Evidence map›Paper›PMID 32772775›Full record

ArticleInnate immunity2020

Contribution of NK cells to HBsAg seroconversion in inactive HBsAg carriers following pegylated IFN therapy.

Zhenhuan Cao, Sha Meng, Yanhong Zheng, Junli Wang, Rui Wang, Xinyue Chen

Abstract read
In one paragraph

Article in Innate immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Observational
  2. Article
  3. Review
  4. Article
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

6 authors.

Zhenhuan CaoInternational Medical Department, Beijing You'an Hospital, Capital Medical University, PR China.ORCID 0000-0003-4204-1049
Sha MengScience and Technology Department, Beijing You'an Hospital, Capital Medical University, PR China.
Yanhong ZhengInternational Medical Department, Beijing You'an Hospital, Capital Medical University, PR China.
Junli WangInternational Medical Department, Beijing You'an Hospital, Capital Medical University, PR China.
Rui WangBeijing Key Laboratory for HIV/AIDS Research, PR China.
Xinyue ChenInternational Medical Department, Beijing You'an Hospital, Capital Medical University, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our recent study showed a high rate of HBsAg seroconversion in inactive HBsAg carriers (IHCs) treated with pegylated IFN (PEG-IFN). To understand the immune-mediated component of the HBsAg seroconversion better, this study investigated the role of NK cells. A total of 44 IHCs were given 48 wk of PEG-IFN. Fifteen cases achieved HBsAg seroconversion (R group), whereas 29 failed (NR group). The proportion and activity (CD107α and IFN-γ production) of NK cells were measured before and during treatment. We found that the proportion of NK cells in the R group was higher than in the NR group at baseline and during PEG-IFN treatment, even when patients were matched for age, sex and treatment period. IFN- γ secretion and CD107α expression from NK cells in cases who achieved HBsAg seroconversion were significantly higher than patients matched for age, sex, HBsAg and treatment period in the NR group at baseline and during PEG-IFN treatment. We also found that in HBsAg seroconversion cases, NK cells activity increased after PEG-IFN treatment, especially before HBsAg seroconversion. These effects were not found in non-responders. In conclusion, we demonstrated that the increase of NK cells accompanied by enhanced activity during PEG-IFN treatment favoured HBsAg seroconversion for IHC, and that NK cells may play a role in HBV seroconversion.

Indexed as

AdultFemaleHepatitis BHepatitis B Surface AntigensHepatitis B virusHumansInterferon-alphaInterferon-gammaKiller Cells, NaturalLymphocyte ActivationLysosomal-Associated Membrane Protein 1MaleMiddle AgedPolyethylene GlycolsRecombinant ProteinsSeroconversionHepatitis B Surface AntigensInterferon-alphaInterferon-gammaLysosomal-Associated Membrane Protein 1peginterferon alfa-2aPolyethylene GlycolsRecombinant ProteinsHBsAginactive HBsAg carriersNK cellsPegylated IFN-α-2aseroconversion

Identifiers

PMID32772775
PMCPMC7556194

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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.