In Vitro and In Vivo Models of CLL-T Cell Interactions: Implications for Drug Testing
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F22%3A00076484" target="_blank" >RIV/65269705:_____/22:00076484 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14740/22:00126282
Result on the web
<a href="https://www.mdpi.com/2072-6694/14/13/3087" target="_blank" >https://www.mdpi.com/2072-6694/14/13/3087</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/cancers14133087" target="_blank" >10.3390/cancers14133087</a>
Alternative languages
Result language
angličtina
Original language name
In Vitro and In Vivo Models of CLL-T Cell Interactions: Implications for Drug Testing
Original language description
T cells are key components in environments that support chronic lymphocytic leukemia (CLL), activating CLL-cell proliferation and survival. Here, we review in vitro and in vivo model systems that mimic CLL-T-cell interactions, since these are critical for CLL-cell division and resistance to some types of therapy (such as DNA-damaging drugs or BH3-mimetic venetoclax). We discuss approaches for direct CLL-cell co-culture with autologous T cells, models utilizing supportive cell lines engineered to express T-cell factors (such as CD40L) or stimulating CLL cells with combinations of recombinant factors (CD40L, interleukins IL4 or IL21, INF gamma) and additional B-cell receptor (BCR) activation with anti-IgM antibody. We also summarize strategies for CLL co-transplantation with autologous T cells into immunodeficient mice (NOD/SCID, NSG, NOG) to generate patient-derived xenografts (PDX) and the role of T cells in transgenic CLL mouse models based on TCL1 overexpression (E mu-TCL1). We further discuss how these in vitro and in vivo models could be used to test drugs to uncover the effects of targeted therapies (such as inhibitors of BTK, PI3K, SYK, AKT, MEK, CDKs, BCL2, and proteasome) or chemotherapy (fludarabine and bendamustine) on CLL-T-cell interactions and CLL proliferation.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30204 - Oncology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancers
ISSN
2072-6694
e-ISSN
2072-6694
Volume of the periodical
14
Issue of the periodical within the volume
13
Country of publishing house
CH - SWITZERLAND
Number of pages
21
Pages from-to
3087
UT code for WoS article
000822116900001
EID of the result in the Scopus database
2-s2.0-85132431440