Interleukin-6 production by human neutrophils after Fc-receptor cross-linking or exposure to granulocyte colony-stimulating factor

被引:50
作者
Ericson, SG
Zhao, Y
Gao, HL
Miller, KL
Gibson, LF
Lynch, JP
Landreth, KS
机构
[1] W Virginia Univ, Blood & Marrow Transplantat Program, Mary Babb Randolph Canc Ctr, Robert C Byrd Hlth Sci Ctr, Morgantown, WV 26506 USA
[2] W Virginia Univ, Mary Babb Randolph Canc Ctr, Dept Med, Morgantown, WV 26506 USA
[3] W Virginia Univ, Mary Babb Randolph Canc Ctr, Dept Immunol Microbiol, Morgantown, WV 26506 USA
[4] W Virginia Univ, Mary Babb Randolph Canc Ctr, Dept Pediat, Morgantown, WV 26506 USA
关键词
D O I
10.1182/blood.V91.6.2099.2099_2099_2107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Polymorphonuclear neutrophils (PMNs) are essential effector cells in host defense and tissue inflammatory responses. These responses may be initiated after cross-linking of cell surface Fc receptors that bind the constant portion of IgG (Fc gamma R). We evaluated the effect of cross-linking Fc gamma RI or Fc gamma RII on interleukin-6 (IL-6) production by purified PMNs from normal donors or from patients being treated with recombinant human granulocyte colony-stimulating factor (rhG-CSF). In PMNs from normal donors, IL-6 mRNA was detected by reverse transcriptase-polymerase chain reaction only after Fc gamma RI or Fc gamma RII cross-linking. We also found that IL-6 mRNA could be detected in PMNs after either in vitro or in vivo rhG-CSF treatment in the absence of Fc gamma R crosslinking. IL-6 protein was found to be produced intracellularly and secreted by PMNs after cross-linking Fc gamma RI or Fc gamma RII or after rhG-CSF stimulation. Cross-linking Fc gamma RI or Fc gamma RII on PMNs from patients treated with rhG-CSF resulted in a synergistic increase in IL-6 secretion. Upregulation of IL-6 production by PMNs after rhG-CSF treatment may contribute to a clinical engraftment syndrome that occurs during periods of rapid increase in PMN numbers in patients receiving rhG-CSF. (C) 1998 by The American Society of Hematology.
引用
收藏
页码:2099 / 2107
页数:9
相关论文
共 48 条
[1]  
AKERLEY WL, 1991, BLOOD, V77, P607
[2]  
ASANO T, 1994, J PHARMACOL EXP THER, V268, P1032
[3]  
Biffl WL, 1996, ARCH SURG-CHICAGO, V131, P24
[4]   A cytokine mRNA-destabilizing element that is structurally and functionally distinct from A+U-rich elements [J].
Brown, CY ;
Lagnado, CA ;
Goodall, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13721-13725
[5]  
BUCKLE AM, 1989, J IMMUNOL, V143, P2295
[6]  
Cahill RA, 1996, BONE MARROW TRANSPL, V18, P177
[7]   THE PRODUCTION OF CYTOKINES BY POLYMORPHONUCLEAR NEUTROPHILS [J].
CASSATELLA, MA .
IMMUNOLOGY TODAY, 1995, 16 (01) :21-26
[8]  
CICCO NA, 1990, BLOOD, V75, P2049
[9]  
DJEU JY, 1990, BLOOD, V76, P1405
[10]   CIRCULATING HUMAN PERIPHERAL-BLOOD GRANULOCYTES SYNTHESIZE AND SECRETE TUMOR NECROSIS FACTOR-ALPHA [J].
DUBRAVEC, DB ;
SPRIGGS, DR ;
MANNICK, JA ;
RODRICK, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6758-6761