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Infection and Immunity, September 2003, p. 5115-5120, Vol. 71, No. 9
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.9.5115-5120.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Preparation and Characterization of Group A Meningococcal Capsular Polysaccharide Conjugates and Evaluation of Their Immunogenicity in Mice

Zhigang Jin,* Chiayung Chu, John B. Robbins, and Rachel Schneerson

Laboratory of Developmental and Molecular Immunity, National Institute of Child Health and Development, National Institutes of Health, Bethesda, Maryland 20892

Received 10 March 2003/ Returned for modification 24 April 2003/ Accepted 30 May 2003

Epidemic and endemic meningitis caused by group A Neisseria meningitidis remains a problem in sub-Saharan Africa. Although group A meningococcal capsular polysaccharide (GAMP) vaccine confers immunity at all ages, the improved immunogenicity of a conjugate and its compatibility with the World Health Organization's Extended Program on Immunization offers advantages over GAMP alone. Conjugates of GAMP bound to bovine serum albumin (BSA) were synthesized, characterized, and evaluated for their immunogenicities in mice. Two methods, involving adipic acid dihydrazide (ADH) as a linker, were used. First, ADH was bound to GAMP activated with cyanogen bromide (CNBr) or with 1-cyano-4(dimethylamino)-pyridinium tetrafluoroborate (CDAP) to form GAMPCNBrAH and GAMPCDAPAH. These derivatives were bound to BSA by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) to form GAMPCNBrAH-BSA and GAMPCDAPAH-BSA. Second, ADH was bound to BSA with EDC to form AHBSA. AHBSA was bound to activated GAMP to form GAMPCNBr-AHBSA and GAMPCDAP-AHBSA. The yield of GAMPCDAP-AHBSA (35 to 40%) was higher than those of the other conjugates (5 to 20%). GAMP conjugates elicited immunoglobulin G (IgG) anti-GAMP in all mice after three injections of 2.5 or 5.0 µg of GAMP: the geometric mean (GM) was highest in recipients of GAMPCDAP-AHBSA (11.40 enzyme-linked immunosorbent assay units). Although the difference was not statistically significant, the 5.0-µg dose elicited a higher GM IgG anti-GAMP than the 2.5-µg dose. Low levels of anti-GAMP were elicited by GAMP alone. GAMPCDAP-AHBSA elicited bactericidal activity roughly proportional to the level of IgG anti-GAMP.


* Corresponding author. Mailing address: National Institute of Child Health and Development, National Institutes of Health, Building 6, Room 424, Bethesda, MD 20892-2720. Phone: (301) 496-6141. Fax: (301) 402-9108. E-mail: jinz{at}mail.nih.gov.

Editor: J. N. Weiser


Infection and Immunity, September 2003, p. 5115-5120, Vol. 71, No. 9
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.9.5115-5120.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

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