Evidence map›Paper›PMID 30060038›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2019

Immune Responses to Middle East Respiratory Syndrome Coronavirus During the Acute and Convalescent Phases of Human Infection.

Hyoung-Shik Shin, Yeonjae Kim, Gayeon Kim, Ji Yeon Lee, Ina Jeong, Joon-Sung Joh, Hana Kim, Eunjin Chang, Soo Yeon Sim, Jun-Sun Park and 1 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing 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

97 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review

37 more citing papers are in PubMed but not listed here.

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.

Hyoung-Shik ShinCenter for Infectious Diseases, Department of Internal Medicine.
Yeonjae KimCenter for Infectious Diseases, Department of Internal Medicine.
Gayeon KimCenter for Infectious Diseases, Department of Internal Medicine.
Ji Yeon LeeDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Ina JeongDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Joon-Sung JohDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Hana KimCenter for Chronic Diseases, Research Institute, National Medical Center, Seoul, Korea.
Eunjin ChangCenter for Chronic Diseases, Research Institute, National Medical Center, Seoul, Korea.
Soo Yeon SimCenter for Chronic Diseases, Research Institute, National Medical Center, Seoul, Korea.
Jun-Sun ParkCenter for Infectious Diseases, Research Institute, National Medical Center, Seoul, Korea.
Dong-Gyun LimCenter for Chronic Diseases, Research Institute, National Medical Center, Seoul, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn understanding of immune responses against the Middle East respiratory syndrome (MERS) is important for the development of treatments and preventive measures. Here, we investigated the spectrum of immune responses occurring in patients with MERS during the early period of infection.

methodsWe obtained peripheral blood samples from 27 hospitalized patients recruited during the epidemic that occurred in 2015 in South Korea. Plasma cytokines/chemokines and antibodies were quantified. Virus-specific T cells were examined by intracellular cytokine staining after stimulation of peripheral blood mononuclear cells with overlapping peptides spanning whole virus structural proteins.

resultsAt the acute phase of infection, elevated levels of plasma proinflammatory cytokines/chemokines were detected in proportion to the severity of the disease. Distinctively high frequencies of MERS coronavirus-reactive CD8+ T cells were also observed in patients with severe/moderate illness, whereas antibody and CD4+ T-cell responses were minimally detected at this stage. At the convalescent phase, disease severity-dependent antibody responses emerged and antigen-reactive cells were identified in both T-cell subsets. These T cells belonged to the T-helper 1 or type 1 cytotoxic T cell subtypes. While CD8+ T cells responded preferentially to the viral S protein compared with E/M/N proteins, especially at the acute stage, slightly more CD4+ T cells recognized E/M/N proteins compared with S protein at the convalescent phase.

conclusionsOur findings show an association between the early CD8+ T-cell response and the severity of the infection, and also provide basic information that may help to prepare effective control strategies for MERS in humans.

Indexed as

AdultAgedAntibodies, NeutralizingAntibodies, ViralCoronavirus InfectionsCytokinesFemaleHost-Pathogen InteractionsHumansMaleMiddle AgedMiddle East Respiratory Syndrome CoronavirusMortalityPatient Outcome AssessmentRepublic of KoreaT-Lymphocyte SubsetsAntibodies, NeutralizingAntibodies, ViralCytokinesacute phase of infectionimmune responseMERS coronavirusT lymphocytes

Identifiers

PMID30060038
PMCPMC7108191

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.