Active vaccination in patients with common variable immunodeficiency (CVID)

被引:77
作者
Goldacker, S.
Draeger, R.
Warnatz, K.
Huzly, D.
Salzer, U.
Thiel, J.
Eibel, H.
Schlesier, M.
Peter, H. H.
机构
[1] Univ Freiburg, Inst Med Microbiol & Hyg, Freiburg, Germany
[2] Univ Hosp, Dept Rheumat & Clin Immunol, Freiburg, Germany
关键词
CVID; vaccination; pneumococcal; polysaccharides; polypeptides; IgM memory B cells;
D O I
10.1016/j.clim.2007.04.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Active vaccination of CVID patients with standard vaccines has rarely been studied in depth although some patients have been shown to develop transient vaccine-specific immunity. We addressed the question whether these patients can be identified by functional classification of their B cell subsets in vitro. Twenty-one CVID patients receiving regular IgG substitution were immunized with anti-peptide and anti-polysaccharide vaccines. Humoral vaccination responses were compared to the numbers of circulating memory B cells, CD21(low) B cells and the capacity to produce antibodies in vitro. Our findings allow four conclusions: (1) positive vaccination responses are not contradictory to the diagnosis of CVID; they occurred against polypeptide vaccines in M and against polysaccharide antigens in 18% of all vaccinations. (2) Class-switched antibody responses occur preferentially in patients of CVID group II. (3) A normal percentage of IgM memory B cells is necessary but not sufficient for a vaccination response to polysaccharide antigens. (4) Active vaccination in addition to IgG replacement therapy should be performed in patients of CVID type II - especially in case of vaccines for which passive protection cannot be guaranteed. (c) 2007 Elsevier Inc. Ail rights reserved.
引用
收藏
页码:294 / 303
页数:10
相关论文
共 40 条
[1]  
Addae-Mensah I, 2005, WHO TECH REP SER, V929, P1
[2]   Antibody response in common variable immunodeficiency [J].
Al-Herz, W ;
McGeady, SJ .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2003, 90 (02) :244-247
[3]  
[Anonymous], EPIDEMIOL B
[4]   CLASSIFICATION OF PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY BY B-CELL SECRETION OF IGM AND IGG IN RESPONSE TO ANTI-IGM AND INTERLEUKIN-2 [J].
BRYANT, A ;
CALVER, NC ;
TOUBI, E ;
WEBSTER, ADB ;
FARRANT, J .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1990, 56 (02) :239-248
[5]   The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency [J].
Carsetti, R ;
Rosado, MM ;
Donnanno, S ;
Guazzi, V ;
Soresina, A ;
Meini, M ;
Plebani, A ;
Aiuti, F ;
Quinti, I .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 115 (02) :412-417
[6]   Peripheral development of B cells in mouse and man [J].
Carsetti, R ;
Rosado, MM ;
Wardemann, H .
IMMUNOLOGICAL REVIEWS, 2004, 197 :179-191
[7]   TACI and BAFF-R mediate isotype switching in B cells [J].
Castigli, E ;
Wilson, SA ;
Scott, S ;
Dedeoglu, F ;
Xu, SL ;
Lam, KP ;
Bram, RJ ;
Jabara, H ;
Geha, RS .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (01) :35-39
[8]  
CHALMERS A, 1994, J RHEUMATOL, V21, P1203
[9]   Primary immunodeficiency diseases: an update [J].
Chapel, H ;
Geha, R ;
Rosen, F .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 132 (01) :9-15
[10]   Pneumococcal type 22F polysaccharide absorption improves the specificity of a pneumococcal-polysaccharide enzyme-linked immunosorbent assay [J].
Concepcion, NF ;
Frasch, CE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (02) :266-272