Reliability of laboratory models in the analysis of TBP2 and other meningococcal antigens
- 1 October 1994
- journal article
- Published by Oxford University Press (OUP) in FEMS Immunology & Medical Microbiology
- Vol. 9 (4) , 299-305
- https://doi.org/10.1111/j.1574-695x.1994.tb00365.x
Abstract
The lack of experimental models suitable for the study of meningococcal pathogenicity led us to investigate if those actually in use (culture in iron-restricted media and animal models) provide results comparable with the responses observed in vivo during infection. In this work we studied three invasive strains cultured both in laboratory media and in human plasma, analysing the immune responses elicited in mice against membrane antigens and comparing them with those seen using homologous human convalescent sera. Outer membrane protein profiles observed after culture in plasma were different and more complex than those obtained after growth in laboratory media. Analogous differences were observed in the antigenic profiles, detecting some antigens recognized by human, but not mouse sera, and vice versa. However, the response to one of the major iron-regulated outer membrane antigens, the transferrin binding protein 2 (TBP2), was unaffected by the culture medium or the model, human or mouse, used for the analysis. In conclusion, we have found that results of antigenic analysis change depending on the culture conditions and animal models used. For the meningococcal antigen TBP2, growth in iron-restricted laboratory media and a mouse model provide results which correlate well with those observed using convalescent human serum from individuals recovered from infections. We suggest that careful analysis and evaluation of experimental results and their comparison with in vivo elicited immune responses are essential in order to get accurate extrapolations for experimental vaccine designs.Keywords
This publication has 16 references indexed in Scilit:
- In vivo human immune response to transferrin-binding protein 2 and other iron-regulated proteins ofNeisseria meningitidisFEMS Immunology & Medical Microbiology, 1994
- The ferric iron‐binding protein of pathogenic Neisseria spp. functions as a periplasmic transport protein in iron acquisition from human transferrinMolecular Microbiology, 1993
- Purification of the Neisseria meningitidis transferrin binding protein-2 (TBP2) to homogeneity using column chromatographyFEMS Microbiology Letters, 1993
- Antigenic relationships of transferrin-binding proteins fromNeisseria meningitisis, N. gonorrhoeaeandHaemophilus influenzae: Cross-reactivity of antibodies to NH2-terminal peptidesFEMS Microbiology Letters, 1993
- Immunogenicity in adult males of a Neisseria meningitidis group B vaccine composed of polysaccharide complexed with outer membrane proteinsVaccine, 1991
- Antigenic and molecular heterogeneity of the transferrin-binding protein ofNeisseria meningitidisFEMS Microbiology Letters, 1990
- Reactogenicity and Immunogenicity of a Quadrivalent Combined Meningococcal Polysaccharide Vaccine in ChildrenThe Journal of Infectious Diseases, 1986
- Clear background and highly sensitive protein staining with Coomassie Blue dyes in polyacrylamide gels: A systematic analysisElectrophoresis, 1985
- Immunologic Response of Man to Group B Meningococcal Polysaccharide VaccinesThe Journal of Infectious Diseases, 1972
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970