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1.
Med Sci (Paris) ; 39(11): 845-854, 2023 Nov.
Article in French | MEDLINE | ID: mdl-38018928

ABSTRACT

The discovery of the unique ability of certain viruses to specifically target cancer cells has led to significant advancements in cancer immunotherapy research. In addition to inducing specific lysis of cancer cells, oncolytic viruses (OV) have been genetically modified to express molecules of interest within the tumor bed. The use of OV as vectors for therapeutic molecules has allowed to enhance antitumor responses while limiting the adverse effects associated with systemic administration of the molecule. Other studies are currently focused on delaying the neutralization and clearance of the virus by the host's immune system and improving its delivery insight tumors.


Title: Les virus oncolytiques : acteurs et vecteurs de protéines thérapeutiques contre les tumeurs. Abstract: La mise en évidence de la capacité unique de certains virus à cibler spécifiquement les cellules cancéreuses a ouvert de nouvelles perspectives pour la recherche en immunothérapie des cancers. Outre leur capacité à induire la destruction spécifique des cellules cancéreuses, les virus oncolytiques (OV) ont été modifiés génétiquement pour exprimer des molécules thérapeutiques directement au sein de la tumeur. L'utilisation des OV comme vecteurs de molécules thérapeutiques a permis d'augmenter les réponses anti-tumorales, tout en limitant les effets indésirables liés à une administration par voie générale de ces molécules. D'autres recherches visent aujourd'hui à limiter la neutralisation et l'élimination du virus par le système immunitaire de l'hôte et à améliorer son accès aux tumeurs.


Subject(s)
Neoplasms , Oncolytic Virotherapy , Oncolytic Viruses , Humans , Oncolytic Viruses/genetics , Oncolytic Virotherapy/adverse effects , Immunotherapy/adverse effects
2.
Semin Immunol ; 69: 101796, 2023 09.
Article in English | MEDLINE | ID: mdl-37356421

ABSTRACT

Tertiary lymphoid structures (TLS) are ectopic aggregates of immune cells that develop in non-lymphoid tissues under persistent inflammation. Since their presence has been associated with a better prognosis in cancer patients, modulating TLS formation is being part of new challenges in immunotherapy. Although mechanisms underlying TLS genesis are still not fully understood, different strategies have been developed in preclinical models to induce their formation and ultimately enhance antitumor responses. Herein, we will discuss a new approach that would consist in using oncolytic viruses (OV). These viruses have the unique feature to preferentially infect, replicate in and kill cancer cells. Their immunoadjuvant property, their use as a vector of therapeutic molecules and their selectivity for cancer cells, make them an attractive strategy to induce TLS in the tumor microenvironment. This review will examine the current knowledge about TLS neogenesis, approaches for inducing them, and relevance of using OV for this purpose, especially in combination with immunotherapy such as immune checkpoint blockade.


Subject(s)
Neoplasms , Oncolytic Virotherapy , Oncolytic Viruses , Tertiary Lymphoid Structures , Humans , Oncolytic Viruses/physiology , Immunotherapy , Tumor Microenvironment
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