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SUMMARYThe CpG motifs of bacterial-derived plasmids augment antigen-specific immune responses and steer those responses towards the T helper 1 ( Th1) type. In this study, we have addressed the immuno-stimulatory effect of intramuscular co-administration of CpG motifs containing vector DNA on the modulation of immune responses to the haemagglutinin (HA) and the nucleoprotein (NP) proteins of influenza virus. The co-administration of vector DNA with a HA-encoding plasmid DNA showed a significant enhancement in the total IgG response, the generation of cytotoxic T lymphocyte (CTL), and the T-cell proliferative response. In the case of NP-encoding plasmid DNA inoculations, the co-administration of vector DNA slightly decreased the total IgG response, although the IgG2a/IgG1 ratio and the CTL responses to NP were significantly increased. These observations suggest that the immuno-stimulatory effects of bacterial-derived plasmids depend upon the nature of the co-administered antigen.

Four polyimides containing hexylene spacer and a fluorostilbene unit in the side chains were prepared in thin‐film form by two‐step condensation of 3,3′‐bis[(4′‐fluoro‐4‐stilbenyl)oxyhexyloxy]‐4,4′‐biphenyldiamine (FS6B) with pyromellitic dianhydride (PMDA), benzophenone‐3,3′,4,4′‐tetracarboxylic dianydride (BTDA), 4,4′‐oxydi(phthalic anhydride) (ODPA), and 4,4′‐hexafluoroisopropylidenedi(phthalic anhydride) (6FDA), respectively, and their controllability of liquid crystal (LC) alignment on rubbed surfaces was investigated. Pretilt angles of LCs were achieved in the 2–9° range, depending on the rubbing density and backbone structures. The effect of the mesogenic stilbene group on the pretilting of LCs was distinctive in FS6B‐PMDA. Contact‐angle measurements on thin films annealed at 120 °C revealed that FS6B‐PMDA potentially had the better alignment stability than FS6B‐6FDA. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3622–3632, 2001

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Four different polyimides with side chains containing undecyl spacers and 4-fluorostilbene mesogen end groups were prepared, and their structures and the controllability of the liquid-crystal (LC) alignment with rubbing were investigated. From X-ray scattering and differential scanning calorimetry data, pyromellitic dianhydride (PMDA)-, benzophenone-3,3Ј,4,4Ј-tetracarboxylic dianhydride (BTDA)-, and 4,4Јoxydi(phthalic anhydride) (ODPA)-based polyimides were shown to have layered structures and short-range ordering. Pretilt angles of LCs on the rubbed surfaces were 1-9°, depending on the rubbing density and backbone. In particular, the long undecyl spacers caused the mesogenic stilbene end groups to lie next to the main chain, resulting in a reduction in the pretilt angles.