Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1782477355272372224 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3767048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sharmaalok autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT gokulchandrannandini autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT sanehemangi autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT nagrajananjana autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT paranjapeamruta autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT kulkarnipooja autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT shettyakshata autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT mishrapriti autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT kalimrudula autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT bijuhema autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy AT badheprerna autologousbonemarrowmononuclearcelltherapyforautismanopenlabelproofofconceptstudy |