Odeberg Jenny, Piao Jing-Hua, Samuelsson Eva-Britt, Falci Scott, Akesson Elisabet
Neurotec Department, Division of Experimental Geriatrics, Karolinska Institutet, Karolinska University Hospital, KFC, 4th floor, Novum, SE-141 86 Stockholm, Sweden.
J Neuroimmunol. 2005 Apr;161(1-2):1-11. doi: 10.1016/j.jneuroim.2004.11.016.
The ability to expand human neural precursor cells in vitro offers new possibilities for future cell therapies. However, concern over immunologically based rejection of in vitro-expanded human neural cells confounds their use as donor cells. Here, we demonstrate that the expression of human leukocyte antigen (HLA) class I and II molecules, but not the co-stimulatory proteins CD40, CD80 and CD86, substantially increase during expansion of neurospheres. Furthermore, peripheral lymphocytes were unresponsive when co-cultured with in vitro-expanded neural cells. Taken together, these results suggest a low immunogenicity of these cultured human neural cells despite HLA incompatibility and high HLA expression.
在体外扩增人神经前体细胞的能力为未来的细胞治疗提供了新的可能性。然而,对体外扩增的人神经细胞基于免疫的排斥反应的担忧,使其作为供体细胞的应用受到困扰。在此,我们证明,在神经球扩增过程中,人类白细胞抗原(HLA)I类和II类分子的表达显著增加,但共刺激蛋白CD40、CD80和CD86的表达并未增加。此外,外周淋巴细胞与体外扩增的神经细胞共培养时无反应。综上所述,尽管存在HLA不相容性和高HLA表达,但这些结果表明这些培养的人神经细胞具有低免疫原性。