Immune checkpoints: Cytotoxic T-lymphocyte antigen 4 and programmed cell death protein 1 in breast cancer surgery

Agnieszka Kolacinska1, Barbara Cebula-Obrzut2, Lukasz Pakula3

  • 1Department of Head and Neck Cancer Surgery, Medical University of Łódź, Łódź 93-509, Poland ; Department of Surgical Oncology, Cancer Center, Łódź 93-509, Poland.

Oncology Letters
|December 2, 2015
PubMed

Insights

Breast cancer patients show altered immune checkpoint levels, with higher Programmed Cell Death Protein 1 (PD-1) in larger, progesterone receptor-negative tumors. Cytotoxic T-lymphocyte antigen 4 (CTLA-4) levels correlate with patient age.

Area of Science:

  • Immunology
  • Oncology
  • Biochemistry

Background:

  • Immune checkpoints are critical inhibitory pathways in the immune system.
  • These checkpoints play a significant role in carcinogenesis.
  • Understanding immune checkpoint involvement in breast cancer is crucial for therapeutic strategies.

Purpose of the Study:

  • To evaluate serum concentrations of two major immune checkpoints, CTLA-4 and PD-1.
  • To assess these markers in patients with stage I and II breast cancer.
  • To compare marker levels between patients and healthy controls at different perioperative time points.

Main Methods:

  • Serum samples were collected from 35 breast cancer patients and 25 healthy controls.
  • Measurements of CTLA-4 and PD-1 were taken preoperatively, intraoperatively, and postoperatively.
  • Flow cytometry was used to assess protein expression levels.

Main Results:

  • Significantly higher PD-1 levels were observed in breast cancer patients compared to controls (P<0.0001).
  • CTLA-4 and PD-1 levels showed a significant association prior to surgery (P=0.0084).
  • Elevated CTLA-4 correlated with older patient age (P=0.0453), and PD-1 decreased post-metastatic sentinel node harvesting (P=0.05).

Conclusions:

  • Breast cancer patients exhibit an altered immune checkpoint profile.
  • Higher PD-1 concentrations are associated with larger, progesterone receptor-negative tumors.
  • These findings warrant further investigation into immune checkpoints in breast cancer.

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