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毛里求斯食蟹猴和印度恒河猴中Tat疫苗方案的比较研究:毛里求斯主要组织相容性复合体单倍型对感染SHIV(89.6P)易感性/抗性的影响

Comparative study of Tat vaccine regimens in Mauritian cynomolgus and Indian rhesus macaques: influence of Mauritian MHC haplotypes on susceptibility/resistance to SHIV(89.6P) infection.

作者信息

Florese Ruth H, Wiseman Roger W, Venzon David, Karl Julie A, Demberg Thorsten, Larsen Kay, Flanary Leon, Kalyanaraman V S, Pal Ranajit, Titti Fausto, Patterson L Jean, Heath Megan J, O'Connor David H, Cafaro Aurelio, Ensoli Barbara, Robert-Guroff Marjorie

机构信息

Vaccine Branch, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

出版信息

Vaccine. 2008 Jun 19;26(26):3312-21. doi: 10.1016/j.vaccine.2008.03.100. Epub 2008 Apr 30.

DOI:10.1016/j.vaccine.2008.03.100
PMID:18486283
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2577850/
Abstract

Protection afforded by HIV Tat-based vaccines has differed in Indian rhesus and Mauritian cynomolgus macaques. We evaluated native Tat and Ad-HIVtat priming/Tat-boosting regimens in both species. Both vaccines were immunogenic. Only the Ad-tat regimen modestly reduced acute viremia in rhesus macaques after SHIV(89.6P) challenge. Confounding variables uncovered in Mauritian macaques included significant associations of susceptibility to infection with MHC class IB and class II H2 and H5 haplotypes, and resistance to infection with class IB haplotypes H3 and H6. Although protection here was limited, Tat-based vaccines incorporating other HIV components have shown greater efficacy. Combination strategies should be further explored.

摘要

基于HIV反式激活因子(Tat)的疫苗在印度恒河猴和毛里求斯食蟹猴中提供的保护作用有所不同。我们评估了两种猴类中天然Tat以及腺病毒载体HIV Tat初免/Tat加强免疫方案。两种疫苗均具有免疫原性。在感染猿猴免疫缺陷病毒(SHIV,89.6P)后,只有腺病毒载体Tat方案适度降低了恒河猴的急性病毒血症。在毛里求斯猴中发现的混杂变量包括,感染易感性与MHC I类B基因以及II类H2和H5单倍型之间存在显著关联,而I类B基因单倍型H3和H6与抗感染性有关。尽管此处的保护作用有限,但包含其他HIV成分的基于Tat的疫苗已显示出更高的效力。应进一步探索联合策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/8c63e0c08fc5/nihms57622f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/c62eddad3bd0/nihms57622f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/fadfee85e2c4/nihms57622f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/f5ae2c158302/nihms57622f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/a5d41d322395/nihms57622f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/8c63e0c08fc5/nihms57622f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/c62eddad3bd0/nihms57622f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/fadfee85e2c4/nihms57622f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/f5ae2c158302/nihms57622f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/a5d41d322395/nihms57622f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd58/2577850/8c63e0c08fc5/nihms57622f5.jpg

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2
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J Exp Med. 2007 Nov 26;204(12):3027-36. doi: 10.1084/jem.20070695. Epub 2007 Nov 19.
3
The major histocompatibility complex class II alleles Mamu-DRB1*1003 and -DRB1*0306 are enriched in a cohort of simian immunodeficiency virus-infected rhesus macaque elite controllers.
实验医学中的食蟹猴 MHC 多态性。
Cells. 2019 Aug 26;8(9):978. doi: 10.3390/cells8090978.
4
Vaccination with the Conserved Caveolin-1 Binding Motif in Human Immunodeficiency Virus Type 1 Glycoprotein gp41 Delays the Onset of Viral Infection and Provides Partial Protection in Simian/Human Immunodeficiency Virus-Challenged Cynomolgus Macaques.用人类免疫缺陷病毒 1 糖蛋白 gp41 中的保守 caveolin-1 结合基序进行免疫接种可延迟病毒感染的发作,并为感染猴免疫缺陷病毒的食蟹猴提供部分保护。
J Virol. 2018 Aug 29;92(18). doi: 10.1128/JVI.00370-18. Print 2018 Sep 15.
5
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PLoS One. 2017 Mar 8;12(3):e0171906. doi: 10.1371/journal.pone.0171906. eCollection 2017.
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J Immunol. 2012 Aug 15;189(4):1878-85. doi: 10.4049/jimmunol.1201026. Epub 2012 Jul 13.
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J Virol. 2007 Jan;81(1):349-61. doi: 10.1128/JVI.01841-06. Epub 2006 Oct 11.