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通过接种部位抗原滞留与免疫应答之间的关系阐明含铝佐剂的免疫增强机制。

Mechanism of immunopotentiation by aluminum-containing adjuvants elucidated by the relationship between antigen retention at the inoculation site and the immune response.

机构信息

Department of Industrial and Physical Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, IN 47907-2091, USA.

出版信息

Vaccine. 2010 Apr 30;28(20):3588-94. doi: 10.1016/j.vaccine.2010.02.085. Epub 2010 Mar 5.

Abstract

The relationship between depot formation and immunopotentiation was studied by comparing the retention of antigen at the inoculation site with antibody production in rats. A model (111)In-labeled alpha casein (IDCAS) antigen was formulated into four vaccines: IDCAS adsorbed onto either aluminum hydroxide adjuvant (AH) or aluminum phosphate adjuvant (AP); non-adsorbed IDCAS with phosphate-treated AP (PTAP); and IDCAS solution. Gamma scintigraphy showed the order of retention following subcutaneous administration to be: AH adsorbed>AP adsorbed>non-adsorbed with PTAP=solution. The antibody titers followed the order: non-adsorbed with PTAP=AP adsorbed>AH adsorbed>>solution. The presence of an aluminum-containing adjuvant was essential for immunopotentiation, but retention of the antigen at the inoculation site was not required.

摘要

我们通过比较抗原在接种部位的保留情况与大鼠的抗体产生情况,研究了贮存库形成与免疫增强之间的关系。将模型(111)In 标记的α-酪蛋白(IDCAS)抗原配制成四种疫苗:吸附于氢氧化铝佐剂(AH)或磷酸铝佐剂(AP)的 IDCAS;用磷酸盐处理的 AP 吸附的非吸附 IDCAS(PTAP);以及 IDCAS 溶液。γ闪烁显像显示,皮下给药后,其在体内的保留顺序为:吸附 AH>吸附 AP>非吸附并用 PTAP=溶液。抗体效价的顺序为:非吸附并用 PTAP=吸附 AP>吸附 AH>>溶液。铝佐剂的存在对免疫增强是必需的,但不需要抗原在接种部位的保留。

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