Pig models of neurodegenerative disorders: Utilization in cell replacement‐based preclinical safety and efficacy studies. Issue 12 (12th April 2014)
- Record Type:
- Journal Article
- Title:
- Pig models of neurodegenerative disorders: Utilization in cell replacement‐based preclinical safety and efficacy studies. Issue 12 (12th April 2014)
- Main Title:
- Pig models of neurodegenerative disorders: Utilization in cell replacement‐based preclinical safety and efficacy studies
- Authors:
- Dolezalova, Dasa
Hruska‐Plochan, Marian
Bjarkam, Carsten R.
Sørensen, Jens Christian H.
Cunningham, Miles
Weingarten, David
Ciacci, Joseph D.
Juhas, Stefan
Juhasova, Jana
Motlik, Jan
Hefferan, Michael P.
Hazel, Tom
Johe, Karl
Carromeu, Cassiano
Muotri, Alysson
Bui, Jack
Strnadel, Jan
Marsala, Martin - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review<abstract abstract-type="main"> <title>ABSTRACT</title> <p>An important component for successful translation of cell replacement‐based therapies into clinical practice is the utilization of large animal models to conduct efficacy and/or safety cell dosing studies. Over the past few decades, several large animal models (dog, cat, nonhuman primate) were developed and employed in cell replacement studies; however, none of these models appears to provide a readily available platform to conduct effective and large‐scale preclinical studies. In recent years, numerous pig models of neurodegenerative disorders were developed using both a transgenic approach as well as invasive surgical techniques. The pig model (naïve noninjured animals) was recently used successfully to define the safety and optimal dosing of human spinal stem cells after grafting into the central nervous system (CNS) in immunosuppressed animals. The data from these studies were used in the design of a human clinical protocol used in amyotrophic lateral sclerosis (ALS) patients in a Phase I clinical trial. In addition, a highly inbred (complete major histocompatibility complex [MHC] match) strain of miniature pigs is available which permits the design of comparable MHC combinations between the donor cells and the graft recipient as used in human patients. Jointly, these studies show that the pig model can represent an effective large animal model to be used in preclinical cell replacement modeling. This review summarizes the available pig models of neurodegenerative disorders and the use of some of these models in cell replacement studies. The challenges and potential future directions in more effective use of the pig neurodegenerative models are also discussed. J. Comp. Neurol. 522:2784–2801, 2014. © 2014 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Journal of comparative neurology. Volume 522:Issue 12(2014:Aug. 15)
- Journal:
- Journal of comparative neurology
- Issue:
- Volume 522:Issue 12(2014:Aug. 15)
- Issue Display:
- Volume 522, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 522
- Issue:
- 12
- Issue Sort Value:
- 2014-0522-0012-0000
- Page Start:
- 2784
- Page End:
- 2801
- Publication Date:
- 2014-04-12
- Subjects:
- Comparative neurobiology -- Periodicals
Neurology -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9861 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cne.23575 ↗
- Languages:
- English
- ISSNs:
- 0021-9967
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4962.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3442.xml