LOW T-CELL RESPONSIVENESS TO ACTIVATION VIA CD3/TCR IS A PROGNOSTIC MARKER FOR ACQUIRED-IMMUNODEFICIENCY-SYNDROME (AIDS) IN HUMAN IMMUNODEFICIENCY VIRUS-1 (HIV-1)-INFECTED MEN

被引:115
作者
SCHELLEKENS, PTA
ROOS, MTL
DEWOLF, F
LANGE, JMA
MIEDEMA, F
机构
[1] UNIV AMSTERDAM,DEPT INTERNAL MED,AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,ACAD MED CTR,DEPT VIROL,1105 AZ AMSTERDAM,NETHERLANDS
关键词
human immunodeficiency virus-1 (HIV-1); prognostic marker; T-cell function; Whole-blood lymphocyte culture;
D O I
10.1007/BF00918194
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In a cohort of 300 HIV-1-infected homosexual men, studied longitudinally, the prognostic value of T-cell proliferative responses for development of AIDS was analyzed. In 15 persons we observed that, at seroconversion, T-cell reactivity to anti-CD3 monoclonal antibody (Mab) and phytohemagglutinin (PHA) was decreased to 20 and 60% of the normal values, respectively. After seroconversion, within 3 months, the response to anti-CD3 Mab and PHA returned to 60 and 80%, respectively, of the normal magnitude and declined thereafter. To investigate whether low T-cell reactivity correlated with progression to AIDS, groups of progressors and nonprogressors were compared. In individuals who progressed to AIDS, already 12 months before diagnosis, responses to anti-CD3 Mab were virtually absent, whereas at that time CD4+ cell numbers and reactivity to horse anti-human lymphocyte serum and PHA were still comparable to values observed for nonprogressors and the asymptomatic population as a whole. In a disease-free survival analysis, low anti-CD3 Mab reactivity predicted progression to AIDS. Our findings demonstrate that low T-cell responsiveness to anti-CD3 Mab is an early marker of progression toward AIDS in HIV-1 infected individuals. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 32 条
[1]   ACQUIRED IMMUNE DYSFUNCTION IN HOMOSEXUAL MEN - IMMUNOLOGICAL PROFILES [J].
AMMANN, AJ ;
ABRAMS, D ;
CONANT, M ;
CHUDWIN, D ;
COWAN, M ;
VOLBERDING, P ;
LEWIS, B ;
CASAVANT, C .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1983, 27 (03) :315-325
[2]   EPIDEMIOLOGICAL PARAMETERS OF HIV TRANSMISSION [J].
ANDERSON, RM ;
MAY, RM .
NATURE, 1988, 333 (6173) :514-519
[3]   IMPAIRMENT IN LYMPHOCYTE-T RESPONSES DURING EARLY INFECTION WITH THE HUMAN IMMUNODEFICIENCY VIRUS [J].
BENTIN, J ;
TSOUKAS, CD ;
MCCUTCHAN, JA ;
SPECTOR, SA ;
RICHMAN, DD ;
VAUGHAN, JH .
JOURNAL OF CLINICAL IMMUNOLOGY, 1989, 9 (02) :159-168
[4]   WHOLE-BLOOD LYMPHOCYTE-CULTURES [J].
BLOEMENA, E ;
ROOS, MTL ;
VANHEIJST, JLAM ;
VOSSEN, JMJJ ;
SCHELLEKENS, PTA .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 122 (02) :161-167
[5]   PHASEOLUS-VULGARIS PHYTOHEMAGGLUTININ (PHA) BINDS TO THE HUMAN LYMPHOCYTE-T ANTIGEN RECEPTOR [J].
CHILSON, OP ;
BOYLSTON, AW ;
CRUMPTON, MJ .
EMBO JOURNAL, 1984, 3 (13) :3239-3245
[6]   CHARACTERIZATION OF LYMPHOCYTE-T RESPONSES DURING PRIMARY INFECTION WITH HUMAN IMMUNODEFICIENCY VIRUS [J].
COOPER, DA ;
TINDALL, B ;
WILSON, EJ ;
IMRIE, AA ;
PENNY, R .
JOURNAL OF INFECTIOUS DISEASES, 1988, 157 (05) :889-896
[7]  
DEWOLF F, 1988, J INFECT DIS, V158, P615, DOI 10.1093/infdis/158.3.615
[8]  
GIORGI JV, 1987, J IMMUNOL, V138, P3725
[9]   3-YEAR INCIDENCE OF AIDS IN 5 COHORTS OF HTLV-III-INFECTED RISK GROUP MEMBERS [J].
GOEDERT, JJ ;
BIGGAR, RJ ;
WEISS, SH ;
EYSTER, ME ;
MELBYE, M ;
WILSON, S ;
GINZBURG, HM ;
GROSSMAN, RJ ;
DIGIOLA, RA ;
SANCHEZ, WC ;
GIRON, JA ;
EBBESEN, P ;
GALLO, RC ;
BLATTNER, WA .
SCIENCE, 1986, 231 (4741) :992-995
[10]   PNEUMOCYSTIS-CARINII PNEUMONIA AND MUCOSAL CANDIDIASIS IN PREVIOUSLY HEALTHY HOMOSEXUAL MEN - EVIDENCE OF A NEW ACQUIRED CELLULAR IMMUNODEFICIENCY [J].
GOTTLIEB, MS ;
SCHROFF, R ;
SCHANKER, HM ;
WEISMAN, JD ;
FAN, PT ;
WOLF, RA ;
SAXON, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (24) :1425-1431