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ICOSLG 与晚期黑色素瘤患者接受抗 PD-1 联合抗组胺治疗应答相关。

ICOSLG Is Associated with Anti-PD-1 and Concomitant Antihistamine Treatment Response in Advanced Melanoma.

机构信息

Melanoma, Cancer Immunotherapy and Development Therapeutics Unit, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Via Mariano Semmola, 53, 80131 Naples, Italy.

Medical Statistics Unit, Universitiy of Campania "Luigi Vanvitelli", 81100 Naples, Italy.

出版信息

Int J Mol Sci. 2024 Nov 19;25(22):12439. doi: 10.3390/ijms252212439.

DOI:10.3390/ijms252212439
PMID:39596506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11594639/
Abstract

We previously demonstrated that patients with metastatic unresectable stage IIIb-IV melanoma receiving cetirizine (a second-generation H1 antagonist antihistamine) premedication with immunotherapy had better outcomes than those not receiving cetirizine. In this retrospective study, we searched for a gene signature potentially predictive of the response to the addition of cetirizine to checkpoint inhibition (nivolumab or pembrolizumab with or without previous ipilimumab). Transcriptomic analysis showed that inducible T cell costimulator ligand (ICOSLG) expression directly correlated with the disease control rate (DCR) when detected with a loading value > 0.3. A multivariable logistic regression model showed a positive association between the DCR and ICOSLG expression for progression-free survival and overall survival. ICOSLG expression was associated with CD64, a specific marker of M1 macrophages, at baseline in the patient samples who received cetirizine concomitantly with checkpoint inhibitors, but this association was not present in subjects who had not received cetirizine. In conclusion, our results show that the clinical advantage of concomitant treatment with cetirizine during checkpoint inhibition in patients with malignant melanoma is associated with high ICOSLG expression, which could predict the response to immune checkpoint inhibitor blockade.

摘要

我们之前的研究表明,接受西替利嗪(第二代 H1 拮抗剂抗组胺药)预先免疫治疗的转移性不可切除 IIIb-IV 期黑色素瘤患者比未接受西替利嗪的患者有更好的结局。在这项回顾性研究中,我们寻找了一种潜在的基因标志物,以预测西替利嗪联合检查点抑制(nivolumab 或 pembrolizumab,联合或不联合之前的 ipilimumab)的反应。转录组分析表明,诱导性 T 细胞共刺激配体(ICOSLG)的表达与疾病控制率(DCR)直接相关,当检测到加载值>0.3 时。多变量逻辑回归模型显示,ICOSLG 表达与无进展生存期和总生存期的 DCR 之间存在正相关。在同时接受检查点抑制剂和西替利嗪治疗的患者样本中,ICOSLG 表达与基线时的 CD64(M1 巨噬细胞的特异性标志物)相关,但在未接受西替利嗪治疗的患者中不存在这种相关性。总之,我们的研究结果表明,在恶性黑色素瘤患者中,同时接受西替利嗪和检查点抑制剂治疗的临床优势与高 ICOSLG 表达相关,这可能预测对免疫检查点抑制剂阻断的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/3ca61bbd75b2/ijms-25-12439-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/624bcad7563b/ijms-25-12439-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/db8944e1eb65/ijms-25-12439-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/7807c2fedb98/ijms-25-12439-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/3ca61bbd75b2/ijms-25-12439-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/624bcad7563b/ijms-25-12439-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/db8944e1eb65/ijms-25-12439-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/7807c2fedb98/ijms-25-12439-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6573/11594639/3ca61bbd75b2/ijms-25-12439-g004a.jpg

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