Evidence map›Paper›PMID 31763042›Full record

ArticleClinical & translational immunology2019

Cross-reactive antibody-dependent cellular cytotoxicity antibodies are increased by recent infection in a household study of influenza transmission.

Sophie A Valkenburg, Vicky J Fang, Nancy Hl Leung, Daniel Kw Chu, Dennis Km Ip, Ranawaka Apm Perera, Yizhuo Wang, Athena Py Li, Js Malik Peiris, Benjamin J Cowling and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Dynamic Natural Killer Cell and T Cell Responses to Influenza Infection.Frontiers in cellular and infection microbiology · 2020
    Review
  9. Review
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

11 authors at 2 institutions in 1 country.

Sophie A ValkenburgLi Ka Shing Faculty of Medicine HKU Pasteur Research Pole School of Public Health The University of Hong Kong Hong Kong.ORCID https://orcid.org/0000-0002-0768-9926
Vicky J FangLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Nancy Hl LeungLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.ORCID https://orcid.org/0000-0001-7314-840X
Daniel Kw ChuLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Dennis Km IpLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Ranawaka Apm PereraLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Yizhuo WangLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Athena Py LiLi Ka Shing Faculty of Medicine HKU Pasteur Research Pole School of Public Health The University of Hong Kong Hong Kong.
Js Malik PeirisLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Benjamin J CowlingLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
Leo Lm PoonLi Ka Shing Faculty of Medicine School of Public Health WHO Collaborating Centre for Infectious Disease Epidemiology and Control The University of Hong Kong Hong Kong.
University of Hong Kong · HKHKU-Pasteur Research Pole · HK

Funding

NIAID NIH HHS HHSN272201400006C
6 · The paper itself

Abstract

objectivesInfluenza causes a spectrum of disease from asymptomatic infection to fatal outcome, and pre-existing immunity can alter susceptibility and disease severity. In a household transmission study, we recruited outpatients with confirmed influenza virus infection and prospectively identified secondary infections in their household contacts, therefore identifying infection cases with baseline samples for determining immune-mediated protection from influenza infection.

methodsWe examined baseline broadly reactive immune correlates of relevance to universal vaccine development, specifically antibody-dependent cytotoxic (ADCC) antibodies and T-cell responses in functional assays. Antibodies were assessed in a cell-based NK cell degranulation assay by flow cytometry, and T-cell responses were assessed by IFN-γ intracellular cytokine staining flow cytometry assay.

resultsThe magnitude of antibody responses and ADCC function for multiple influenza-specific proteins was lower in participants who became infected, consolidating the role of pre-existing antibodies in protection from seasonal influenza virus infection. Among H1N1-infected contacts, we found that higher levels of pre-existing H1-haemagglutinin ADCC responses correlated with reduced symptom severity. Recent infection boosted the titre and magnitude of haemagglutinin-, neuraminidase- and nucleoprotein-specific ADCC antibodies. Limited T-cell samples precluded conclusions on the role of pre-existing T-cell responses.

conclusionsOverall, ADCC responses are a protective correlate against influenza virus infection that should be considered in future vaccine development and evaluation.Influenza-specific ADCC responses are elevated in uninfected subjects, associated with reduced symptoms and boosted by recent infection, whilst HA stem and NA IgG are also elevated in uninfected participants irrespective of ADCC function.

Indexed as

antibody‐dependent cellular cytotoxicitybaseline immunityHA stem antibodiesinfluenza virus infectionT cellsuniversal immune correlate

Identifiers

PMID31763042
PMCPMC6864499
OpenAlexW2989728614

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.