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Investigation of the pathogen-specific antibody response in periprosthetic joint infection.
Janz, Viktor; Rakow, Anastasia; Schröder, Leonie; Hofer, André; Wiebe, Sergej; Schoon, Janosch; Weiss, Stefan; Bröker, Barbara M; Wassilew, Georgi I; Raafat, Dina.
Affiliation
  • Janz V; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Rakow A; Sporthopaedicum, 93053, Regensburg, Germany.
  • Schröder L; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Hofer A; Institute of Immunology, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Wiebe S; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Schoon J; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Weiss S; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Bröker BM; Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Wassilew GI; Institute of Immunology, University Medicine Greifswald, 17475, Greifswald, Germany.
  • Raafat D; Center for Orthopaedics, Trauma Surgery and Rehabilitation Medicine, University Medicine Greifswald, 17475, Greifswald, Germany.
Infection ; 2024 May 31.
Article in En | MEDLINE | ID: mdl-38819638
ABSTRACT

PURPOSE:

Periprosthetic joint infections (PJIs) are a very demanding complication of arthroplasty. Diagnosis of PJI and pathogen identification pose considerable challenges in clinical practice. We hypothesized that the pathogen-specific immune response to PJI reflects the infection process, provides clinically relevant information on disease course, and has the potential to further optimize antimicrobial therapy.

METHODS:

We conducted a prospective matched cohort pilot study with 13 patients undergoing two-stage septic revision arthroplasty (PJI patients) between 06/2020 and 06/2021, as well as 11 control patients undergoing one-stage aseptic revision arthroplasty (Non-PJI patients). Pre-, intra- and postoperative serum samples were collected at standardized time points. We developed a custom Luminex®-based quantitative bead-based suspension array (Infection Array; IA), and used it for simultaneous measurement of antibody specificities against 32 pathogens commonly associated with PJI in 267 serum samples.

RESULTS:

The IA was able to trace the dynamics of the pathogen-specific humoral immune response in all patients against PJI-related pathogens, prominently coagulase-negative staphylococci and streptococci. Pathogen-specific serum antibody titers declined in 62% of PJI patients over the course of treatment, while no changes in antibody titers were observed in 82% of Non-PJI patients during this study. Our serological data strongly suggested that antibody signatures reflect an immune response to microbial invasion.

CONCLUSION:

Our results provide insights into the pathophysiology of PJI and information on the individual disease courses. The IA is therefore a promising and novel serological tool of high resolution for monitoring the immunoproteomic footprints of infectious pathogens in the course of PJI.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Infection Year: 2024 Type: Article Affiliation country: Germany

Full text: 1 Database: MEDLINE Language: En Journal: Infection Year: 2024 Type: Article Affiliation country: Germany