2021
DOI: 10.1016/j.semcancer.2019.11.010
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Nano-immunotherapy: Overcoming tumour immune evasion

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Cited by 62 publications
(48 citation statements)
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“…In recent years, many studies have demonstrated that dying cancer cells have the ability to elicit an immune response through the release or exposure of immunostimulatory DAMPs, resulting in T cell activation and proliferation, eventually culminating in eradication of the tumour [ 30 , 90 , 91 ].…”
Section: Immunogenic Cell Death-inducers For Anti-tumour In Situ Vaccinationmentioning
confidence: 99%
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“…In recent years, many studies have demonstrated that dying cancer cells have the ability to elicit an immune response through the release or exposure of immunostimulatory DAMPs, resulting in T cell activation and proliferation, eventually culminating in eradication of the tumour [ 30 , 90 , 91 ].…”
Section: Immunogenic Cell Death-inducers For Anti-tumour In Situ Vaccinationmentioning
confidence: 99%
“…Immunogenic cell death (ICD)-mediated immune priming and activation is characterized by the induction of a distinct cascade of molecular events, including (i) the relocation on the plasma membrane of the endoplasmic reticulum (ER)-resident chaperone calreticulin (CRT) and the exposition of heat-shock protein 70 (HSP70) and HSP90, which together act as “eat me” signals upon binding to their transmembrane receptor CD91 (also known as LRP1) on immature DCs and macrophages, promoting phagocytosis [ 90 , 91 , 92 , 93 ]; (ii) the secretion of adenosine-5′-triphosphate (ATP) that will bind to the purinergic receptor P2RX7 expressed on DCs, leading to their recruitment at the tumour site [ 90 , 91 , 92 , 93 ]; (iii) the activation of a cancer cell-intrinsic type I IFN response and consequent secretion of CXC-chemokine ligand 10 (CXCL10), stimulating T cell recruitment; and (iv) the release of the non-histone chromatin-binding protein high-mobility group box 1 (HMGB1) into the extracellular environment that will bind to toll-like receptor 4 (TLR4) on DCs to promote maturation, antigen processing, and presentation ( Figure 6 ) [ 30 , 90 , 91 ].…”
Section: Immunogenic Cell Death-inducers For Anti-tumour In Situ Vaccinationmentioning
confidence: 99%
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“…Release and presentation of TAs are the preconditions of cellular immune response. However, many tumors have poor immunogenicity due to down-regulation of antigen expression, antigen loss, and antigen modulation 32 , 33 . Also, antigen presentation to T cells by dysfunctional DCs induces antigen-specific immunotolerance.…”
Section: Antigen Release and Presentationmentioning
confidence: 99%
“…The dispatched immunotherapies struggle for optimal function in eradicating the tumor cells. 70 Consequently, there may be a competition among how speedy the immunotherapy gets to the intracellular space, via each energetic (active) delivery system, likewise the talent of the receptor interceded endocytosis, and the way rapidly it will proceed to malignant cells. 71 Thus, for an effective outcome to be achieved, the delivery system has to be modified in such a way that the immunotherapeutic carrier gets into the intracellular space before dispatching the immunotherapy.…”
Section: Transport Of Nanoparticle-immunotherapy Complex To Malignantmentioning
confidence: 99%