Ex vivo-expanded autologous bone marrow-derived mesenchymal stromal cells in human spinal cord injury/paraplegia: a pilot clinical study

被引:183
|
作者
Pal, Rakhi [2 ]
Venkataramana, Neelam K. [1 ]
Jaan, Majahar [1 ,2 ]
Bansal, Abhilash [3 ]
Balaraju, Sudheer [2 ]
Jaan, Majahar [1 ,2 ]
Chandra, Ravi [3 ]
Dixit, Ashish [3 ]
Rauthan, Amit [3 ]
Murgod, Uday [3 ]
Totey, Satish [2 ]
机构
[1] BGS Global Hosp, Adv Neurosci Inst, Bangalore 560060, Karnataka, India
[2] Stempeut Res Private Ltd, Bangalore, Karnataka, India
[3] Manipal Hosp, Bangalore, Karnataka, India
关键词
autologous; bone marrow; mesenchymal stromal cells; spinal cord injury; MAGNETIC-RESONANCE TRACKING; LUMBAR PUNCTURE TECHNIQUE; STEM-CELLS; NEURONAL DIFFERENTIATION; IN-VIVO; INJURY; ADULT; TRANSPLANTATION; BIOLOGY; RAT;
D O I
10.3109/14653240903253857
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims Spinal cord injury (SCI) is a medically untreatable condition for which stem cells have created hope in the last few years. Earlier preclinical reports have shown that transplantation of bone marrow (BM) mesenchymal stromal cells (MSC) in SCI-simulated models can produce encouraging results. In a clinical pilot study, we investigated the growth kinetics of BM MSC from SCI patients, their safety and functional improvement post-transplantation. Methods Thirty patients with clinically complete SCI at cervical or thoracic levels were recruited and divided into two groups based on the duration of injury. Patients with < 6 months of post-SCI were recruited into group 1 and patients with > 6 months of post-SCI were included into group 2. Autologous BM was harvested from the iliac crest of SCI patients under local anesthesia and BM MSC were isolated and expanded ex vivo. BM MSC were tested for quality control, characterized for cell surface markers and transplanted back to the patient via lumbar puncture at a dose of 1 x 10(6) cells/kg body weight. Results At the time of writing, three patients had completed 3 years of follow-up post-BM MSC administration, 10 patients 2 years follow-up and 10 patients 1 year follow-up. Five patients have been lost to follow-up. None of the patients have reported any adverse events associated with BM MSC transplantation. Conclusions The results indicate that our protocol is safe with no serious adverse events following transplantation in SCI patients. The number of patients recruited and the uncontrolled nature of the trial do not permit demonstration of the effectiveness of the treatment involved. However, the results encourage further trials with higher doses and different routes of administration in order to demonstrate the recovery/efficacy if any, in SCI patients.
引用
收藏
页码:897 / 911
页数:15
相关论文
共 50 条
  • [41] The use of unlicensed bone marrow-derived platelet lysate-expanded mesenchymal stromal cells in colitis: a pre-clinical study
    Salmenkari, Hanne
    Laitinen, Anita
    Forsgard, Richard A.
    Holappa, Mervi
    Linden, Jere
    Pasanen, Lauri
    Korhonen, Matti
    Korpela, Riitta
    Nystedt, Johanna
    CYTOTHERAPY, 2019, 21 (02) : 175 - 188
  • [42] Bone marrow stromal cells (bone marrow-derived multipotent mesenchymal stromal cells) for bone tissue engineering: Basic science to clinical translation
    Kagami, Hideaki
    Agata, Hideki
    Tojo, Arinobu
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2011, 43 (03): : 286 - 289
  • [43] Standard toxicity study of clinical-grade allogeneic human bone marrow-derived clonal mesenchymal stromal cells
    Tayebi, Behnoosh
    Babaahmadi, Mahnaz
    Pakzad, Mohammad
    Hajinasrollah, Mostafa
    Mostafaei, Farhad
    Jahangiri, Shahrbanoo
    Kamali, Amir
    Baharvand, Hossein
    Baghaban Eslaminejad, Mohamadreza
    Hassani, Seyedeh-Nafiseh
    Hajizadeh-Saffar, Ensiyeh
    STEM CELL RESEARCH & THERAPY, 2022, 13 (01)
  • [44] Standard toxicity study of clinical-grade allogeneic human bone marrow-derived clonal mesenchymal stromal cells
    Behnoosh Tayebi
    Mahnaz Babaahmadi
    Mohammad Pakzad
    Mostafa Hajinasrollah
    Farhad Mostafaei
    Shahrbanoo Jahangiri
    Amir Kamali
    Hossein Baharvand
    Mohamadreza Baghaban Eslaminejad
    Seyedeh-Nafiseh Hassani
    Ensiyeh Hajizadeh-Saffar
    Stem Cell Research & Therapy, 13
  • [45] Application of ex-vivo expanded autologous bone marrow derived mesenchymal stem cells for repair of transected tendon in caprine
    Adhikari, Yogita
    Jadon, N. S.
    Shukla, Priyanka
    Singh, Parul
    Verma, A. K.
    INDIAN JOURNAL OF ANIMAL SCIENCES, 2014, 84 (06): : 629 - 634
  • [46] Transplantation of human bone marrow-derived stromal cells into the contused spinal cord of nude rats - Laboratory investigation
    Sheth, Rishi N.
    Manzano, Glen
    Li, Xiuming
    Levi, Allan D.
    JOURNAL OF NEUROSURGERY-SPINE, 2008, 8 (02) : 153 - 162
  • [47] Endogenous bone morphogenetic proteins in human bone marrow-derived multipotent mesenchymal stromal cells
    Seib, F. Philipp
    Franke, Martina
    Jing, Duohui
    Werner, Carsten
    Bornhaeuser, Martin
    EUROPEAN JOURNAL OF CELL BIOLOGY, 2009, 88 (05) : 257 - 271
  • [48] Comparison of functional and histological outcomes after intralesional, intracisternal, and intravenous transplantation of human bone marrow-derived mesenchymal stromal cells in a rat model of spinal cord injury
    Dong Ah Shin
    Jin-Myung Kim
    Hyoung-Ihl Kim
    Seong Yi
    Yoon Ha
    Do Heum Yoon
    Keung Nyun Kim
    Acta Neurochirurgica, 2013, 155 : 1943 - 1950
  • [49] Comparison of functional and histological outcomes after intralesional, intracisternal, and intravenous transplantation of human bone marrow-derived mesenchymal stromal cells in a rat model of spinal cord injury
    Shin, Dong Ah
    Kim, Jin-Myung
    Kim, Hyoung-Ihl
    Yi, Seong
    Ha, Yoon
    Yoon, Do Heum
    Kim, Keung Nyun
    ACTA NEUROCHIRURGICA, 2013, 155 (10) : 1943 - 1950
  • [50] Comparison of mesenchymal stromal cells from human bone marrow and adipose tissue for the treatment of spinal cord injury
    Zhou, Zhilai
    Chen, Yinhai
    Zhang, Hui
    Min, Shaoxiong
    Yu, Bo
    He, Bing
    Jin, Anmin
    CYTOTHERAPY, 2013, 15 (04) : 434 - 448