Isoform‐Level Analysis Reveals Reproducible Early Changes in Transcript Usage During Human Vaccine Responses. [[{“value”:”Lennart Riemann, Ahmed Hassan, Swantje Hammerschmidt, Anja Schimrock, Gunnar Schmidt, Nataliya Di Donato, Reinhold Förster”}]]

mRNA vaccination triggers an early, transient wave of altered transcript isoform usage peaking at 24 h and resolving by Day 14, affecting genes involved in innate immunity. Confirmed by long-read sequencing and reproduced across influenza, Ebola, and MVA-based vaccine cohorts, these results highlight a previously underappreciated feature of vaccine-induced transcriptional regulation. ABSTRACT Vaccine-induced transcriptional responses have … Read more

Cover Story: Eur. J. Immunol. 9’26.

Our cover features images related to flow cytometry techniques widely used for analysis of function and phenotypes of major human and murine immune cell subsets, superimposed on a multidimensional immune cell population scatter plot. These images are taken from the third edition of EJI’s Flow Cytometry Guidelines by Cossarizza et al., a comprehensive resource prepared … Read more

Single‐Cell Profiling Identifies Skin‐Resident Memory CD4+ T Cells as a Potential Correlate of Immunity During Staphylococcus aureus Skin Infection. [[{“value”:”Jonah Clegg, Giovanni Cova, Alberto Carignano, Megan Smith, Emiliano Chiarot, Simona Tavarini, Chiara Sammicheli, Nicholas Rachmaninoff, Serena Vastola, Silvia Guidotti, Emilio Siena, Monia Bardelli, Fabio Bagnoli, Michela Brazzoli, Rachel M. McLoughlin, Elisabetta Soldaini”}]]

Staphylococcus aureus skin infection generates long-lived tissue-resident memory T cells that provide enhanced local recall responses to reinfection, leading to improved bacterial clearance. Skin Trm could therefore be a potential correlate of protective immunity and targeted in future vaccine development. ABSTRACT Staphylococcus aureus is a leading cause of skin and soft tissue infections (SSTIs), yet … Read more

Serological Predictors of Protection from Infection Upon Household Exposure to SARS‐CoV‐2. [[{“value”:”Henrike Maaß, Imke Hinrichs, Martina Pavletic, Manuela Harries, Tatjana Prinke, Najat Bdeir, Richard Egelkamp, Berit Lange, Yannic C. Bartsch, Mate Lerga, Luka Cicin‐Sain”}]]

Household members of SARS-CoV-2 positive index persons donated a serum sample (t = 0). Within 14 days, the household members reported if COVID-19-like symptoms appeared and returned after 2 weeks to be retested. Serum responses were comprehensively measured and elevated variant-specific IgA1 and neutralizing antibody responses identified in the noninfected group. ABSTRACT Correlates of protection … Read more

IL‐9 Is Essential for ILC2‐Mediated but Not Th2‐ and Th17‐Cell‐Mediated Allergic Airway Inflammation in Mice. [[{“value”:”Nikolaos D. Sidiropoulos, Franziska Ampenberger, Christoph Schlapbach, Christoph Schneider, Manfred Kopf”}]]

Autocrine IL-9 production by ILC2s promotes their expansion and effector responses, including IL-5-driven eosinophilia, in response to airway allergens. In contrast, Th2 cell-intrinsic IL-9R signaling is dispensable for type 2 lung inflammation. Lung monocytes, macrophages, and DCs do not respond to IL-9 in asthma models due to the absence of IL-9R expression. ABSTRACT Interleukin-9 (IL-9) … Read more

A Bacterial Microbiome Is Dispensable for the Induction of CD8 T Cell Exhaustion. [[{“value”:”Miriam Kuhlmann, Daphne Del Carmen Kolland, Gustavo Pereira de Almeida, Christian Hoffmann, Madlaina von Hoesslin, Jacqueline Berner, Christine Wurmser, Anna Akulich, Anna M. Schulz, Carl‐Philipp Hackstein, Caspar Ohnmacht, Dietmar Zehn”}]]

We infected Germ-free and normal SPF mice infected with strains of LCMV that cause chronic infections. In both types of mice, T cell exhaustion progressed to similar levels. Thus, the microbiome is dispensable for the induction of T cell exhaustion. ABSTRACT Prolonged antigen exposure in chronic viral infections reduces the effector capacity of cytotoxic T … Read more

The Glucose Transporter GLUT3 Controls Regulatory T Cell Function. [[{“value”:”Katrin Sinning, Miriam Eckstein, Xiufeng Zhao, Alexandra Freitag, Mathias Rosenfeldt, Sophia M. Hochrein, Martin Vaeth”}]]

GLUT3 is essential for T regulatory (Treg) cell metabolic fitness, supporting both glycolysis and mitochondrial function required for their suppressive activity and effector differentiation. Loss of GLUT3 in Treg cells leads to impaired immune regulation and systemic autoimmunity, highlighting a critical role for glucose uptake in maintaining immune tolerance. ABSTRACT Regulatory T (Treg) cells are … Read more

Impact of Chronic Infection‐Induced Inflammation on TREG Cell Homeostasis. [[{“value”:”Zachary R. Lanzar, Daniel L. Aldridge, Julia N. Eberhard, Elisa Cruz‐Morales, Isabella O. Conway, Molly E. Bunkofske, Joseph A. Pereira, Melissa Parker, Chryssa Kanellopoulou, Christopher A. Hunter”}]]

Acute T. gondii infection caused thymic atrophy, reduced IL-2, and a sharp decline in Treg cells. As infection resolves, IL-2 and thymic function recover, which partially restores Tregs. Fate-mapping shows thymic Treg generation remains intact, but surviving peripheral Tregs chiefly rebuild the pool. Antiparasitic treatment can enhance thymic Treg generation. ABSTRACT Thymically-derived regulatory T (Treg) … Read more

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