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Characterization of immunogenic properties of haptenated liposomal model membranes in mice. V. Effect of membrane composition on humoral and cellular immunogenicity.

机译:小鼠半抗原脂质体模型膜的免疫原性表征。 V.膜组成对体液和细胞免疫原性的影响。

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摘要

This paper describes the effect of altering liposomal membrane composition on humoral and cellular immunogenicity of haptenated liposomes in mice. Antibody formation was determined by enumeration of direct, plaque-forming cells in the spleen and delayed-type hypersensitivity (DH) was measured with a footpad swelling test. Humoral immunogenicity of haptenated liposomes was strongly influenced by membrane phospholipid, cholesterol and charged amphiphile composition. Haptenated liposomes prepared from phospholipids with a low (dioleoyl- and dilauroyl-phosphatidylcholine) or high (distearoyl phosphatidylcholine) phase-transition temperature were less immunogenic than those prepared from phospholipids with an intermediate phase-transition temperature (dipalmitoyl phosphatidylcholine and sphingomyelin). In general, increasing the amount of liposomal membrane cholesterol induced a higher humoral response. These results are discussed in relation to liposomal membrane fluidity. Induction of an optimal DH with haptenated liposomes did not occur in the absence of the adjuvant dimethyl dioctadecyl ammonium bromide (DDA). When DDA was used, alterations in membrane composition did not influence cellular immunogenicity. From these results it was concluded that 'intermediate' liposomal membrane fluidity is the most important requirement for induction of optimal antibody formation with haptenated liposomes and that a certain physicochemical configuration of the antigen, provided by the adjuvant DDA, is a prerequisite for induction of DH.
机译:本文描述了改变脂质体膜组成对小鼠半抗原脂质体的体液和细胞免疫原性的影响。通过枚举脾脏中直接形成斑块的细胞来确定抗体的形成,并通过脚垫肿胀测试测量迟发型超敏反应(DH)。半透明脂质体的体液免疫原性受到膜磷脂,胆固醇和带电两亲物组成的强烈影响。由具有低(二油酰基和二月桂酰-磷脂酰胆碱)相或高(二硬脂酰基磷脂酰胆碱)相转变温度的磷脂制备的半抗原化脂质体的免疫原性低于由具有中间相转变温度的磷脂(二棕榈酰磷脂酰胆碱和鞘磷脂)制备的脂质体的免疫原性。通常,增加脂质体膜胆固醇的量会引起更高的体液反应。这些结果与脂质体膜的流动性有关。在没有佐剂二甲基二十八烷基溴化铵(DDA)的情况下,未用半抗原脂质体诱导最佳DH。当使用DDA时,膜组成的改变不影响细胞免疫原性。从这些结果可以得出结论,“中间”脂质体膜流动性是诱导半抗原脂质体形成最佳抗体的最重要条件,佐剂DDA提供的抗原的某些理化构型是诱导DH的前提条件。

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