Akashdip Singh

ORCID: 0000-0001-5326-8826
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • vaccines and immunoinformatics approaches
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Immunotherapy and Biomarkers
  • T-cell and B-cell Immunology
  • Cell Adhesion Molecules Research
  • Glycosylation and Glycoproteins Research
  • CAR-T cell therapy research

University Medical Center Utrecht
2020-2024

Utrecht University
2020-2024

Oncode Institute
2020-2024

Collagens are a primary component of the extracellular matrix and functional ligands for inhibitory immune receptor leukocyte-associated immunoglobulin-like (LAIR)-1. LAIR-2 is secreted protein that can act as decoy by binding collagen with higher affinity than LAIR-1. We propose collagens promote evasion interacting LAIR-1 expressed on cells, releases LAIR-1-mediated suppression. Analysis public human datasets shows collagens, have unique overlapping associations survival in certain tumors....

10.7554/elife.62927 article EN cc-by eLife 2021-06-14

The tumor microenvironment (TME) is a complex structure comprised of tumor, immune and stromal cells, vasculature, extracellular matrix (ECM). During development, ECM homeostasis dysregulated. Collagen remodeling by metalloproteinases (MMPs) generates specific collagen fragments, that can be detected in the circulation cancer patients correlate with poor disease outcome. Leukocyte-Associated Immunoglobulin-like Receptor-1 (LAIR-1) an inhibitory receptor expressed on cells TME circulation. We...

10.3389/fimmu.2021.733561 article EN cc-by Frontiers in Immunology 2021-10-07

Abstract Collagen expression and structure in the tumour microenvironment are associated with development therapy response. Leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1) is a widely expressed inhibitory collagen receptor. LAIR-2 soluble homologue of LAIR-1 that competes for binding. Multiple studies mice implicate blockade LAIR-1:collagen interaction cancer as promising therapeutic strategy. Here, we investigated role anti-tumour responses. We show although inhibits...

10.1007/s00262-023-03600-6 article EN cc-by Cancer Immunology Immunotherapy 2024-01-01

Despite major successes with inhibitory receptor blockade in cancer, the identification of novel receptors as putative drug targets is needed due to lack durable responses, therapy resistance, and side effects. Most signal via immunoreceptor tyrosine-based motifs (ITIMs) previous studies estimated that our genome contains over 1600 ITIM-bearing transmembrane proteins. However, testing development these candidates requires increased understanding their expression patterns likelihood function...

10.7554/elife.92870.3 article EN cc-by eLife 2024-10-08

Despite major successes with inhibitory receptor blockade in cancer, the identification of novel receptors as putative drug targets is needed due to lack durable responses, therapy resistance, and side effects. Most signal via immunoreceptor tyrosine-based motifs (ITIMs) previous studies estimated that our genome contains over 1600 ITIM-bearing transmembrane proteins. However, testing development these candidates requires increased understanding their expression patterns likelihood function...

10.7554/elife.92870 article EN cc-by eLife 2024-03-13

Blocking inhibitory receptors like PD-1 and CTLA-4 has revolutionized cancer treatment in recent years. However, despite major successes melanoma lung cancer, the majority of types are not responsive to these immunotherapies. As such, there is an ongoing need for identification novel as drug targets. Most signal via immunoreceptor tyrosine-based motifs (ITIMs) previous studies have estimated that our genome contains over 1600 ITIM-bearing transmembrane proteins. further testing development...

10.7554/elife.92870.1 preprint EN 2024-03-13

Blocking inhibitory receptors like PD-1 and CTLA-4 has revolutionized cancer treatment in recent years. However, despite major successes melanoma lung cancer, the majority of types are not responsive to these immunotherapies. As such, there is an ongoing need for identification novel as drug targets. Most signal via immunoreceptor tyrosine-based motifs (ITIMs) previous studies have estimated that our genome contains over 1600 ITIM- bearing transmembrane proteins. further testing development...

10.7554/elife.92870.2 preprint EN 2024-09-25

Abstract Collagens are a primary component of the extracellular matrix and functional ligands for inhibitory immune receptor leukocyte associated immunoglobulin-like receptor-1 (LAIR-1). Leukocyte receptor-2 (LAIR-2) is secreted protein that can act as decoy by binding collagen with higher affinity than LAIR-1. We propose collagens promote evasion interacting LAIR-1 LAIR-2 could release mediated suppression. Analysis public datasets shows high expression being favorable outcome in certain...

10.1101/2020.10.21.349480 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2020-10-22

Abstract Blocking inhibitory receptors like PD-1 and CTLA-4 has revolutionized cancer treatment in recent years. However, despite major successes melanoma lung cancer, the majority of types are not responsive to these immunotherapies. As such, there is an ongoing need for identification novel as drug targets. Most signal via immunoreceptor tyrosine-based motifs (ITIMs) previous studies have estimated that our genome contains over 1600 ITIM- bearing transmembrane proteins. further testing...

10.1101/2023.10.24.563834 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2023-10-28
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