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CD56 CD16自然杀伤细胞在乳腺癌术前化疗反应中的积累

Accumulation of CD56 CD16 Natural Killer Cells in Response to Preoperative Chemotherapy for Breast Cancer.

作者信息

Kim Ryungsa, Kawai Ami, Wakisaka Megumi, Shimoyama Mika, Yasuda Naomi, Ito Mitsuya, Kin Takanori, Arihiro Koji

机构信息

Department of Breast Surgery, Hiroshima Mark Clinic, Hiroshima, Japan.

Department of Breast Surgery, Hiroshima City Hospital, Hiroshima, Japan.

出版信息

World J Oncol. 2024 Aug;15(4):682-694. doi: 10.14740/wjon1885. Epub 2024 Jul 5.

Abstract

BACKGROUND

The activation of the antitumor immune responses of T cells and natural killer (NK) cells is important to induce breast tumor shrinkage via preoperative chemotherapy. We evaluated how antitumor immune responses contribute to the effects of such therapy.

METHODS

Forty-three patients with stages I - IV breast cancer who underwent surgery between August 2018 and Jun 2023 after preoperative chemotherapy were enrolled. Peripheral natural killer (pNK) cell activity was assessed by Cr-release assay, and the counts and percentages of CD4, CD8, and NK cells and their subsets in peripheral blood were measured before and after chemotherapy by two-color flow cytometry. Associations of cell population changes with chemotherapy responses were analyzed.

RESULTS

On univariate analysis, relative to grade (G) ≤ 1 effects, G ≥ 2 therapeutic effects were associated significantly with human epidermal growth factor receptor 2 (HER-2) breast cancer (P = 0.024) and post-chemotherapy CD56 CD16 NK cell accumulation (8.4% vs. 5.5%, P = 0.042), and tended to be associated with increased pre-chemotherapy CD56 CD16 NK cell percentages (5.4% vs. 3.3%, P = 0.054) and pNK cell activity (42.0% vs. 34.5%, P = 0.057). The accumulation and increased percentage of CD56 CD16 NK cells in patients with G ≥ 2 effects were not associated with changes in pNK cell activity or the disappearance of axillary lymph-node metastases. On multivariate analysis, G ≥ 2 therapeutic effects tended to be associated with higher pre-chemotherapy pNK levels (odds ratio = 0.96; 95% confidence interval: 0.921 - 1.002; P = 0.067).

CONCLUSIONS

The accumulation of the immunoregulatory CD56 CD16 NK cell subset in the peripheral blood before and after chemotherapy may lead to the production of cytokines that induce an antitumor immune response. Activation of the immune response mediated by CD56 CD16 pNK cells after chemotherapy and their high counts before chemotherapy may contribute to the improvement of therapeutic effects against breast cancer.

摘要

背景

T细胞和自然杀伤(NK)细胞的抗肿瘤免疫反应激活对于通过术前化疗诱导乳腺肿瘤缩小至关重要。我们评估了抗肿瘤免疫反应如何促进此类治疗的效果。

方法

纳入2018年8月至2023年6月期间接受术前化疗后行手术的43例I - IV期乳腺癌患者。通过铬释放试验评估外周自然杀伤(pNK)细胞活性,并在化疗前后通过双色流式细胞术测量外周血中CD4、CD8和NK细胞及其亚群的计数和百分比。分析细胞群体变化与化疗反应的相关性。

结果

单因素分析显示,相对于分级(G)≤1的疗效,G≥2的治疗效果与人类表皮生长因子受体2(HER-2)乳腺癌显著相关(P = 0.024)以及化疗后CD56 CD16 NK细胞积累(8.4%对5.5%,P = 0.042),并且倾向于与化疗前CD56 CD16 NK细胞百分比增加(5.4%对3.3%,P = 0.054)和pNK细胞活性增加(42.0%对34.5%,P = 0.057)相关。G≥2疗效患者中CD56 CD16 NK细胞的积累和百分比增加与pNK细胞活性变化或腋窝淋巴结转移消失无关。多因素分析显示,G≥2的治疗效果倾向于与化疗前较高的pNK水平相关(比值比 = 0.96;95%置信区间:0.921 - 1.002;P = 0.067)。

结论

化疗前后外周血中免疫调节性CD56 CD16 NK细胞亚群的积累可能导致诱导抗肿瘤免疫反应的细胞因子产生。化疗后由CD56 CD16 pNK细胞介导的免疫反应激活及其化疗前的高计数可能有助于提高乳腺癌治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd7d/11236370/e02cab3017db/wjon-15-682-g001.jpg

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