Allergy Immunotherapy Researches

Discover Genes Enhancing Immunotherapy in Lymphomas Through CRISPR Screening

Discover genes enhancing lymphoma immunotherapy through CRISPR screening. Learn how genome-wide screens identify tumor-specific regulators of MHC-I and MHC-II immunosurveillance, uncovering potential therapeutic targets like SUGT1 and inhibitors of EZH2 for advanced cancer treatment.

Written and prepared by:

Devin Dersh, James D. Phelan, Megan E. Gumina, Boya Wang, Jesse H. Arbuckle, Jaroslav Holly, Rigel J. Kishton, Tovah E. Markowitz, Mina O. Seedhom, Nathan Fridlyand, George W. Wright, Da Wei Huang, Michele Ceribelli, Craig J. Thomas, Justin B. Lack, Nicholas P. Restifo, Thomas M. Kristie, Louis M. Staudt, Jonathan W. Yewdell

What’s inside

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Explore the discovery of genes modulating MHC-I and MHC-II immunosurveillance in human lymphomas through genome-wide CRISPR screening. This study identifies numerous regulators of antigen presentation, revealing tumor-specific mechanisms affecting immune evasion and suggesting potential therapeutic targets. The findings highlight the role of SUGT1 and pharmacological inhibitors of EZH2 and thymidylate synthase in enhancing tumor immunogenicity, promising advancements in cancer immunotherapy.

MHC-I and MHC-II Regulation in Lymphomas

Discover lineage- and tumor-specific genes modulating MHC-I and MHC-II immunosurveillance in human lymphomas.

Genome-Wide CRISPR Screening in DLBCL

Using genome-wide CRISPR screens to identify novel MHC-I regulators in diffuse large B cell lymphoma.

SUGT1's Role in Antigen Presentation

Study reveals SUGT1 as a key positive regulator of both MHC-I and MHC-II surface expression in lymphomas.

Enhancing Immunotherapy in DLBCL

Targeting EZH2 and thymidylate synthase to enhance antigen presentation and immunotherapy in DLBCL.

Genetic Alterations in MHC-I Pathway

Analysis of genetic mutations and alterations in MHC-I regulators across 574 DLBCL patient samples.

Pharmacological Targets for DLBCL

Exploring the potential of EZH2 and thymidylate synthase inhibitors to improve immunotherapy in DLBCL.

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