Serum Bactericidal Antibody Response 1 Year after Meningococcal Polysaccharide Vaccination of Patients with Common Variable Immunodeficiency
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Published:2010-04
Issue:4
Volume:17
Page:524-528
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ISSN:1556-6811
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Container-title:Clinical and Vaccine Immunology
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language:en
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Short-container-title:Clin Vaccine Immunol
Author:
Rezaei Nima12345, Siadat Seyed Davar12345, Aghamohammadi Asghar12345, Moin Mostafa12345, Pourpak Zahra12345, Norouzian Dariush12345, Mobarakeh Jalal Izadi12345, Aghasadeghi Mohammad Reza12345, Nejati Mehdi12345, Read Robert C.12345
Affiliation:
1. Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran 2. Department of Pediatrics, Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran 3. Department of Infection and Immunity, School of Medicine and Biomedical Sciences, The University of Sheffield, Sheffield, United Kingdom 4. Department of Bacterial Vaccine and Antigen Production, Pasteur Institute of Iran, Tehran, Iran 5. Department of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran
Abstract
ABSTRACT
Some patients with common variable immunodeficiency (CVID) can generate an antibody response following vaccination with
Neisseria meningitidis
polysaccharide, but the duration of this protection is unknown. In this study, serum bactericidal antibody (SBA) responses to serogroup C
N. meningitidis
of 23 patients with CVID and 23 sex- and age-matched controls were measured 1 year after vaccination with the plain A/C meningococcal polysaccharide vaccine. The fold rise in serum bactericidal antibody geometric mean titers of the control group from prevaccination to 1 year postvaccination was significantly higher than that of the patient group (5.41- versus 2.96-fold,
P
= 0.009). Of 23 CVID patients, 8 had a poor response to vaccine (<4-fold rise) 3 weeks after vaccination, and low titers remained when measured 1 year later. Of the 15 CVID patients who had a normal response to vaccine (≥4-fold rise) 3 weeks after vaccination, 6 cases failed to maintain protective SBA titers, whereas the remaining 9 had protective titers 1 year after vaccination. Only one of the 23 controls, who developed protective SBA titers after 3 weeks, lost the protective titers after 1 year. Among the patients, the presence of bronchiectasis and/or splenomegaly at enrollment was associated with poor SBA response to vaccine at 3 weeks and/or failure to maintain protective levels at 1 year. The results of this study demonstrate that a number of CVID patients can produce protective antibody titers that can persist for 1 year after vaccination, which lends strong support to the inclusion of polysaccharide vaccine in the immunization program for CVID patients.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
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