TY - JOUR
T1 - Immunolocalization of CD80 and CD86 in Non-Small Cell Lung Carcinoma
T2 - CD80 as a Potent Prognostic Factor
AU - Sato, Takashi
AU - Takagi, Kiyoshi
AU - Higuchi, Mitsunori
AU - Abe, Hiroko
AU - Kojimahara, Michie
AU - Sagawa, Miho
AU - Tanaki, Megumi
AU - Miki, Yasuhiro
AU - Suzuki, Takashi
AU - Hojo, Hiroshi
N1 - Publisher Copyright:
© 2022 The Japan Society of Histochemistry and Cytochemistry.
PY - 2022
Y1 - 2022
N2 - 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 carci-nomas (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 metasta-sis, 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.
AB - 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 carci-nomas (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 metasta-sis, 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.
KW - CD80
KW - CD86
KW - Immunohistochemistry
KW - Lung cancer
KW - PD-L1
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U2 - 10.1267/ahc.21-00075
DO - 10.1267/ahc.21-00075
M3 - Article
AN - SCOPUS:85126019644
SN - 0044-5991
VL - 55
SP - 25
EP - 35
JO - Acta Histochemica et Cytochemica
JF - Acta Histochemica et Cytochemica
IS - 1
ER -