Patrick Taeschler

ORCID: 0000-0003-0522-7629
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About
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Research Areas
  • SARS-CoV-2 and COVID-19 Research
  • COVID-19 Clinical Research Studies
  • Long-Term Effects of COVID-19
  • T-cell and B-cell Immunology
  • Immunotherapy and Immune Responses
  • Immune responses and vaccinations
  • Vagus Nerve Stimulation Research
  • COVID-19 and Mental Health

University Hospital of Zurich
2021-2024

University of Zurich
2021-2024

Abstract Following acute infection with severe respiratory syndrome coronavirus 2 (SARS-CoV-2) a significant proportion of individuals develop prolonged symptoms, serious condition termed post-acute disease 2019 (COVID-19) (PACS) or long COVID. Predictors PACS are needed. In prospective multicentric cohort study 215 individuals, we COVID-19 patients during primary and up to one year later, compared healthy subjects. We discover an immunoglobulin (Ig) signature, based on total IgM IgG3...

10.1038/s41467-021-27797-1 article EN cc-by Nature Communications 2022-01-25

Long Covid is a debilitating condition of unknown etiology. We performed multimodal proteomics analyses blood serum from COVID-19 patients followed up to 12 months after confirmed severe acute respiratory syndrome coronavirus 2 infection. Analysis >6500 proteins in 268 longitudinal samples revealed dysregulated activation the complement system, an innate immune protection and homeostasis mechanism, individuals experiencing Covid. Thus, active was characterized by terminal system...

10.1126/science.adg7942 article EN cc-by Science 2024-01-18

Abstract Immunological memory is a hallmark of adaptive immunity and facilitates an accelerated enhanced immune response upon re-infection with the same pathogen 1,2 . Since outbreak ongoing COVID-19 pandemic, key question has focused on which SARS-CoV-2-specific T cells stimulated during acute infection give rise to long-lived 3 Here, using spectral flow cytometry combined cellular indexing transcriptomes cell receptor sequencing, we longitudinally characterized individual CD8 + patients...

10.1038/s41586-021-04280-x article EN cc-by Nature 2021-12-07

Abstract Infection with severe acute respiratory syndrome coronavirus 2 associates diverse symptoms, which can persist for months. While antiviral antibodies are protective, those targeting interferons and other immune factors associated adverse disease 2019 (COVID-19) outcomes. Here we discovered that against specific chemokines were omnipresent post-COVID-19, favorable outcome negatively correlated the development of long COVID at 1 yr post-infection. Chemokine also present in HIV-1...

10.1038/s41590-023-01445-w article EN cc-by Nature Immunology 2023-03-06

Several autoimmune features occur during coronavirus disease 2019 (COVID-19), with possible implications for course, immunity, and pathology. In this study, we longitudinally screened clinically relevant systemic autoantibodies to assess their prevalence, temporal trajectory, association comorbidities, severity of COVID-19.We performed highly sensitive indirect immunofluorescence assays detect antinuclear antibodies (ANA) antineutrophil cytoplasmic (ANCA), along serum proteomics virome-wide...

10.1111/all.15302 article EN cc-by-nc-nd Allergy 2022-04-01

Abstract The B cell response to different pathogens uses tailored effector mechanisms and results in functionally specialized memory (B m ) subsets, including CD21 + resting, – CD27 activated cells. interrelatedness between these subsets remains unknown. Here we showed that single severe acute respiratory syndrome coronavirus 2-specific clones plasticity upon antigen rechallenge previously exposed individuals. cells were the predominant during infection early after immunization. At months 6...

10.1038/s41590-023-01497-y article EN cc-by Nature Immunology 2023-04-27

T-cell lymphopenia and functional impairment is a hallmark of severe acute coronavirus disease 2019 (COVID-19). How numbers function evolve at later timepoints after clinical recovery remains poorly investigated.

10.1111/all.15372 article EN cc-by-nc-nd Allergy 2022-05-14

Abstract Background Several autoimmune features occur during coronavirus disease 2019 (COVID-19), with possible implications for course, immunity, and pathology. In this study, we longitudinally screened clinically relevant systemic autoantibodies to assess their prevalence, temporal trajectory, association comorbidities, severity of COVID-19. Methods We performed highly sensitive indirect immunofluorescence assays detect anti-nuclear antibodies (ANA) anti-neutrophil cytoplasmic (ANCA),...

10.1101/2022.01.08.22268901 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2022-01-10

Abstract Infection by SARS-CoV-2 leads to diverse symptoms, which can persist for months. While antiviral antibodies are protective, those targeting interferons and other immune factors associated with adverse COVID-19 outcomes. Instead, we discovered that against specific chemokines omnipresent after COVID-19, favorable disease, predictive of lack long COVID symptoms at one year post infection. Anti-chemokine present also in HIV-1 infection autoimmune disorders, but they target different...

10.1101/2022.05.23.493121 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-05-23

Following acute infection with severe respiratory syndrome coronavirus 2 (SARS-CoV-2) a significant proportion of individuals develop prolonged symptoms, serious condition termed post-acute disease 2019 (COVID-19) (PACS) or long COVID.Predictors PACS are needed.In prospective multicentric cohort study 215 individuals, we COVID-19 patients during primary and up to one year later, compared healthy subjects.We discover an immunoglobulin (Ig) signature, based on total IgM IgG3 levels,...

10.2139/ssrn.3850036 article EN SSRN Electronic Journal 2021-01-01

Abstract B cell responses to different pathogens recruit tailored effector mechanisms, resulting in functionally specialized subsets. For human memory cells (MBCs), these include CD21 + resting, − CD27 activated, and atypical cells. Whether subsets follow deterministic or interconnected fates is unknown. We demonstrate COVID-19 patients that single clones of SARS-CoV-2-specific MBCs followed multiple with distinctive phenotypic functional characteristics. 6–12 months after infection, most...

10.1101/2022.10.07.511336 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-10-07

Abstract Immunological memory is a hallmark of adaptive immunity and facilitates an accelerated enhanced immune response upon re-infection with the same pathogen 1,2 . Since outbreak ongoing coronavirus disease 19 (COVID-19) pandemic, key question has focused on whether severe acute respiratory syndrome 2 (SARS-CoV-2)-specific T cells stimulated during infection give rise to long-lived 3 Using spectral flow cytometry combined cellular indexing transcriptomes cell receptor (TCR) sequencing we...

10.1101/2021.07.22.453029 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-07-22
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