Rat models are often used to study liver allograft rejection. We have
established a model for rat liver allograft rejection, monitored by fi
ne needle aspiration biopsy (FNAB), in the strain combination PVG-to-B
N with a mean survival time of 37 +/- 20 days. In this model. we obser
ved acute rejection with an intense peak of lymphoid blasts and lympho
cyte-dominated inflammation in the FNAB [9.1 +/- 3.0 corrected increme
nt units (CIU)], and an eventual increase in macrophages (up to 4.2 +/
- 4.4 CIU), together with fibrosis and parenchymal necrosis in the gra
ft. Markers of immune activation, such as an increase in IL-2-receptor
(from 1% +/- 2% to 21% +/- 13%) and class II (from 20% +/- 9% to 43%
+ 13%) expressing lymphoid cells and induction of ICAM-1 in the graft,
were consistent with the overall cellular response. The FNAB correlat
ed well with parallel graft histology. In this rat model, the atraumat
ic monitoring makes a close follow-up possible without having to sacri
fice the experimental animals, This saves work, animals, and costs in
the study of liver rejection.