Evidence map›Paper›PMID 33928221›Full record

ArticleAntibody therapeutics2019

Induction of neutralizing antibodies by human papillomavirus vaccine generated in mammalian cells.

Xilin Wu, Xiaohua Ma, Yanlei Li, Yue Xu, Nan Zheng, Shijie Xu, Waqas Nawaz, Zhiwei Wu

Open access · goldAbstract read
In one paragraph

Article in Antibody therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 15 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

8 authors at 1 institution in 1 country.

Xilin WuCenter for Public Health Research, Medical School, Nanjing University, Nanjing, PR, China.
Xiaohua MaAntibody Department, Y-Clone Medical Science Co.Ltd., Suzhou, PR, China.
Yanlei LiAntibody Department, Y-Clone Medical Science Co.Ltd., Suzhou, PR, China.
Yue XuAntibody Department, Y-Clone Medical Science Co.Ltd., Suzhou, PR, China.
Nan ZhengCenter for Public Health Research, Medical School, Nanjing University, Nanjing, PR, China.
Shijie XuCenter for Public Health Research, Medical School, Nanjing University, Nanjing, PR, China.
Waqas NawazCenter for Public Health Research, Medical School, Nanjing University, Nanjing, PR, China.
Zhiwei WuCenter for Public Health Research, Medical School, Nanjing University, Nanjing, PR, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer caused by human papillomavirus (HPV) infections is one of the most common cancers affecting women worldwide. Current preventative HPV vaccines on the market are composed of HPV L1 protein produced either in the yeast such as Gardasil or in the insect cells such as Cervarix. The duration of efficacy and cross-protection remain highly desirable for the improvement of current prophylactic HPV vaccine. Given that HPV carries out infection and replicates in mammalian cells, L2 protein, which is not included in the current licensed vaccines, is included in the third generation of HPV vaccine in pursuing of providing broader prevention. We hypothesize that a virus-like particle (VLP) consisting of HPV L1 plus L2 proteins generated in mammalian cells will present conformations more closely to native HPV, thus it will provide more durable and broader efficacy of prevention.

methodsWe took advantage of 293TT cells to produce VLP containing L1 and L2 proteins of HPV16 and HPV18, respectively.

resultsVLP particles of uniformed size and morphology were observed, and potent and broadly neutralizing antibodies were induced in mice and rabbits. In addition, compared to bivalent HPV vaccine of Cervarix, our HPV L1-L2 VLPs elicited higher titer of anti-sera, and the anti-sera also presented comparable neutralization potency against HPV16 and HPV18 infections even a much less potent adjuvant was used in our case.

conclusionOur VLPs were capable of eliciting stronger and more broadly neutralizing activities against various HPV subtypes and were potential candidate HPV vaccines.

Indexed as

cervical cancerHPVmammalian cellsneutralizing antibodiesvaccine

Identifiers

PMID33928221
PMCPMC7990147
OpenAlexW2918361966

What OpenQuestion holds

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Registered trials

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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.