Effects of immune complex formation and complement activation on circulating platelets in the primate

被引:10
作者
Birmingham, DJ [1 ]
Hebert, LA
Shen, XP
Higgins, P
Yeh, CG
Creasey, AA
机构
[1] Ohio State Univ, Columbus, OH 43210 USA
[2] Cytomed Inc, Cambridge, MA 02139 USA
[3] Chiron Corp, Emeryville, CA 94608 USA
关键词
primate platelets; complement; immune complexes;
D O I
10.1006/clim.1998.4677
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primate platelets are different from rodent and rabbit platelets in that they do not express receptors for C3a or C5a or immune adherence receptors. This study assessed the effects of immune complex (IC)-induced complement activation on primate platelets in the circulation. Cynomolgus monkeys (CYN, N = 4) immunized to bovine gamma globulin (BGG) were infused with EGG over 5 min to induce acute intravascular IC formation and complement activation. The studies were carried out under normal complement conditions (N = 12), partial complement inhibition (CAB-2 treated, N = 3), or total complement inhibition (CVF treated, N = 1). Under normal complement conditions, EGG; infusion increased C3a levels from undetectable to an average of 11.9 +/- 2.6 mu g/ml. At this time, decreases occurring in both circulating neutrophils (85 +/- 6%) and monocytes (78 +/- 6%) were significantly greater than decreases in circulating platelets (13 +/- 3%, p < 0.001). Partial complement inhibition had an equivocal effect on the EGG-induced changes in circulating leukocytes, while total complement inhibition abrogated these changes. In contrast, platelet changes were unaffected by complement inhibition. We conclude that, compared to circulating leukocytes, circulating platelets are insensitive to intravascular complement activation induced by IC in the nonhuman primate. These results contrast with previous studies in rodents which demonstrate strong effects of IC-induced intravascular complement activation on both circulatingneutrophils and platelets. (C) 1999 Academic Press.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 31 条
[1]  
Birmingham DJ, 1996, J IMMUNOL, V157, P2586
[2]   ERYTHROCYTE COMPLEMENT RECEPTORS [J].
BIRMINGHAM, DJ .
CRITICAL REVIEWS IN IMMUNOLOGY, 1995, 15 (02) :133-154
[3]  
BIRMINGHAM DJ, 1990, J LAB CLIN MED, V116, P242
[4]   CR3-RECEPTOR ON PLATELETS AND ITS ROLE IN THE PROSTAGLANDIN METABOLIC PATHWAY [J].
COSGROVE, LJ ;
DAPICE, AJF ;
HADDAD, A ;
PEDERSEN, J ;
MCKENZIE, IFC .
IMMUNOLOGY AND CELL BIOLOGY, 1987, 65 :453-460
[5]  
COUSER WG, 1995, J AM SOC NEPHROL, V5, P1888
[6]  
FERNANDEZGALLARDO S, 1989, LAB INVEST, V60, P705
[7]   DETERMINANTS OF IMMUNE COMPLEX-MEDIATED GLOMERULONEPHRITIS [J].
FRIES, JWU ;
MENDRICK, DL ;
RENNKE, HG .
KIDNEY INTERNATIONAL, 1988, 34 (03) :333-345
[8]  
FUKUOKA Y, 1988, J IMMUNOL, V140, P3496
[9]   CHARACTERIZATION OF C3A RECEPTOR-PROTEINS ON GUINEA-PIG PLATELETS AND HUMAN POLYMORPHONUCLEAR LEUKOCYTES [J].
GERARDYSCHAHN, R ;
AMBROSIUS, D ;
SAUNDERS, D ;
CASARETTO, M ;
MITTLER, C ;
KARWARTH, G ;
GORGEN, S ;
BITTERSUERMANN, D .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (06) :1095-1102
[10]  
HAMMERSCHMIDT DE, 1981, AM J PATHOL, V102, P146