Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

A Novel Immune Checkpoint Siglec-15 Antibody Inhibits LUAD by Modulating mφ Polarization in TME

View through CrossRef
Abstract Background Siglec-15 (S15) is a type-I transmembrane protein and is considered a new candidate of immune checkpoint inhibitor for cancer immunotherapy. Methods In the present study, we first constructed and characterized a chimeric S15-specific monoclonal antibody (S15-4E6A). Then, the antitumor effectiveness and modulatory role of S15-4E6A in macrophages (mφs) were explored in vitro and in vivo. Finally, the underlying mechanism by which S15mAb inhibits LUAD was preliminarily explored. Results The results demonstrated the successful construction of S15-4E6A, and S15-4E6A exerted an efficacious tumor-inhibitory effect on LUAD cells and xenografts. S15-4E6A could promote M1-mφ polarization while inhibiting M2-mφ polarization, both in vitro and in vivo. Conclusions S15-based immunotherapy that functions by modulating mφ polarization may be a promising strategy for the treatment of S15-positive LUAD.
Title: A Novel Immune Checkpoint Siglec-15 Antibody Inhibits LUAD by Modulating mφ Polarization in TME
Description:
Abstract Background Siglec-15 (S15) is a type-I transmembrane protein and is considered a new candidate of immune checkpoint inhibitor for cancer immunotherapy.
Methods In the present study, we first constructed and characterized a chimeric S15-specific monoclonal antibody (S15-4E6A).
Then, the antitumor effectiveness and modulatory role of S15-4E6A in macrophages (mφs) were explored in vitro and in vivo.
Finally, the underlying mechanism by which S15mAb inhibits LUAD was preliminarily explored.
Results The results demonstrated the successful construction of S15-4E6A, and S15-4E6A exerted an efficacious tumor-inhibitory effect on LUAD cells and xenografts.
S15-4E6A could promote M1-mφ polarization while inhibiting M2-mφ polarization, both in vitro and in vivo.
Conclusions S15-based immunotherapy that functions by modulating mφ polarization may be a promising strategy for the treatment of S15-positive LUAD.

Related Results

Transcriptional analysis of small cell lung cancer transformation in epidermal growth factor receptor mutated lung adenocarcinomas.
Transcriptional analysis of small cell lung cancer transformation in epidermal growth factor receptor mutated lung adenocarcinomas.
e21100 Background: Epidermal growth factor receptor ( EGFR)-mutated lung adenocarcinoma (LUAD) could benefit from EGFR-TKIs (tyrosine kinase inhibitors) treatment, but drug resist...
Abstract 1634: Siglec-15 knockout inhibits tumor growth in mouse model
Abstract 1634: Siglec-15 knockout inhibits tumor growth in mouse model
Abstract Several immune checkpoint blockers have been approved for treatment of certain cancers, which benefits a lot of patients with malignancies. However, the ove...
Analysis of CAFs‑related Genes Identifies COL11A1 Associated with Lung Adenocarcinoma Diagnosis and Prognosis
Analysis of CAFs‑related Genes Identifies COL11A1 Associated with Lung Adenocarcinoma Diagnosis and Prognosis
Abstract Background Difficulties in the treatment of lung adenocarcinoma(LUAD) are due to lack of understanding of relevant molecular mechanisms and limited potential ther...
Siglecs in Brain Function and Neurological Disorders
Siglecs in Brain Function and Neurological Disorders
Siglecs (Sialic acid-binding immunoglobulin-type lectins) are a I-type lectin that typically binds sialic acid. Siglecs are predominantly expressed in immune cells and generate act...
Abstract 1819: The immunosuppressive role of YAP1 on the tumor immune microenvironment
Abstract 1819: The immunosuppressive role of YAP1 on the tumor immune microenvironment
Abstract Background and aims: Lung adenocarcinoma (LUAD), the most prevalent histologic subtype of non-small cell lung cancer, is one of the most fatal malignancies....

Back to Top