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Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients

Background. Multiple myeloma (MM) and its therapies may induce a severely compromised humoral immunity. We have performed a longitudinal analysis of IgG-antibody responses against influenza virus (FLU) and tetanus toxoid (TT) as surrogate markers for the B cell-mediated immunity in MM patients. Meth...

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Autores principales: Kobold, Sebastian, Luetkens, Tim, Bartels, Britta Marlen, Cao, Yanran, Hildebrandt, York, Sezer, Orhan, Reinhard, Henrike, Templin, Julia, Bartels, Katrin, Lajmi, Nesrine, Haag, Friedrich, Bokemeyer, Carsten, Kröger, Nicolaus, Atanackovic, Djordje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310258/
https://www.ncbi.nlm.nih.gov/pubmed/22481961
http://dx.doi.org/10.1155/2012/134081
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author Kobold, Sebastian
Luetkens, Tim
Bartels, Britta Marlen
Cao, Yanran
Hildebrandt, York
Sezer, Orhan
Reinhard, Henrike
Templin, Julia
Bartels, Katrin
Lajmi, Nesrine
Haag, Friedrich
Bokemeyer, Carsten
Kröger, Nicolaus
Atanackovic, Djordje
author_facet Kobold, Sebastian
Luetkens, Tim
Bartels, Britta Marlen
Cao, Yanran
Hildebrandt, York
Sezer, Orhan
Reinhard, Henrike
Templin, Julia
Bartels, Katrin
Lajmi, Nesrine
Haag, Friedrich
Bokemeyer, Carsten
Kröger, Nicolaus
Atanackovic, Djordje
author_sort Kobold, Sebastian
collection PubMed
description Background. Multiple myeloma (MM) and its therapies may induce a severely compromised humoral immunity. We have performed a longitudinal analysis of IgG-antibody responses against influenza virus (FLU) and tetanus toxoid (TT) as surrogate markers for the B cell-mediated immunity in MM patients. Methods. 1094 serum samples of 190 MM patients and samples from 100 healthy donors were analyzed by ELISA for FLU- and TT-specific antibodies. Results. MM patients evidenced lower levels of FLU- and TT-specific antibodies than healthy controls (P < 0.001). Immunoreactivity decreased with progressing disease and worsening clinical status. Levels of FLU- and TT-specific antibodies increased shortly (0-6 months) after alloSCT (P < 0.001), a time-period during which intravenous immunoglobulin (IVIG) is routinely applied. Thereafter, antibody concentrations declined and remained suppressed for 3 years in the case of FLU-specific and for more than 5 years in the case of TT-specific antibodies. Conclusions. We found that MM is associated with a profound disease- and therapy-related immunosuppression, which is compensated for a few months after alloSCT, most likely by application of IVIG. This and the differences regarding the recovery of anti-FLU and anti-TT antibody titers during the following years need to be taken into account for optimizing IVIG application and immunization after alloSCT.
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spelling pubmed-33102582012-04-05 Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients Kobold, Sebastian Luetkens, Tim Bartels, Britta Marlen Cao, Yanran Hildebrandt, York Sezer, Orhan Reinhard, Henrike Templin, Julia Bartels, Katrin Lajmi, Nesrine Haag, Friedrich Bokemeyer, Carsten Kröger, Nicolaus Atanackovic, Djordje Clin Dev Immunol Clinical Study Background. Multiple myeloma (MM) and its therapies may induce a severely compromised humoral immunity. We have performed a longitudinal analysis of IgG-antibody responses against influenza virus (FLU) and tetanus toxoid (TT) as surrogate markers for the B cell-mediated immunity in MM patients. Methods. 1094 serum samples of 190 MM patients and samples from 100 healthy donors were analyzed by ELISA for FLU- and TT-specific antibodies. Results. MM patients evidenced lower levels of FLU- and TT-specific antibodies than healthy controls (P < 0.001). Immunoreactivity decreased with progressing disease and worsening clinical status. Levels of FLU- and TT-specific antibodies increased shortly (0-6 months) after alloSCT (P < 0.001), a time-period during which intravenous immunoglobulin (IVIG) is routinely applied. Thereafter, antibody concentrations declined and remained suppressed for 3 years in the case of FLU-specific and for more than 5 years in the case of TT-specific antibodies. Conclusions. We found that MM is associated with a profound disease- and therapy-related immunosuppression, which is compensated for a few months after alloSCT, most likely by application of IVIG. This and the differences regarding the recovery of anti-FLU and anti-TT antibody titers during the following years need to be taken into account for optimizing IVIG application and immunization after alloSCT. Hindawi Publishing Corporation 2012 2012-03-12 /pmc/articles/PMC3310258/ /pubmed/22481961 http://dx.doi.org/10.1155/2012/134081 Text en Copyright © 2012 Sebastian Kobold et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Kobold, Sebastian
Luetkens, Tim
Bartels, Britta Marlen
Cao, Yanran
Hildebrandt, York
Sezer, Orhan
Reinhard, Henrike
Templin, Julia
Bartels, Katrin
Lajmi, Nesrine
Haag, Friedrich
Bokemeyer, Carsten
Kröger, Nicolaus
Atanackovic, Djordje
Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title_full Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title_fullStr Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title_full_unstemmed Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title_short Longitudinal Analysis of Tetanus- and Influenza-Specific IgG Antibodies in Myeloma Patients
title_sort longitudinal analysis of tetanus- and influenza-specific igg antibodies in myeloma patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310258/
https://www.ncbi.nlm.nih.gov/pubmed/22481961
http://dx.doi.org/10.1155/2012/134081
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