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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.
Abstract:
Purpose: The immune checkpoint PD-1 and its receptor B7-H1 (PD-L1) are successful therapeutic targets in cancer but less is known about other B7 family members. Here, we determined the expression level of B7-H3 protein in non-small cell lung cancer (NSCLC) and evaluated its association with tumor-infiltrating lymphocytes (TIL), PD-L1, B7-H4, and major clinicopathologic characteristics is in 3 NSCLC cohorts.Experimental design: We used multiplexed automated quantitative immunofluorescence (QIF) to assess the levels of B7-H3, PD-L1, B7-H4, and TILs in 634 NSCLC cases with validated antibodies. Associations between the marker levels, major clinicopathologic variables and survival were analyzed.Results: Expression of B7-H3 protein was found in 80.4% (510/634) of the cases. High B7-H3 protein level (top 10 percentile) was associated with poor overall survival (P < 0.05). Elevated B7-H3 was consistently associated with smoking history across the 3 cohorts, but not with sex, age, clinical stage, and histology. Coexpression of B7-H3 and PD-L1 was found in 17.6% of the cases (112/634) and with B7-H4 in 10% (63/634). B7-H4 and PD-L1 were simultaneously detected only in 1.8% of NSCLCs (12/634). The expression of B7-H3 was not associated with the levels of CD3-, CD8-, and CD20-positive TILs.Conclusions: B7-H3 protein is expressed in the majority of NSCLCs and is associated with smoking history. High levels of B7-H3 protein have a negative prognostic impact in lung carcinomas. Coexpression of B7-H3 with PD-L1 and B7-H4 is relatively low, suggesting a nonredundant biological role of these targets. Clin Cancer Res; 23(17); 5202-9. ©2017 AACR.
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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