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Åsa Sjöling

Researcher at Karolinska Institutet

Publications -  94
Citations -  2856

Åsa Sjöling is an academic researcher from Karolinska Institutet. The author has contributed to research in topics: Enterotoxigenic Escherichia coli & Helicobacter pylori. The author has an hindex of 26, co-authored 85 publications receiving 2416 citations. Previous affiliations of Åsa Sjöling include University of Gothenburg & World Health Organization.

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Mucosal FOXP3-Expressing CD4+ CD25high Regulatory T Cells in Helicobacter pylori-Infected Patients

TL;DR: It is shown that H. pylori-infected individuals have increased frequencies of CD4+ CD25high T cells in both the stomach and duodenal mucosa compared to uninfected controls, suggesting that regulatory T cells may suppress mucosal immune responses and thereby contribute to the persistence of H.pylori infections.
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Identification of enterotoxigenic Escherichia coli (ETEC) clades with long-term global distribution

TL;DR: Whole-genome sequencing of a representative collection of ETEC isolated between 1980 and 2011 identified globally distributed lineages characterized by distinct colonization factor and enterotoxin profiles that might harbor chromosome and plasmid combinations that optimize fitness and transmissibility.
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Comparative Analyses of Phenotypic and Genotypic Methods for Detection of Enterotoxigenic Escherichia coli Toxins and Colonization Factors

TL;DR: Established phenotypic and genotypic detection methods and newly developed PCR detection methods are compared with respect to sensitivity, specificity, positive predictive value, and ease of performance for Enterotoxigenic Escherichia coli.
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Oral Tolerance Induction with Antigen Conjugated to Cholera Toxin B Subunit Generates Both Foxp3+CD25+ and Foxp3−CD25− CD4+ Regulatory T Cells

TL;DR: It is demonstrated that oral tolerance induced by CTB-conjugated Ag is associated with increase in TGF-β and in both the frequency and suppressive capacity of Foxp3+ and CTLA-4+ CD25+ Treg together with the generation of both Foxp 3+ andFoxp3−CD25− CD4+ T Reg.