Moll Guido, Geißler Sven, Catar Rusan, Ignatowicz Lech, Hoogduijn Martin J, Strunk Dirk, Bieback Karen, Ringdén Olle
Berlin-Brandenburg Center/School for Regenerative Therapies (BCRT/BSRT), Charité Universitätsmedizin, Berlin, Germany.
Therapeutic Immunology (TIM), Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Adv Exp Med Biol. 2016;951:77-98. doi: 10.1007/978-3-319-45457-3_7.
Mesenchymal stromal cells (MSCs) harbor great therapeutic potential for numerous diseases. From early clinical trials, success and failure analysis, bench-to-bedside and back-to-bench approaches, there has been a great gain in knowledge, still leaving a number of questions to be answered regarding optimal manufacturing and quality of MSCs for clinical application. For treatment of many acute indications, cryobanking may remain a prerequisite, but great uncertainty exists considering the therapeutic value of freshly thawed (thawed) and continuously cultured (fresh) MSCs. The field has seen an explosion of new literature lately, outlining the relevance of the topic. MSCs appear to have compromised immunomodulatory activity directly after thawing for clinical application. This may provide a possible explanation for failure of early clinical trials. It is not clear if and how quickly MSCs recover their full therapeutic activity, and if the "cryo stun effect" is relevant for clinical success. Here, we will share our latest insights into the relevance of these observations for clinical practice that will be discussed in the context of the published literature. We argue that the differences of fresh and thawed MSCs are limited but significant. A key issue in evaluating potency differences is the time point of analysis after thawing. To date, prospective double-blinded randomized clinical studies to evaluate potency of both products are lacking, although recent progress was made with preclinical assessment. We suggest refocusing therapeutic MSC development on potency and safety assays with close resemblance of the clinical reality.
间充质基质细胞(MSCs)对多种疾病具有巨大的治疗潜力。从早期临床试验、成败分析、从 bench 到 bedside 再回到 bench 的方法中,我们已经获得了很多知识,但在临床应用中关于 MSCs 的最佳制造和质量仍有许多问题有待解答。对于许多急性适应症的治疗,细胞冻存可能仍然是一个先决条件,但考虑到新鲜解冻(解冻)和持续培养(新鲜)的 MSCs 的治疗价值,仍存在很大的不确定性。最近该领域出现了大量新文献,概述了该主题的相关性。用于临床应用的 MSCs 在解冻后似乎免疫调节活性受损。这可能为早期临床试验的失败提供了一个可能的解释。目前尚不清楚 MSCs 是否以及多快能恢复其全部治疗活性,以及“冷冻休克效应”是否与临床成功相关。在此,我们将分享我们对这些观察结果与临床实践相关性的最新见解,并将在已发表文献的背景下进行讨论。我们认为新鲜和解冻的 MSCs 之间的差异是有限但显著的。评估效力差异的一个关键问题是解冻后的分析时间点。迄今为止,虽然在临床前评估方面取得了进展,但仍缺乏评估两种产品效力的前瞻性双盲随机临床研究。我们建议将治疗性 MSCs 的开发重点重新放在与临床实际情况密切相似的效力和安全性检测上。