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用减毒活猿猴免疫缺陷病毒(SIV)疫苗进行黏膜免疫可在恒河猴体内引发抗病毒细胞毒性T淋巴细胞和抗体。

Mucosal immunization with a live, virulence-attenuated simian immunodeficiency virus (SIV) vaccine elicits antiviral cytotoxic T lymphocytes and antibodies in rhesus macaques.

作者信息

Lohman B L, McChesney M B, Miller C J, Otsyula M, Berardi C J, Marthas M L

机构信息

California Regional Primate Research Center, University of California, Davis 95616.

出版信息

J Med Primatol. 1994 Feb-May;23(2-3):95-101. doi: 10.1111/j.1600-0684.1994.tb00108.x.

DOI:10.1111/j.1600-0684.1994.tb00108.x
PMID:7966240
Abstract

An effective AIDS vaccine must protect against sexual transmission of human immunodeficiency virus (HIV). Therefore, vaccine regimens which stimulate antiviral immunity in the genital tract as well as in peripheral blood and systemic lymphoid tissues are needed. Here, we describe a method of immunization by direct inoculation of the vaginal submucosa with a live attenuated SIV, SIVmac1A11. Immunization by this route generated low levels of SIV-specific IgG and IgA antibodies in serum and vaginal secretions and viral specific cytotoxic T lymphocyte (CTL) activity in peripheral blood.

摘要

一种有效的艾滋病疫苗必须能够预防人类免疫缺陷病毒(HIV)的性传播。因此,需要能在生殖道以及外周血和全身淋巴组织中激发抗病毒免疫的疫苗方案。在此,我们描述了一种通过向阴道黏膜下层直接接种减毒活猴免疫缺陷病毒(SIV)SIVmac1A11进行免疫的方法。通过这种途径进行免疫可在血清和阴道分泌物中产生低水平的SIV特异性IgG和IgA抗体,并在外周血中产生病毒特异性细胞毒性T淋巴细胞(CTL)活性。

相似文献

1
Mucosal immunization with a live, virulence-attenuated simian immunodeficiency virus (SIV) vaccine elicits antiviral cytotoxic T lymphocytes and antibodies in rhesus macaques.用减毒活猿猴免疫缺陷病毒(SIV)疫苗进行黏膜免疫可在恒河猴体内引发抗病毒细胞毒性T淋巴细胞和抗体。
J Med Primatol. 1994 Feb-May;23(2-3):95-101. doi: 10.1111/j.1600-0684.1994.tb00108.x.
2
Antiviral CD8+ T cells in the genital tract control viral replication and delay progression to AIDS after vaginal SIV challenge in rhesus macaques immunized with virulence attenuated SHIV 89.6.在经减毒活SHIV 89.6免疫的恒河猴中,生殖道中的抗病毒CD8 + T细胞可控制病毒复制,并延缓阴道感染SIV后向艾滋病的进展。
J Intern Med. 2009 Jan;265(1):67-77. doi: 10.1111/j.1365-2796.2008.02051.x.
3
Targeted lymph-node immunization with whole inactivated simian immunodeficiency virus (SIV) or envelope and core subunit antigen vaccines does not reliably protect rhesus macaques from vaginal challenge with SIVmac251.用全灭活猴免疫缺陷病毒(SIV)或包膜及核心亚单位抗原疫苗进行靶向淋巴结免疫,不能可靠地保护恒河猴免受SIVmac251的阴道攻击。
AIDS. 1998 Jan 1;12(1):1-10. doi: 10.1097/00002030-199801000-00001.
4
Simian-human immunodeficiency virus SHIV89.6-induced protection against intravaginal challenge with pathogenic SIVmac239 is independent of the route of immunization and is associated with a combination of cytotoxic T-lymphocyte and alpha interferon responses.猿猴-人类免疫缺陷病毒SHIV89.6诱导的针对致病性SIVmac239阴道内攻击的保护作用与免疫途径无关,且与细胞毒性T淋巴细胞和α干扰素反应的组合有关。
J Virol. 2003 Mar;77(5):3099-118. doi: 10.1128/jvi.77.5.3099-3118.2003.
5
Live-attenuated lentivirus immunization modulates innate immunity and inflammation while protecting rhesus macaques from vaginal simian immunodeficiency virus challenge.减毒慢病毒免疫调节先天免疫和炎症,同时保护恒河猴免受阴道猴免疫缺陷病毒挑战。
J Virol. 2012 Sep;86(17):9188-200. doi: 10.1128/JVI.00532-12. Epub 2012 Jun 13.
6
Immunogenicity of a vaccine regimen composed of simian immunodeficiency virus DNA, rMVA, and viral particles administered to female rhesus macaques via four different mucosal routes.四种不同黏膜途径给予雌性恒河猴的猴免疫缺陷病毒 DNA、rMVA 和病毒颗粒疫苗方案的免疫原性。
J Virol. 2013 Apr;87(8):4738-50. doi: 10.1128/JVI.03531-12. Epub 2013 Feb 13.
7
Protective attenuated lentivirus immunization induces SIV-specific T cells in the genital tract of rhesus monkeys.保护性减毒慢病毒免疫可诱导恒河猴生殖道中的SIV特异性T细胞。
Mucosal Immunol. 2008 May;1(3):219-28. doi: 10.1038/mi.2008.6. Epub 2008 Mar 5.
8
Live simian immunodeficiency virus vaccine correlate of protection: immune complex-inhibitory Fc receptor interactions that reduce target cell availability.活猿猴免疫缺陷病毒疫苗的保护相关因素:降低靶细胞可用性的免疫复合物抑制性Fc受体相互作用。
J Immunol. 2014 Sep 15;193(6):3126-33. doi: 10.4049/jimmunol.1400822. Epub 2014 Aug 20.
9
With minimal systemic T-cell expansion, CD8+ T Cells mediate protection of rhesus macaques immunized with attenuated simian-human immunodeficiency virus SHIV89.6 from vaginal challenge with simian immunodeficiency virus.在全身T细胞扩增极少的情况下,CD8+ T细胞介导了对用减毒猿猴-人类免疫缺陷病毒SHIV89.6免疫的恒河猴的保护,使其免受猿猴免疫缺陷病毒的阴道攻击。
J Virol. 2008 Nov;82(22):11181-96. doi: 10.1128/JVI.01433-08. Epub 2008 Sep 10.
10
Both mucosal and systemic routes of immunization with the live, attenuated NYVAC/simian immunodeficiency virus SIV(gpe) recombinant vaccine result in gag-specific CD8(+) T-cell responses in mucosal tissues of macaques.用减毒活疫苗NYVAC/猴免疫缺陷病毒SIV(gpe)重组疫苗进行黏膜免疫和全身免疫,均可在猕猴的黏膜组织中引发针对gag的CD8(+) T细胞应答。
J Virol. 2002 Nov;76(22):11659-76. doi: 10.1128/jvi.76.22.11659-11676.2002.

引用本文的文献

1
Stone age diseases and modern AIDS.石器时代的疾病与现代艾滋病
Virol J. 2008 Aug 7;5:93. doi: 10.1186/1743-422X-5-93.
2
An adenovirus-simian immunodeficiency virus env vaccine elicits humoral, cellular, and mucosal immune responses in rhesus macaques and decreases viral burden following vaginal challenge.一种腺病毒-猴免疫缺陷病毒包膜疫苗可在恒河猴中引发体液免疫、细胞免疫和黏膜免疫反应,并在阴道攻毒后降低病毒载量。
J Virol. 1997 Nov;71(11):8531-41. doi: 10.1128/JVI.71.11.8531-8541.1997.
3
Viral factors determine progression to AIDS in simian immunodeficiency virus-infected newborn rhesus macaques.
病毒因素决定了感染猿猴免疫缺陷病毒的新生恒河猴向艾滋病的进展。
J Virol. 1995 Jul;69(7):4198-205. doi: 10.1128/JVI.69.7.4198-4205.1995.