TLR4-dependent adjuvant activity of Neisseria meningitidis lipid A

被引:19
|
作者
Zughaier, Susu
Steeghs, Liana
van der Ley, Peter
Stephens, David S.
机构
[1] Emory Univ, Sch Med, Div Infect Dis, Dept Med, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Labs Microbial Pathogenesis, Dept Vet Affairs Med Ctr, Atlanta, GA 30322 USA
[3] Univ Utrecht, Dept Infect Dis & Immunol, Utrecht, Netherlands
关键词
lipid A; IgG titer; adjuvanticity; TLR4;
D O I
10.1016/j.vaccine.2007.03.029
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The adjuvant activity of Neisseria meningitidis serogroup B lipopoly(oligo)saccharide (LOS) from wild-type and genetically defined LOS mutants and unglycosylated meningococcal lipid A was assessed in C3H/HeN and C3H/HeJ mice. Meningococcal lipid A, a weak agonist for TLR4/MD-2 in human macrophages, was found to have adjuvant activity similar to that of wild-type and KDO2-lipid A LOS in C3H/HeN mice. All meningococcal LOS structures as adjuvants induced high titers of IgG1, IgG2a and IgG2b but very little IgG3 to OMP compared to no adjuvant PBS controls. In addition, induced OMP antibodies were shown to have high bactericidal activity against serogroup B meningococci. Purified LOS and lipid A structures failed to induce any adjuvant activity in C3H/HeJ mice indicating that meningococcal LOS as an adjuvant was TLR4-dependent. Unglycosylated meningococcal lipid A because of its weak agonist activity for human macrophages and retention of adjuvant activity may be a candidate for use in serogroup B meningococcal OMP and OMV vaccines and for use as an adjuvant in other vaccines. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4401 / 4409
页数:9
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