4.8 Review

Checkpoint inhibitors as immunotherapy for fungal infections: Promises, challenges, and unanswered questions

期刊

FRONTIERS IN IMMUNOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2022.1018202

关键词

immunotherapy; fungal sepsis; candidiasis; aspergillosis; mucormycosis; checkpoint inhibitors; T cells; immune exhaustion

资金

  1. MD Anderson Cancer Center, Division of Internal Medicine Research and Quality Improvement Award
  2. MD Anderson Cancer Center Institutional Research Grant [2022-00060729-Y1]
  3. Robert C. Hickey Chair for Clinical Care endowment
  4. NIH [R01 AI133822, R56 AI109294, R03 AI166285]

向作者/读者索取更多资源

Opportunistic fungal infections have high mortality in patients with severe immune dysfunction. Evidence suggests that immune checkpoint pathways play a role in the immunopathology of fungal sepsis, opportunistic mold infections, and dimorphic fungal infections. The use of immune checkpoint inhibitors as antifungal immunotherapy shows potential but also has limitations that require further research.
Opportunistic fungal infections have high mortality in patients with severe immune dysfunction. Growing evidence suggests that the immune environment of invasive fungal infections and cancers share common features of immune cell exhaustion through activation of immune checkpoint pathways. This observation gave rise to several preclinical studies and clinical case reports describing blockade of the Programmed Cell Death Protein 1 and Cytotoxic T-Lymphocyte Antigen 4 immune checkpoint pathways as an adjunct immune enhancement strategy to treat opportunistic fungal infections. The first part of this review summarizes the emerging evidence for contributions of checkpoint pathways to the immunopathology of fungal sepsis, opportunistic mold infections, and dimorphic fungal infections. We then review the potential merits of immune checkpoint inhibitors (ICIs) as an antifungal immunotherapy, including the incomplete knowledge of the mechanisms involved in both immuno-protective effects and toxicities. In the second part of this review, we discuss the limitations of the current evidence and the many unknowns about ICIs as an antifungal immune enhancement strategy. Based on these gaps of knowledge and lessons learned from cancer immunology studies, we outline a research agenda to determine a sweet spot for ICIs in medical mycology. We specifically discuss the importance of more nuanced animal models, the need to study ICI-based combination therapy, potential ICI resistance, the role of the immune microenvironment, and the impact of ICIs given as part of oncological therapies on the natural immunity to various pathogenic fungi.

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