TY - JOUR
T1 - Human Brain Organoids as Models for Central Nervous System Viral Infection
AU - Depla, Josse A.
AU - Mulder, Lance A.
AU - de Sá, Renata Vieira
AU - Wartel, Morgane
AU - Sridhar, Adithya
AU - Evers, Melvin M.
AU - Wolthers, Katja C.
AU - Pajkrt, Dasja
N1 - Funding Information: Funding: This research was co-funded by the European Union’s Horizon 2020 Research and Innovation Program under the Marie Sklowdowska-Curie Grant Agreement OrganoVIR (grant 812673) and uniQure Biopharma B.V. Publisher Copyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - Pathogenesis of viral infections of the central nervous system (CNS) is poorly understood, and this is partly due to the limitations of currently used preclinical models. Brain organoid models can overcome some of these limitations, as they are generated from human derived stem cells, differentiated in three dimensions (3D), and can mimic human neurodevelopmental characteristics. Therefore, brain organoids have been increasingly used as brain models in research on various viruses, such as Zika virus, severe acute respiratory syndrome coronavirus 2, human cytomegalovirus, and herpes simplex virus. Brain organoids allow for the study of viral tropism, the effect of infection on organoid function, size, and cytoarchitecture, as well as innate immune response; therefore, they provide valuable insight into the pathogenesis of neurotropic viral infections and testing of antivirals in a physiological model. In this review, we summarize the results of studies on viral CNS infection in brain organoids, and we demonstrate the broad application and benefits of using a human 3D model in virology research. At the same time, we describe the limitations of the studies in brain organoids, such as the heterogeneity in organoid generation protocols and age at infection, which result in differences in results between studies, as well as the lack of microglia and a blood brain barrier.
AB - Pathogenesis of viral infections of the central nervous system (CNS) is poorly understood, and this is partly due to the limitations of currently used preclinical models. Brain organoid models can overcome some of these limitations, as they are generated from human derived stem cells, differentiated in three dimensions (3D), and can mimic human neurodevelopmental characteristics. Therefore, brain organoids have been increasingly used as brain models in research on various viruses, such as Zika virus, severe acute respiratory syndrome coronavirus 2, human cytomegalovirus, and herpes simplex virus. Brain organoids allow for the study of viral tropism, the effect of infection on organoid function, size, and cytoarchitecture, as well as innate immune response; therefore, they provide valuable insight into the pathogenesis of neurotropic viral infections and testing of antivirals in a physiological model. In this review, we summarize the results of studies on viral CNS infection in brain organoids, and we demonstrate the broad application and benefits of using a human 3D model in virology research. At the same time, we describe the limitations of the studies in brain organoids, such as the heterogeneity in organoid generation protocols and age at infection, which result in differences in results between studies, as well as the lack of microglia and a blood brain barrier.
KW - Dengue virus (DENV)
KW - Japanese encephalitis virus (JEV)
KW - La crosse virus (LACV)
KW - Measles virus (MeV)
KW - Zika virus (ZIKV)
KW - brain organoids
KW - cerebral organoids
KW - herpes simplex virus 1 (HSV1)
KW - human cytomegalovirus (HCMV)
KW - severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
UR - http://www.scopus.com/inward/record.url?scp=85127168294&partnerID=8YFLogxK
U2 - https://doi.org/10.3390/v14030634
DO - https://doi.org/10.3390/v14030634
M3 - Review article
C2 - 35337041
SN - 1999-4915
VL - 14
JO - Viruses
JF - Viruses
IS - 3
M1 - 634
ER -