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用于预防性疫苗接种的小鼠模型中的全灭活gp120缺失型HIV-1抗原。

Whole-killed gp120-depleted HIV-1 antigen in a murine model for prophylactic vaccination.

作者信息

Lanza P, Moss R B, Giermakowska W, Hancock R B, Richieri S P, Theofa G, Jensen F C, Salk P L, Carlo D J

机构信息

Immune Response Corporation, Carlsbad, CA 92008, USA.

出版信息

Vaccine. 1998 Apr;16(7):727-31. doi: 10.1016/s0264-410x(97)00256-9.

Abstract

In this study, the effects were examined of dose and adjuvant of whole-killed gp120-depleted HIV-1 antigen on antibody and cytokine responses in a murine model. Immunization with increasing doses of inactivated HIV-1 antigen in Incomplete Freund's Adjuvant (IFA) resulted in increased production of IL-4 and IgG1 antibody with decreased production of interferon gamma. Immunization with inactivated HIV-1 antigen in Detox PC adjuvant produced TH1 type predominant cytokine patterns along with IgG2a subclass antibody. Higher levels of interferon gamma were associated with immunization with inactivated HIV-1 antigen in Detox PC compared with inactivated HIV-1 in IFA or inactivated HIV-1 in saline. Inactivated HIV-1 antigen in Detox PC adjuvant produced a trend of lower levels of the beta-chemokine MIP-1 alpha compared with inactivated HIV-1 in IFA or saline. Dose and adjuvant play an important role in the type of immune response elicited to a whole-killed HIV vaccine. Low doses of inactivated HIV-1 antigen in Detox PC adjuvant are currently being studied in animal models in order to optimize cell-mediated immunity against HIV infection.

摘要

在本研究中,在小鼠模型中检测了全灭活的gp120缺失型HIV-1抗原的剂量和佐剂对抗体及细胞因子反应的影响。用递增剂量的灭活HIV-1抗原与不完全弗氏佐剂(IFA)免疫,导致IL-4和IgG1抗体产生增加,而干扰素γ产生减少。用去毒PC佐剂中的灭活HIV-1抗原免疫产生以TH1型为主的细胞因子模式以及IgG2a亚类抗体。与IFA中的灭活HIV-1或盐水中的灭活HIV-1相比,去毒PC中的灭活HIV-1抗原免疫与更高水平的干扰素γ相关。与IFA或盐水中的灭活HIV-1相比,去毒PC佐剂中的灭活HIV-1抗原产生β趋化因子MIP-1α水平较低的趋势。剂量和佐剂在对全灭活HIV疫苗引发的免疫反应类型中起重要作用。目前正在动物模型中研究去毒PC佐剂中低剂量的灭活HIV-1抗原,以优化针对HIV感染的细胞介导免疫。

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