Ximena Díaz

ORCID: 0000-0001-9036-4868
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About
Contact & Profiles
Research Areas
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • CAR-T cell therapy research
  • Cancer Research and Treatments
  • Cancer Immunotherapy and Biomarkers

Universidad de Santiago de Chile
2021

Fundación Ciencia and Vida
2018-2019

Abstract Tissue-resident memory CD8 + T (Trm) cells mediate potent local innate and adaptive immune responses play a central role against solid tumors. However, whether Trm cross-talk with dendritic (DCs) to support anti-tumor immunity remains unclear. Here we show that antigen-specific activation of skin leads maturation migration draining lymph nodes cross-presenting dermal DCs. Tumor rejection mediated by triggers the spread cytotoxic cell tumor-derived neo- self-antigens via These...

10.1038/s41467-019-12319-x article EN cc-by Nature Communications 2019-09-27

Memory CD8+ T cell responses have the potential to mediate long-lasting protection against cancers. Resident memory (Trm) cells stably reside in non-lymphoid tissues and superior innate adaptive immunity pathogens. Emerging evidence indicates that Trm develop human solid cancers play a key role controlling tumor growth. However, specific contribution of anti-tumor is incompletely understood. Moreover, clinically applicable vaccination strategies efficiently establish remain largely...

10.1080/2162402x.2018.1442163 article EN OncoImmunology 2018-02-20

Active immunotherapy against cancer is based on immune system stimulation, triggering efficient and long-lasting antigen-specific responses. Immunization strategies using whole dead cells from tumor tissue, containing specific antigens inside, have become a promising approach, providing lymphocyte activation through dendritic (DCs). In this work, we generate CT26, E.G7, EL4 live as antigen sources, which termed immunogenic cell bodies (ICBs), generated by simple cost-efficient...

10.1155/2021/6626851 article EN cc-by BioMed Research International 2021-02-03
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