PD-1, PD-L1, IDO, CD70 and microsatellite instability as potential targets to prevent immune evasion in sarcomas

Author:

Siozopoulou Vasiliki12ORCID,Smits Evelien23,Zwaenepoel Karen12,Liu Jimmy1,Pouliakis Abraham4,Pauwels Patrick A12,Marcq Elly2

Affiliation:

1. Department of Pathology, Antwerp University Hospital, Edegem, 2650, Belgium

2. Center for Oncological Research, Integrated Personalized & Precision Oncology Network, University of Antwerp, Wilrijk, 2610, Belgium

3. Center for Cell Therapy & Regenerative Medicine, Antwerp University Hospital, Edegem, 2650, Belgium

4. Second Department of Pathology, National & Kapodistrian University of Athens, “Attikon” University Hospital, Athens, 12464, Greece

Abstract

Background: Soft tissue and bone sarcomas are rare entities, hence, standardized therapeutic strategies are difficult to assess. Materials & methods: Immunohistochemistry was performed on 68 sarcoma samples to assess the expression of PD-1, PD-L1, IDO and CD70 in different tumor compartments and molecular analysis was performed to assess microsatellite instability status. Results: PD-1/PD-L1, IDO and CD70 pathways are at play in the immune evasion of sarcomas in general. Soft tissue sarcomas more often show an inflamed phenotype compared with bone sarcomas. Specific histologic sarcoma types show high expression levels of different markers. Finally, this is the first presentation of a microsatellite instability-high Kaposi sarcoma. Discussion/conclusion: Immune evasion occurs in sarcomas. Specific histologic types might benefit from immunotherapy, for which further investigation is needed.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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