Immunolocalization of CD80 and CD86 in Non-Small Cell Lung Carcinoma: CD80 as a Potent Prognostic Factor.

CD80 CD86 PD-L1 immunohistochemistry lung cancer

Journal

Acta histochemica et cytochemica
ISSN: 0044-5991
Titre abrégé: Acta Histochem Cytochem
Pays: Japan
ID NLM: 0147110

Informations de publication

Date de publication:
26 Feb 2022
Historique:
received: 03 09 2021
accepted: 10 12 2021
entrez: 21 4 2022
pubmed: 22 4 2022
medline: 22 4 2022
Statut: ppublish

Résumé

It has been demonstrated that tumor cells express programed cell death protein 1 (PD-L1) to escape T lymphocytes that express programed cell protein 1 (PD-1), and PD-1/PD-L1 immune checkpoint inhibitors have been regarded in lung cancer patients. CD80 and CD86 are members of B7 superfamily which regulates T lymphocyte activation and tolerance. However, immunolocalization of CD80 and CD86 has not been examined in the lung carcinoma tissues and their clinical significance remains unknown. Therefore, to clarify clinical significance of CD80 and CD86, we immunolocalized these in 75 non-small cell lung carcinomas (NSCLC) in this study. Immunoreactivities of CD80 and CD86 were mainly detected in tumor-infiltrating macrophages. Immunohistochemical CD80 status was high in 56% of NSCLC, and it was positively associated with stage, pathological T factor, distant metastasis, histological type and PD-L1 status. Moreover, multivariate analysis turned out that the CD80 status was an independent worse prognostic factor. CD86 status was high in 53% of the cases, but it was not significantly associated with any clinicopathological parameters. These findings suggest that CD80 is a potent worse prognostic factor possibly in association with escape from immune attack in NSCLC.

Identifiants

pubmed: 35444349
doi: 10.1267/ahc.21-00075
pii: JST.JSTAGE/ahc/21-00075
pmc: PMC8913274
doi:

Types de publication

Journal Article

Langues

eng

Pagination

25-35

Informations de copyright

2022 The Japan Society of Histochemistry and Cytochemistry.

Déclaration de conflit d'intérêts

VThe authors declare that there are no conflicts of interest.

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Auteurs

Takashi Sato (T)

Department of Clinical Laboratory, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.
Department of Pathology and Histotechnology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Kiyoshi Takagi (K)

Department of Pathology and Histotechnology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Mitsunori Higuchi (M)

Department of Thoracic Surgery, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Hiroko Abe (H)

Department of Clinical Laboratory, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Michie Kojimahara (M)

Department of Clinical Laboratory, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Miho Sagawa (M)

Department of Clinical Laboratory, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Megumi Tanaki (M)

Department of Clinical Laboratory, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Yasuhiro Miki (Y)

Department of Disaster Obstetrics and Gynecology, International Research Institute of Disaster Science, Tohoku University, Sendai, Japan.

Takashi Suzuki (T)

Department of Pathology and Histotechnology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Hiroshi Hojo (H)

Department of Pathology, Aizu Medical Center, Fukushima Medical University, Aizuwakamatsu, Japan.

Classifications MeSH