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Pneumococcal Polysaccharide Vaccine Ameliorates Murine Lupus.
Cantarelli, Chiara; Guglielmo, Chiara; Hartzell, Susan; Salem, Fadi El; Andrighetto, Sofia; Gazivoda, Victor P; Fiaccadori, Enrico; La Manna, Gaetano; Zaza, Gianluigi; Leventhal, Jeremy; Tassiulas, Ioannis; Cravedi, Paolo.
Afiliação
  • Cantarelli C; Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Guglielmo C; Unità Operativa Complessa di Nefrologia, Azienda Ospedaliera-Universitaria Parma, Dipartimento di Medicina e Chirurgia, Università di Parma, Parma, Italy.
  • Hartzell S; Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Salem FE; Department of Experimental Diagnostic and Specialty Medicine (DIMES), Nephrology, Dialysis and Renal Transplant Unit, St. Orsola Hospital, University of Bologna, Bologna, Italy.
  • Andrighetto S; Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Gazivoda VP; Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
  • Fiaccadori E; Renal Unit, Department of Medicine, University-Hospital of Verona, Verona, Italy.
  • La Manna G; Department of Surgery, Maimonides Medical Center, New York, NY, United States.
  • Zaza G; Unità Operativa Complessa di Nefrologia, Azienda Ospedaliera-Universitaria Parma, Dipartimento di Medicina e Chirurgia, Università di Parma, Parma, Italy.
  • Leventhal J; Department of Experimental Diagnostic and Specialty Medicine (DIMES), Nephrology, Dialysis and Renal Transplant Unit, St. Orsola Hospital, University of Bologna, Bologna, Italy.
  • Tassiulas I; Renal Unit, Department of Medicine, University-Hospital of Verona, Verona, Italy.
  • Cravedi P; Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Front Immunol ; 10: 2695, 2019.
Article em En | MEDLINE | ID: mdl-31824490
ABSTRACT
Current guidelines encourage administering pneumococcal vaccine Prevnar-13 to patients with lupus, but whether such vaccinations affect disease severity is unclear. To address this issue, we treated 3-month-old MRL-lpr mice, that spontaneously develop a lupus-like syndrome, with Prevnar-13 or vehicle control. After 3 months, we quantified circulating anti-Pneumococcal polysaccharide capsule (PPS) antibodies and signs of disease severity, including albuminuria, renal histology and skin severity score. We also compared immunophenotypes and function of T and B cells from treated and untreated animals. Prevnar-13 elicited the formation of anti-pneumococcal IgM and IgG. Prevnar-13 treated animals showed reduced albuminuria, renal histological lesions, and milder dermatitis compared to vehicle-treated controls. Mitigated disease severity was associated with reduced and increased T follicular helper cells (TFH) and T follicular regulatory cells (TFR), respectively, in Prevnar-treated animals. T cells from Prevnar-13 vaccinated mice showed differential cytokine production after aCD3/aCD28 stimulation, with significantly decreased IL-17 and IL-4, and increased IL-10 production compared to non-vaccinated mice. In conclusion, pneumococcal vaccination elicits anti-pneumococcal antibody response and ameliorates disease severity in MRL-lpr mice, which associates with fewer TFH and increased TFR. Together, the data support use of Prevnar vaccination in individuals with SLE.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Pneumocócicas / Lúpus Eritematoso Sistêmico Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Pneumocócicas / Lúpus Eritematoso Sistêmico Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article