Evidence map›Paper›PMID 39770286›Full record

ArticlePathogens (Basel, Switzerland)2024

Establishment of an Immortalized Porcine Alveolar Macrophage Cell Line That Supports Efficient Replication of Porcine Reproductive and Respiratory Syndrome Viruses.

Nguyen Van Diep, Yuiko Hayakawa-Sugaya, Shingo Ishikawa, Hiroaki Kawaguchi, Yasuo Suda, Mana Esaki, Kosuke Okuya, Makoto Ozawa

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

8 authors.

Nguyen Van DiepJoint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.ORCID 0000-0002-8833-1693
Yuiko Hayakawa-SugayaIDEAS Swine Clinic, Asahi 289-2505, Japan.
Shingo IshikawaInstitute of Veterinary Science, Osaka Metropolitan University, Izumisano 598-8531, Japan.
Hiroaki KawaguchiLaboratory of Veterinary Pathology, Kitasato University School of Veterinary Medicine, Towada 034-8628, Japan.
Yasuo SudaGraduate School of Science and Engineering, Kagoshima University, Kagoshima 890-0065, Japan.
Mana EsakiJoint Graduate School of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.
Kosuke OkuyaJoint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.ORCID 0000-0002-7987-9884
Makoto OzawaJoint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.ORCID 0000-0002-7731-5321

Funding

the NARO Bio-oriented Technology Research Advancement Institution "Integration Research for Agriculture and Interdisciplinary Fields" and "R&D matching funds on the field for Knowledge Integration and innovation"
6 · The paper itself

Abstract

Porcine reproductive and respiratory syndrome (PRRS), which is caused by the porcine reproductive and respiratory syndrome virus (PRRSV), has a significant impact on the global pork industry. It results in reproductive failure in sows and respiratory issues in pigs of all ages. Despite the availability of vaccines, controlling the PRRSV remains challenging, partly owing to the limitations of cell culture systems. Current methods largely rely on primary porcine alveolar macrophages (PAMs), which must be harvested from piglets and have limited proliferative capacity. Although some simian cell lines support PRRSV replication, their inability to express porcine CD163, which is a key receptor for PRRSV entry, compromises their effectiveness, because the virus replicates differently in these non-target cells. To address these issues, we established an immortalized PAM cell line, PAM-T43, using SV40 large T antigen for immortalization and porcine serum as a culture supplement. PAM-T43 cells maintain essential macrophage functions, including CD163 expression and phagocytic activity, and exhibit high sensitivity to the PRRSV, efficiently supporting viral replication. This novel cell line offers significant potential for advancing PRRSV research, particularly in vaccine development and field strain isolation, by overcoming the limitations of current systems.

Indexed as

Macrophages, AlveolarPorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusVirus ReplicationAnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCell Culture TechniquesCell LineCell Line, TransformedReceptors, Cell SurfaceSwineAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenReceptors, Cell Surfaceimmortalizationporcine alveolar macrophageporcine reproductive and respiratory syndrome virus

Identifiers

PMID39770286
PMCPMC11678208

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.