IMMUNOGLOBULIN ISOTYPE-SPECIFIC ANTIBODY-RESPONSES TO PNEUMOCOCCAL POLYSACCHARIDE VACCINE IN PATIENTS WITH RECURRENT BACTERIAL RESPIRATORY-TRACT INFECTIONS

被引:52
作者
SANDERS, LAM
RIJKERS, GT
TENBERGENMEEKES, AM
VOORHORSTOGINK, MM
ZEGERS, BJM
机构
[1] Department of Immunology, University Hospital for Children, Het Wilhelmina Kinderziekenhuis, Utrecht
关键词
D O I
10.1203/00006450-199506000-00023
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Anti-pneumococcal IgM, IgG1, IgG2, and IgA antibody titers were determined in 61 pediatric patients with recurrent bacterial respiratory tract infections. The patients were divided in those with normal serum Ig levels (group I, n = 46) and patients with dysimmunoglobulinemia (group II, n = 15). Antibody titers to five pneumococcal serotypes (3, 4, 6A, 9N, and 19F) of different immunogenicity were determined by ELISA, before and 14 d after immunization with pneumococcal polysaccharide vaccine. In the patients of group I, IgM responses did not vary between the various serotypes. IgG1 antibodies reached high levels for pneumococcal types 3, 4, and 9N compared with an adult reference hyperimmune plasma pool, but remained low for the weak immunogenic types 6A and 19F. IgG2 antibody titers remained low and were nearly absent in 20/46 patients. The fold increase in IgA was high, but the ultimate IgA antibody levels remained low. IgA levels remained low to absent in 10/46 patients. Two patients (4%) of group I failed to show antipneumococcal antibodies of all Ig isotypes. In group II, 6/15 patients (40%) made no anti-pneumococcal antibodies of any isotype, whereas the remaining patients made no IgG2 and/or IgA anti-pneumococcal antibodies. We conclude that the frequency of nonresponders to pneumococcal vaccination in patients with normal serum Ig is low (4%). However, low IgG2 anti-pneumococcal levels are found in approximately 50% of the patients. In patients with dysimmunoglobulinemia, IgA and IgG2 responses were absent in virtually all patients, whereas 40% made no anti-pneumococcal antibodies of any isotype.
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页码:812 / 819
页数:8
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共 43 条
[31]  
Lortan J.E., Kaniuk A., Monteil M.A., Relationship of in vitro phagocytosis of serotype 14 Streptococcus pneumoniae to specific class and IgG subclass antibody levels in healthy adults, Clin Exp Immunol, 91, pp. 54-57, (1993)
[32]  
Bredius R.G., De Vries C., Troelstra A., Van Alphen L., Weening R.S., Van De Winkel J., Out T.A., Phagocytosis of Staphylococcus aureus and Haemophilus influenzae type B opsonized with polyclonal human IgGl and IgG2 antibodies, J Immunol, 151, pp. 1463-1472, (1993)
[33]  
Givner L.B., Baker C.J., Edwards M.S., Type III group B Streptococcus: Functional interaction with IgG subclass antibodies, J Infect Dis, 155, pp. 532-539, (1987)
[34]  
Chudwin D.S., Artrip S.G., Schiffman G., Immunoglobulin G class and subclass antibodies to pneumococcal capsular polysaccharides, Clin Immunol Immunopathol, 44, pp. 114-121, (1987)
[35]  
Van De Winkel J., Capel P., Human IgG Fc receptor heterogeneity: Molecular aspects and clinical implications, Immunol Today, 14, pp. 215-221, (1993)
[36]  
Sanders E., Van De Winkel J., Rijkers G.T., Voorhorst-Ogink M.M., De Haas M., Capel P.J., Zegers B., Fey receptor IIA (CD32) heterogeneity in patients with recurrent bacterial respiratory tract infections, J Infect Dis, 170, pp. 854-861, (1994)
[37]  
Lue C., Tarkowski A., Mestecky J., Systemic immunization with pneumococcal polysaccharide vaccine induces a predominant IgA2 response of peripheral blood lymphocytes and increases of both serum and secretory anti-pneumococcal antibodies, J Immunol, 140, pp. 3793-3800, (1988)
[38]  
Shen L., Receptors for IgA on phagocytic cells, Immunol Res, 11, pp. 273-277, (1992)
[39]  
Kilian M., Mestecky J., Russell M.W., Defense against involving Fc-dependent functions of immunoglobulin A and their subversion by bacterial immunoglobulin A proteases, Microbiol Rev, 52, pp. 296-303, (1988)
[40]  
Stewart W.W., Kerr M.A., The specificity of the human neutrophil IgA receptor (FcaR) determined by measurement of chemiluminescence induced by serum or secretory IgAl or IgA2, Immunology, 71, pp. 328-334, (1990)