Evidence map›Paper›PMID 30148455›Full record

ArticleThe Journal of clinical investigation2018

TLR3 agonist and CD40-targeting vaccination induces immune responses and reduces HIV-1 reservoirs.

Liang Cheng, Qi Wang, Guangming Li, Riddhima Banga, Jianping Ma, Haisheng Yu, Fumihiko Yasui, Zheng Zhang, Giuseppe Pantaleo, Matthieu Perreau and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 71 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 5 countries.

Liang ChengLineberger Comprehensive Cancer Center, and.
Qi WangLineberger Comprehensive Cancer Center, and.
Guangming LiLineberger Comprehensive Cancer Center, and.
Riddhima BangaService of Immunology and Allergy and.
Jianping MaLineberger Comprehensive Cancer Center, and.
Haisheng YuLineberger Comprehensive Cancer Center, and.
Fumihiko YasuiLineberger Comprehensive Cancer Center, and.
Zheng ZhangLineberger Comprehensive Cancer Center, and.
Giuseppe PantaleoService of Immunology and Allergy and.
Matthieu PerreauService of Immunology and Allergy and.
Sandra ZurawskiVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France.
Gerard ZurawskiVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France.
Yves LevyVaccine Research Institute, Université Paris-Est, Faculté de Médecine, INSERM U955, Créteil, France.
Lishan SuLineberger Comprehensive Cancer Center, and.
Segeberger Kliniken · DEInserm · FRSwiss Vaccine Research Institute · CHUniversity of North Carolina at Chapel Hill · US302 Military Hospital of China · CN

Funding

Protein Expression/Dengue Virology CoreU19AI109784 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TING, JENNY P · 2014 to 2018
$20.8M
Novel therapeutic approaches to treating chronic hepatitis B virus infectionR01DK095962 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FU, YANG-XIN, SU, LISHAN · 2013 to 2016
$2.1M
NIAID NIH HHS U19 AI109784NIDDK NIH HHS R01 DK095962
6 · The paper itself

Abstract

Activation of HIV-1 reservoirs and induction of anti-HIV-1 T cells are critical to control HIV-1 rebound after combined antiretroviral therapy (cART). Here we evaluated in humanized mice (hu-mice) with persistent HIV-1 infection the therapeutic effect of TLR3 agonist and a CD40-targeting HIV-1 vaccine, which consists of a string of 5 highly conserved CD4+ and CD8+ T cell epitope-rich regions of HIV-1 Gag, Nef, and Pol fused to the C-terminus of a recombinant anti-human CD40 antibody (αCD40.HIV5pep). We show that αCD40.HIV5pep vaccination coadministered with poly(I:C) adjuvant induced HIV-1-specific human CD8+ and CD4+ T cell responses in hu-mice. Interestingly, poly(I:C) treatment also reactivated HIV-1 reservoirs. When administrated in therapeutic settings in HIV-1-infected hu-mice under effective cART, αCD40.HIV5pep with poly(I:C) vaccination induced HIV-1-specific CD8+ T cells and reduced the level of cell-associated HIV-1 DNA (or HIV-1 reservoirs) in lymphoid tissues. Most strikingly, the vaccination significantly delayed HIV-1 rebound after cART cessation. In summary, the αCD40.HIV5pep with poly(I:C) vaccination approach both activates replication of HIV-1 reservoirs and enhances the anti-HIV-1 T cell response, leading to a reduced level of cell-associated HIV-1 DNA or reservoirs. Our proof-of-concept study has significant implication for the development of CD40-targeting HIV-1 vaccine to enhance anti-HIV-1 immunity and reduce HIV-1 reservoirs in patients with suppressive cART.

Indexed as

AIDS VaccinesEpitopes, T-LymphocyteHuman Immunodeficiency Virus ProteinsAnimalsCD40 AntigensHIV-1HumansImmunity, CellularMiceMice, KnockoutPoly I-CToll-Like Receptor 3AIDS VaccinesCD40 AntigensEpitopes, T-LymphocyteHuman Immunodeficiency Virus ProteinsPoly I-CTLR3 protein, humanToll-Like Receptor 3AIDS/HIVAIDS vaccineCellular immune responseVaccines

Identifiers

PMID30148455
PMCPMC6159955
OpenAlexW2888061414

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.