Response to a heptavalent conjugate Streptococcus pneumoniae vaccine in children with recurrent infections who are unresponsive to the polysaccharide vaccine

被引:92
作者
Sorensen, RU
Leiva, LE
Giangrosso, PA
Butler, B
Javier, FC
Sacerdote, DM
Bradford, N
Moore, C
机构
[1] Louisiana State Univ, Med Ctr, Dept Pediat, Div Allergy & Immunol, New Orleans, LA 70112 USA
[2] Childrens Hosp, New Orleans, LA USA
关键词
Streptococcus pneumoniae; recurrent infections; immunization; polysaccharide vaccine; conjugate vaccine;
D O I
10.1097/00006454-199808000-00005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective, To determine whether children with recurrent respiratory infections who failed to respond to the conventional polysaccharide vaccine would respond to a pneumococcal conjugate vaccine. Methods. Children referred to our clinic for recurrent respiratory infections who had no known primary or secondary immunodeficiencies mere immunized with a 23-valent pneumococcal polysaccharide vaccine. IgG antibodies to pneumococcal serotypes 1, 3, 4, 6B, 9V, 14, 18C, 19F and 23F were determined by enzyme-linked immunosorbent assay before and 4 to 6 weeks after immunization. An adequate IgG antibody response to an individual serotype was arbitrarily defined as a postimmunization antibody titer greater than or equal to 1.3 mu g/ml Or at least 4 times the preimmunization value. Immunization with an experimental CRM197-heptavalent pneumococcal conjugate vaccine was offered to patients without an adequate response to 4 or more vaccine serotypes (nonresponders). Post-conjugate immunization antibody concentrations were measured 4 to 6 weeks later. Results. In nonresponder patients (n = 17) geometric mean post-conjugate immunization (C) serum antibody concentrations (mu g/ml) compared with post-polysaccharide (PS) concentrations were: (serotype, C vs, PS) 4, 1.11 vs. 0.30 (P = 0.000227); 6B, 0.46 vs, 0.20 (P = 0.017267); 9V, 0.82 vs. 0.29 (P = 0.002163); 14, 1.88 vs. 0.27 (P = 0.000615); 18C, 0.98 us, 0.32 (P = 0.021962); 19F, 1.24 vs. 0.34 (P = 0.002844); and 23F, 0.87 us. 0.16 (P = 0.000194), In responder patients (n = 67), after 1 dose of the polysaccharide vaccine, geometric mean antibody concentrations were: 4, 1.05; 6B, 0.96; 9V, 1.55; 14, 1.65; 18C, 1.62; 19F, 1.30; and 23F, 1.02, Conclusions. Our results show that a pneumococcal conjugate vaccine is capable of inducing an IgG response in patients with recurrent infections who had failed to mount an adequate response to the polysaccharide vaccine. Conjugate vaccines may be of value in the management of children with recurrent pneumococcal respiratory infections.
引用
收藏
页码:685 / 691
页数:7
相关论文
共 34 条
[1]   Pentavalent pneumococcal oligosaccharide conjugate vaccine PncCRM is well-tolerated and able to induce an antibody response in infants [J].
Ahman, H ;
Kayhty, H ;
Tamminen, P ;
Vuorela, A ;
Malinoski, F ;
Eskola, J .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1996, 15 (02) :134-139
[2]   AN IMMUNODEFICIENCY CHARACTERIZED BY IMPAIRED ANTIBODY-RESPONSES TO POLYSACCHARIDES [J].
AMBROSINO, DM ;
SIBER, GR ;
CHILMONCZYK, BA ;
JERNBERG, JB ;
FINBERG, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (13) :790-793
[3]   Immunogenicity of heptavalent pneumococcal conjugate vaccine in infants [J].
Anderson, EL ;
Kennedy, DJ ;
Geldmacher, KM ;
Donnelly, J ;
Mendelman, PM .
JOURNAL OF PEDIATRICS, 1996, 128 (05) :649-653
[4]  
BARRETT DJ, 1986, CLIN EXP IMMUNOL, V63, P127
[5]   SEROTYPE DISTRIBUTION OF STREPTOCOCCUS-PNEUMONIAE INFECTIONS AMONG PRESCHOOL-CHILDREN IN THE UNITED-STATES, 1978-1994 - IMPLICATIONS FOR DEVELOPMENT OF A CONJUGATE VACCINE [J].
BUTLER, JC ;
BREIMAN, RF ;
LIPMAN, HB ;
HOFMANN, J ;
FACKLAM, RR .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (04) :885-889
[6]  
*CDCP, 1996, WHO WORKSH PNEUM ELI
[7]   Safety and immunogenicity of tetravalent pneumococcal vaccines containing 6B, 14, 19F and 23F polysaccharides conjugated to either tetanus toxoid or diphtheria toxoid in young infants and their boosterability by native polysaccharide antigens [J].
Dagan, R ;
Melamed, R ;
Zamir, O ;
Leroy, O .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1997, 16 (11) :1053-1059
[8]   Reduction of nasopharyngeal carriage of pneumococci during the second year of life by a heptavalent conjugate pneumococcal vaccine [J].
Dagan, R ;
Melamed, R ;
Muallem, M ;
Piglansky, L ;
Greenberg, D ;
Abramson, O ;
Mendelman, PM ;
Bohidar, N ;
Yagupsky, P .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (06) :1271-1278
[9]  
EPSTEIN M, 1996, ANN ALLERG ASTHMA IM, V75, P125
[10]  
FRIEDLAND IR, 1994, NEW ENGL J MED, V331, P337