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Reduced number of IFN‐γ producing cells in peripheral blood is a biomarker for patients with renal cell carcinoma

Authors :
Kun‐Jin Wu
Kun Yang
Feng‐Ping Zhang
Si‐Nan Liu
Kai‐Bo Yang
Xiao‐Hua Ma
Xing Zhang
Yan‐Fen Ma
Hui Geng
Zheng Wang
Chang Liu
Ting Lin
Source :
Immunity, Inflammation and Disease, Vol 10, Iss 7, Pp n/a-n/a (2022)
Publication Year :
2022
Publisher :
Wiley, 2022.

Abstract

Abstract Renal cell cancer (RCC) is the most lethal of all the common urologic cancers and constitutes 2.2% of all malignancy diagnoses. The incidence of RCC has been steadily increasing in recent decades. The classic risk factors of RCC include smoking, hypertension, obesity, genetics, and genetic mutations. Recent studies also revealed that RCC was an immunogenic tumor and affected by host immune status. Among the pan‐cance, RCC presented with the highest degree of immune infiltration, indicating RCC patients might benefit from immunotherapy. A new immune classification of RCC has been developed by Su et al. based on tumor‐infiltrating lymphocytes to guide clinical practice. However, these studies mainly focus on biomarkers derived from tumor microenvironment (TME), the biomarkers based on peripheral blood samples to RCC have rarely been described. We collected peripheral blood samples from RCC patients and their matched healthy controls and detected the number of IL‐2 and IFN‐γ producing cells by implementing an enzyme‐linked immunospot (ELISPOT) assay. This is the first study to report blood‐based immune biomarkers for RCC using an ELISPOT assay. Our results suggested the frequency of IFN‐γ producing cells but not IL‐2 producing cells was associated with RCC risk. These findings warrant further validation in larger prospective studies.

Details

Language :
English
ISSN :
20504527
Volume :
10
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Immunity, Inflammation and Disease
Publication Type :
Academic Journal
Accession number :
edsdoj.4bf01222fb764a3287cdbd64b4fe0678
Document Type :
article
Full Text :
https://doi.org/10.1002/iid3.637