Oral immunization with PspA elicits protective humoral immunity against Streptococcus pneumoniae infection

被引:53
作者
Yamamoto, M
McDaniel, LS
Kawabata, K
Briles, DE
Jackson, RJ
McGhee, JR
Kiyono, H
机构
[1] UNIV ALABAMA,DEPT MICROBIOL,IMMUNOBIOL VACCINE CTR,MED CTR,BIRMINGHAM,AL 35294
[2] UNIV MISSISSIPPI,MED CTR,DEPT SURG,JACKSON,MS 39216
[3] UNIV MISSISSIPPI,MED CTR,DEPT MICROBIOL,JACKSON,MS 39216
[4] OSAKA UNIV,DEPT MUCOSAL IMMUNOL,MICROBIAL DIS RES INST,SUITA,OSAKA 565,JAPAN
关键词
D O I
10.1128/IAI.65.2.640-644.1997
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Streptococcus pneumoniae is a major respiratory mucosal pathogen affecting infants and children, Although a polysaccharide-based vaccine has been useful in adult populations, it does not elicit protective immunity in infants and young children, Pneumococcal surface protein A (PspA) is a highly immunogenic surface protein produced by all strains of Streptococcus pneumoniae. Previous studies have shown that systemic immunization of mice with PspA can elicit protective immunity against fatal pneumococcal infection, In this study, we demonstrated that oral immunization with PspA could elicit protective immune responses against pneumococcal infection, When mice were orally immunized with PspA alone, low levels of PspA-specific immunoglobulin G (IgG) responses were induced in serum; none was induced in secretion, On the other hand, when PspA was given orally with the mucosal adjuvant cholera toxin (CT), significant levels of IgG and IgA anti-PspA responses were induced in serum, The major IgG subclass was IgG1, followed by IgG2b, a profile of antibody response supported by Th2-type cells, In addition, all mice orally immunized with PspA and CT were protected from the lethal challenge with capsular serotype 3 S. pneumoniae A66, These results suggested that an oral PspA vaccine may be a useful means of preventing pneumococcal disease.
引用
收藏
页码:640 / 644
页数:5
相关论文
共 37 条
[1]  
ANDERSON P, 1977, J INFECT DIS, V136, P557
[2]   PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE CAUSES CHRONIC BACTEREMIA RATHER THAN ACUTE SEPSIS IN MICE [J].
BENTON, KA ;
EVERSON, MP ;
BRILES, DE .
INFECTION AND IMMUNITY, 1995, 63 (02) :448-455
[3]   CONTRIBUTION OF AUTOLYSIN TO VIRULENCE OF STREPTOCOCCUS-PNEUMONIAE [J].
BERRY, AM ;
LOCK, RA ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1989, 57 (08) :2324-2330
[4]   REDUCED VIRULENCE OF A DEFINED PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE [J].
BERRY, AM ;
YOTHER, J ;
BRILES, DE ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1989, 57 (07) :2037-2042
[5]   PspA, a protection-eliciting pneumococcal protein: Immunogenicity of isolated native PspA in mice [J].
Briles, DE ;
King, JD ;
Gray, MA ;
McDaniel, LS ;
Swiatlo, E ;
Benton, KA .
VACCINE, 1996, 14 (09) :858-867
[6]  
BRILES DE, IN PRESS INFECT AGEN
[7]   PNEUMOCOCCAL BACTEREMIA - REVIEW OF 111 CASES, 1957-1969, WITH SPECIAL REFERENCE TO CASES WITH UNDETERMINED FOCUS [J].
BURKE, JP ;
KLEIN, JO ;
GEZON, HM ;
FINLAND, M .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1971, 121 (04) :353-+
[8]  
COWAN MJ, 1978, PEDIATRICS, V62, P721
[9]   PNEUMOCOCCAL SURFACE PROTEIN-A (PSPA) IS SEROLOGICALLY HIGHLY VARIABLE AND IS EXPRESSED BY ALL CLINICALLY IMPORTANT CAPSULAR SEROTYPES OF STREPTOCOCCUS-PNEUMONIAE [J].
CRAIN, MJ ;
WALTMAN, WD ;
TURNER, JS ;
YOTHER, J ;
TALKINGTON, DF ;
MCDANIEL, LS ;
GRAY, BM ;
BRILES, DE .
INFECTION AND IMMUNITY, 1990, 58 (10) :3293-3299
[10]  
DAMME MC, 1992, GASTROENTEROLOGY, V103, P520