Influence of maternal antibodies on vaccine responses: Inhibition of antibody but not T cell responses allows successful early prime-boost strategies in mice

European Journal of Immunology

Volumn 28, Issue 12, 1998, Pages 4138-4148

  Siegrist, Claire Anne ^a,b   Barrios, Christy ^a   Martinez, Xavier ^a   Brandt, Christian ^a   Berney, Monika ^a   Córdova, Marco ^a   Kovarik, Jiri ^a   Lambert, Paul Henri ^a  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b WORLD HEALTH ORGANIZATION   (Switzerland)

Author keywords

Immunization; Infant; Maternal antibody; Measles; Vaccine

Indexed keywords

ANTIBODY; DNA VACCINE; GAMMA INTERFERON; HEMAGGLUTININ; INTERLEUKIN 5; LIVE VACCINE; MATERNAL ANTIBODY; MEASLES VACCINE; TETANUS TOXOID;

ANIMAL CELL; ANIMAL EXPERIMENT; ANTIBODY RESPONSE; ANTIBODY TITER; ARTICLE; CELLULAR IMMUNITY; CONTROLLED STUDY; EXPRESSION VECTOR; FEMALE; IMMUNIZATION; LYMPHOCYTE PROLIFERATION; MOUSE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; T LYMPHOCYTE;

EID: 0031768411     PISSN: 00142980     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-4141(199812)28:12<4138::aid-immu4138>3.0.co;2-l     Document Type: Article

References (33)

1. Leach, J. L., Sedmak, D. D., Osborne, J. M., Rahill, B., Lairmore, M. D. and Anderson, C. L., Isolation from human placenta of the IgG transporter, FcRn, and localization to the syncytiotrophoblast. J. Immunol. 1996. 157: 337-332.
2. Osborn, J. J., Dancis, J. and Julia, J. F., Studies of the immunology of the newborn infant. II Interference with active immunization by passive transplacental circulating antibody. Pediatrics 1952. 10: 328-334.
3. Albrecht, P., Ennis, F. A., Saltzman, E. J. and Krugman, S., Persistence of maternal antibody in infants beyond 12 months: mechanism of measles vaccine failure. J. Pediatr. 1977. 91: 715-718.
4. Burström, B., Aaby, P., Mutie, D. M., Kimani, G. and Bjerregaard, P., Severe measles outbreak in Western Kenya. East Afr. Med. J. 1992. 69: 419-423.
5. Malfait, P., Jataou, I. M., Jollet, M. C., Margot, A., De Benoist, A. C. and Moren, A., Measles epidemic in the urban community of Niamey: transmission patterns, vaccine efficacy and immunization strategies, Niger 1990 to 1991. Pediatr. Infect. Dis. J. 1994. 13: 38-45.
6. WHO Study Group on oral polio vaccine, Factors affecting the immunogenicity of oral poliovirus vaccine: a prospective evaluation in Brazil and the Gambia. J. Infect. Dis. 1995. 171: 1097-1106.
7. Booy, R., Aitken, S. J. M., Taylor, S., Tudor-Williams, G., Macfarlane, J. A., Moxon, E. R., Ashworth, L. A., Mayon-White, R. T., Griffiths, H. and Chapel, H. M., Immunogenicity of combined diphtheria, tetanus, and pertussis vaccine given at 2, 3, and 4 months versus 3, 5, and 9 months of age. Lancet 1992. 339: 507-510.
8. Sarvas, H., Kurikka, S., Seppala, I. J., Makela, P. H. and Makela, O., Maternal antibodies partly inhibit an active antibody response to routine tetanus toxoid immunization in infants. J. Infect. Dis. 1992. 165: 977-979.
9. Björkholm, B., Granström, M., Taranger, J., Wahl, M. and Hagberg, L., Influence of high titers of maternal antibody on the serologic response of infants to diphtheria vaccination at three, five and twelve months of age. Ped. Infect. Dis. J. 1995. 14: 846-850.
10. Englund, J. A., Anderson, E. L., Reed, G., Decker, M. D., Edwards, K. M., Pichichero, M. E., Steinhoff, M. C., Rennels, M. B., Deforest, A. and Meade, B., The effect of maternal antibody on the serologic response and the incidence of adverse reactions after primary immunization with a cellular and whole-cell pertussis vaccines combined with diphtheria and tetanus toxoids. Pediatrics 1995. 96 (suppl): 580-584.
11. Uhr, J. W. and Baumann, J., Antibody formation. I. The suppression of antibody formation by passively administered antibody. J. Exp. Med. 1961. 113: 395-397.
12. Mills, K. H. G., Inhibitory effects of monoclonal antibodies to a synthetic peptide of influenza hemagglutinin on the processing and presentation of viral antigens to class II-restricted T-cell clones. Immunology 1988. 65: 365-371.
13. Jemmerson, R., Johnson, J. G., Burrell, E., Taylor, P. S. and Jenkins, M. K., A monoclonal antibody specific for a cytochrome c T cell stimulatory peptide inhibits T cell responses and affects the way the peptide associates with antigen-presenting cells. Eur. J. Immunol. 1991. 21: 143-151.
14. Watts, C. and Lanzavecchia, A., Suppressive effect of antibody on processing of T cell epitopes. J. Exp. Med. 1993. 178: 1459-1463.
15. Celis, E., Zurawsky, Jr. V. R. and Chang, T. W., Regulation of T cell function by antibodies: enhancement of the response of human T-cell clones to hepatitis B surface antigen by antigen-specific monoclonal antibodies. Proc. Natl. Acad. Sci. USA 1984. 81: 6846-6850.
16. Schalke, B. C. G., Klinkert, W. E. F., Wekerle, H. and Dwyer, D. S., Enhanced activation of a T cell line specific for acetylcholine receptor (AChR) by using anti-AChR monoclonal antibodies plus receptors. J. Immunol. 1985. 134: 3643-3648.
17. Simitsek, P. D., Campbell, D. G., Lanzavecchia, A., Fairweather, N. and Watts, C., Modulation of antigen processing by bound antibodies can boost or suppress class II Major Histocompatibility Complex presentation of different T cell determinants. J. Exp. Med. 1995. 181: 1957-1963.
18. Duc, H. T., Rucay, P., Righenzi, S., Halle-Pannenko, O. and Kourilsky, P., Monoclonal antibodies directed against T cell epitopes presented by class I MHC antigens. Int. Immunol. 1993. 5: 427-431.
19. Harte, P. G. and Playfair, J. H. L., Failure of malaria vaccination in mice born to immune mothers. II. Induction of specific suppressor cells by maternal IgG. Clin. Exp. Immunol. 1983. 51: 157-164.
20. Xiang, Z. Q. and Ertl, H. C. J., Transfer of maternal antibodies results in inhibition of specific immune responses in the offspring. Virus Res. 1992. 24: 297-314.
21. Bangham, C. R. M., Passively acquired antibodies to Respiratory Syncytial virus impair the secondary cytotoxic T cell response in the neonatal mice. Immunology 1986. 59: 37-41.
22. Hasset, D. E., Zhang, J. and Whitton, J. L., Neonatal DNA immunization with a plasmid encoding an internal viral protein is effective in the presence of maternal antibodies and protects against subsequent viral challenge. J. Virol. 1997. 71: 7881-7888.
23. Manickan, E., Yu, Z. and Rouse, B. T., DNA immunization of neonates induces immunity despite the presence of maternal antibody. J. Clin. Invest. 1997. 100: 2371-2375.
24. Wang, Y., Xiang, Z., Pasquini, S. and Ertl, H. C. J., Effect of passive immunization or maternally transferred immunity on the antibody response to a genetic vaccine to rabies virus. J. Virol. 1998. 72: 1790-1796.
25. Monteil, M., Le Potier, M. F., Guillotin, J., Cariolet, R., Houdayer, C. and Eloit, M., Genetic immunization of seronegative one-day-old piglets against pseudorabies induces neutralizing antibodies but not protection and is ineffective in piglets from immune dams. Vet. Res. 1996. 27: 443-452.
26. Le Potier, M. F., Monteil, M., Houdayer, C. and Eloit, M., Study of the delivery of the gD gene of pseudorabies virus to one-day-old piglets by adenovirus or plasmid DNA as ways to bypass the inhibition of immune responses by colostral antibodies. Vet. Microbiol. 1997. 55: 75-80.
27. Barrios, C., Brawand, P., Berney, M., Brandt, C., Lambert, P. H. and Siegrist, C. A., Neonatal and early life immune responses to various forms of vaccine antigens qualitatively differ from adult responses: predominance of a TH2-biased pattern which persists after adult boosting. Eur. J. Immunol. 1996. 26: 1489-1496.
28. Martinez, X., Brandt, C., Saddallah, F., Tougne, C., Barrios, C., Wild, F., Dougan, G., Lambert, P. H. and Siegrist, C. A., DNA immunization circumvents deficient induction of TH1 and CTL responses in early life. Proc. Natl. Acad. Sci. USA 1997. 94: 8726-8731.
29. Davis, H. L., Brazolot Millan, C. L. and Watkins, S. C., Immune-mediated destruction of transfected muscle fibers after direct gene transfer with antigen-expressing plasmid DNA. Gene Ther. 1997. 4: 181-188.
30. van Binnendijk, R. S., Peolen, M. C. M., van Amerongen, G., de Vries, P. and Osterhaus, A. D. M. E., Protective immunity in macaques vaccinated with live attenuated, recombinant and subunit measles vaccines in the presence of passively acquired antibodies. J. Infect. Dis. 1997. 175: 534-542.
31. Cherry, J. D., Feigin, R. D., Schackelford, P. G., Hinthorn, D. R. and Schmidt, R. R., A clinical and serologic study of 103 children with measles vaccine failure. J. Pediatr. 1973. 82: 802-808.
32. McGraw, T. T., Reimmunization following early immunization with measles vaccine: a prospective study. Pediatrics 1986. 77: 45-48.
33. Stetler, H. C., Orenstein, W. A., Bernier, R. H., Herrmann, K. L., Sirotkin, B., Hopfensperger, D., Schuh, R., Albrecht, P., Lievens, A. W. and Brunell, P. A., Impact of revaccinating children who initially received measles vaccine before 10 months of age. Pediatrics 1986. 77: 471-476.