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Published on: February 24, 2023
Tumor CD155 Expression Is Associated with Resistance to Anti-PD1 Immunotherapy in Metastatic Melanoma
Ailin Lepletier1, Jason Madore1, Jake S O'Donnell1,2,3
1Immunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Queensland, Australia.
Purpose:
Resistance to anti-PD1-based immune checkpoint blockade (ICB) remains a problem for the treatment of metastatic melanoma. Tumor cells as well as host myeloid cells can express the immune checkpoint ligand CD155 to regulate immune cell function. However, the effect of tumor CD155 on the immune context of human melanoma has not been well described. This observational study characterizes tumor CD155 ligand expression by metastatic melanoma tumors and correlates results with differences in immune cell features and response to ICB.
Experimental Design:
Pretreatment tumor specimens, from 155 patients with metastatic melanoma treated with ICB and from 50 patients treated with BRAF/MEK-directed targeted therapy, were assessed for CD155 expression by IHC. Intratumor T-cell features were analyzed using multiplex-immunohistofluorescence for CD8, PD1, and SOX10. Correlations were made between CD155 tumor level and bulk tumor RNA sequencing results, as well as clinical RECIST response and progression-free survival.
Results:
High pretreatment CD155 tumor levels correlated with high parenchymal PD1+CD8+/CD8+ T-cell ratios (PD1tR) and poor response to anti-PD1 therapy. In PDL1 negative tumors, high CD155 tumor expression was associated with patients who had poor response to combination anti-PD1/CTLA4 therapy.
Conclusions:
Our findings are the first to suggest that tumor CD155 supports an increase in the fraction of PD1+CD8+ T cells in anti-PD1 refractory melanoma tumors and, further, that targeting the CD155 pathway might improve response to anti-PD1 therapy for patients with metastatic melanoma.
Insights
High CD155 tumor expression in melanoma is linked to poor response to anti-PD1 therapy. Targeting CD155 may improve treatment outcomes for metastatic melanoma patients.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Resistance to anti-PD1 immune checkpoint blockade (ICB) is a significant challenge in metastatic melanoma treatment.
- Tumor and myeloid cells express CD155, a ligand that regulates immune cell function, but its role in melanoma immunity is not fully understood.
Purpose of the Study:
- To characterize tumor CD155 ligand expression in metastatic melanoma.
- To correlate CD155 expression with immune cell features and response to ICB.
Main Methods:
- Assessed CD155 expression in pretreatment tumor specimens from 155 patients treated with ICB and 50 with targeted therapy using IHC.
- Analyzed intratumor T-cell features (CD8, PD1) via multiplex-immunohistofluorescence.
- Correlated CD155 levels with RNA sequencing, RECIST response, and progression-free survival.
Main Results:
- High pretreatment CD155 tumor levels correlated with increased PD1+CD8+/CD8+ T-cell ratios (PD1tR).
- Elevated CD155 expression was associated with poor response to anti-PD1 therapy.
- In PDL1-negative tumors, high CD155 predicted poor response to combined anti-PD1/CTLA4 therapy.
Conclusions:
- Tumor CD155 promotes a higher fraction of PD1+CD8+ T cells in anti-PD1 refractory melanoma.
- Targeting the CD155 pathway may enhance anti-PD1 therapy response in metastatic melanoma.
