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Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study

Cellular therapy is an emerging therapeutic modality with a great potential for the treatment of autism. Recent findings show that the major underlying pathogenetic mechanisms of autism are hypoperfusion and immune alterations in the brain. So conceptually, cellular therapy which facilitates counter...

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Autores principales: Sharma, Alok, Gokulchandran, Nandini, Sane, Hemangi, Nagrajan, Anjana, Paranjape, Amruta, Kulkarni, Pooja, Shetty, Akshata, Mishra, Priti, Kali, Mrudula, Biju, Hema, Badhe, Prerna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767048/
https://www.ncbi.nlm.nih.gov/pubmed/24062774
http://dx.doi.org/10.1155/2013/623875
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author Sharma, Alok
Gokulchandran, Nandini
Sane, Hemangi
Nagrajan, Anjana
Paranjape, Amruta
Kulkarni, Pooja
Shetty, Akshata
Mishra, Priti
Kali, Mrudula
Biju, Hema
Badhe, Prerna
author_facet Sharma, Alok
Gokulchandran, Nandini
Sane, Hemangi
Nagrajan, Anjana
Paranjape, Amruta
Kulkarni, Pooja
Shetty, Akshata
Mishra, Priti
Kali, Mrudula
Biju, Hema
Badhe, Prerna
author_sort Sharma, Alok
collection PubMed
description Cellular therapy is an emerging therapeutic modality with a great potential for the treatment of autism. Recent findings show that the major underlying pathogenetic mechanisms of autism are hypoperfusion and immune alterations in the brain. So conceptually, cellular therapy which facilitates counteractive processes of improving perfusion by angiogenesis and balancing inflammation by immune regulation would exhibit beneficial clinical effects in patients with autism. This is an open label proof of concept study of autologous bone marrow mononuclear cells (BMMNCs) intrathecal transplantation in 32 patients with autism followed by multidisciplinary therapies. All patients were followed up for 26 months (mean 12.7). Outcome measures used were ISAA, CGI, and FIM/Wee-FIM scales. Positron Emission Tomography-Computed Tomography (PET-CT) scan recorded objective changes. Out of 32 patients, a total of 29 (91%) patients improved on total ISAA scores and 20 patients (62%) showed decreased severity on CGI-I. The difference between pre- and postscores was statistically significant (P < 0.001) on Wilcoxon matched-pairs signed rank test. On CGI-II 96% of patients showed global improvement. The efficacy was measured on CGI-III efficacy index. Few adverse events including seizures in three patients were controlled with medications. The encouraging results of this leading clinical study provide future directions for application of cellular therapy in autism.
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spelling pubmed-37670482013-09-23 Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study Sharma, Alok Gokulchandran, Nandini Sane, Hemangi Nagrajan, Anjana Paranjape, Amruta Kulkarni, Pooja Shetty, Akshata Mishra, Priti Kali, Mrudula Biju, Hema Badhe, Prerna Stem Cells Int Clinical Study Cellular therapy is an emerging therapeutic modality with a great potential for the treatment of autism. Recent findings show that the major underlying pathogenetic mechanisms of autism are hypoperfusion and immune alterations in the brain. So conceptually, cellular therapy which facilitates counteractive processes of improving perfusion by angiogenesis and balancing inflammation by immune regulation would exhibit beneficial clinical effects in patients with autism. This is an open label proof of concept study of autologous bone marrow mononuclear cells (BMMNCs) intrathecal transplantation in 32 patients with autism followed by multidisciplinary therapies. All patients were followed up for 26 months (mean 12.7). Outcome measures used were ISAA, CGI, and FIM/Wee-FIM scales. Positron Emission Tomography-Computed Tomography (PET-CT) scan recorded objective changes. Out of 32 patients, a total of 29 (91%) patients improved on total ISAA scores and 20 patients (62%) showed decreased severity on CGI-I. The difference between pre- and postscores was statistically significant (P < 0.001) on Wilcoxon matched-pairs signed rank test. On CGI-II 96% of patients showed global improvement. The efficacy was measured on CGI-III efficacy index. Few adverse events including seizures in three patients were controlled with medications. The encouraging results of this leading clinical study provide future directions for application of cellular therapy in autism. Hindawi Publishing Corporation 2013 2013-08-25 /pmc/articles/PMC3767048/ /pubmed/24062774 http://dx.doi.org/10.1155/2013/623875 Text en Copyright © 2013 Alok Sharma et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Sharma, Alok
Gokulchandran, Nandini
Sane, Hemangi
Nagrajan, Anjana
Paranjape, Amruta
Kulkarni, Pooja
Shetty, Akshata
Mishra, Priti
Kali, Mrudula
Biju, Hema
Badhe, Prerna
Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title_full Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title_fullStr Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title_full_unstemmed Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title_short Autologous Bone Marrow Mononuclear Cell Therapy for Autism: An Open Label Proof of Concept Study
title_sort autologous bone marrow mononuclear cell therapy for autism: an open label proof of concept study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767048/
https://www.ncbi.nlm.nih.gov/pubmed/24062774
http://dx.doi.org/10.1155/2013/623875
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