Characterization of a multi-lipopeptides mixture used as an HIV-1 vaccine candidate

被引:41
作者
Klinguer, C
David, D
Kouach, M
Wieruszeski, JM
Tartar, A
Marzin, D
Levy, JP
Gras-Masse, H [1 ]
机构
[1] Univ Lille 2, Fac Pharmaceut Sci, F-59045 Lille, France
[2] Inst Pasteur Lille, IBL, UMR 8528, F-59021 Lille, France
[3] Inst Pasteur Lille, Toxicol Lab, F-59021 Lille, France
[4] Univ Lille 2, Fac Med Henri Warembourg, Lab Spectrometrie Masse, F-59045 Lille, France
[5] Inst Cochin Genet Mol, INSERM, Lab Immunol Pathol Infect & Tumorale, U445, F-75014 Paris, France
关键词
lipopeptide; synthetic vaccine; characterization;
D O I
10.1016/S0264-410X(99)00196-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A multi-component vaccine has been defined, which contains six different synthetic 24- to 32-amino acid lipopeptides derived from the sequence of HIV-I proteins. The physicochemical properties of the lipopeptide components were compatible with multi-dimensional analysis, using RP-HPLC, Edman sequencing, electrospray mass spectrometry, and 2D-NMR. Detailed analysis of the impurity profiles led to the detection and evaluation of the relative proportions of most by-products: several contaminants resulted from the formation of acetylated fragments, transpeptidation reactions with succinimide or piperidide formation, or methionine and/or tryptophan mono-oxidations. The first batch to be produced underwent extensive pharmacotoxicological testings to confirm its safety; this vaccine candidate has now been used in phase I clinical trials. Despite the complexity of such multi-lipopeptide vaccines, our findings suggest the possibility of preparing a clear and precise assignment of by-products to toxicologically qualified impurities in the eventuality of a future production of several successive batches. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:259 / 267
页数:9
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