Imaging in Stem Cell Transplant and Cell-based Therapy

(Nancy Kaufman) #1

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with hematopoietic stem cell therapy and mesenchymal stem cell therapy, significant
improvement in nerve conduction velocities was noted, suggesting that mesenchy-
mal stem cells facilitate the action of hematopoietic stem cells and may differentiate
into Schwann cells or produce the enzyme arylsulfatase themselves [ 55 ].


4.10 Conclusion


Mesenchymal stem cells have the unique ability to differentiate into various cell
lines, selectively home in injured/inflamed tissues, promote growth of endogenous
cells by producing trophic factors, possess anti inflammatory and immune modula-
tory effects and; have found various applications in multiple organ systems. Several
animal models and ongoing human clinical trials have all mostly established the
safety of mesenchymal stem cells, although the long term efficacy remains to be
well established and thus far has only been studied in small groups of human subjects.
Larger multi center randomized controlled studies are needed to validate the results
of smaller studies. Although imaging modalities such as MRI have been described
in evaluating response to musculoskeletal and neurological applications of mesen-
chymal stem cells, further studies to validate the preliminary findings are pending.


References



  1. Dominici MLBK, Le Blanc K, Mueller I, Slaper-Cortenbach I, Marini FC, Krause DS, Deans
    R, Keating A, Prockop DJ, Horwitz EM. Minimal criteria for defining multipotent mesenchy-
    mal stromal cells. The International Society for Cellular Therapy position statement.
    Cytotherapy. 2006;8(4):315–7.

  2. Toma C, Pittenger MF, Cahill KS, Byrne BJ, Kessler PD. Human mesenchymal stem cells dif-
    ferentiate to a cardiomyocyte phenotype in the adult murine heart. Circulation.
    2002;105(1):93–8.

  3. Satake K, Lou J, Lenke LG. Migration of mesenchymal stem cells through cerebrospinal fluid
    into injured spinal cord tissue. Spine. 2004;29(18):1971–9.

  4. Kim N, Cho SG.  Clinical applications of mesenchymal stem cells. Korean J  Intern Med.
    2013;28(4):387–402.

  5. Sohni A, Verfaillie CM. Mesenchymal stem cells migration homing and tracking. Stem Cells
    Int. 2013;2013:130763.

  6. Hajivalili M, Pourgholi F, Kafil HS, Jadidi-Niaragh F, Yousefi M. Mesenchymal stem cells in
    the treatment of amyotropic lateral sclerosis. Curr Stem Cell Res Ther. 2016;11:41–50.

  7. Levy M, et al. Regenerative cellular therapies for neurologic diseases. Brain Res. 2016;1638(Pt
    A):88–96.

  8. Rushkevich YN, et al. The use of autologous mesenchymal stem cells for cell therapy of patients
    with amyotrophic lateral sclerosis in Belarus. Bull Exp Biol Med. 2015;159(4):576–81.

  9. Böttcher C, Priller J. Myeloid cell-based therapies in neurological disorders: how far have we
    come? Biochim Biophys Acta. 2016;1862(3):323–8.

  10. Reston JT, Uhl S, Treadwell JR, et al. Autologous hematopoietic cell transplantation for mul-
    tiple sclerosis: a systematic review. Mult Scler. 2011;17(2):204–13.


R. Ram et al.
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