Evidence map›Paper›PMID 16051831›Full record

ArticleJournal of virology2005

Influence of glycosylation on the efficacy of an Env-based vaccine against simian immunodeficiency virus SIVmac239 in a macaque AIDS model.

Kazuyasu Mori, Chie Sugimoto, Shinji Ohgimoto, Emi E Nakayama, Tatsuo Shioda, Shigeru Kusagawa, Yutaka Takebe, Munehide Kano, Tetsuro Matano, Takae Yuasa and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

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  8. Review and hypothesis: does Graves' disease develop in non-human great apes?Thyroid : official journal of the American Thyroid Association · 2011
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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

18 authors at 8 institutions in 1 country.

Kazuyasu MoriAIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan. mori@nibio.go.jp
Chie Sugimoto
Shinji Ohgimoto
Emi E Nakayama
Tatsuo Shioda
Shigeru Kusagawa
Yutaka Takebe
Munehide Kano
Tetsuro Matano
Takae Yuasa
Daisuke Kitaguchi
Masaaki Miyazawa
Yumiko Takahashi
Michio Yasunami
Akinori Kimura
Naoki Yamamoto
Yasuo Suzuki
Yoshiyuki Nagai
National Institute of Infectious Diseases · JPKindai University · JPTokyo Medical and Dental University · JPOsaka University · JPJapan Science and Technology Agency · JPKobe University · JPThe University of Tokyo · JPToyama Institute of Health · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The envelope glycoprotein (Env) of human immunodeficiency viruses (HIVs) and simian immunodeficiency viruses (SIVs) is heavily glycosylated, and this feature has been speculated to be a reason for the insufficient immune control of these viruses by their hosts. In a macaque AIDS model, we demonstrated that quintuple deglycosylation in Env altered a pathogenic virus, SIVmac239, into a novel attenuated mutant virus (delta5G). In delta5G-infected animals, strong protective immunity against SIVmac239 was elicited. These HIV and SIV studies suggested that an understanding of the role of glycosylation is critical in defining not only the virological properties but also the immunogenicity of Env, suggesting that glycosylation in Env could be modified for the development of effective vaccines. To examine the effect of deglycosylation, we constructed prime-boost vaccines consisting of Env from SIVmac239 and delta5G and compared their immunogenicities and vaccine efficacies by challenge infection with SIVmac239. Vaccination-induced immune responses differed between the two vaccine groups. Both Env-specific cellular and humoral responses were higher in wild-type (wt)-Env-immunized animals than in delta5G Env-immunized animals. Following the challenge, viral loads in SIVmac239 Env (wt-Env)-immunized animals were significantly lower than in vector controls, with controlled viral replication in the chronic phase. Unexpectedly, viral loads in delta5G Env-immunized animals were indistinguishable from those in vector controls. This study demonstrated that the prime-boost Env vaccine was effective against homologous SIVmac239 challenge. Changes in glycosylation affected both cell-mediated and humoral immune responses and vaccine efficacy.

Indexed as

AnimalsAntibodies, ViralCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalGene Products, envGlycosylationImmunizationMacaca mulattaResearch DesignSAIDS VaccinesSimian Immunodeficiency VirusViral LoadVirus ReplicationAntibodies, ViralGene Products, envSAIDS Vaccines

Identifiers

PMID16051831
PMCPMC1182680
OpenAlexW2160723909

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.