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Kidney-resident innate-like memory γδ T cells control chronic Staphylococcus aureus infection of mice.
Bertram, Tabea; Reimers, Daniel; Lory, Niels C; Schmidt, Constantin; Schmid, Joanna; C Heinig, Lisa; Bradtke, Peter; Rattay, Guido; Zielinski, Stephanie; Hellmig, Malte; Bartsch, Patricia; Rohde, Holger; Nuñez, Sarah; Rosemblatt, Mariana V; Bono, Maria Rosa; Gagliani, Nicola; Sandrock, Inga; Panzer, Ulf; Krebs, Christian F; Meyer-Schwesinger, Catherine; Prinz, Immo; Mittrücker, Hans-Willi.
Afiliación
  • Bertram T; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Reimers D; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Lory NC; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Schmidt C; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Schmid J; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • C Heinig L; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Bradtke P; Institute for Immunology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Rattay G; I. Department of Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Zielinski S; Institute of Cellular and Integrative Physiology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Hellmig M; III. Department of Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Bartsch P; III. Department of Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Rohde H; Institute for Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Nuñez S; Institute for Medical Microbiology, Virology and Hygiene, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Rosemblatt MV; Facultad de Medicina y Ciencia, Universidad San Sebastián 7510602, Sede Los Leones, Chile.
  • Bono MR; Centro Ciencia & Vida 7780272, Santiago, Chile.
  • Gagliani N; Facultad de Medicina y Ciencia, Universidad San Sebastián 7510602, Sede Los Leones, Chile.
  • Sandrock I; Department of Biology, Faculty of Sciences, Universidad de Chile, Las Palmeras 3425, Nunoa 7800003, Chile.
  • Panzer U; I. Department of Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Krebs CF; Immunology and Allergy Unit, Department of Medicine, Karolinska Institute and University Hospital, Solna, Stockholm 17176, Sweden.
  • Meyer-Schwesinger C; Institute of Immunology, Hannover Medical School, 30625 Hannover, Germany.
  • Prinz I; III. Department of Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
  • Mittrücker HW; Hamburg Center for Translational Immunology (HCTI), University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Proc Natl Acad Sci U S A ; 120(1): e2210490120, 2023 01 03.
Article en En | MEDLINE | ID: mdl-36574651
ABSTRACT
γδ T cells are involved in the control of Staphylococcus aureus infection, but their importance in protection compared to other T cells is unclear. We used a mouse model of systemic S. aureus infection associated with high bacterial load and persistence in the kidney. Infection caused fulminant accumulation of γδ T cells in the kidney. Renal γδ T cells acquired tissue residency and were maintained in high numbers during chronic infection. At day 7, up to 50% of renal γδ T cells produced IL-17A in situ and a large fraction of renal γδ T cells remained IL-17A+ during chronic infection. Controlled depletion revealed that γδ T cells restricted renal S. aureus replication in the acute infection and provided protection during chronic renal infection and upon reinfection. Our results demonstrate that kidney-resident γδ T cells are nonredundant in limiting local S. aureus growth during chronic infection and provide enhanced protection against reinfection.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Interleucina-17 Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2023 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones Estafilocócicas / Interleucina-17 Límite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2023 Tipo del documento: Article País de afiliación: Alemania