Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats

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Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats. / Søe, Niels Henrik; Jensen, Nina Vendel; Lundorff Jensen, Asger; Koch, Janne; Poulsen, Steen Seier; Pier, Gerald B; Johansen, Helle Krogh.

I: In Vivo, Bind 31, Nr. 1, 2017, s. 45-50.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Søe, NH, Jensen, NV, Lundorff Jensen, A, Koch, J, Poulsen, SS, Pier, GB & Johansen, HK 2017, 'Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats', In Vivo, bind 31, nr. 1, s. 45-50. https://doi.org/10.21873/invivo.11023

APA

Søe, N. H., Jensen, N. V., Lundorff Jensen, A., Koch, J., Poulsen, S. S., Pier, G. B., & Johansen, H. K. (2017). Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats. In Vivo, 31(1), 45-50. https://doi.org/10.21873/invivo.11023

Vancouver

Søe NH, Jensen NV, Lundorff Jensen A, Koch J, Poulsen SS, Pier GB o.a. Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats. In Vivo. 2017;31(1):45-50. https://doi.org/10.21873/invivo.11023

Author

Søe, Niels Henrik ; Jensen, Nina Vendel ; Lundorff Jensen, Asger ; Koch, Janne ; Poulsen, Steen Seier ; Pier, Gerald B ; Johansen, Helle Krogh. / Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats. I: In Vivo. 2017 ; Bind 31, Nr. 1. s. 45-50.

Bibtex

@article{65e8031e87b74797ac05627d83ad4546,
title = "Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats",
abstract = "BACKGROUND/AIM: Staphylococcus aureus infection associated with orthopedic implants cannot always be controlled. We used a knee prosthesis model with implant-related osteomyelitis in rats to explore induction of an effective immune response with active and passive immunization.MATERIALS AND METHODS: Fifty-two Sprague-Dawley rats were divided into active (N=28) and passive immunization groups (N=24). A bacterial inoculum of 10(3) S. aureus MN8 was injected into the tibia and the femur marrow before insertion of a non-constrained knee prosthesis in each rat. The active-immunization group received a synthetic oligosaccharide of polysaccharide poly-N-acetylglucosamine (PNAG), 9G1cNH2 and the passive-immunization group received immunization with immunoglobulin from rabbits infected with S. aureus.RESULTS/CONCLUSION: Active immunization against PNAG significantly reduced the consequences of osteomyelitis infection from PNAG-producing intercellular adhesion (ica(+)) but not ica(-) S. aureus. Passive immunization resulted in better clinical assessments in animals challenged with either ica(+) or ica(-) S. aureus, suggesting a lack of specificity in this antiserum.",
author = "S{\o}e, {Niels Henrik} and Jensen, {Nina Vendel} and {Lundorff Jensen}, Asger and Janne Koch and Poulsen, {Steen Seier} and Pier, {Gerald B} and Johansen, {Helle Krogh}",
note = "Copyright{\textcopyright} 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.",
year = "2017",
doi = "10.21873/invivo.11023",
language = "English",
volume = "31",
pages = "45--50",
journal = "In Vivo",
issn = "0258-851X",
publisher = "International Institute of Anticancer Research",
number = "1",

}

RIS

TY - JOUR

T1 - Active and Passive Immunization Against Staphylococcus aureus Periprosthetic Osteomyelitis in Rats

AU - Søe, Niels Henrik

AU - Jensen, Nina Vendel

AU - Lundorff Jensen, Asger

AU - Koch, Janne

AU - Poulsen, Steen Seier

AU - Pier, Gerald B

AU - Johansen, Helle Krogh

N1 - Copyright© 2017, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

PY - 2017

Y1 - 2017

N2 - BACKGROUND/AIM: Staphylococcus aureus infection associated with orthopedic implants cannot always be controlled. We used a knee prosthesis model with implant-related osteomyelitis in rats to explore induction of an effective immune response with active and passive immunization.MATERIALS AND METHODS: Fifty-two Sprague-Dawley rats were divided into active (N=28) and passive immunization groups (N=24). A bacterial inoculum of 10(3) S. aureus MN8 was injected into the tibia and the femur marrow before insertion of a non-constrained knee prosthesis in each rat. The active-immunization group received a synthetic oligosaccharide of polysaccharide poly-N-acetylglucosamine (PNAG), 9G1cNH2 and the passive-immunization group received immunization with immunoglobulin from rabbits infected with S. aureus.RESULTS/CONCLUSION: Active immunization against PNAG significantly reduced the consequences of osteomyelitis infection from PNAG-producing intercellular adhesion (ica(+)) but not ica(-) S. aureus. Passive immunization resulted in better clinical assessments in animals challenged with either ica(+) or ica(-) S. aureus, suggesting a lack of specificity in this antiserum.

AB - BACKGROUND/AIM: Staphylococcus aureus infection associated with orthopedic implants cannot always be controlled. We used a knee prosthesis model with implant-related osteomyelitis in rats to explore induction of an effective immune response with active and passive immunization.MATERIALS AND METHODS: Fifty-two Sprague-Dawley rats were divided into active (N=28) and passive immunization groups (N=24). A bacterial inoculum of 10(3) S. aureus MN8 was injected into the tibia and the femur marrow before insertion of a non-constrained knee prosthesis in each rat. The active-immunization group received a synthetic oligosaccharide of polysaccharide poly-N-acetylglucosamine (PNAG), 9G1cNH2 and the passive-immunization group received immunization with immunoglobulin from rabbits infected with S. aureus.RESULTS/CONCLUSION: Active immunization against PNAG significantly reduced the consequences of osteomyelitis infection from PNAG-producing intercellular adhesion (ica(+)) but not ica(-) S. aureus. Passive immunization resulted in better clinical assessments in animals challenged with either ica(+) or ica(-) S. aureus, suggesting a lack of specificity in this antiserum.

U2 - 10.21873/invivo.11023

DO - 10.21873/invivo.11023

M3 - Journal article

C2 - 28064219

VL - 31

SP - 45

EP - 50

JO - In Vivo

JF - In Vivo

SN - 0258-851X

IS - 1

ER -

ID: 172266256