2018
DOI: 10.1007/s40257-018-0402-5
|View full text |Cite
|
Sign up to set email alerts
|

Antibody-Based Therapies for Cutaneous T-Cell Lymphoma

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
22
0
3

Year Published

2019
2019
2023
2023

Publication Types

Select...
8
1
1

Relationship

0
10

Authors

Journals

citations
Cited by 22 publications
(25 citation statements)
references
References 41 publications
0
22
0
3
Order By: Relevance
“…The IPH4102, a humanized monoclonal antibody directed against the KIR3DL2 cell receptor (CD158K), has also been proposed. Finally, histone deacetylase (HDAC) inhibitors (romidepsin and vorinostat) and demethylating agents have demonstrated efficacy in inducing cell cycle arrest, differentiation, and/or apoptosis of tumor cells [35][36][37][38].…”
Section: Therapiesmentioning
confidence: 99%
“…The IPH4102, a humanized monoclonal antibody directed against the KIR3DL2 cell receptor (CD158K), has also been proposed. Finally, histone deacetylase (HDAC) inhibitors (romidepsin and vorinostat) and demethylating agents have demonstrated efficacy in inducing cell cycle arrest, differentiation, and/or apoptosis of tumor cells [35][36][37][38].…”
Section: Therapiesmentioning
confidence: 99%
“…Genomic analysis in mycosis fungoides [33] A Oncogenes upregulated MALAT1, MECOM, PBX1, TTK, WWTR1 gets the immune receptor KIR3DL2/CD158k). [36][37][38][39][40][41] Targeting CD47 is expressed on all normal cells, targets SIRPα on the surface of myeloid cells and may be a new cancer therapeutic strategy also in cutaneous T-cell lymphoma.…”
Section: How Ha S the Field Pur Sued This Line Of Re S E Arch In Thmentioning
confidence: 99%
“…The IPH4102, a humanized monoclonal antibody directed against the KIR3DL2 cell receptor (CD158K) has been also proposed. Finally, histone deacetylase (HDAC) inhibitors (romidepsin and vorinostat) and demethylating agents have demonstrated efficacy in inducing cell cycle arrest, differentiation and / or apoptosis of tumor cells [37][38][39][40][41].…”
Section: Therapiesmentioning
confidence: 99%