Mesenchymal stem/stromal cell therapy improves immune recovery in a feline model of severe coronavirus infection.

IF 5.4 2区 医学 Q1 CELL & TISSUE ENGINEERING
Patrawin Wanakumjorn, Kazuto Kimura, Diego Castillo, Ehren McLarty, Rachel Formaker, Rachel Qiao, Katherine Farrell, Terza Brostoff, Raneesh Ramarapu, Jully Pires, Tamar Cohen-Davidyan, Jennifer Cassano, Brian Murphy, Krystle Reagan, Amir Kol
{"title":"Mesenchymal stem/stromal cell therapy improves immune recovery in a feline model of severe coronavirus infection.","authors":"Patrawin Wanakumjorn, Kazuto Kimura, Diego Castillo, Ehren McLarty, Rachel Formaker, Rachel Qiao, Katherine Farrell, Terza Brostoff, Raneesh Ramarapu, Jully Pires, Tamar Cohen-Davidyan, Jennifer Cassano, Brian Murphy, Krystle Reagan, Amir Kol","doi":"10.1093/stcltm/szaf025","DOIUrl":null,"url":null,"abstract":"<p><p>Severe coronavirus infections, including SARS-CoV-2, are marked by systemic inflammation, T-cell exhaustion, lymphopenia, and chronic immune dysfunction, with limited therapeutic options for recovery. Feline infectious peritonitis (FIP), a naturally occurring feline coronavirus infection, mirrors these immune pathologies, providing a valuable translational model. This study evaluated the safety and efficacy of allogeneic mesenchymal stem/stromal cell (MSC) therapy combined with antiviral treatment in cats with effusive FIP. Hematologic, virologic, and immunologic analyses were conducted over 12 weeks. Antiviral therapy reduced cytotoxic T-cell exhaustion by downregulating inhibitory receptors PD-1, TIM-3, and LAG-3. MSC-treated cats demonstrated enhanced immune recovery, evidenced by reduced expression of exhaustion-related transcription factors (IKZF2, ZEB2, PRDM1) and increased regulatory T-cell populations, promoting immune homeostasis. Single-cell RNA sequencing of mesenteric lymph nodes revealed transcriptomic shifts indicative of immune rejuvenation, including elevated memory T-cell markers (IKZF1, GZMK, IL7R) and reduced hyperproliferative lymphocyte subsets. Serum cytokine analysis revealed 3 distinct inflammatory mediator patterns using principal component analysis. Both treatment groups showed transitions toward cytokine profiles resembling those of healthy controls. Notably, residual cytokine elevations persisted at the study's end, mirroring features of chronic immune dysregulation. PDGF-bb, a marker of tissue repair, was uniquely associated with higher lymphocyte counts, suggesting its role in lymphoid recovery. This study highlights the potential of MSC therapy to modulate immune dysfunction and support durable immune recovery. The findings underscore its translational relevance for addressing severe viral diseases characterized by chronic inflammation and immune dysregulation, advancing both veterinary and human medicine.</p>","PeriodicalId":21986,"journal":{"name":"Stem Cells Translational Medicine","volume":"14 7","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12259234/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem Cells Translational Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/stcltm/szaf025","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
引用次数: 0

Abstract

Severe coronavirus infections, including SARS-CoV-2, are marked by systemic inflammation, T-cell exhaustion, lymphopenia, and chronic immune dysfunction, with limited therapeutic options for recovery. Feline infectious peritonitis (FIP), a naturally occurring feline coronavirus infection, mirrors these immune pathologies, providing a valuable translational model. This study evaluated the safety and efficacy of allogeneic mesenchymal stem/stromal cell (MSC) therapy combined with antiviral treatment in cats with effusive FIP. Hematologic, virologic, and immunologic analyses were conducted over 12 weeks. Antiviral therapy reduced cytotoxic T-cell exhaustion by downregulating inhibitory receptors PD-1, TIM-3, and LAG-3. MSC-treated cats demonstrated enhanced immune recovery, evidenced by reduced expression of exhaustion-related transcription factors (IKZF2, ZEB2, PRDM1) and increased regulatory T-cell populations, promoting immune homeostasis. Single-cell RNA sequencing of mesenteric lymph nodes revealed transcriptomic shifts indicative of immune rejuvenation, including elevated memory T-cell markers (IKZF1, GZMK, IL7R) and reduced hyperproliferative lymphocyte subsets. Serum cytokine analysis revealed 3 distinct inflammatory mediator patterns using principal component analysis. Both treatment groups showed transitions toward cytokine profiles resembling those of healthy controls. Notably, residual cytokine elevations persisted at the study's end, mirroring features of chronic immune dysregulation. PDGF-bb, a marker of tissue repair, was uniquely associated with higher lymphocyte counts, suggesting its role in lymphoid recovery. This study highlights the potential of MSC therapy to modulate immune dysfunction and support durable immune recovery. The findings underscore its translational relevance for addressing severe viral diseases characterized by chronic inflammation and immune dysregulation, advancing both veterinary and human medicine.

间充质干细胞/基质细胞治疗可改善严重冠状病毒感染猫模型的免疫恢复
包括SARS-CoV-2在内的严重冠状病毒感染的特征是全身性炎症、t细胞衰竭、淋巴细胞减少和慢性免疫功能障碍,康复治疗选择有限。猫传染性腹膜炎(FIP)是一种自然发生的猫冠状病毒感染,反映了这些免疫病理,提供了一个有价值的转化模型。本研究评估了同种异体间充质干细胞/基质细胞(MSC)治疗联合抗病毒治疗对渗出性FIP猫的安全性和有效性。在12周内进行血液学、病毒学和免疫学分析。抗病毒治疗通过下调抑制受体PD-1、TIM-3和LAG-3来减少细胞毒性t细胞衰竭。骨髓间质干细胞治疗的猫表现出增强的免疫恢复,其证据是耗竭相关转录因子(IKZF2, ZEB2, PRDM1)的表达减少,调节性t细胞群增加,促进免疫稳态。肠系膜淋巴结的单细胞RNA测序显示,转录组变化表明免疫年轻化,包括记忆t细胞标志物(IKZF1、GZMK、IL7R)升高和超增殖淋巴细胞亚群减少。血清细胞因子分析显示3种不同的炎症介质模式使用主成分分析。两个治疗组都表现出细胞因子谱的转变,与健康对照组相似。值得注意的是,在研究结束时,残留的细胞因子升高持续存在,反映了慢性免疫失调的特征。PDGF-bb是组织修复的标志,与较高的淋巴细胞计数有独特的关联,表明其在淋巴细胞恢复中的作用。这项研究强调了间充质干细胞治疗在调节免疫功能障碍和支持持久免疫恢复方面的潜力。这些发现强调了其在解决以慢性炎症和免疫失调为特征的严重病毒性疾病方面的转化相关性,从而推动了兽医和人类医学的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Stem Cells Translational Medicine
Stem Cells Translational Medicine CELL & TISSUE ENGINEERING-
CiteScore
12.90
自引率
3.30%
发文量
140
审稿时长
6-12 weeks
期刊介绍: STEM CELLS Translational Medicine is a monthly, peer-reviewed, largely online, open access journal. STEM CELLS Translational Medicine works to advance the utilization of cells for clinical therapy. By bridging stem cell molecular and biological research and helping speed translations of emerging lab discoveries into clinical trials, STEM CELLS Translational Medicine will help move applications of these critical investigations closer to accepted best patient practices and ultimately improve outcomes. The journal encourages original research articles and concise reviews describing laboratory investigations of stem cells, including their characterization and manipulation, and the translation of their clinical aspects of from the bench to patient care. STEM CELLS Translational Medicine covers all aspects of translational cell studies, including bench research, first-in-human case studies, and relevant clinical trials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信