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Lymph Nodes Draining Infections Investigated by PET and Immunohistochemistry in a Juvenile Porcine Model
Authors:Pia Afzelius  Malene Kjelin Morsing  Ole Lerberg Nielsen  Aage Kristian Olsen Alstrup  Svend Borup Jensen  Lars Jdal
Abstract:Background: 18F]FDG and 11C]methionine accumulate in lymph nodes draining S. aureus -infected foci. The lymph nodes were characterized by weight, 11C]methionine- and 18F]FDG-positron emissions tomography (PET)/computed tomography (CT), and immunohistochemical (IHC)-staining. Methods: 20 pigs inoculated with S. aureus into the right femoral artery were PET/CT-scanned with 18F]FDG, and nine of the pigs were additionally scanned with 11C]methionine. Mammary, medial iliac, and popliteal lymph nodes from the left and right hind limbs were weighed. IHC-staining for calculations of area fractions of Ki-67, L1, and IL-8 positive cells was done in mammary and popliteal lymph nodes from the nine pigs. Results: The pigs developed one to six osteomyelitis foci. Some pigs developed contiguous infections of peri-osseous tissue and inoculation-site abscesses. Weights of mammary and medial iliac lymph nodes and their 18F]FDG maximum Standardized Uptake Values (SUVFDGmax) showed a significant increase in the inoculated limb compared to the left limb. Popliteal lymph node weight and their FDG uptake did not differ significantly between hind limbs. Area fractions of Ki-67 and IL-8 in the right mammary lymph nodes and SUVMetmax in the right popliteal lymph nodes were significantly increased compared with the left side. Conclusion: The PET-tracers 18F]FDG and 11C]methionine, and the IHC- markers Ki-67 and IL-8, but not L1, showed increased values in lymph nodes draining soft tissues infected with S. aureus. The increase in 11C]methionine may indicate a more acute lymph node response, whereas an increase in 18F]FDG may indicate a more chronic response.
Keywords:PET  [18F]FDG  [11C]methionine  lymph nodes  pig model  Staphylococcus aureus  Ki-67  calcium-binding leukocyte L1  IL-8  immunohistochemistry
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