Carola G. Vinuesa

ORCID: 0000-0001-9799-0298
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About
Contact & Profiles
Research Areas
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Systemic Lupus Erythematosus Research
  • Immunodeficiency and Autoimmune Disorders
  • Immune Response and Inflammation
  • Monoclonal and Polyclonal Antibodies Research
  • interferon and immune responses
  • Cytokine Signaling Pathways and Interactions
  • Diabetes and associated disorders
  • NF-κB Signaling Pathways
  • CAR-T cell therapy research
  • RNA Research and Splicing
  • MicroRNA in disease regulation
  • Cancer-related molecular mechanisms research
  • Blood disorders and treatments
  • RNA modifications and cancer
  • IL-33, ST2, and ILC Pathways
  • Cell death mechanisms and regulation
  • Inflammasome and immune disorders
  • Immune responses and vaccinations
  • Genomics and Rare Diseases
  • RNA regulation and disease
  • SARS-CoV-2 and COVID-19 Research
  • HIV Research and Treatment

The Francis Crick Institute
2021-2024

Australian National University
2015-2024

Renji Hospital
2015-2024

Shanghai Jiao Tong University
2019-2024

Curtin University
2019-2024

Hackensack University Medical Center
2024

University at Buffalo, State University of New York
2024

Royal Society
2024

University of Cambridge
2023

Personalis (United States)
2021-2022

During T cell–dependent responses, B cells can either differentiate extrafollicularly into short-lived plasma or enter follicles to form germinal centers (GCs). Interactions with follicular helper (Tfh) are required for GC formation and selection of somatically mutated cells. Interleukin (IL)-21 has been reported play a role in Tfh cell growth, survival, isotype switching. To date, it is unclear whether the effect IL-21 on predominantly consequence this cytokine acting directly if influences...

10.1084/jem.20091738 article EN cc-by-nc-sa The Journal of Experimental Medicine 2010-02-08

Abstract Objective In the sanroque mouse model of lupus, pathologic germinal centers (GCs) arise due to increased numbers follicular helper T (Tfh) cells, resulting in high‐affinity anti–double‐stranded DNA antibodies that cause end‐organ inflammation, such as glomerulonephritis. The purpose this study was examine hypothesis pathway could account for a subset patients with systemic lupus erythematosus (SLE). Methods An expansion Tfh cells is causal, and therefore consistent, component...

10.1002/art.25032 article EN Arthritis & Rheumatism 2009-12-28

The incidence of food allergies in western countries has increased dramatically recent decades. Tolerance to antigens relies on mucosal CD103(+) dendritic cells (DCs), which promote differentiation regulatory T (Treg) cells. We show that high-fiber feeding mice improved oral tolerance and protected from allergy. High-fiber reshaped gut microbial ecology the release short-chain fatty acids (SCFAs), particularly acetate butyrate. enhanced against allergy by enhancing retinal dehydrogenase...

10.1016/j.celrep.2016.05.047 article EN cc-by-nc-nd Cell Reports 2016-06-01

Production of high-affinity pathogenic autoantibodies appears to be central the pathogenesis lupus. Because normal antibodies arise from germinal centers (GCs), aberrant selection GC B cells, caused by either failure negative or enhanced positive follicular helper T (T(FH)) is a plausible explanation for these autoantibodies. Mice homozygous san allele Roquin, which encodes RING-type ubiquitin ligase, develop GCs in absence foreign antigen, excessive T(FH) cell numbers, and features We...

10.1084/jem.20081886 article EN The Journal of Experimental Medicine 2009-02-16

Abstract Although circumstantial evidence supports enhanced Toll-like receptor 7 (TLR7) signalling as a mechanism of human systemic autoimmune disease 1–7 , lupus-causing TLR7 gene variants is lacking. Here we describe lupus erythematosus caused by gain-of-function variant. sensor viral RNA 8 9 and binds to guanosine 10 – 12 . We identified de novo, previously undescribed missense Y264H variant in child with severe additional other patients lupus. The selectively increased sensing 2',3'-cGMP...

10.1038/s41586-022-04642-z article EN cc-by Nature 2022-04-27

Regnase-1 and Roquin are RNA binding proteins essential for degradation of inflammation-related mRNAs maintenance immune homeostasis. However, their mechanistic relationship has yet to be clarified. Here, we show that, although regulate an overlapping set via a common stem-loop structure, they function in distinct subcellular locations: ribosome/endoplasmic reticulum processing-body/stress granules, respectively. Moreover, specifically cleaves degrades translationally active requires the...

10.1016/j.cell.2015.04.029 article EN publisher-specific-oa Cell 2015-05-01

T follicular helper cells (Tfh cells) localize to follicles where they provide growth and selection signals mutated germinal center (GC) B cells, thus promoting their differentiation into high affinity long-lived plasma memory cells. T-dependent cell also occurs extrafollicularly, giving rise unmutated that are important for early protection against microbial infections. Bcl-6 expression in has been shown be essential the formation of Tfh GC but little is known about its requirement...

10.1084/jem.20102065 article EN The Journal of Experimental Medicine 2011-06-27

The clinical course and eventual outcome, or prognosis, of complex diseases varies enormously between affected individuals. This variability critically determines the impact a disease has on patient's life but is very poorly understood. Here, we exploit existing genome-wide association study data to gain insight into role genetics in prognosis. We identify noncoding polymorphism FOXO3A (rs12212067: T > G) at which minor (G) allele, despite not being associated with susceptibility, milder...

10.1016/j.cell.2013.08.034 article EN cc-by-nc-nd Cell 2013-09-01
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