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1.
Exp Hematol Oncol ; 13(1): 48, 2024 May 09.
Artigo em Inglês | MEDLINE | ID: mdl-38725070

RESUMO

BACKGROUND: Cancer is the leading cause of death among older adults. Although the integration of immunotherapy has revolutionized the therapeutic landscape of cancer, the complex interactions between age and immunotherapy efficacy remain incompletely defined. Here, we aimed to elucidate the relationship between aging and immunotherapy resistance. METHODS: Flow cytometry was performed to evaluate the infiltration of immune cells in the tumor microenvironment (TME). In vivo T cell proliferation, cytotoxicity and migration assays were performed to evaluate the antitumor capacity of tumor antigen-specific CD8+ T cells in mice. Real-time quantitative PCR (qPCR) was used to investigate the expression of IFN-γ-associated gene and natural killer (NK)-associated chemokine. Adoptive NK cell transfer was adopted to evaluate the effects of NK cells from young mice in overcoming the immunotherapy resistance of aged mice. RESULTS: We found that elderly patients with advanced non-small cell lung cancer (aNSCLC) aged ≥ 75 years exhibited poorer progression-free survival (PFS), overall survival (OS) and a lower clinical response rate after immunotherapy. Mechanistically, we showed that the infiltration of NK cells was significantly reduced in aged mice compared to younger mice. Furthermore, the aged NK cells could also suppress the activation of tumor antigen-specific CD8+ T cells by inhibiting the recruitment and activation of CD103+ dendritic cells (DCs). Adoptive transfer of NK cells from young mice to aged mice promoted TME remodeling, and reversed immunotherapy resistance. CONCLUSION: Our findings revealed the decreased sensitivity of elderly patients to immunotherapy, as well as in aged mice. This may be attributed to the reduction of NK cells in aged mice, which inhibits CD103+ DCs recruitment and its CD86 expression and ultimately leads to immunotherapy resistance.

2.
Front Immunol ; 15: 1371559, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38576625

RESUMO

Anti-PD-(L)1 therapy has shown great efficacy in some patients with cancer. However, a significant proportion of patients with cancer do not respond to it. Another unmet clinical need for anti-PD-(L)1 therapy is the dynamic monitoring of treatment effects. Therefore, identifying biomarkers that can stratify potential responders before PD-(L)1 treatment and timely monitoring of the efficacy of PD-(L)1 treatment are crucial in the clinical setting. The identification of biomarkers by liquid biopsy has attracted considerable attention. Among the identified biomarkers, circulating T cells are one of the most promising because of their indispensable contribution to anti-PD-(L)1 therapy. The present review aimed to thoroughly explore the potential of circulating T cells as biomarkers of anti-PD-(L)1 therapy and its advantages and limitations.


Assuntos
Neoplasias , Linfócitos T , Humanos , Biomarcadores , Imunoterapia , Neoplasias/tratamento farmacológico
3.
Forensic Sci Res ; 3(3): 194-201, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30483669

RESUMO

As a result of the many developments in information technology, digital evidence plays an increasingly important role in criminal and civil litigation. Because digital evidence is necessary for litigation, the judicial system must be assured of its accuracy, reliability, and verifiability, which can be assured by accreditation. This paper focuses on a comparison of the evolution of the accreditation of digital forensics internationally and domestically, discusses the existing problems that such accreditation encounters, and proposes the corresponding solutions. Moreover, this paper discusses the future of digital forensic laboratory accreditation and its implementation.

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