The common Cryptococcus neoformans glucuronoxylomannan M2 motif elicits non-protective antibodies

被引:24
|
作者
Nakouzi, Antonio [2 ]
Zhang, Tong [2 ]
Oscarson, Stefan [3 ]
Casadevall, Arturo [1 ,2 ]
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Div Infect Dis, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[3] Univ Coll Dublin, UCD Sch Chem & Chem Biol, Ctr Synth & Chem Biol, Dublin 4, Ireland
关键词
Antibody; Cryptococcus neoformans; Immune response; Vaccine; TOXOID CONJUGATE VACCINE; CAPSULAR POLYSACCHARIDE; MONOCLONAL-ANTIBODIES; FINE SPECIFICITY; INFECTION; FUNGAL; MICE; IMMUNOGENICITY; MIMOTOPE; EFFICACY;
D O I
10.1016/j.vaccine.2009.03.089
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 Cryptococcus neoformans capsular glucuronoxylomannan (GXM) is a potential vaccine antigen that can elicit protective and non-protective antibodies. In an attempt to focus the immune response on a single antigenic component, a heptasaccharide oligosaccharide representing the major structural motif (M2) of the most common clinical isolate was synthesized and conjugated to human serum albumin (HSA). Monoclonal antibodies (mAbs) generated from mice immunized with M2-HSA produced the characteristic punctuate immunofluorescence associated with non-protective mAbs. None of the mAbs elicited by M2 immunization was opsonic. Passive administration of mAbs elicited by M2-HSA was not protective and there was no difference in the Survival Of Mice immunized with M2-HSA and HSA. Hence, we conclude that the M2 motif represents an antigenic determinant in C. neoformans GXM that elicits non-protective responses and is not a suitable vaccine candidate. Furthermore, the results illustrate the first molecular assignment of a C. neoformans polysaccharide epitope and suggest a general strategy for the identification of GXM epitopes. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3513 / 3518
页数:6
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