Thomas E. Starzl Transplantation Institute, University of Pittsburgh Medical Center, Pittsburgh, PA 15261, USA.
Xenotransplantation. 2012 Sep-Oct;19(5):273-85. doi: 10.1111/xen.12000.
Allogeneic mesenchymal stem (stromal) cells (MSC) are a promising therapy for various pathological conditions. Genetically modified pig MSC have been demonstrated to downregulate the human T-cell response to pig antigens in vitro. Before genetically modified pig MSC can be used clinically, however, evidence needs to be provided to indicate whether they will survive in a human (xenogeneic) host.
A literature search through the end of 2011 identified 94 reports of the in vivo cross-species administration of MSC in a variety of experimental models. The majority (n = 89) involved the use of human MSC in various other species, with an occasional study using pig, rat, or guinea-pig MSC. When human MSC were used, they were largely derived from the bone marrow, adipose tissue, or umbilical cord blood. The routes of administration were varied, although almost half of the studies utilized the intravenous route. In 88 experiments (93.6%), there was evidence that the MSC engrafted and functioned across the species barrier, and in only six cases (6.4%) was there evidence of failure to function. Importantly, MSC function was confirmed in several different cross-species models. For example, human MSC functioned in no fewer than seven different recipient species.
The data provided by this literature search strengthen the hypothesis that pig MSC will function satisfactorily in a different species, for example, humans. The data also suggest that our own in vitro observations on the efficacy of pig MSC in downregulating the strength of the human T-cell response to pig antigens will likely be reproduced in vivo in pre-clinical large animal models and in clinical trials.
同种异体间充质干细胞(MSC)是一种治疗多种病理状态的有前途的疗法。已经证明,遗传修饰的猪 MSC 可以在体外下调人 T 细胞对猪抗原的反应。然而,在将遗传修饰的猪 MSC 用于临床之前,需要提供证据表明它们是否能在人类(异种)宿主中存活。
截至 2011 年底的文献检索确定了 94 份关于 MSC 在各种实验模型中异种体内给药的报告。大多数(n=89)涉及各种其他物种中使用人 MSC,偶尔有研究使用猪、大鼠或豚鼠 MSC。当使用人 MSC 时,它们主要来自骨髓、脂肪组织或脐带血。给药途径多种多样,尽管近一半的研究采用静脉途径。在 88 项实验(93.6%)中,有证据表明 MSC 跨越物种屏障植入和发挥功能,只有 6 项(6.4%)有功能失败的证据。重要的是,MSC 功能在几个不同的异种模型中得到了证实。例如,人 MSC 在不少于七种不同的受者物种中发挥作用。
该文献检索提供的数据支持这样一种假设,即猪 MSC 将在不同的物种中(例如人类)令人满意地发挥功能。这些数据还表明,我们在体外观察到的猪 MSC 下调人 T 细胞对猪抗原反应强度的有效性很可能在临床前大型动物模型和临床试验中得到体内复制。