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Ryan Englander

@ryan-englander

MD/PhD candidate at UConn/JAX studying the intersection between tumor immunology and RNA splicing. Interested in all things oncology, splicing, immunology, and health policy.

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Latest posts by Ryan Englander @ryan-englander

Text on a yellow background states ACIP's vote to weaken the Hepatitis B vaccine birth-dose recommendation is reckless and undermines public confidence. The AMA urges the CDC to reject this action, citing it's not based on scientific evidence.

Text on a yellow background states ACIP's vote to weaken the Hepatitis B vaccine birth-dose recommendation is reckless and undermines public confidence. The AMA urges the CDC to reject this action, citing it's not based on scientific evidence.

Today’s action to weaken the birth-dose recommendation for the Hepatitis B vaccine disregards data supporting the effectiveness of the Hepatitis B vaccine, and creates confusion for parents about how best to protect their newborns. Full statement: spr.ly/633227f3XE

05.12.2025 17:04 πŸ‘ 113 πŸ” 52 πŸ’¬ 2 πŸ“Œ 3

THIS IS HUGE! Researchers at The Jackson Laboratory and UConn Health have successfully discovered a molecular switch that can actually SHUT DOWN cancer growth signals and STOP tumor growth at the RNA LEVEL. The discovery could pave the way for a groundbreaking RNA-based multi-cancer treatment. πŸ§ͺπŸ§΅β¬‡οΈ

23.03.2025 16:00 πŸ‘ 5286 πŸ” 1682 πŸ’¬ 101 πŸ“Œ 127
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Antisense oligonucleotide-mediated TRA2Ξ² poison exon inclusion induces the expression of a lncRNA with anti-tumor effects Nature Communications - The oncogenic splicing factor TRA2Ξ² is reported to be upregulated in human cancers partly by increased TRA2Ξ² poison exon (PE) skipping. Here the authors show that...

Our latest work on targeting the poison exon in #RNA #splicing factor TRA2B in #cancer reveals a role for this non coding transcript and opportunities for targeting splicing factor levels across multiple tumor types
rdcu.be/d90Ra
#RNAsky @jacksonlab.bsky.social

16.02.2025 14:37 πŸ‘ 25 πŸ” 11 πŸ’¬ 2 πŸ“Œ 0
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Intratumoral immune triads are required for immunotherapy-mediated elimination of solid tumors Tumor-specific CD8+ TΒ cells are dysfunctional within tumors. Espinosa-Carrasco etΒ al. show that CD4+ TΒ cells must engage with CD8+ TΒ cells on the same antigen-presenting cell (APC) during the effector phase, forming a three-cell-cluster (triad) to license CD8+ TΒ cell cytotoxicity and CD8+ TΒ cell-mediated cancer cell elimination.

www.cell.com/cancer-cell/...

Such a cool paper!!!

05.12.2024 17:32 πŸ‘ 3 πŸ” 0 πŸ’¬ 0 πŸ“Œ 0
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Spatial proteomics identifies JAKi as treatment for a lethal skin disease Nature - Cell-type-resolved spatial proteomics of the skin from patients with toxic epidermal necrolysis reveals that it is driven by JAK/STAT signaling, leading to successful treatment of this...

This is a cool story - spatial proteomics to identify over-expressed pathways (type I IFN & JAK/STAT) proposing new therapies (JAKi) for Toxic Epidermal Necrolysis

🌟 Discovery science translated into clincial benfit. Love it! 🌟

#MedSky πŸ§ͺ #ImmunoSky #dermatology
www.nature.com/artic...

30.11.2024 12:54 πŸ‘ 32 πŸ” 4 πŸ’¬ 2 πŸ“Œ 1
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A splicing isoform of PD-1 promotes tumor progression as a potential immune checkpoint - Nature Communications Whether PD-1 splicing isoforms impact T cell anti-tumor capacity has not been fully illustrated. Here the authors identify a human PD-1 isoform, PD-1^28, which functions to suppress anti-cancer immuni...

"Here, we identify an alternative splicing isoform of human PD-1, which carries a 28-base pairs extension retained from 5β€² region of intron 2 (PD-1^28), is expressed in peripheral T cells and tumor infiltrating lymphocytes."
#Immunology #Immunotherapy
www.nature.com/articles/s41...

29.11.2024 21:32 πŸ‘ 27 πŸ” 9 πŸ’¬ 2 πŸ“Œ 0
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Complementation of a human disease phenotype in vitro by intercellular mRNA transfer https://www.biorxiv.org/content/10.1101/2024.11.06.622258v1 There is growing evidence that full-length mRNAs undergo intercellular transfer through long, thin c

Complementation of a human disease phenotype in vitro by intercellular mRNA transfer https://www.biorxiv.org/content/10.1101/2024.11.06.622258v1

07.11.2024 02:30 πŸ‘ 2 πŸ” 1 πŸ’¬ 0 πŸ“Œ 2