Instillation of allogeneic lung macrophages and dendritic cells cause differential effects on local IFN-γ production, lymphocytic bronchitis, and vasculitis in recipient murine lungs

被引:13
作者
Wilkes, DS
Thompson, LK
Cummings, OW
Bragg, S
Heidler, KM
机构
[1] Indiana Univ, Sch Med, Div Pulm & Crit Care & Occupat Med, Dept Med, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Pathol, Indianapolis, IN 46202 USA
关键词
allograft rejection; C57BL/6; mouse; BALB/c mouse;
D O I
10.1002/jlb.64.5.578
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lung allograft rejection is believed to be initiated by donor lung accessory cells, namely macrophages and dendritic cells, interacting with recipient lymphocytes leading to up-regulated Th1 type (IFN-gamma) cellular immunity culminating in graft destruction. The purpose of this study Tvas to determine the individual role of donor lung macrophages and dendritic cells in the rejection response. Utilizing a murine model that reproduces the immunology and histology of acute rejection, C57BL/6 mouse (I-a(b), H-2(b)) lung dendritic cells (DC-enriched lung cells), purified alveolar macrophages (I-a-negative macrophages), or various ratios of I-a-negative macrophages/DC were instilled into BALB/c mouse (I-a(d), H-2(d)) lungs followed by an assessment of local IFN-gamma production and grading of rejection pathology. The data show that DC, and not I-a-negative macrophages, induced IFN-gamma production in recipient lungs, However, the local production of IFN-gamma was not always associated with histological changes characteristic of rejection pathology. In contrast to either cell type alone, instillation of C57BL/6 I-a-negative macrophages and DC, together, were required to induce rejection pathology in BALB/c lungs. In addition, the rejection response was dependent on interactions between donor I-a-negative macrophages and DC.
引用
收藏
页码:578 / 586
页数:9
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