B7-H3 Expression in NSCLC and Its Association with B7-H4, PD-L1 and Tumor-Infiltrating Lymphocytes

Mehmet Altan1,2, Vasiliki Pelekanou3, Kurt A Schalper1,3

  • 1Section of Medical Oncology, Yale School of Medicine, New Haven, Connecticut.

Insights

High B7-H3 protein expression in non-small cell lung cancer (NSCLC) is linked to poorer survival and smoking history. Its coexpression with PD-L1 and B7-H4 is low, suggesting distinct roles in lung cancer.

Area of Science:

  • Oncology
  • Immunology
  • Cancer Research

Background:

  • Immune checkpoint inhibitors targeting PD-1/PD-L1 are effective cancer therapies.
  • The role of other B7 family members, like B7-H3, in non-small cell lung cancer (NSCLC) remains less understood.
  • Understanding B7 family member expression is crucial for developing novel cancer immunotherapies.

Purpose of the Study:

  • To determine the expression level of B7-H3 protein in NSCLC.
  • To evaluate the association of B7-H3 with tumor-infiltrating lymphocytes (TIL), PD-L1, B7-H4, and clinicopathologic characteristics.
  • To assess the prognostic significance of B7-H3 in NSCLC patients.

Main Methods:

  • Multiplexed automated quantitative immunofluorescence (QIF) was employed.
  • B7-H3, PD-L1, B7-H4, and TIL levels were assessed in 634 NSCLC cases.
  • Statistical analyses were performed to correlate marker levels with clinicopathologic variables and survival.

Main Results:

  • B7-H3 protein was expressed in 80.4% of NSCLC cases.
  • High B7-H3 levels correlated with poor overall survival and were associated with smoking history.
  • Coexpression of B7-H3 with PD-L1 was observed in 17.6% and with B7-H4 in 10% of cases, while simultaneous B7-H4 and PD-L1 detection was rare (1.8%).
  • B7-H3 expression was not associated with CD3, CD8, or CD20 positive TILs.

Conclusions:

  • B7-H3 is frequently expressed in NSCLC and linked to smoking history.
  • Elevated B7-H3 protein levels indicate a negative prognostic impact in lung cancer.
  • The low coexpression rates of B7-H3 with PD-L1 and B7-H4 suggest these targets may have non-redundant biological functions in NSCLC.

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