2015
DOI: 10.1016/j.jcyt.2015.02.010
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Human allogeneic AB0/Rh-identical umbilical cord blood cells in the treatment of juvenile patients with cerebral palsy

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Cited by 52 publications
(34 citation statements)
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“…The dose‐escalation trial of UCB‐MSCs for BPD did not find evidence of dose‐dependent toxicity, but, interestingly, a trend toward greater benefit with the lower dose was observed (a similar inverse relationship was seen in the adult POSEIDON trial of BM‐MSCs for myocardial infarction ). In contrast, administration of UC‐MSCs for cerebral palsy showed a significant positive correlation between number of doses of UC‐MSCs and likelihood of experiencing improvement . Finally, the meta‐analysis of MSC therapy for acute GvHD did not find response to be dose‐dependent .…”
Section: Clinical Studies Of Msc Therapymentioning
confidence: 83%
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“…The dose‐escalation trial of UCB‐MSCs for BPD did not find evidence of dose‐dependent toxicity, but, interestingly, a trend toward greater benefit with the lower dose was observed (a similar inverse relationship was seen in the adult POSEIDON trial of BM‐MSCs for myocardial infarction ). In contrast, administration of UC‐MSCs for cerebral palsy showed a significant positive correlation between number of doses of UC‐MSCs and likelihood of experiencing improvement . Finally, the meta‐analysis of MSC therapy for acute GvHD did not find response to be dose‐dependent .…”
Section: Clinical Studies Of Msc Therapymentioning
confidence: 83%
“…No further complications arose over a 6‐month follow‐up period. An efficacy case series of 80 patients found that allogeneic, ABO/Rh‐matched, HLA‐mismatched UC‐MSCs administered intravenously resulted in 69% of patients improving muscle tone, strength, speech, memory, attention, or cognition in a dose‐dependent manner, with no worsening of symptoms . No treatment‐related adverse effects were reported, giving further credence to the possibility that the fever and vomiting reported earlier were indeed related to the general anesthesia and intrathecal administration.…”
Section: Clinical Studies Of Msc Therapymentioning
confidence: 90%
“…Interestingly, they noted that the higher the cell dose given to the patient the better the outcome, suggesting that cell dose is critical for efficacy. This is confirmed by a further study in which administration of greater number of allogeneic UCB cells was associated with better outcome at 36 months [142]. A handful of smaller, non-RCT trials have also added to our knowledge on the efficacy of UCB for treating established CP [142][143][144].…”
Section: Ucb In Clinical Trialsmentioning
confidence: 67%
“…There is currently no specific treatment for CP except for rehabilitation training in the clinic (Maclennan et al, ). Since the first transplantation of UCBCs was performed in 1988 (Mreboredo, Diaz, Castro, & Villaescusa, ), UCB‐SC therapy has been widely studied in children with CP, and improved brain cognition and gross motor function have been shown with no serious side effects indicating that the therapy is neuroprotective and safe (Feng et al, ; Huang et al, ; Kang et al, ; Lee et al, ; Min et al, ; Romanov et al, ; Sun et al, ) (Table ). However, current clinical trials focused on UCB‐SC therapy in children with CP have not considered the gestational age partition of the patients, and thus further research is needed regarding children with CP who were born prematurely.…”
Section: Ucb‐sc Therapy In Preterm Brain Injuries and Neurological Sementioning
confidence: 99%