Magnetic resonance imaging detection of rat renal transplant rejection by monitoring macrophage infiltration

被引:68
作者
Zhang, YQ
Dodd, SJ
Hendrich, KS
Williams, M
Ho, C
机构
[1] Carnegie Mellon Univ, Dept Biol Sci, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Pittsburgh NMR Ctr Biomed Res, Pittsburgh, PA 15213 USA
关键词
immune cells; T cell; ultrasmall superparamagnetic iron oxide; kidney transplantation; acute rejection;
D O I
10.1046/j.1523-1755.2000.00286.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. A rat renal transplantation model was studied by noninvasive magnetic resonance imaging (MRI) with an infusion of ultrasmall superparamagnetic iron oxide (USPIO) particles to test whether the accumulation of immune cells, such as macrophages, could be detected in vivo while the kidney transplant was being rejected. Methods. Major histocompatibility disparate DA to BN male rat renal transplantation recipients were infused with USPIO particles, with magnetic resonance (MR) images acquired before, immediately after, and one day following infusion. Results. When the USPIO infusion was on the fourth day post-transplantation. some rejecting allografts showed a decrease of MR signal intensity one day later. Isografts and allografts with triple immunosuppressant treatment had no MR signal reduction. Immunohistologic staining for ED1(+) macrophages and CD4(+) and CD8(+) T cells in allogeneic transplanted kidneys indicated the accumulation of these immune cells as acute rejection occurred. Morphological studies by electron microscopy confirmed the existence of iron inside the lysosomes of macrophages of rejecting kidneys, while Prussian blue staining detected the presence of iron plaques in macrophages. Isografts and allografts with a triple immunosuppressant treatment exhibited smaller MR signal reductions with minimal histologic changes. Conclusions. The concurrence of MR signal reduction following USPIO infusion with pathological manifestation in a rat renal allograft model suggests the possibility that renal transplantation status may be assessed by MRI using USPIO particles as markers for the accumulation of immune cells, such as macrophages.
引用
收藏
页码:1300 / 1310
页数:11
相关论文
共 38 条
[11]  
2-C
[12]  
Hughes J, 1997, J IMMUNOL, V158, P4389
[13]   A RANDOMIZED TRIAL COMPARING CYCLOSPORINE WITH ANTILYMPHOBLAST-GLOBULIN AZATHIOPRINE FOR RENAL-ALLOGRAFT RECIPIENTS - RESULTS AT 2-1/2-6 YEARS [J].
JOHNSON, CP ;
SIMMONS, RL ;
SUTHERLAND, DER ;
CANAFAX, DM ;
ASCHER, NL ;
PAYNE, WD ;
FLICK, B ;
NAJARIAN, JS ;
FRYD, DS .
TRANSPLANTATION, 1988, 45 (02) :380-385
[14]   DEOXYSPERGUALIN SUPPRESSES LOCAL MACROPHAGE PROLIFERATION IN RAT RENAL-ALLOGRAFT REJECTION [J].
KERR, PG ;
NIKOLICPATERSON, DJ ;
LAN, HY ;
TESCH, G ;
RAINONE, S ;
ATKINS, RC .
TRANSPLANTATION, 1994, 58 (05) :596-601
[15]  
LEE S, 1967, SURGERY, V61, P771
[16]   PHARMACOKINETICS OF SUPERPARAMAGNETIC IRON-OXIDE MR CONTRAST AGENTS IN THE RAT [J].
MAJUMDAR, S ;
ZOGHBI, SS ;
GORE, JC .
INVESTIGATIVE RADIOLOGY, 1990, 25 (07) :771-777
[17]   Uptake of dextran-coated monocrystalline iron oxides in tumor cells and macrophages [J].
Moore, A ;
Weissleder, R ;
Bogdanov, A .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 1997, 7 (06) :1140-1145
[18]  
MOROZUMI K, 1992, CLIN NEPHROL, V38, P1
[19]  
NADASDY T, 1989, Orvosi Hetilap, V130, P2369
[20]  
NADASDY T, 1991, PATHOL RES PRACT, V187, P178