The coiled-coil N-terminal domain of the heparin-binding haemagglutinin is required for the humoral and cellular immune responses in mice

被引:11
作者
Guerrero, Gloria G. [1 ,2 ,3 ]
F, P. Feunou [1 ,3 ]
Locht, C. [1 ,3 ]
机构
[1] Inst Pasteur, F-59019 Lille, France
[2] UJED, Fac Quim, Durango, Dgo, Mexico
[3] INSERM, U629, F-59045 Lille, France
关键词
alpha-helical; Coiled coil; HBHA; M; tuberculosis; Immunogenicity;
D O I
10.1016/j.molimm.2008.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Heparin-binding haemagglutinin (HBHA) is a 28-kDa mycobacterial adhesin, composed of three functional domains. Previous work has shown that the C-terminal methylated domain is important for adherence, and it is involved in protective T cell immunity in mouse models. However, the role of the coiled-coil N-terminal domain of HBHA in its overall immunogenic capacity remains elusive. Herein, a comparison of the antibody and cellular immune responses after subcutaneous and intranasal immunization of mice with HBHA (native and recombinant) revealed that the methylation pattern is important but not essential for this property. Subcutaneous immunization of mice with a truncated protein, rHBHA Delta C, which lacks the C-terminal methylated domain, was sufficient to trigger humoral and cellular immune responses to HBHA in mice. Altogether we provide evidence that the coiled-coil N-terminal domain is required for HBHA immunogenicity in vivo. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:116 / 124
页数:9
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