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Quentin Riller

@quentinriller.bsky.social
44 followers 34 following 9 posts

MD, internal medicine and clinical immunology resident @APHP. PhD immunology, post-doc in Frédéric Rieux-Laucat's lab, Imagine Insitute, Necker Paris #SingleCell #Rstats

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Quentin Riller @quentinriller.bsky.social · 06/07/2026
Eosinophilic fasciitis induced by checkpoint inhibitors: a retrospective multicenter case-series, comparison with eosinophilic fasciitis unrelated to checkpoint inhibition and literature review - Journal of the American Academy of Dermatology www.jaad.org/article/S019...
jaad.org
Eosinophilic fasciitis induced by checkpoint inhibitors: a retrospective multicenter case-series, comparison with eosinophilic fasciitis unrelated to checkpoint inhibition and literature review
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Reposted by Quentin Riller
Megan Cooper @macattacklab.bsky.social · 04/04/2026
1/5 Here we show in work led by Dani Arnold- 1) the first female patient with TLR8 GOF/INFLTR8- an X linked DOMINANT #inbornerrorofimmunity Clinical characteristics, management, and hematopoietic cell transplantation of patients with TLR8 gain-of-function url: ashpublications.org/bloodadvance...
ashpublications.org
Clinical characteristics, management, and hematopoietic cell transplantation of patients with TLR8 gain-of-function
Key PointsTLR8 GOF is an X-linked dominant disease that should be considered in both male and female patients with cytopenia and immune dysregulation.Patie
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Reposted by Quentin Riller
alexandrebelot.bsky.social @alexandrebelot.bsky.social · 02/04/2026
When pediatric lupus behaves like a Mendelian disease: #Monogeniclupus, @hcl-recherche.bsky.social @ciri-lyon.bsky.social, @frl-lab.bsky.social Important implications for personalized care👇 WES enables molecular diag in 10% of pediatric SLE cases eBioMedicine www.thelancet.com/journals/ebi...
thelancet.com
Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus cases
This study expands our understanding of causes of lupus, highlighting its genetic heterogeneity. It also supports the systematic use of genetic testing in cases of juvenile lupus, especially those wit...
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Quentin Riller @quentinriller.bsky.social · 04/04/2026
Congrats to the whole team! This is an important contribution, not only for pediatricians, but for the entire systemic lupus erythematosus community.
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Quentin Riller @quentinriller.bsky.social · 28/05/2025
Congratulations @damien-glon.bsky.social ! Very happy to be involved in this study with @frl-lab.bsky.social ! 🔥
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Quentin Riller @quentinriller.bsky.social · 27/05/2025
🔥🔥
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Quentin Riller @quentinriller.bsky.social · 24/05/2025
🎉 Excited to share the publication of our study in @bloodjournal.bsky.social , highlighted by an accompanying editorial! 📄 Article: doi.org/10.1182/bloo... 🖋 Editorial: doi.org/10.1182/bloo...
doi-org.proxy.insermbiblio.inist.fr
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Blood Journals Portfolio @bloodjournals.hematology.org · 23/05/2025
Graft failure remains challenging, with CI of grade 2 to 4 acute GVHD, but not grade 3 to 4, being significantly higher after PTCY. buff.ly/7VcLjgd #hemesky #transplantation
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Journal of Experimental Medicine @jem.org · 11/04/2025
@quentinriller.bsky.social, @frl-lab.bsky.social et al. present the first case of biallelic CHUK mutations disrupting IKKα kinase function, broadening the understanding of non-canonical NF-κB defects rupress.org/jem/article/... 📘 In Genes & Immunity collection: rupress.org/jem/collecti... #HKS2025
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Waggoner Lab @labwaggoner.bsky.social · 15/01/2025
Mutations disrupting the kinase domain of IKKα lead to immunodeficiency and immune dysregulation in humans @jem.org‪ @quentinriller.bsky.social @frl-lab.bsky.social doi.org/10.1084/jem....
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Quentin Riller @quentinriller.bsky.social · 15/01/2025
Thrilled to share our latest in @jem.org! 🚨 A single patient with syndromic immunodeficiency led us to uncover that biallelic point mutations in the IKKα kinase domain disrupt the non-canonical and partially the canonical NF-kB pathway activation. Dive into the details! 🧬 #NFkB #Immunology
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