Evidence map›Paper›PMID 27929748›Full record

ArticleHuman vaccines & immunotherapeutics2017

Evaluation of inflammatory and immune responses in long-term cultured human precision-cut lung slices.

Angela Temann, Tatiana Golovina, Vanessa Neuhaus, Carolann Thompson, Jessica A Chichester, Armin Braun, Vidadi Yusibov

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Modeling Immunity In Vitro: Slices, Chips, and Engineered Tissues.Annual review of biomedical engineering · 2021
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Tools of the trade: leveraging 3DFrontiers in pharmacology · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Transcriptional Host Responses to Infection withPathogens (Basel, Switzerland) · 2023
    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

7 authors at 2 institutions in 2 countries.

Angela Temanna Fraunhofer USA Center for Molecular Biotechnology , Newark , DE , USA.
Tatiana Golovinaa Fraunhofer USA Center for Molecular Biotechnology , Newark , DE , USA.
Vanessa Neuhausb Fraunhofer Institute for Toxicology and Experimental Medicine , Hannover , Germany.
Carolann Thompsona Fraunhofer USA Center for Molecular Biotechnology , Newark , DE , USA.
Jessica A Chichestera Fraunhofer USA Center for Molecular Biotechnology , Newark , DE , USA.
Armin Braunb Fraunhofer Institute for Toxicology and Experimental Medicine , Hannover , Germany.
Vidadi Yusibova Fraunhofer USA Center for Molecular Biotechnology , Newark , DE , USA.
Fraunhofer USA Center for Molecular Biotechnology · USFraunhofer Institute for Toxicology and Experimental Medicine · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of systems that are more accurate and time-efficient in predicting safety and efficacy of target products in humans are critically important in reducing the cost and duration of pharmaceutical development. To circumvent some of the limitations imposed by the use of animal models, ex vivo systems, such as precision-cut lung slices (PCLS), have been proposed as an alternative for evaluating safety, immunogenicity and efficacy of vaccines and pharmaceuticals. In this study, we have established a human PCLS system and methodology for PCLS cultivation that can provide long-term viability and functionality in culture. Using these techniques, we found that cultured PCLS remained viable for at least 14 d in culture and maintained normal metabolic activity, tissue homeostasis and structural integrity. To investigate whether cultured PCLS remained functional, lipopolysaccharide (LPS) was used as a target stimulating compound. We observed that after an 18-hour incubation with LPS, cultured PCLS produced a set of pro-inflammatory cytokines, including TNF-α, IL-1β, IL-6 and IL-10 as well as the enzyme COX-2. Furthermore, cultured PCLS were shown to be capable of generating re-call immune responses, characterized by cytokine production, against antigens commonly found in routine vaccinations against influenza virus and tetanus toxoid. Taken together, these results suggest that human PCLS have the potential to be used as an alternative, high-throughput, ex vivo system for evaluating the safety, and potentially immunogenicity, of vaccines and pharmaceuticals.

Indexed as

Drug Evaluation, PreclinicalHumansLungOrgan Culture Techniquesimmune responseinflammationLPSlungprecision-cut lung slices

Identifiers

PMID27929748
PMCPMC5328235
OpenAlexW2560670986

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.