Author/Authors :
Goldacker، نويسنده , , S. and Draeger، نويسنده , , R. and Warnatz، نويسنده , , K. and Huzly، نويسنده , , Wolf D. and Salzer، نويسنده , , U. and Thiel، نويسنده , , J. and Eibel، نويسنده , , H. and Schlesier، نويسنده , , M. and Peter، نويسنده , , H.H.، نويسنده ,
Abstract :
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, CD21low 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 23% 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.
Keywords :
Pneumococcal polysaccharides , Polypeptides , IgM memory B cells , CVID , Vaccination