CHRONIC REJECTION OF MHC-INCOMPATIBLE RAT-KIDNEY GRAFTS BY ALLOREACTIVE CD4 T-CELLS ACTIVATED BY THE DIRECT PATHWAY OF SENSITIZATION [J].
BRAUN, MY ;
MCCORMACK, A ;
WEBB, G ;
BATCHELOR, JR .
TRANSPLANTATION, 1993, 55 (01) :177-182
[10]   Mechanisms of indirect allorecognition in graft rejection - Class II MHC allopeptide-specific T cell clones transfer delayed-type hypersensitivity responses in vivo [J].
Chen, WJ ;
Murphy, B ;
Waaga, AM ;
Willett, TA ;
Russell, ME ;
Khoury, SJ ;
Sayegh, MH .
TRANSPLANTATION, 1996, 62 (06) :705-710