2022
DOI: 10.1007/s13402-022-00700-w
|View full text |Cite
|
Sign up to set email alerts
|

Immunotherapy and immunoengineering for breast cancer; a comprehensive insight into CAR-T cell therapy advancements, challenges and prospects

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 199 publications
0
4
0
Order By: Relevance
“…However, due to the constant threat of developing cytokine release syndrome (CRS) and early relapse of antigen-positive leukemia (loss of active CAR T cell-mediated surveillance) or later relapse (loss of antigen) of the tumor, limited the range of specific CAR T cells [175]. However recent cotreatment of CAR T cells with immunomodulators (immune check point inhibitors like PDL1-PD1 blockage) has shown to be promising in terms of the depth and durability of the treatment clinically [176][177][178][179]. The above description insights us into the importance of the 'CSC-TME-immune' triangular (Fig.…”
Section: Cscs Control the Host Immune System And Mediate Drug Resistancementioning
confidence: 99%
“…However, due to the constant threat of developing cytokine release syndrome (CRS) and early relapse of antigen-positive leukemia (loss of active CAR T cell-mediated surveillance) or later relapse (loss of antigen) of the tumor, limited the range of specific CAR T cells [175]. However recent cotreatment of CAR T cells with immunomodulators (immune check point inhibitors like PDL1-PD1 blockage) has shown to be promising in terms of the depth and durability of the treatment clinically [176][177][178][179]. The above description insights us into the importance of the 'CSC-TME-immune' triangular (Fig.…”
Section: Cscs Control the Host Immune System And Mediate Drug Resistancementioning
confidence: 99%
“…M2 macrophages, on the other hand, activated by IL-4, IL-10, and IL-13, promote tumor growth and suppress anti-tumor immune responses [ 129 ]. TAMs suppress T-cells by secreting factors such as IL-10, ARG1, iNOS, PGE2, and TGFβ and recruiting T regs [ 165 , 166 , 167 ]. TAMs can also express PD-L1, CD80/86, or death receptor ligands that engage with inhibitory receptors on effector cells [ 166 ].…”
Section: Overcoming the Tumor Microenvironmentmentioning
confidence: 99%
“…Folate receptor, MUC1, c-Met, integrin, HER2, ROR1, and TEM8 are among the targeted receptors in breast cancer in recent studies [ 181 ]. Several recent publications have reviewed the advancements of this approach in breast cancer [ 182 , 183 , 184 , 185 , 186 , 187 ].…”
Section: The Unchartedmentioning
confidence: 99%