Quantitative Interactomics in Primary T Cells Provides a Rationale for Concomitant PD-1 and BTLA Coinhibitor Blockade in Cancer Immunotherapy (Q92686032)

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scientific article published on 01 June 2019

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English	Quantitative Interactomics in Primary T Cells Provides a Rationale for Concomitant PD-1 and BTLA Coinhibitor Blockade in Cancer Immunotherapy	scientific article published on 01 June 2019

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1 May 2020

Quantitative Interactomics in Primary T Cells Provides a Rationale for Concomitant PD-1 and BTLA Coinhibitor Blockade in Cancer Immunotherapy (English)

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Peter Blattmann

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Romain Roncagalli

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Bernard Malissen

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Frédéric Fiore

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Javier Celis-Gutierrez

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Yunhao Zhai

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Nicolas Jarmuzynski

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Kilian Ruminski

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Claude Grégoire

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Matthias Gstaiger

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1 May 2020

PD-1 Primarily Targets TCR Signal in the Inhibition of Functional T Cell Activation

1 reference

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Restriction of PD-1 function by cis-PD-L1/CD80 interactions is required for optimal T cell responses

1 reference

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Subsets of exhausted CD8+ T cells differentially mediate tumor control and respond to checkpoint blockade

1 reference

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Intratumoral Tcf1+PD-1+CD8+ T Cells with Stem-like Properties Promote Tumor Control in Response to Vaccination and Checkpoint Blockade Immunotherapy

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FBXO38 mediates PD-1 ubiquitination and regulates anti-tumour immunity of T cells

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Crispr/Cas Mediated Deletion of PTPN22 in Jurkat T Cells Enhances TCR Signaling and Production of IL-2

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Antigen-Presenting Cell-Intrinsic PD-1 Neutralizes PD-L1 in cis to Attenuate PD-1 Signaling in T Cells

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Shp-2 Is Dispensable for Establishing T Cell Exhaustion and for PD-1 Signaling In Vivo.

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CD8 T Cell Exhaustion in Chronic Infection and Cancer: Opportunities for Interventions.

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11 February 2021

Affinity purification mass spectrometry analysis of PD-1 uncovers SAP as a new checkpoint inhibitor

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CD4+ T Cell Help Confers a Cytotoxic T Cell Effector Program Including Coinhibitory Receptor Downregulation and Increased Tissue Invasiveness

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In vitro reconstitution of T cell receptor-mediated segregation of the CD45 phosphatase.

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11 February 2021

The diverse functions of the PD1 inhibitory pathway

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Enhanced differential expression statistics for data-independent acquisition proteomics

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PD-1 Blockade Promotes Emerging Checkpoint Inhibitors in Enhancing T Cell Responses to Allogeneic Dendritic Cells.

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Biophysical assay for tethered signaling reactions reveals tether-controlled activity for the phosphatase SHP-1.

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Precise Temporal Profiling of Signaling Complexes in Primary Cells Using SWATH Mass Spectrometry.

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A DNA-Based T Cell Receptor Reveals a Role for Receptor Clustering in Ligand Discrimination.

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11 February 2021

T cell costimulatory receptor CD28 is a primary target for PD-1-mediated inhibition.

1 reference

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11 February 2021

In situ and in silico kinetic analyses of programmed cell death-1 (PD-1) receptor, programmed cell death ligands, and B7-1 protein interaction network.

1 reference

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Social network architecture of human immune cells unveiled by quantitative proteomics

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Defining CD8+ T cells that provide the proliferative burst after PD-1 therapy

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Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinases

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The cytotoxic T cell proteome and its shaping by the kinase mTOR.

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A human interactome in three quantitative dimensions organized by stoichiometries and abundances

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mapDIA: Preprocessing and statistical analysis of quantitative proteomics data from data independent acquisition mass spectrometry

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11 February 2021

Genetic absence of PD-1 promotes accumulation of terminally differentiated exhausted CD8+ T cells

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Bioorthogonal mimetics of palmitoyl-CoA and myristoyl-CoA and their subsequent isolation by click chemistry and characterization by mass spectrometry reveal novel acylated host-proteins modified by HIV-1 infection

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Combinatorial proteomic analysis of intercellular signaling applied to the CD28 T-cell costimulatory receptor.

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A THEMIS:SHP1 complex promotes T-cell survival

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aLFQ: an R-package for estimating absolute protein quantities from label-free LC-MS/MS proteomics data

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Quantitative proteomics analysis of signalosome dynamics in primary T cells identifies the surface receptor CD6 as a Lat adaptor-independent TCR signaling hub

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The CRAPome: a contaminant repository for affinity purification-mass spectrometry data

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Strength of PD-1 signaling differentially affects T-cell effector functions.

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Programmed cell death 1 forms negative costimulatory microclusters that directly inhibit T cell receptor signaling by recruiting phosphatase SHP2.

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CD8(+) T cells specific for tumor antigens can be rendered dysfunctional by the tumor microenvironment through upregulation of the inhibitory receptors BTLA and PD-1.

1 reference

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Global quantification of mammalian gene expression control

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BTLA mediates inhibition of human tumor-specific CD8+ T cells that can be partially reversed by vaccination

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SOCS-6 negatively regulates T cell activation through targeting p56lck to proteasomal degradation

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PD-1 signaling in primary T cells

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B and T lymphocyte attenuator regulates CD8+ T cell-intrinsic homeostasis and memory cell generation

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1 reference

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T cell receptor ligation induces the formation of dynamically regulated signaling assemblies

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10.1016/J.CELREP.2019.05.041

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1 May 2020

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