The secret ally: immunostimulation by anticancer drugs
By L. Galluzzi, L. Senovilla, L. Zitvogel, Guido Kroemer. Nature reviews. Drug discovery, 2012
664 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/665586bca7d45de32bb8f04673a85f3c1b33d8d5
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In Oncology
Citations in the corpus
- Immune evasion in cancer: Mechanistic basis and therapeutic strategies. (2015, neutral): “[98] Galluzzi L, Senovilla L, Zitvogel L, Kroemer G.”
- The tumor microenvironment at a glance (2012, background): “In mouse cancers and clinical trials, there is evidence that chemotherapy is most successful when it causes a form of cell death that stimulates an anti-tumor immune response (Galluzzi et al., 2012).”
- Neutrophil: A Cell with Many Roles in Inflammation or Several Cell Types? (2018, background): “Through immunogenic cell death, after some types of anticancer therapy (Galluzzi et al., 2012; Bezu et al., 2015; Garg et al., 2017a), a damaged cancer cell produces specific inflammatory chemokines to recruit neutrophils as first innate immune cells (Kolaczkowska and Kubes, 2013; Garg et al.”
- Consensus guidelines for the detection of immunogenic cell death (2014, background): “Indeed, even the activity of antineoplastic regimens that fail to render dying cells immunogenic but induce other immunostimulatory effects is negatively affected by the absence of a functional immune system.(104,105) Among other molecules, this applies to the microtubular inhibitor paclitaxel and t”
- Mechanism of action of conventional and targeted anticancer therapies: reinstating immunosurveillance. (2013, background): “A comprehensive compendium of chemotherapeutic agents that mediate immunostimulatory effects can be found in Galluzzi et al. (2012c) and Vanneman and Dranoff, (2012).”
- Immunological Effects of Conventional Chemotherapy and Targeted Anticancer Agents. (2015, background): “…contrary, specific immunosuppressive circuits were inactivated demonstrate that many chemotherapeutic agents that were initially developed according to a purely cancer cell-autonomous logics mediate antineoplastic effects via immunological mechanisms (Galluzzi et al., 2012; Zitvogel et al., 2013).”
- Immunogenic cell death and DAMPs in cancer therapy (2012, background): “These authors showed that a recombinant N-terminal fragment of CRT (39-272) is a potent inducer of activation and maturation of B cells and macrophages and can trigger Ig class switching in B cells without T cell help in vitro and in vivo72.”