First-pass extracted concept

PD-1/PD-L1 axis

Candidate: concept label1 source documents6 linked claims
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Aliases

PD-1/PD-L1 signaling, PD-L1

Extracted Explainers

What the tool is doing

The paper discusses the PD-1/PD-L1 axis as part of the immune-suppressive tumor microenvironment in LUAD metastases, especially in lymph node and liver metastases.

Source 1DOIPubMed

What problem it solves

It helps frame biomarker-guided interpretation of immune suppression and possible therapeutic response in metastatic LUAD.

Source 1DOIPubMed

What it does not solve

The abstract does not present this axis as a standalone intervention or engineered platform.

Source 1DOIPubMed

Alternatives

Other biomarker classes mentioned in the abstract include cytokine profiles, immune cell ratios, and metabolic markers.

Source 1DOIPubMed

Evidence Snippets

Lymph node metastases are characterized by ... high programmed death ligand-1 (PD-L1) expression ... liver metastases show Kupffer cell-driven PD-L1/ programmed death 1(PD-1) axis suppression.
Evidence 1Source 1DOIPubMedprovenance

Supporting Sources

Linked Claims

Claim 1biomarker associationsupports2025Source 1DOIPubMed

Key biomarkers across LUAD metastatic sites include PD-L1, cytokine profiles, immune cell ratios, and metabolic markers.

Quoted textsource-backed
Key biomarkers across all types of metastases include PD-L1, cytokine profiles, immune cell ratios, and metabolic markers.
Claim 2disease biologysupports2025Source 1DOIPubMed

Brain metastases in LUAD display an immune-desert phenotype associated with blood-brain barrier constraints, reduced T-cell infiltration, and microglia-mediated immunosuppression.

Quoted textsource-backed
Brain metastases display an "immune desert" phenotype due to blood-brain barrier constraints, reduced T-cell infiltration, and microglia-mediated immunosuppression.
Claim 3disease biologysupports2025Source 1DOIPubMed

Liver metastases in LUAD show Kupffer cell-driven PD-L1/PD-1 axis suppression and elevated Treg infiltration.

Quoted textsource-backed
liver metastases show Kupffer cell-driven PD-L1/ programmed death 1(PD-1) axis suppression and elevated Treg infiltration.
Claim 4disease biologysupports2025Source 1DOIPubMed

Lung adenocarcinoma metastases to lymph node, brain, bone, and liver share immune suppression but show distinct tumor microenvironment heterogeneity that affects treatment efficacy and prognosis.

Quoted textsource-backed
Metastasis to these locations exhibits some common features, such as immune suppression, and distinct tumor microenvironment (TME) heterogeneity involving differentiation of immune cells, impacting treatment efficacy and prognosis.
Claim 5disease biologysupports2025Source 1DOIPubMed

Lymph node metastases in LUAD are characterized by immune suppression with exhausted CD8+ T cells, expanded Tregs, M2-polarized macrophages, and high PD-L1 expression.

Quoted textsource-backed
Lymph node metastases are characterized by immune suppression with exhausted CD8+ T cells, expanded regulated T cell (Tregs), M2-polarized macrophages, and high programmed death ligand-1 (PD-L1) expression.
Claim 6therapeutic strategysupports2025Source 1DOIPubMed

Therapeutic strategies for metastatic LUAD tumor microenvironments focus on immune checkpoint inhibitors combined with metabolic modulators, localized drug delivery, and biomarker-guided approaches.

Quoted textsource-backed
Therapeutic strategies focus on combination therapies such as immune checkpoint inhibitors (ICIs) with metabolic modulators, localized drug delivery, and biomarker-guided approaches.