Alveolar macrophages in sarcoidosis coexpress high levels of CD86 (B7.2), CD40, and CD30L

被引:55
作者
Nicod, LP
Isler, P
机构
[1] Pulmonary Division, University Hospital of Geneva, Geneva
[2] Pulmonary Division, University Hospital
关键词
D O I
10.1165/ajrcmb.17.1.2781
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alveolar macrophages (AM) from sarcoid patients have been shown to be good antigen presenting cells (APC) unlike normal AM which are usually ineffective. We demonstrate in ten consecutive sarcoid patients that most of their AM, unlike normal AM, do coexpress high levels of CD86, CD40, and CD30L, all known to be important for T-cell activation. CD80 is also slightly more expressed on sarcoid AM than on normal AM, but is detected on only 26 +/- 6% (mean +/- SEM) of sarcoid AM. A good correlation is present between the percentage of sarcoid AM expressing CD86 and CD40 or CD86 and CD30L. However, no correlation is found between the percentage of CD80 and CD86 positive AM in these same patients. Blocking antibodies against CD86 were able to reduce by more than 80% allogeneic T-cell proliferation induced by the AM of sarcoid patients. This study provides evidence that AM can, in pathologic states such as sarcoidosis, express functional costimulatory molecules for T-cell activation such as CD86, thought to be rather specific for more professional APC such as dendritic cells.
引用
收藏
页码:91 / 96
页数:6
相关论文
共 23 条
[1]   THE YIN AND YANG OF T-CELL COSTIMULATION [J].
ALLISON, JP ;
KRUMMEL, MF .
SCIENCE, 1995, 270 (5238) :932-933
[2]  
BACHWICH PR, 1986, AM J PATHOL, V125, P421
[3]   Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation [J].
Cella, M ;
Scheidegger, D ;
PalmerLehmann, K ;
Lane, P ;
Lanzavecchia, A ;
Alber, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :747-752
[4]   HUMAN ALVEOLAR MACROPHAGES PRESENT ANTIGEN INEFFECTIVELY DUE TO DEFECTIVE EXPRESSION OF B7 COSTIMULATORY CELL-SURFACE MOLECULES [J].
CHELEN, CJ ;
FANG, Y ;
FREEMAN, GJ ;
SECRIST, H ;
MARSHALL, JD ;
HWANG, PT ;
FRANKEL, LR ;
DEKRUYFF, RH ;
UMETSU, DT .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (03) :1415-1421
[5]   B7-1 AND B7-2 DO NOT DELIVER IDENTICAL COSTIMULATORY SIGNALS, SINCE B7-2 BUT NOT B7-1 PREFERENTIALLY COSTIMULATES THE INITIAL PRODUCTION OF IL-4 [J].
FREEMAN, GJ ;
BOUSSIOTIS, VA ;
ANUMANTHAN, A ;
BERNSTEIN, GM ;
KE, XY ;
RENNERT, PD ;
GRAY, GS ;
GRIBBEN, JG ;
NADLER, LM .
IMMUNITY, 1995, 2 (05) :523-532
[6]   Tumor necrosis factor soluble receptor 75: The principal receptor form released by human alveolar macrophages and monocytes in the presence of interferon gamma [J].
GalvedeRochemonteix, B ;
Nicod, LP ;
Dayer, JM .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1996, 14 (03) :279-287
[7]   IMPAIRMENT OF ANTIGEN-SPECIFIC T-CELL PRIMING IN MICE LACKING CD40 LIGAND [J].
GREWAL, IS ;
XU, JC ;
FLAVELL, RA .
NATURE, 1995, 378 (6557) :617-620
[8]  
Hamann D, 1996, J IMMUNOL, V156, P1387
[9]  
KIENER PA, 1995, J IMMUNOL, V155, P4917
[10]  
LEM VM, 1985, J IMMUNOL, V135, P1766