Global control and prevention of meningococcal disease depends on the furth
er development of vaccines that overcome the Limitations of the current pol
ysaccharide vaccines. Protein-polysaccharide conjugate vaccines likely will
address the marginal protective antibody responses and short duration of i
mmunity in young children derived from the A, C, T, and W-135 capsular poly
saccharides, but they will be expensive to produce and purchase and may not
offer a practical solution to the countries with greatest need. In additio
n, outer membrane proteins vaccines have been tested extensively in humans
and hold some promise in the development of a serogroup B vaccine but are L
imited by the antigenic variability of these subcapsular antigens and the r
esulting strain-specific protection. Elimination of meningococcal disease l
ikely will require a novel approach to vaccine development, ideally incorpo
rating a safe and effective antigen or antigens common to all meningococcal
serogroups. As a solely human pathogen, however, N. meningitidis has devel
oped many teals with which to evade the human immune system and likely will
pose a formidable challenge for years to come.