2010
DOI: 10.1007/s12072-010-9210-6
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Fluidized-bed bioartificial liver assist devices (BLADs) based on microencapsulated primary porcine hepatocytes have risk of porcine endogenous retroviruses transmission

Abstract: The kind of fluidized-bed BLADs based on microencapsulated primary porcine hepatocytes have risk of PERVs transmission. Further extensive pre-clinical study focused on biosafety is warranted.

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Cited by 19 publications
(11 citation statements)
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“…Various efforts have been made to maintain the functional performance of hepatocytes by providing proper extracellular matrix for attachment either as scaffolds , microcarriers or cell entrapment/encapsulation devices . The main concerns in using xenogenic porcine hepatocytes is the transfer of zoonotic diseases , protein–protein incompatibility and the possible immune responses generated during treatment . There is therefore a compelling need to seek alternative cell sources.…”
Section: Cell Sources For Liver Tissue Engineeringmentioning
confidence: 99%
“…Various efforts have been made to maintain the functional performance of hepatocytes by providing proper extracellular matrix for attachment either as scaffolds , microcarriers or cell entrapment/encapsulation devices . The main concerns in using xenogenic porcine hepatocytes is the transfer of zoonotic diseases , protein–protein incompatibility and the possible immune responses generated during treatment . There is therefore a compelling need to seek alternative cell sources.…”
Section: Cell Sources For Liver Tissue Engineeringmentioning
confidence: 99%
“…In order to protect cells from toxic exposures to perfused blood, microencapsulated hepatocytes have been used in fluidized bed-type bioreactors for BAL support recently [51,52]. The advantage of fluidized bed-type bioreactors is the large mass transfer area provided by spherical capsules that contain the cells.…”
Section: Development Of Bal Devicesmentioning
confidence: 99%
“…VIRIONS BY PORCINE CELLS RNA expression of PERV has been found in several types of tissue, including kidney, lung, skin, liver, and pancreatic islands (Le Tissier et al, 1997;Patience et al, 1997;Akiyoshi et al, 1998;Martin et al, 1998a;van der Laan et al, 2000;Yang et al, 2010). Neverthe less, expression of viral RNA cannot be correlated with the isolation of infection particles.…”
Section: Rna Expression and Release Of Pervmentioning
confidence: 99%