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1.
Cancer Immunol Immunother ; 72(3): 527-542, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36066649

ABSTRACT

Neutrophils have recently gained recognition for their potential in the fight against cancer. Neutrophil plasticity between the N1 anti-tumor and N2 pro-tumor subtypes is now apparent, as is the ability to polarize these individual subtypes by interventions such as intratumoral injection of various agents including bacterial products or pro-oxidants. Metabolic responses and the production of reactive oxygen species (ROS) such as hydrogen peroxide act as potent chemoattractants and activators of N1 neutrophils that facilitates their recruitment and ensuing activation of a toxic respiratory burst in tumors. Greater understanding of the precise mechanism of N1 neutrophil activation, recruitment and regulation is now needed to fully exploit their anti-tumor potential against cancers both locally and at distant sites. This systematic review critically analyzes these new developments in cancer immunotherapy.


Subject(s)
Neoplasms , Neutrophils , Humans , Reactive Oxygen Species/metabolism , Neutrophils/metabolism , Respiratory Burst , Immunotherapy , Neoplasms/metabolism
2.
Virology ; 495: 18-32, 2016 08.
Article in English | MEDLINE | ID: mdl-27152479

ABSTRACT

West Nile Virus (WNV) is a mosquito-borne flavivirus that can cause neuroinvasive disease in humans and animals for which no therapies are currently available. We studied an established combination of monoterpene alcohols (CMA) derived from Melaleuca alternifolia, against WNV infection. The in vitro results show that CMA exhibits virucidal activity, as well as reduces the viral titres and percentage of infected cells. The antiviral mechanism of action of CMA was studied. We found that CMA did not alter the intracellular pH, neither induced apoptosis, but did induce cell cycle arrest in the G0/G1-phase although that was not the antiviral mechanism. Furthermore, we tested CMA in vivo using IRF 3(-)(/)(-)/7(-/-)mice and it was found that CMA treatment significantly delayed morbidity due to WNV infection, reduced the loss of body weight and reduced the viral titres in brain. These findings suggest that CMA could be a therapeutic agent against WNV infection.


Subject(s)
Alcohols/pharmacology , Antiviral Agents/pharmacology , Monoterpenes/pharmacology , West Nile Fever/virology , West Nile virus/drug effects , Alcohols/chemistry , Animals , Antiviral Agents/chemistry , Apoptosis , Cell Cycle Checkpoints/drug effects , Cell Line , Cell Survival/drug effects , Chlorocebus aethiops , Disease Models, Animal , Hydrogen-Ion Concentration , Mice , Mice, Knockout , Monoterpenes/chemistry , Vero Cells , Virus Replication/drug effects , West Nile Fever/drug therapy , West Nile Fever/mortality , West Nile Fever/pathology , West Nile virus/physiology
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