Immune activation with peptide assemblies carrying Lewis y tumor-associated carbohydrate antigen.

J Pept Sci

Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto Daigaku-Katsura, Nishikyo-ku, Kyoto, 615-8510, Japan.

Published: February 2017

Molecular assemblies varying morphologies in a wide range from spherical micelle, nanosheet, curved sheet, nanotube and vesicle were prepared and loaded with Lewis y (Le ) tumor-associated carbohydrate antigen on the assembly surface. The molecular assemblies were composed of poly(sarcosine) -block-poly(L-lactic acid) (m = 15 or 50, Lactosome), poly(sarcosine) -block-(D/L-Leu-Aib) (m = 22 or 30, n = 6 or 8) and their combinations. The molecular assemblies carrying Le on the surface were administered in BALB/c nu/nu mice. The major epitopes of the molecular assemblies are commonly Le and poly(sarcosine). IgM productions upon administrations of the molecular assemblies were assayed by ELISA, showing that anti-poly(sarcosine) IgM was highly produced by Lactosome of spherical micelle but with a negligible amount of anti-Le IgM. On the other hand, the nanosheet of the interdigitated monolayer triggered the production of anti-Le IgM but with less anti-poly(sarcosine) IgM production. Taken together, IgM specificity differs according to the molecular environment of the epitopes in the molecular assemblies. The antigenicity of poly(sarcosine) was augmented in polymeric micelle providing loose environment for B cells to penetrate in, whereas a high density of Le on the molecular assembly was required for anti-Le IgM production. The antigenicity of Le is therefore dependent on the molecular assemblies on which Le is displayed on the surface. Copyright © 2016 European Peptide Society and John Wiley & Sons, Ltd.

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http://dx.doi.org/10.1002/psc.2926DOI Listing

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