T cell receptor biases and clonal proliferations among lung transplant recipients with obliterative bronchiolitis

被引:29
作者
Duncan, SR
Valentine, V
Roglic, M
Elias, DJ
Pekny, KW
Theodore, J
Kono, DH
Theofilopoulos, AN
机构
[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA
[2] SCRIPPS RES INST, DEPT EXPTL MED, LA JOLLA, CA 92037 USA
[3] STANFORD UNIV, MED CTR, DEPT MED, STANFORD, CA 94305 USA
关键词
allograft rejection; chronic; T cell antigen receptors; alpha beta; organ transplantation;
D O I
10.1172/JCI118714
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Obliterative bronchiolitis (OB) is the most serious late complication of lung transplantation, but the pathogenesis of this disorder has not been elucidated, We sought evidence that OB is mediated by a cellular immunologic response by characterizing T cell antigen receptor beta-chain variable gene (TCRBV) repertoires in lung allograft recipients. Expression levels of 27 TCRBV among recipients were determined by multiprobe RNase protection assay after PCR amplification, In comparison to recipients with no evidence of rejection (n=9), the PBL TCRBV repertoires of OB subjects (n=16) exhibited more frequent expansions (16 vs. 9% of all measured TCRBV, P<0.02), and the magnitudes of these abnormalities were greater (8.2+/-0.8 vs, 4.5+/-0.3 SD from mean normal values, P<0.01). TCRBV sequencing showed these expansions were composed of clonal or oligoclonal populations, Thus, T cell responses in the recipients are marked by highly selective clonal expansions, presumably driven by indirect recognition of a limited number of immunodominant alloantigens. These processes are exaggerated among allograft recipients with OB, implying that cognate immune mechanisms are important in the pathogenesis of the disorder. Furthermore, the prominence of finite, distinct TCR phenotypes raise possibilities for development of novel diagnostic modalities and targeted immunotherapies for OB and other manifestations of chronic allograft rejection.
引用
收藏
页码:2642 / 2650
页数:9
相关论文
共 39 条
[1]   SELECTIVE IMMUNOSUPPRESSION (REPRINTED FROM TRENDS IN PHARMACOLOGICAL SCIENCES, VOL 14, PG 178-1828, 1993) [J].
ADORINI, L ;
GUERY, JC ;
RODRIGUEZTARDUCHY, G ;
TREMBLEAU, S .
IMMUNOLOGY TODAY, 1993, 14 (06) :285-289
[2]   DOMINANT SELECTION OF AN INVARIANT T-CELL ANTIGEN RECEPTOR IN RESPONSE TO PERSISTENT INFECTION BY EPSTEIN-BARR-VIRUS [J].
ARGAET, VP ;
SCHMIDT, CW ;
BURROWS, SR ;
SILINS, SL ;
KURILLA, MG ;
DOOLAN, DL ;
SUHRBIER, A ;
MOSS, DJ ;
KIEFF, E ;
SCULLEY, TB ;
MISKO, IS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) :2335-2340
[3]   CHRONIC GRAFT-REJECTION [J].
AZUMA, H ;
TILNEY, NL .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (05) :770-776
[4]  
BENCHELOU G, 1992, J EXP MED, V175, P305
[5]   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
[6]   POST-TRANSPLANT OBLITERATIVE BRONCHIOLITIS AND OTHER LATE LUNG SEQUELAE IN HUMAN HEART-LUNG TRANSPLANTATION [J].
BURKE, CM ;
THEODORE, J ;
DAWKINS, KD ;
YOUSEM, SA ;
BLANK, N ;
BILLINGHAM, ME ;
VANKESSEL, A ;
JAMIESON, SW ;
OYER, PE ;
BALDWIN, JC ;
STINSON, EB ;
SHUMWAY, NE ;
ROBIN, ED .
CHEST, 1984, 86 (06) :824-829
[7]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[8]  
COLVIN RB, 1990, ANNU REV MED, V41, P361
[9]   ALLORECOGNITION OF ISOLATED, DENATURED CHAINS OF CLASS-I AND CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX-MOLECULES - EVIDENCE FOR AN IMPORTANT ROLE FOR INDIRECT ALLORECOGNITION IN TRANSPLANTATION [J].
DALCHAU, R ;
FANGMANN, J ;
FABRE, JW .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (03) :669-677
[10]   SEQUELAE OF CYTOMEGALOVIRUS PULMONARY INFECTIONS IN LUNG ALLOGRAFT RECIPIENTS [J].
DUNCAN, SR ;
PARADIS, IL ;
YOUSEM, SA ;
SIMILO, SL ;
GRGURICH, WF ;
WILLIAMS, PA ;
DAUBER, JH ;
GRIFFITH, BP .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (06) :1419-1425