HLA-DR-mediated apoptosis susceptibility discriminates differentiation stages of dendritic/monocytic APC

被引:55
作者
Bertho, N
Drénou, B
Laupeze, B
Le Berre, C
Amiot, L
Grosset, JM
Fardel, O
Charron, D
Mooney, N
Fauchet, R
机构
[1] INSERM, U396, Inst Cordeliers, Paris, France
[2] Univ Rennes 1, INSERM, U456, Rennes, France
[3] Etablissement Transfus Sanguine Bretagne, Rennes, France
[4] INSERM, CRI 9606 UPRES EA 22 33, Lab Univ Hematol & Biol Cellules Sanguines, Rennes, France
关键词
D O I
10.4049/jimmunol.164.5.2379
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Professional APC are characterized by their ability to present peptide via HLA class II in the presence of costimulatory molecules (CD40, CD80, and CD86), The efficiency of Ag presentation can be classed as follows: mature dendritic cells (DC) are most efficient, immature DC and macrophages are intermediate, and monocytes are considered poor APC, There is a large body of evidence demonstrating that HLA-DR transmits signals in the APC, In this study, we have addressed the question of the outcome of HLA-DR signals on APC of the monocyte/DC lineages throughout their differentiation from immature to mature APC, DC were generated from both monocytes and CD34(+) cells of the same individual, macrophages were differentiated from monocytes, Immunophenotypical analysis clearly distinguished these populations. HLA-DR-mediated signals led to marked apoptosis in mature DC of either CD34 or monocytic origin. Significantly less apoptosis was observed in immature DC of either origin, Nonetheless, even immature DC were more susceptible to HLA-DR-mediated apoptosis than macrophages, whereas monocytes were resistant to HLA-DR-mediated apoptosis, The mechanism of HLA-DR-mediated apoptosis was independent of caspase activation. Taken together, these data lead to the notion that signals generated via HLA-DR lead to the demise of mature professional APC, thereby providing a means of limiting the immune response.
引用
收藏
页码:2379 / 2385
页数:7
相关论文
共 51 条
[1]
Anti-adhesive signals are mediated via major histocompatibility complex class II molecules in normal and neoplastic human B cells: correlation with B cell differentiation stage [J].
Ahsmann, EJM ;
Boom, SE ;
Lokhorst, HM ;
Rijksen, G ;
Bloem, AC .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (10) :2688-2695
[2]
GM-CSF AND TNF-ALPHA COOPERATE IN THE GENERATION OF DENDRITIC LANGERHANS CELLS [J].
CAUX, C ;
DEZUTTERDAMBUYANT, C ;
SCHMITT, D ;
BANCHEREAU, J .
NATURE, 1992, 360 (6401) :258-261
[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]
Drénou B, 1999, J IMMUNOL, V163, P4115
[5]
Garban F, 1998, EXP HEMATOL, V26, P874
[6]
CD28/B7 costimulation: A review [J].
Greenfield, EA ;
Nguyen, KA ;
Kuchroo, VK .
CRITICAL REVIEWS IN IMMUNOLOGY, 1998, 18 (05) :389-418
[7]
Dendritic cells: Unique leukocyte populations which control the primary immune response [J].
Hart, DNJ .
BLOOD, 1997, 90 (09) :3245-3287
[8]
Vaccination of patients with B-cell lymphoma using autologous antigen-pulsed dendritic cells [J].
Hsu, FJ ;
Benike, C ;
Fagnoni, F ;
Liles, TM ;
Czerwinski, D ;
Taidi, B ;
Engleman, EG ;
Levy, R .
NATURE MEDICINE, 1996, 2 (01) :52-58
[9]
In vivo detection of dendritic cell antigen presentation to CD4(+) T cells [J].
Ingulli, E ;
Mondino, A ;
Khoruts, A ;
Jenkins, MK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (12) :2133-2141
[10]
ESTABLISHMENT AND CHARACTERIZATION OF A UNIQUE HUMAN CELL-LINE THAT PROLIFERATES DEPENDENTLY ON GM-CSF, IL-3, OR ERYTHROPOIETIN [J].
KITAMURA, T ;
TANGE, T ;
TERASAWA, T ;
CHIBA, S ;
KUWAKI, T ;
MIYAGAWA, K ;
PIAO, YF ;
MIYAZONO, K ;
URABE, A ;
TAKAKU, F .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 140 (02) :323-334