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Quantification of Tumor Cell Adhesion in Lymph Node Cryosections
Published on: February 9, 2020
Active macromolecule uptake by lymph node antigen-presenting cells: a novel mechanism in determining sentinel lymph
M B Faries1, I Bedrosian, C Reynolds
1Department of Surgery, University of Pennsylvania, Philadelphia, USA.
Annals of Surgical Oncology
|April 13, 2000
Summary
Sentinel lymph node (SLN) biopsy effectiveness relies on antigen-presenting cells (APCs) actively taking up macromolecules. This mechanism explains differential radioactivity in SLNs and impacts SLN biopsy techniques.
Area of Science:
- Oncology
- Immunology
- Surgical Pathology
Background:
- Sentinel lymph node (SLN) biopsy is crucial for staging melanoma and breast cancer.
- Technique-related controversies persist in SLN biopsy.
- The role of antigen-presenting cells (APCs) in differential radiotracer retention in SLNs requires clarification.
Purpose of the Study:
- To investigate if active particle uptake by APCs explains differential radioactivity retention in SLNs versus nonsentinel lymph nodes (NSLNs).
Main Methods:
- Pigs were injected with vital blue dye, FITC-labeled human serum albumin (FITC-HSA), and 99mTc-labeled tracers (macromolecule or sulfur colloid).
- In vitro APC uptake of FITC-HSA was assessed using fluorescence-activated cell sorting (FACS).
- SLNs and NSLNs were analyzed via fluorescence microscopy and FACS, with leukocyte markers for cell identification.
Main Results:
- Both radiotracers proved effective for SLN mapping.
- APCs demonstrated rapid uptake of FITC-HSA in vitro.
- Microscopy revealed FITC-HSA in SLN subcapsular sinuses and interfollicular areas; FACS confirmed increasing SLN uptake over time.
- APCs expressing MHC class II were identified as the primary cells responsible for uptake.
Conclusions:
- Active macromolecule uptake by APCs is a key mechanism determining SLN status.
- Understanding this mechanism is vital for optimizing SLN biopsy procedures.
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