Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response

Infections are a major cause of morbidity and mortality in multiple myeloma (MM), a cancer of the immune system. Vaccination clinical efficacy endpoints have not been demonstrated, and there are limited data on surrogate markers of efficacy. This pilot study evaluated sequential immunologic markers...

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Main Authors: Michael A. Thompson, Martin K. Oaks, Maharaj Singh, Karen M. Michel, Michael P. Mullane, Husam S. Tarawneh, Angi Kraut, Kayla J. Hamm
Format: Article
Language:English
Published: Advocate Aurora Health 2017-08-01
Series:Journal of Patient-Centered Research and Reviews
Subjects:
Online Access:http://digitalrepository.aurorahealthcare.org/cgi/viewcontent.cgi?article=1453&context=jpcrr
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author Michael A. Thompson
Martin K. Oaks
Maharaj Singh
Karen M. Michel
Michael P. Mullane
Husam S. Tarawneh
Angi Kraut
Kayla J. Hamm
author_facet Michael A. Thompson
Martin K. Oaks
Maharaj Singh
Karen M. Michel
Michael P. Mullane
Husam S. Tarawneh
Angi Kraut
Kayla J. Hamm
author_sort Michael A. Thompson
collection DOAJ
description Infections are a major cause of morbidity and mortality in multiple myeloma (MM), a cancer of the immune system. Vaccination clinical efficacy endpoints have not been demonstrated, and there are limited data on surrogate markers of efficacy. This pilot study evaluated sequential immunologic markers after standard pneumococcal vaccination (PV) in patients with MM and non-MM controls. Vaccination was standard for PV (PCV13 or PPV23), with laboratory testing at baseline and at 2, 4, 12 and 24 weeks after vaccination. Immunoglobulin G (IgG) antibodies to pneumococcal antigens were detected by ELISA. Prevaccination total IgG levels and IgG subclass levels were also measured by ELISA. Four of 6 controls responded with at least a 2-fold increase in antibody concentration; only 2 controls had a sustained increase in concentration. Six of 8 patients with MM had at least a 2-fold antibody increase; however, only 2 of these patients showed a sustained increase of antipneumococcal antibody. Response rate differences were not statistically significant in this small pilot, and there was no relationship between responsiveness to PV and initial serum total IgG levels or IgG subclasses at study entry. Future prospective studies are needed to ascertain the immunological and clinical efficacy and effectiveness of various vaccines and vaccination strategies in MM.
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spelling doaj.art-f5d1f077220c45c1aeac3805563647842023-02-02T15:28:58ZengAdvocate Aurora HealthJournal of Patient-Centered Research and Reviews2330-06982017-08-014313113510.17294/2330-0698.1453Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody ResponseMichael A. Thompson0Martin K. Oaks1Maharaj Singh2Karen M. Michel3Michael P. Mullane4Husam S. Tarawneh5Angi Kraut6Kayla J. Hamm7Aurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIAurora Health Care, Milwaukee, WIInfections are a major cause of morbidity and mortality in multiple myeloma (MM), a cancer of the immune system. Vaccination clinical efficacy endpoints have not been demonstrated, and there are limited data on surrogate markers of efficacy. This pilot study evaluated sequential immunologic markers after standard pneumococcal vaccination (PV) in patients with MM and non-MM controls. Vaccination was standard for PV (PCV13 or PPV23), with laboratory testing at baseline and at 2, 4, 12 and 24 weeks after vaccination. Immunoglobulin G (IgG) antibodies to pneumococcal antigens were detected by ELISA. Prevaccination total IgG levels and IgG subclass levels were also measured by ELISA. Four of 6 controls responded with at least a 2-fold increase in antibody concentration; only 2 controls had a sustained increase in concentration. Six of 8 patients with MM had at least a 2-fold antibody increase; however, only 2 of these patients showed a sustained increase of antipneumococcal antibody. Response rate differences were not statistically significant in this small pilot, and there was no relationship between responsiveness to PV and initial serum total IgG levels or IgG subclasses at study entry. Future prospective studies are needed to ascertain the immunological and clinical efficacy and effectiveness of various vaccines and vaccination strategies in MM.http://digitalrepository.aurorahealthcare.org/cgi/viewcontent.cgi?article=1453&context=jpcrrmultiple myelomavaccinationpneumococcalclinical efficacyimmunologyantibodyimmunoglobulin G
spellingShingle Michael A. Thompson
Martin K. Oaks
Maharaj Singh
Karen M. Michel
Michael P. Mullane
Husam S. Tarawneh
Angi Kraut
Kayla J. Hamm
Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
Journal of Patient-Centered Research and Reviews
multiple myeloma
vaccination
pneumococcal
clinical efficacy
immunology
antibody
immunoglobulin G
title Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
title_full Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
title_fullStr Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
title_full_unstemmed Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
title_short Multiple Myeloma Baseline Immunoglobulin G Level and Pneumococcal Vaccination Antibody Response
title_sort multiple myeloma baseline immunoglobulin g level and pneumococcal vaccination antibody response
topic multiple myeloma
vaccination
pneumococcal
clinical efficacy
immunology
antibody
immunoglobulin G
url http://digitalrepository.aurorahealthcare.org/cgi/viewcontent.cgi?article=1453&context=jpcrr
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