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乳香(BOS 2000)对卵清蛋白特异性抗体和细胞应答的免疫佐剂效应在小鼠体内的研究。

Immunological adjuvant effect of Boswellia serrata (BOS 2000) on specific antibody and cellular response to ovalbumin in mice.

机构信息

Division of Pharmacology, Indian Institute of Integrative Medicine, Canal Road, Jammu Tawi, Pin code 180001, India.

出版信息

Int Immunopharmacol. 2011 Aug;11(8):968-75. doi: 10.1016/j.intimp.2011.02.011. Epub 2011 Mar 1.

Abstract

In this study, the biopolymeric fraction BOS 2000 from Boswellia serrata was evaluated for its potential ability as adjuvants on the immune responses to ovalbumin (OVA) in mice. Balb/c mice were immunized subcutaneously with OVA 100 μg alone or with OVA 100 μg dissolved in saline containing alum (200 μg) or BOS 2000 (10, 20, 40 and 80 μg) on Days 1 and 15. Two weeks later, OVA specific antibodies in serum; concanavalin A (Con A), OVA stimulated splenocyte proliferation, CD4/CD8/CD80/CD86 analysis in spleen cells and its estimation of cytokines (IL-2 and IFN gamma) from cell culture supernatant were measured. OVA specific IgG, IgG1 and IgG2a antibody levels in serum were significantly enhanced by BOS 2000 (80 μg) compared with OVA control group. Moreover, the adjuvant effect of BOS 2000 (80 μg) on the OVA-specific IgG, IgG1, and IgG2a antibody responses to OVA in mice were more significant than those of alum. BOS 2000 significantly enhanced the Con A and OVA induced splenocyte proliferation in the OVA immunized mice especially at a dose of 80 μg (p<0.001). However, no significant differences were observed among the OVA group and OVA/alum group. At a dose of 80 μg (p<0.001), there was a significant increase in the CD4/CD8 and CD80/CD86 analysis in spleen cells and cytokine (IL-2 and IFN-gamma) profile in the spleen cell culture supernatant was observed. In conclusion, BOS 2000 seems to be a promising balanced Th1 and Th2 directing immunological adjuvants which can enhance the immunogenicity of vaccine.

摘要

在这项研究中,评估了乳香树 Boswellia serrata 的生物聚合物部分 BOS 2000 作为佐剂对卵清蛋白(OVA)在小鼠免疫反应中的潜在能力。Balb/c 小鼠通过皮下免疫用 OVA 100 μg 单独或用 OVA 100 μg 溶解在含明矾(200 μg)或 BOS 2000(10、20、40 和 80 μg)的盐水中在第 1 天和第 15 天免疫。两周后,测量血清中的 OVA 特异性抗体;刀豆蛋白 A(Con A)、OVA 刺激的脾细胞增殖、脾细胞中 CD4/CD8/CD80/CD86 的分析及其细胞培养上清液中细胞因子(IL-2 和 IFNγ)的估计。与 OVA 对照组相比,BOS 2000(80 μg)显著增强了血清中的 OVA 特异性 IgG、IgG1 和 IgG2a 抗体水平。此外,BOS 2000(80 μg)对 OVA 免疫小鼠 OVA 特异性 IgG、IgG1 和 IgG2a 抗体反应的佐剂作用比明矾更显著。BOS 2000 显著增强了 OVA 免疫小鼠的 Con A 和 OVA 诱导的脾细胞增殖,尤其是在 80 μg 剂量下(p<0.001)。然而,OVA 组和 OVA/明矾组之间没有观察到显著差异。在 80 μg 剂量下(p<0.001),观察到脾细胞中 CD4/CD8 和 CD80/CD86 分析显著增加,脾细胞培养上清液中的细胞因子(IL-2 和 IFN-γ)谱也显著增加。总之,BOS 2000 似乎是一种有前途的平衡 Th1 和 Th2 导向的免疫佐剂,可以增强疫苗的免疫原性。

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