Publications by authors named "Allison Seeger"

Article Synopsis
  • The study analyzes the molecular composition of polyclonal IgG anti-spike antibodies from SARS-CoV-2 infection, vaccination, and their combination, termed "hybrid immunity."
  • It finds that infection mainly triggers antibodies reactive to the spike S2 and N-terminal domain, while vaccination predominantly induces antibodies that target the receptor-binding domain (RBD).
  • The research also shows how original IgG antibodies can enhance their effectiveness against SARS-CoV-2 variants after subsequent exposures, highlighted by the SC27 antibody's improved neutralization capabilities and binding affinity.
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Unlabelled: We used plasma IgG proteomics to study the molecular composition and temporal durability of polyclonal IgG antibodies triggered by ancestral SARS-CoV-2 infection, vaccination, or their combination ("hybrid immunity"). Infection, whether primary or post-vaccination, mainly triggered an anti-spike antibody response to the S2 domain, while vaccination predominantly induced anti-RBD antibodies. Immunological imprinting persisted after a secondary (hybrid) exposure, with >60% of the ensuing serological response originating from the initial antibodies generated during the first exposure.

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Persons living with HIV (PLWH) have an increased risk for tuberculosis (TB). After prolonged and repeated exposure, some PLWH never develop TB and show no evidence of immune sensitization to Mycobacterium tuberculosis (Mtb) as defined by persistently negative tuberculin skin tests (TST) and interferon gamma release assays (IGRA). This group has been identified and defined as HIV+ persistently TB, tuberculin and IGRA negative (HITTIN).

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Certain individuals are able to resist infection despite persistent and intense exposure. These persons do not exhibit adaptive immune priming as measured by tuberculin skin test (TST) and interferon-γ (IFN-γ) release assay (IGRA) responses, nor do they develop active tuberculosis (TB). Genetic investigation of individuals who are able to resist infection shows there are likely a combination of genetic variants that contribute to the phenotype.

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Treatment of invasive fungal infections often fails due to the limited number of therapeutic options. In this study, we have analyzed the impact of agents activating the High Osmolarity Glycerol (HOG) pathway on molds that cause infections in humans and livestock. We found that agents like fludioxonil and iprodione, have a clear anti-fungal activity against pathogenic Aspergillus, Lichtheimia, Rhizopus and Scedosporium species.

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