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Eterna Therapeutics to Present at the ASGCT 27th Annual Meeting on Development of Beta 2 Microglobulin-Knockout (B2M-KO) IMSC Line With Enhanced Immunosuppressive Activity and Stealthing Features That May Further Augment the Therapeutic Potential of...

Eterna Therapeutics to Present at the ASGCT 27th Annual Meeting on Development of Beta 2 Microglobulin-Knockout (B2M-KO) IMSC Line With Enhanced Immunosuppressive Activity and Stealthing Features That May Further Augment the Therapeutic Potential of...

Eterna Therapeutics将在ASGCT第27届年会上介绍β2微球蛋白基因敲除(B2M-KO)IMSC系列的开发情况,该系列具有增强的免疫抑制活性和隐身功能,可能会进一步增强... 的治疗潜力
GlobeNewswire ·  05/07 08:00

Eterna Therapeutics to Present at the ASGCT 27th Annual Meeting on Development of Beta 2 Microglobulin-Knockout (B2M-KO) IMSC Line With Enhanced Immunosuppressive Activity and Stealthing Features That May Further Augment the Therapeutic Potential of MSCs in Inflammatory Diseases

Eterna Therapeutics将在ASGCT第27届年会上介绍β2微球蛋白基因敲除(B2M-KO)IMSC系列的开发情况,该系列具有增强的免疫抑制活性和隐身功能,可能会进一步增强间充质干细胞在炎性疾病中的治疗潜力

  • The presentation reports the development of a beta 2 microglobulin-knockout (B2M-KO) iMSC line with enhanced immunosuppressive activity and stealthing features that may further augment the therapeutic potential of MSCs in treating inflammatory diseases by precluding batch-to-batch inconsistencies, promoting in vivo persistence, and enhancing the effector function of the cells
  • The presentation is on Saturday, May 11th, 2024
  • 该演讲报告了具有增强免疫抑制活性和隐身特征的β2微球蛋白基因敲除(B2M-KO)iMSC系列的开发情况,该系列可以通过排除批次间的不一致性、促进体内持久性和增强细胞的效应器功能,进一步增强间充质干细胞治疗炎症性疾病的治疗潜力
  • 演讲将于5月11日星期六举行第四,2024

CAMBRIDGE, Mass., May 07, 2024 (GLOBE NEWSWIRE) -- Eterna Therapeutics Inc. (Nasdaq: ERNA) ("Eterna" or the "Company"), a biopharmaceutical company using advanced cell engineering technology to develop transformational new medicines, today announces that Raven Hinkel will present at the 27th Annual Meeting of the American Society of Gene & Cell Therapy, taking place in Baltimore, Maryland.

马萨诸塞州剑桥,2024年5月7日(环球新闻专线)——使用先进细胞工程技术开发变革性新药的生物制药公司Eterna Therapeutics Inc.(纳斯达克股票代码:ERNA)(“Eterna” 或 “公司”)今天宣布,Raven Hinkel将出席27届会议第四 美国基因与细胞疗法学会年会,在马里兰州巴尔的摩举行。

While mesenchymal stem cells (MSCs) have repeatedly demonstrated significant therapeutic potential in numerous preclinical models, their clinical translation has been greatly impeded by variability in therapeutic responses. This variability is often attributed to donor and source heterogeneity and limited expansion potential. Furthermore, MSCs can exhibit limited in vivo persistence due to clearance by host immune cells, which can also contribute to deficient therapeutic responses. Induced pluripotent stem cell (iPSC)-derived MSCs (iMSCs) promise to directly address many of the fundamental challenges facing MSC translation.

尽管间充质干细胞(MSC)在许多临床前模型中一再显示出巨大的治疗潜力,但其临床转化却因治疗反应的变异而受到极大阻碍。这种变异性通常归因于捐赠者和来源的异质性以及有限的扩张潜力。此外,由于宿主免疫细胞的清除,间充质干细胞在体内的持久性可能有限,这也可能导致治疗反应不足。诱导多能干细胞 (iPSC) 衍生的间充质干细胞 (IMSC) 有望直接解决 MSC 翻译面临的许多基本挑战。

Here, we report the development of a beta 2 microglobulin-knockout (B2M-KO) iMSC line with enhanced immunosuppressive activity and stealthing features that may further augment the therapeutic potential of MSCs in treating inflammatory diseases by precluding batch-to-batch inconsistencies, promoting in vivo persistence, and enhancing the effector function of the cells.

在这里,我们报告了一种具有增强免疫抑制活性和隐身特征的β2微球蛋白基因敲除(B2M-KO)iMSC系列的开发情况,该系列可以通过排除批次间的不一致性、促进体内持久性和增强细胞的效应功能,进一步增强间充质干细胞治疗炎症性疾病的治疗潜力。

The abstract concludes that B2M-KO iMSCs are more likely to evade immune clearance and exert their immunomodulatory effects, as demonstrated by their enhanced sensitivity of IDO1 expression and their improved ability to inhibit PBMC proliferation. Our data suggest that B2M-KO iMSCs may be a promising therapeutic agent for T-cell mediated autoimmune and inflammatory indications.

摘要得出结论,B2M-KO IMSC更有可能逃避免疫清除并发挥其免疫调节作用,其增强的IDO1表达灵敏度以及抑制PBMC增殖的能力提高就证明了这一点。我们的数据表明,B2M-KO IMSC可能是治疗T细胞介导的自身免疫和炎症适应症的有前途的治疗药物。

"We are thrilled to advance our iMSC research," says Sanjeev Luther, President and CEO. "iPSC-Derived iMSCs drive our Multiple Sclerosis pipeline candidate and are an important scientific focus for our team."

总裁兼首席执行官桑杰夫·路德说:“我们很高兴能推进我们的iMSC研究。”“iPSC衍生的IMSC推动了我们的多发性硬化症候选药物的发展,也是我们团队重要的科学重点。”

Presentation Details

演示详情

Title: iMSCs Derived from mRNA-Engineered B2M-KO iPSCs Exhibit Enhanced Immunosuppressive Activity and Stealthing Features

标题:源自 mRNA 设计的 B2M-KO iPSC 的 IMSC 具有增强的免疫抑制活性和隐身特性

Presenter: Raven Dance Hinkel, Research Associate II

主持人:Raven Dance Hinkel,二级研究助理

Date: Saturday, May 11, 2024

日期:2024 年 5 月 11 日星期六

Time: 10:30am - 10:45am

时间:上午 10:30-上午 10:45

Session Title: Novel Immune Effector Cell Manufacturing

会议标题:新型免疫效应细胞制造

Session Room: Ballroom 2

会议室:宴会厅 2

Location: Baltimore Convention Center in Baltimore, MD

地点:马里兰州巴尔的摩的巴尔的摩会议中心

About Eterna Therapeutics Inc.

关于 Eterna Therapeutics公司

Eterna Therapeutics is a life science company committed to realizing the potential of mRNA cell engineering to provide patients with transformational new medicines. Eterna has in-licensed a portfolio of over 100 patents covering key mRNA cell engineering technologies, including technologies for mRNA cell reprogramming, mRNA gene editing, the NoveSlice and UltraSlice gene-editing proteins, and the ToRNAdo mRNA delivery system from Factor Bioscience. NoveSlice, UltraSlice, and ToRNAdo are trademarks of Factor Bioscience. For more information, please visit .

Eterna Therapeutics是一家生命科学公司,致力于实现mRNA细胞工程的潜力,为患者提供革命性新药。Eterna已许可了100多项专利,涵盖关键的mRNA细胞工程技术,包括mRNA细胞重编程技术、mRNA基因编辑技术、noveSlice和UltraSlice基因编辑蛋白以及Factor Bioscience的龙卷风mRNA递送系统。noveSlice、UltraSlice 和 TornaDo 是 Factor Bioscience 的商标。欲了解更多信息,请访问。

Forward-Looking Statements

前瞻性陈述

This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which are intended to be covered by the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are any statements that are not statements of historical fact and may be identified by terminology such as "believe," "could," "estimate," "anticipate," "expect," "plan," "possible," "potential," "project," "will" or other similar words and the negatives of such words. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those stated or implied in any forward-looking statement as a result of various factors, including, but not limited to, uncertainties related to: (i) the evolution of Eterna's business model into a platform company focused on mRNA, iPS cell and gene editing technologies; (ii) Eterna's ability to successfully, cost-effectively and efficiently develop its technology and products; (iii) Eterna's ability to successfully commence clinical trials of any products on a timely basis or at all; (iv) Eterna's ability to successfully fund and manage the growth of its development activities; and (v) Eterna 's ability to obtain regulatory approvals of its products for commercialization. You should not rely upon forward-looking statements as predictions of future events. The forward-looking statements made in this communication speak only as of the date on which they were made, and Eterna does not undertake any obligation to update the forward-looking statements contained herein to reflect events that occur or circumstances that exist after the date hereof, except as required by applicable law. Factors that may cause Eterna's actual results to differ from those expressed or implied in forward-looking statements contained in this press release are more fully disclosed in Eterna's periodic public filings with the U.S. Securities and Exchange Commission, particularly under the heading "Risk Factors" in Eterna's Annual Report on Form 10-K for the year ended December 31, 2022, as well as under similar headings in Eterna's subsequently filed Quarterly Reports on Form 10-Q and Current Reports on Form 8-K.

本新闻稿包含经修订的1933年《证券法》第27A条和经修订的1934年《证券交易法》第21E条所指的前瞻性陈述,这些陈述旨在由1995年《私人证券诉讼改革法》的安全港条款所涵盖。前瞻性陈述是指任何不是历史事实陈述的陈述,可以用 “相信”、“可以”、“估计”、“预期”、“期望”、“计划”、“可能”、“潜力”、“项目”、“意愿” 或其他类似词语以及这些词语的否定词来识别。前瞻性陈述基于当前的信念和假设,这些信念和假设受风险和不确定性的影响,不能保证未来的表现。由于各种因素,包括但不限于与以下方面的不确定性,实际结果可能与任何前瞻性陈述中陈述或暗示的结果存在重大差异:(i)Eterna的商业模式演变为专注于mRNA、iPS细胞和基因编辑技术的平台公司;(ii)Eterna成功、具有成本效益和高效地开发其技术和产品的能力;(iii)Eterna成功开始任何产品的临床试验的能力及时或根本没有;(iv) Eterna 的能力成功地为其开发活动的增长提供资金和管理;以及(v)Eterna有能力获得监管部门对其产品的商业化批准。您不应依赖前瞻性陈述来预测未来事件。本通讯中的前瞻性陈述仅代表截至其发表之日,除非适用法律要求,否则Eterna不承担任何义务更新此处包含的前瞻性陈述以反映本通讯发布之日之后发生的事件或存在的情况。可能导致Eterna实际业绩与本新闻稿中包含的前瞻性陈述中表达或暗示的结果不同的因素,在Eterna向美国证券交易委员会提交的定期公开文件中,特别是在Eterna截至2022年12月31日的10-K表年度报告中 “风险因素” 标题下,以及Eterna随后提交的10-Q表季度报告和表单最新报告中的类似标题下 8-K。

Investor Relations Contact:

投资者关系联系人:

investors@eternatx.com

investors@eternatx.com


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