DESCRIPTION OF A HYBRIDOMA BANK TOWARDS BORDETELLA-PERTUSSIS TOXIN AND SURFACE-ANTIGENS

被引:31
作者
POOLMAN, JT
KUIPERS, B
VOGEL, ML
HAMSTRA, HJ
NAGEL, J
机构
[1] Laboratory of Bacterial Vaccines, National Institute of Public Health and Environmental Protection (RIVM), 3720 BA Bilthoven
关键词
Bordetella pertussis; monoclonal antibody; surface antigen;
D O I
10.1016/0882-4010(90)90024-K
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
This paper describes the development of a murine bank of monoclonal antibodies against Bordetella pertussis toxin, filamentous hemagglutinin (FHA), pili, lipopolysaccharide (LPS), or outer membrane proteins (OMPs). Subunits S1, S2, S3 of pertussis toxin (PT) bound immunoglobulins and glycoproteins such as fetuin and haptoglobin in an unspecific manner. The specificity of monoclonal antibodies towards subunits S1, S2, S3 or S4 of PT could be demonstrated by using purified immunoglobulins or their Fab2 fragments. A set of FHA-specific monoclonal antibodies could be differentiated on the basis of their binding to the various breakdown products present in FHA preparations. Pili-specific monoclonal antibodies reacted with either native pili or denatured pilin, and both demonstrated serotype specificity. Monoclonal antibodies to Bordetella pertussis OMPs were directed to either the virulent phase-regulated trypsin-sensitive, detergent-extractable OMPs 92 kDa, 32 kDa, and 30 kDa or the non-virulent phase-expressed, not-trypsin sensitive OMPs 38 kDa, 33kDa, and 18 kDa. © 1990.
引用
收藏
页码:377 / 382
页数:6
相关论文
共 20 条
[1]   NEISSERIA-MENINGITIDIS GROUP-B SEROSUBTYPING USING MONOCLONAL-ANTIBODIES IN WHOLE-CELL ELISA [J].
ABDILLAHI, H ;
POOLMAN, JT .
MICROBIAL PATHOGENESIS, 1988, 4 (01) :27-32
[2]   BORDETELLA-PERTUSSIS MAJOR OUTER-MEMBRANE PORIN PROTEIN FORMS SMALL, ANION-SELECTIVE CHANNELS IN LIPID BILAYER-MEMBRANES [J].
ARMSTRONG, SK ;
PARR, TR ;
PARKER, CD ;
HANCOCK, REW .
JOURNAL OF BACTERIOLOGY, 1986, 166 (01) :212-216
[3]   SURFACE-PROTEINS OF BORDETELLA-PERTUSSIS - COMPARISON OF VIRULENT AND AVIRULENT STRAINS AND EFFECTS OF PHENOTYPIC MODULATION [J].
ARMSTRONG, SK ;
PARKER, CD .
INFECTION AND IMMUNITY, 1986, 54 (02) :308-314
[4]   IDENTIFICATION OF A 69-KILODALTON NONFIMBRIAL PROTEIN AS AN AGGLUTINOGEN OF BORDETELLA-PERTUSSIS [J].
BRENNAN, MJ ;
LI, ZM ;
COWELL, JL ;
BISHER, ME ;
STEVEN, AC ;
NOVOTNY, P ;
MANCLARK, CR .
INFECTION AND IMMUNITY, 1988, 56 (12) :3189-3195
[5]   SOLUBILIZATION OF CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI BY IONIC DETERGENT SODIUM-LAURYL SARCOSINATE [J].
FILIP, C ;
FLETCHER, G ;
WULFF, JL ;
EARHART, CF .
JOURNAL OF BACTERIOLOGY, 1973, 115 (03) :717-722
[6]  
IRONS LI, 1983, J GEN MICROBIOL, V129, P2769
[7]   CHARACTERIZATION OF FIMBRIAL SUBUNITS FROM BORDETELLA SPECIES [J].
MOOI, FR ;
VANDERHEIDE, HGJ ;
TERAVEST, AR ;
WELINDER, KG ;
LIVEY, I ;
VANDERZEIJST, BAM ;
GAASTRA, W .
MICROBIAL PATHOGENESIS, 1987, 2 (06) :473-484
[8]   PEROXIDASE-LABELED ANTIBODY - NEW METHOD OF CONJUGATION [J].
NAKANE, PK ;
KAWAOI, A .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1974, 22 (12) :1084-1091
[9]   SEPARATION OF UNIVALENT FRAGMENTS FROM THE BIVALENT RABBIT ANTIBODY MOLECULE BY REDUCTION OF DISULFIDE BONDS [J].
NISONOFF, A ;
WISSLER, FC ;
LIPMAN, LN ;
WOERNLEY, DL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1960, 89 (02) :230-244
[10]  
PARKER CD, 1988, REV INFECT DIS, V10, pS327