Lymph Nodes Draining Infections Investigated by PET and Immunohistochemistry in a Juvenile Porcine Model
- PMID: 35566137
- PMCID: PMC9104488
- DOI: 10.3390/molecules27092792
Lymph Nodes Draining Infections Investigated by PET and Immunohistochemistry in a Juvenile Porcine Model
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: IL-8; Ki-67; PET; Staphylococcus aureus; [11C]methionine; [18F]FDG; calcium-binding leukocyte L1; immunohistochemistry; lymph nodes; pig model.
Conflict of interest statement
The authors declare no conflict of interest.
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References
-
- Stöber B., Tanase U., Herz M., Seidl C., Schwaiger M., Senekowitsch-Schmidtke R. Differentiation of tumour and inflammation: Characterisation of [methyl-3H]methionine (MET) and O-(2-[18F]fluoroethyl)-L- tyrosine (FET) uptake in human tumour and inflammatory cells. Eur. J. Nucl. Med. Mol. Imaging. 2006;33:932–939. doi: 10.1007/s00259-005-0047-5. - DOI - PubMed
-
- Hoffman R.M. L-[Methyl-11C] Methionine-Positron-Emission Tomography (MET-PET) In: Hoffman R.M., editor. Methionine Dependence of Cancer and Aging: Methods and Protocols. Methods in Molecular Biology. Volume 1866. Humana Press; New York, NY, USA: 2019. pp. 267–271. - PubMed
-
- Hatzenbuehler J., Pulling T.J. Diagnosis and management of osteomyelitis. Am. Fam. Physician. 2011;84:1027–1033. - PubMed
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