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5-氨基酮戊酸光动力疗法对 2 级宫颈上皮内瘤变女性局部免疫反应的影响。

The effects of 5-aminolevulinic acid photodynamic therapy on the local immune response of women with cervical intraepithelial neoplasia grade 2.

机构信息

Department of Obstetrics and Gynecology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Shanghai Key Laboratory of Gynecologic Oncology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

出版信息

Front Immunol. 2023 Oct 20;14:1211114. doi: 10.3389/fimmu.2023.1211114. eCollection 2023.


DOI:10.3389/fimmu.2023.1211114
PMID:37928525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10623119/
Abstract

OBJECTIVE: To evaluate and elucidate the effects and mechanism of 5-aminolevulinic acid photodynamic therapy (ALA-PDT) on the local immune response of women with cervical intraepithelial neoplasia grade 2 (CIN2). MATERIALS AND METHODS: Immunofluorescence staining was used to compare immune cells infiltration before and after ALA-PDT in 23 patients with CIN2. The infiltration of immune cells into the cervical tissues of patients with different outcomes was also compared at the 6-month follow-up period. Immune cell counts in samples collected before and after treatment were compared. RESULTS: We found an increased number of CD8 T cell infiltration, an increased proportion of CD8 T cells expressing Granzyme B (GrB), Chemokine receptor 3 (CXCR3), and CD8 tissue-resident memory T (T) cells, and a decreased proportion of CD8 T cells expressing PD-1 in patients with CIN2 compared to that before ALA-PDT. Moreover, at the 6-month follow-up, there was higher infiltration of CD8 T and CD8 T cells, higher expression of GrB and CXCR3, and lower expression of PD-1 on CD8 T cells in the HPV clearance and CIN2 disappearance groups than in the HPV-positive and CIN2 regression groups. However, no significant difference was observed in the number of CD8 T following ALA-PDT. CONCLUSION: ALA-PDT could activate CD8 T cell responses by modulating the expression of CXCR3 and PD-1 in CD8 T cells and increasing the infiltration of CD8 T cells. And the infiltration of CD8 T cells is correlated with the prognosis of CIN2.

摘要

目的:评估并阐明 5-氨基酮戊酸光动力疗法(ALA-PDT)对 2 级宫颈上皮内瘤变(CIN2)女性局部免疫反应的影响和机制。

材料和方法:采用免疫荧光染色法比较 23 例 CIN2 患者 ALA-PDT 前后免疫细胞浸润情况,并在 6 个月随访期比较不同结局患者宫颈组织中免疫细胞的浸润情况,比较治疗前后采集样本中免疫细胞的计数。

结果:我们发现 CIN2 患者 CD8 T 细胞浸润增加,CD8 T 细胞表达颗粒酶 B(GrB)、趋化因子受体 3(CXCR3)和 CD8 组织驻留记忆 T(T)细胞的比例增加,表达 PD-1 的 CD8 T 细胞比例降低,与 ALA-PDT 前相比。此外,在 6 个月随访时,HPV 清除和 CIN2 消失组 CD8 T 和 CD8 T 细胞浸润更高,GrB 和 CXCR3 表达更高,CD8 T 细胞上 PD-1 表达更低,而 HPV 阳性和 CIN2 消退组则更低。然而,ALA-PDT 后 CD8 T 细胞数量没有显著差异。

结论:ALA-PDT 可通过调节 CD8 T 细胞中 CXCR3 和 PD-1 的表达,增加 CD8 T 细胞浸润,激活 CD8 T 细胞反应。并且 CD8 T 细胞浸润与 CIN2 的预后相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/3da6f55e2872/fimmu-14-1211114-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/0959c5022a95/fimmu-14-1211114-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/c0fef8b58043/fimmu-14-1211114-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/48aa10ee1720/fimmu-14-1211114-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/3da6f55e2872/fimmu-14-1211114-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/0959c5022a95/fimmu-14-1211114-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/c0fef8b58043/fimmu-14-1211114-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/48aa10ee1720/fimmu-14-1211114-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d27/10623119/3da6f55e2872/fimmu-14-1211114-g004.jpg

相似文献

[1]
The effects of 5-aminolevulinic acid photodynamic therapy on the local immune response of women with cervical intraepithelial neoplasia grade 2.

Front Immunol. 2023

[2]
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[3]
Effect and rational application of topical photodynamic therapy (PDT) with 5-aminolevulinic acid (5-ALA) for treatment of cervical intraepithelial neoplasia with vaginal intraepithelial neoplasia.

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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
Efficacy of photodynamic therapy with 5-aminolevulinic acid for the treatment of cervical high-grade squamous intraepithelial lesions with high-risk HPV infection: A retrospective study.

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引用本文的文献

[1]
Photodynamic Therapy in Cancer: Insights into Cellular and Molecular Pathways.

Curr Issues Mol Biol. 2025-1-21

[2]
Emerging trends and hotspots in cervical intraepithelial neoplasia research from 2013 to 2023: A bibliometric analysis.

Heliyon. 2024-5-29

[3]
The efficacy and safety of local 5-aminolevulinic acid-based photodynamic therapy in the treatment of cervical high-grade squamous intraepithelial lesion: a single center retrospective observational study.

Front Oncol. 2024-4-16

[4]
Targeting immunogenic cell stress and death for cancer therapy.

Nat Rev Drug Discov. 2024-6

本文引用的文献

[1]
Graphdiyne Oxide-Mediated Photodynamic Therapy Boosts Enhancive T-Cell Immune Responses by Increasing Cellular Stiffness.

Int J Nanomedicine. 2023

[2]
Cancer statistics, 2023.

CA Cancer J Clin. 2023-1

[3]
Combination of a novel heat shock protein 90-targeted photodynamic therapy with PD-1/PD-L1 blockade induces potent systemic antitumor efficacy and abscopal effect against breast cancers.

J Immunother Cancer. 2022-9

[4]
BET bromodomain inhibition rescues PD-1-mediated T-cell exhaustion in acute myeloid leukemia.

Cell Death Dis. 2022-8-2

[5]
Infiltration Patterns of Cervical Epithelial Microenvironment Cells During Carcinogenesis.

Front Immunol. 2022

[6]
Topical 5-aminolevulinic acid photodynamic therapy for cervical high-grade squamous intraepithelial lesions.

Photodiagnosis Photodyn Ther. 2022-9

[7]
Targeting tissue-resident memory CD8 T cells in the kidney is a potential therapeutic strategy to ameliorate podocyte injury and glomerulosclerosis.

Mol Ther. 2022-8-3

[8]
Targeting CD96 overcomes PD-1 blockade resistance by enhancing CD8+ TIL function in cervical cancer.

J Immunother Cancer. 2022-3

[9]
Importance of the Immune Microenvironment in the Spontaneous Regression of Cervical Squamous Intraepithelial Lesions (cSIL) and Implications for Immunotherapy.

J Clin Med. 2022-3-5

[10]
Recent advances in nanomedicines for photodynamic therapy (PDT)-driven cancer immunotherapy.

Theranostics. 2022

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