2020
DOI: 10.3389/fimmu.2020.00519
|View full text |Cite
|
Sign up to set email alerts
|

Editorial: HIV and Cancer Immunotherapy: Similar Challenges and Converging Approaches

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0
1

Year Published

2020
2020
2023
2023

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 7 publications
(6 citation statements)
references
References 63 publications
0
5
0
1
Order By: Relevance
“…Further, the venetoclax + ixazomib combination had synergistic in vitro efficacy, but did not make it to in vivo testing because ex vivo toxicity with PBMCs was too great [485]. Nevertheless, new combinations must still be tested and given the parallels between cancer and HIV, particularly in relation to the role of immune dysfunction in both disease paradigms, it is imperative that we work closely together to achieve greater results [745]. In addition, the field should take note from its own research on ART and try to find combinations that target different mechanisms of HIV latency persistence or immune dysfunction, similar to how there is an antiretroviral for each step of the HIV life cycle.…”
Section: Crosstalk Between Macrophages and Exhausted T Cellsmentioning
confidence: 99%
“…Further, the venetoclax + ixazomib combination had synergistic in vitro efficacy, but did not make it to in vivo testing because ex vivo toxicity with PBMCs was too great [485]. Nevertheless, new combinations must still be tested and given the parallels between cancer and HIV, particularly in relation to the role of immune dysfunction in both disease paradigms, it is imperative that we work closely together to achieve greater results [745]. In addition, the field should take note from its own research on ART and try to find combinations that target different mechanisms of HIV latency persistence or immune dysfunction, similar to how there is an antiretroviral for each step of the HIV life cycle.…”
Section: Crosstalk Between Macrophages and Exhausted T Cellsmentioning
confidence: 99%
“… 33 These include the persistence of replication-competent viral genomes in latent or intermittently transcribing states, enabling infected cells to avoid detection by CTLs, the accumulation of genetic mutations in CD8 + T cell epitopes that may impair recognition, and effector T cell exhaustion, manifested by upregulation of co-inhibitory receptors. 34 Furthermore, in the case of HIV, replication-competent proviruses persist in rare, long-lived CD4 + T cell clones with a central memory phenotype, which may be selected for survival through immune-editing. 35 These similarities lend support for exploring the potential to use TCR-bispecifics to eliminate virus-infected cells ( Fig.…”
Section: Application Of Tcr-adapted Therapies To Viral Infectionsmentioning
confidence: 99%
“…Tento pool je přibližně 60× větší, než se původně předpokládalo, a představuje asi 10 6 -10 8 latentně infikovaných buněk, které podléhají klonální expanzi, a jejich počet se kontinuálně zvyšuje (13,14). Jeho hlavní komponentou jsou paměťové CD4+ lymfocyty s extrémně dlouhým poločasem (10,17), další subpopulace T lymfocytů (např. gama/delta T buňky, T regulační buňky), dendritické buňky, makrofágy, buňky mikroglie a další (8,15,18,19), na jejichž povrchu jsou exprimovány různé receptory v závislosti na stadiu jejich maturace, aktivace a diferen- Jak ukázaly studie, intenzifikace léčby současnými AR režimy není efektivní (13,14).…”
Section: Rezervoár Latentně Infikovaných Buněkunclassified