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合成硫酸化和萘基磺化碳硅烷树枝状聚合物作为局部抗微生物剂以预防 HIV-1 性传播。

Development of sulphated and naphthylsulphonated carbosilane dendrimers as topical microbicides to prevent HIV-1 sexual transmission.

机构信息

Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Madrid, Spain.

出版信息

AIDS. 2013 May 15;27(8):1219-29. doi: 10.1097/QAD.0b013e32835f2b7a.

Abstract

OBJECTIVES

For the last 20 years, the idea of alternative prevention strategies based on the use of topical vaginally products to inhibit HIV-1 infection in women has been established. The concept of a 'microbicide' product has been born out of the unavailability of a vaccine against HIV-1 and the problems of women in negotiating the use of preventive prophylaxis by their partners, especially in developing countries.

DESIGN

We have developed and evaluated polyanionic carbosilane dendrimers G3-S16 and G2-NF16 with sulphated and naphthylsulphonated end groups as nonspecific microbicides.

METHODS

Cellular in-vitro or in-vivo models were used to evaluate the safety, biocompatibility and anti-HIV ability of two polyanionic carbosilane dendrimers.

RESULTS

Both dendrimers showed high biosafety in human epithelial cell lines derived from uterus and vagina and in primary blood human cells (PBMC). These dendrimers not only have a partial capacity to block the entry of different X4 and R5 HIV-1 isolates inside epithelial cells but protect the epithelial monolayer from cell disruption and also reduce HIV-1 infection of activated PBMC. Additionally, treatment of epithelial cells with G3-S16 or G2-NF16 dendrimers did not produce changes in proinflammatory cytokines profile, in proliferation of PBMC, on microbiota or sperm survival. Finally, no irritation or vaginal lesions were detected in female CD1(ICR) mice after dendrimers vaginal administration.

CONCLUSION

These interesting results suggest that G3-S16 or G2-NF16 could be effective to inhibit HIV infection and transmission within genital mucosa as well as the spread of HIV transmission to human PBMC.

摘要

目的

在过去的 20 年中,基于使用局部阴道产品来抑制女性 HIV-1 感染的替代预防策略的想法已经确立。“杀微生物剂”产品的概念源自 HIV-1 疫苗的不可用性以及女性在与伴侣协商使用预防措施时所面临的问题,尤其是在发展中国家。

设计

我们开发并评估了带有硫酸化和萘基磺化端基的聚阴离子碳硅烷树枝状大分子 G3-S16 和 G2-NF16,作为非特异性杀微生物剂。

方法

使用细胞体外或体内模型来评估两种聚阴离子碳硅烷树枝状大分子的安全性、生物相容性和抗 HIV 能力。

结果

两种树枝状大分子在源自子宫和阴道的人上皮细胞系和原代血液人细胞(PBMC)中均显示出高度的生物安全性。这些树枝状大分子不仅具有部分能力来阻止不同 X4 和 R5 HIV-1 分离株进入上皮细胞,而且还可以保护上皮细胞单层免受细胞破坏,并减少激活的 PBMC 中的 HIV-1 感染。此外,用 G3-S16 或 G2-NF16 树枝状大分子处理上皮细胞不会导致促炎细胞因子谱、PBMC 增殖、微生物群或精子存活发生变化。最后,在阴道给予树枝状大分子后,雌性 CD1(ICR)小鼠未检测到刺激或阴道损伤。

结论

这些有趣的结果表明,G3-S16 或 G2-NF16 可能有效抑制生殖器黏膜内的 HIV 感染和传播,以及 HIV 向人类 PBMC 的传播。

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