抗原掺入脂质体导致IL-4和IgG1分泌增强:Th-2细胞优先扩增的证据。

Cytokines and molecular therapy Pub Date : 1996-03-01
J N Agrewala, M Owais, C M Gupta, G C Mishra
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引用次数: 0

摘要

脂质体已被用来修饰许多抗原的免疫行为。本研究旨在通过监测淋巴因子和IgG同型的分泌来评估卵清蛋白脂质体化对诱导Th-1和th -2细胞反应的影响。脂质体具有不同的物理化学性质(带正电荷和负电荷,中性和ph敏感)用于此目的。以这种方式传递的卵清蛋白诱导IL-4的优先分泌和抗原特异性IgG1同种型的产生。这与脂质体的表面电荷性质无关。此外,在脂质体中包封后,激活Th细胞所需的抗原浓度降低了10(2)至10(3)倍。这些结果表明脂质体可能被证明是启动th2样免疫反应的有用佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antigen incorporation into liposomes results in the enhancement of IL-4 and IgG1 secretion: evidence for preferential expansion of Th-2 cells.

Liposomes have been used to modify the immunological behaviour of a number of antigens. The present study was designed to evaluate the effect of liposomization of ovalbumin on the induction of Th-1 and Th-2-cell response by monitoring the secretion of lymphokines and IgG Isotypes. Liposomes having varied physicochemical properties (positively and negatively charged, neutral and pH-sensitive) were used for this purpose. Ovalbumin delivered in this way induced preferential secretion of IL-4 and production of antigen-specific IgG1 isotypes. This was observed irrespective of the surface charge properties of the liposomes. Further, the concentration of antigen required for the activation of Th cells was 10(2)- to 10(3)-fold lower after encapsulating it in liposomes. These results suggest that liposomes may prove useful adjuvants to prime Th2-like immune responses.

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