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https://doi.org/10.3389/fmicb.2018.01612
Title: | Immunomodulation as therapy for fungal infection: Are we closer? | Authors: | Sam, Q.H. Yew, W.S. Seneviratne, C.J. Chang, M.W. Chai, L.Y.A. |
Keywords: | auranofin colony stimulating factor 1 cytokine receptor agonist deferasirox ebselen efungumab gamma interferon granulocyte colony stimulating factor granulocyte macrophage colony stimulating factor interleukin 12p40 interleukin 6 molgramostim probiotic agent recombinant gamma interferon recombinant granulocyte macrophage colony stimulating factor retinol sargramostim suppressor of cytokine signaling 3 tamoxifen toll like receptor 9 toll like receptor agonist tumor necrosis factor vitamin D adoptive T cell therapy antifungal therapy cell therapy chimeric antigen receptor natural killer cell immunotherapy chimeric antigen receptor T-cell immunotherapy clinical trial (topic) cryptococcal meningitis cryptococcosis Cryptococcus neoformans drug repositioning granulocyte transfusion human immunomodulation microbiome nonhuman phase 1 clinical trial (topic) phase 2 clinical trial (topic) Review systemic mycosis T lymphocyte |
Issue Date: | 2018 | Publisher: | Frontiers Media S.A. | Citation: | Sam, Q.H., Yew, W.S., Seneviratne, C.J., Chang, M.W., Chai, L.Y.A. (2018). Immunomodulation as therapy for fungal infection: Are we closer?. Frontiers in Microbiology 9 (JUL) : 1612. ScholarBank@NUS Repository. https://doi.org/10.3389/fmicb.2018.01612 | Abstract: | Invasive fungal disease (IFD) causes significant morbidity in immunocompromised patients due to their weakened immune system. Immunomodulatory therapy, in synergy with existing antifungal therapy, is an attractive option to enhance their immune system and aid clearance of these opportunistic pathogens. From a scientific and clinical perspective, we explore the immunotherapeutic options to augment standard antifungal drugs for patients with an IFD. We discuss the range of immunomodulatory therapies being considered in IFD - from cytokines, including G-CSF, GM-CSF, M-CSF, IFN-?, and cytokine agonists, to cellular therapies, consisting of granulocyte transfusion, adoptive T-cell, CAR T-cell, natural killer cell therapies, and monoclonal antibodies. Adjunct pharmaceutical agents which augment the immunity are also being considered. Lastly, we explore the likelihood of the use of probiotics and manipulation of the microbiome/mycobiome to enhance IFD treatment outcomes. © 2018 Sam, Yew, Seneviratne, Chang and Chai. | Source Title: | Frontiers in Microbiology | URI: | https://scholarbank.nus.edu.sg/handle/10635/174534 | ISSN: | 1664302X | DOI: | 10.3389/fmicb.2018.01612 |
Appears in Collections: | Elements Staff Publications |
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