Alexander Beller

ORCID: 0000-0002-4453-2223
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • IL-33, ST2, and ILC Pathways
  • Eosinophilic Esophagitis
  • Peripheral Artery Disease Management
  • Neurological Disorders and Treatments
  • T-cell and B-cell Immunology
  • Venous Thromboembolism Diagnosis and Management
  • Uterine Myomas and Treatments
  • Endometrial and Cervical Cancer Treatments
  • Myasthenia Gravis and Thymoma
  • Pediatric health and respiratory diseases
  • Vascular anomalies and interventions
  • Reproductive System and Pregnancy
  • Diagnosis and Treatment of Venous Diseases
  • Adrenal and Paraganglionic Tumors
  • Ovarian cancer diagnosis and treatment
  • Gut microbiota and health
  • Diabetic Foot Ulcer Assessment and Management
  • Hematopoietic Stem Cell Transplantation
  • Asthma and respiratory diseases
  • Pituitary Gland Disorders and Treatments
  • Cancer Immunotherapy and Biomarkers

German Rheumatism Research Centre
2011-2024

Leibniz Association
2011-2024

Charité - Universitätsmedizin Berlin
2016

Leipzig University
2012

University Hospital Leipzig
2010-2012

Abstract In humans and mice, mucosal immune responses are dominated by IgA antibodies the cytokine TGF‐β, suppressing unwanted reactions but also targeting Ig class switching to IgA. It had been suggested that eosinophils promote generation maintenance of IgA‐expressing plasma cells. Here, we demonstrate not eosinophils, specific bacteria determine production. Co‐housing eosinophil‐deficient mice with having high intestinal levels, as well intentional microbiota transfer induces TGF‐β...

10.1002/eji.201948474 article EN cc-by European Journal of Immunology 2020-02-17
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