Abstract

A subgroup of patients with common variable immunodeficiencies (CVIDs) responds to vaccination. The aim of this study was to try to identify predictive markers for those with a humoral immune response after influenza vaccination. Forty-eight patients with CVID (29 female and 19 male patients; mean age, 57.7years) were vaccinated with the A(H1N1) influenza vaccine Pandemrix (GlaxoSmithKline, Wavre, Belgium) and boosted after 1month. Blood samples were collected before each vaccination and 2months later. Patients with a 4-fold titer increase in results on the hemagglutinin inhibition test (≥1:40) were considered responders and compared with nonresponders for clinical, immunologic, and genetic markers. Eight (16.7%) patients responded to the vaccination. Asignificantly higher proportion of the responders, who showed a EUROclass SmB-Trnorm21norm profile (P=.03) with a post-germinal center B-cell pattern (P=.04) in blood, experienced enteropathies (P=.04) compared with nonresponders. On the other hand, bronchiectasis was found exclusively among nonresponders (n=7), as was autoimmune cytopenia (n=5). Nonresponders with a EUROclass SmB-Trnorm21low profile (P=.02) had a significantly greater prevalence of progressive antibody deficiency (P=.048) and, at diagnosis, a higher mean serum IgM level (P=.03), lower mean serum IgG1 level (P=.007), expansion of absolute counts of cytotoxic CD8+ T cells (P=.033), and increased proportion of memory CD8+ T cells (P=.044) in blood. CVID-associated HLA markers were not detected in responders (P=.03). About one fifth of the patients with CVIDs achieved protective antibody levels after A(H1N1) vaccination and selected clinical, and immunologic markers were identified thatmight predict a positive outcome of influenza vaccination. Patients with CVID should be offered vaccination also against seasonal influenza because of the potential severity of the infection and risk for bacterial complications.

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