Clonotypic analysis of human antibodies specific for Neisseria meningitidis polysaccharides A and C in adults

Serum antibodies to the capsular polysaccharides A and C (PSA and PSC) of N. meningitidis in healthy adults before and after vaccination with the sole polysaccharides were analysed by isoelectric focusing (IEF). Before vaccination, 49% and 28% had naturally acquired antibodies against PSA and PSC, respectively, whereas 18 days after vaccine administration 84% and 91%, respectively, showed a detectable spectrotypic pattern. Oligoclonality appeared to be the main feature of naturally acquired and vaccine‐induced antibodies for both polysaccharides. In all subjects the anti‐PSA response, showing dominant bands at the same pH position, was more homogeneous than anti‐PSC one. Most subjects with naturally acquired antibodies (25 out of 38 for PSA and 20 out of 22 for PSC) showed a spectrotypic pattern after vaccination, similar to that observed before vaccination (any differences were just related to band intensity), suggesting that PSA and PSC are able to recruit the same B cell clones previously primed with a T‐dependent form of the antigen, i.e. the whole bacterium. However, in one‐third of subjects with naturally acquired anti‐PSA antibodies, the appearance of new alkaline bands after vaccination was observed. Furthermore, in subjects with absence of detectable natural antibodies, the vaccine‐induced antibody response started in correspondence of alkaline pH areas, subsequently extending to neutral and acidic areas. Therefore, it may be hypothesized that alkaline antibody‐secreting B cell clones are the first to be recruited. The final spectrotype in these subjects was similar to that observed in subjects with naturally acquired antibodies. This observation, together with the above reported data, allow us to conclude that natural (T‐dependent pathway) and vaccine (T‐independenl pathway) immunization induce the expression of the same antibody repertoire, for both meningococcal PSA and PSC.

[1]  P. Lambert,et al.  Spectrotypic analysis of humoral response in human hydatidosis. , 1989, Clinical and experimental immunology.

[2]  C. Taylor,et al.  T-cell modulation of the antibody response to bacterial polysaccharide antigens , 1989, Infection and immunity.

[3]  P. Lambert,et al.  Igh-C allotype-linked control of anti-DNA production and clonotype expression in mice infected with Plasmodium yoelii. , 1988, Journal of immunology.

[4]  M. Apicella,et al.  T-cell modulation of the murine antibody response to Neisseria meningitidis group A capsular polysaccharide , 1988, Infection and immunity.

[5]  C. von Hunolstein,et al.  IgG subclasses to group B streptococci in normals, colonized woman and IgG2 subclass-deficient patients. , 1988, Monographs in allergy.

[6]  S. Datta,et al.  Induction of a cationic shift in IgG anti-DNA autoantibodies. Role of T helper cells with classical and novel phenotypes in three murine models of lupus nephritis , 1987, The Journal of experimental medicine.

[7]  D. Granoff,et al.  Subclass distribution of human antibodies to Haemophilus influenzae type b capsular polysaccharide. , 1987, Journal of immunology.

[8]  P. Anderson,et al.  Oligosaccharide-protein conjugate vaccines induce and prime for oligoclonal IgG antibody responses to the Haemophilus influenzae b capsular polysaccharide in human infants , 1986, The Journal of experimental medicine.

[9]  P. Baker,et al.  The role of antigen in the activation of regulatory T cells by immune B cells. , 1985, Cellular immunology.

[10]  P. Anderson,et al.  Isoelectric focusing of human antibody to the Haemophilus influenzae b capsular polysaccharide: restricted and identical spectrotypes in adults. , 1985, Journal of immunology.

[11]  M. Cadoz,et al.  Tetravalent (A, C, Y, W 135) meningococcal vaccine in children: immunogenicity and safety. , 1985, Vaccine.

[12]  C. Adamsbaum,et al.  AGE-SPECIFIC DIFFERENCES IN DURATION OF CLINICAL PROTECTION AFTER VACCINATION WITH MENINGOCOCCAL POLYSACCHARIDE A VACCINE , 1985, The Lancet.

[13]  P. Mäkelä,et al.  Serum antibodies after vaccination with Haemophilus influenzae type b capsular polysaccharide and responses to reimmunization: no evidence of immunologic tolerance or memory. , 1984, Pediatrics.

[14]  C. Frasch Immunization against Neisseria meningitidis , 1983 .

[15]  M. Hilleman,et al.  Vaccination and Revaccination with Polyvalent Pneumococcal Polysaccharide Vaccines in Adults and Infants , 1978, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[16]  E. Gotschlich,et al.  Immune Response of human infants of polysaccharide vaccines of group A and C Neisseria meningitidis. , 1977, The Journal of infectious diseases.

[17]  D. Briles,et al.  Clonal dominance. I. Restricted nature of the IgM antibody response to group A streptococcal carbohydrate in mice , 1975, The Journal of experimental medicine.

[18]  D. Smith,et al.  Responses of children immunized with the capsular polysaccharide of Hemophilus influenzae, type b. , 1973, Pediatrics.

[19]  R. Axén,et al.  Chemical fixation of enzymes to cyanogen halide activated polysaccharide carriers. , 1971, European journal of biochemistry.

[20]  A. Williamson,et al.  Selection of a single antibody-forming cell clone and its propagation in syngeneic mice. , 1970, Proceedings of the National Academy of Sciences of the United States of America.

[21]  F. Greenwood,et al.  THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY. , 1963, The Biochemical journal.