» Articles » PMID: 27384771

Stem Cell Therapy and Administration Routes After Stroke

Overview
Publisher Springer
Date 2016 Jul 8
PMID 27384771
Citations 56
Authors
Affiliations
Soon will be listed here.
Abstract

Cell-based therapy has demonstrated safety and efficacy in experimental animal models of stroke, as well as safety in stroke patients. However, various questions remain regarding the therapeutic window, dosage, route of administration, and the most appropriate cell type and source, as well as mechanisms of action and immune-modulation to optimize treatment based on stem cell therapy. Various delivery routes have been used in experimental stroke models, including intracerebral, intraventricular, subarachnoid, intra-arterial, intraperitoneal, intravenous, and intranasal routes. From a clinical point of view, it is necessary to demonstrate which is the most feasible, safest, and most effective for use with stroke patients. Therefore, further experimental studies concerning the safety, efficacy, and mechanisms of action involved in these therapeutic effects are required to determine their optimal clinical use.

Citing Articles

Critical criteria for improvising the efficacy of transplanted cells; Significance of route of administration and microenvironment at the target site.

J Stem Cells Regen Med. 2025; 20(2):24-25.

PMID: 39850637 PMC: 11750065. DOI: 10.46582/jsrm.2002004.


Research progress and challenges of stem cell therapy for ischemic stroke.

Cha Z, Qiao Y, Lu Q, Wang Q, Lu X, Zhou H Front Cell Dev Biol. 2024; 12:1410732.

PMID: 39040041 PMC: 11260720. DOI: 10.3389/fcell.2024.1410732.


Probing Multiple Transplant Delivery Routes of CD+34 Stem Cells for Promoting Behavioral and Histological Benefits in Experimental Ischemic Stroke.

Lee J, Cho J, DEgidio F, Vignon C, Streefkerk H, de Kalbermatten M Stem Cells Transl Med. 2023; 13(2):177-190.

PMID: 38016184 PMC: 10872715. DOI: 10.1093/stcltm/szad081.


Hypoxia and interleukin-1-primed mesenchymal stem/stromal cells as novel therapy for stroke.

Salaudeen M, Allan S, Pinteaux E Hum Cell. 2023; 37(1):154-166.

PMID: 37987924 PMC: 10764391. DOI: 10.1007/s13577-023-00997-1.


Comparison of the Administration Route of Stem Cell Therapy for Ischemic Stroke: A Systematic Review and Meta-Analysis of the Clinical Outcomes and Safety.

Fauzi A, Thamrin A, Permana A, Ranuh I, Hidayati H, Hamdan M J Clin Med. 2023; 12(7).

PMID: 37048818 PMC: 10094955. DOI: 10.3390/jcm12072735.


References
1.
Leu S, Lin Y, Yuen C, Yen C, Kao Y, Sun C . Adipose-derived mesenchymal stem cells markedly attenuate brain infarct size and improve neurological function in rats. J Transl Med. 2010; 8:63. PMC: 2913939. DOI: 10.1186/1479-5876-8-63. View

2.
Cui L, Kerkela E, Bakreen A, Nitzsche F, Andrzejewska A, Nowakowski A . The cerebral embolism evoked by intra-arterial delivery of allogeneic bone marrow mesenchymal stem cells in rats is related to cell dose and infusion velocity. Stem Cell Res Ther. 2015; 6:11. PMC: 4429328. DOI: 10.1186/scrt544. View

3.
Rabinovich S, Seledtsov V, Banul N, Poveshchenko O, Senyukov V, Astrakov S . Cell therapy of brain stroke. Bull Exp Biol Med. 2005; 139(1):126-8. DOI: 10.1007/s10517-005-0229-y. View

4.
Ohshima M, Taguchi A, Tsuda H, Sato Y, Yamahara K, Harada-Shiba M . Intraperitoneal and intravenous deliveries are not comparable in terms of drug efficacy and cell distribution in neonatal mice with hypoxia-ischemia. Brain Dev. 2014; 37(4):376-86. DOI: 10.1016/j.braindev.2014.06.010. View

5.
Sun J, Wei Z, Gu X, Zhang J, Zhang Y, Li J . Intranasal delivery of hypoxia-preconditioned bone marrow-derived mesenchymal stem cells enhanced regenerative effects after intracerebral hemorrhagic stroke in mice. Exp Neurol. 2015; 272:78-87. DOI: 10.1016/j.expneurol.2015.03.011. View