Evidence map›Paper›PMID 33527793›Full record

ArticleYonsei medical journal2021

Systemic Immunomodulatory Effects of Combinatorial Treatment of Thalidomide and Dexamethasone on T Cells and Other Immune Cells.

Eun Jee Kim, Joon Ye Kim, Hoon Young Choi, Hyojung Lee, Juhan Lee, Myoung Soo Kim, Yu Seun Kim, Kyu Ha Huh, Beom Seok Kim

Open access · goldAbstract read
In one paragraph

Article in Yonsei medical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 1 institution in 1 country.

Eun Jee KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3027-2571
Joon Ye KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-1180-2899
Hoon Young ChoiDivision of Nephrology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-4245-0339
Hyojung LeeThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-3110-3718
Juhan LeeDepartment of Transplantation Surgery, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4910-2596
Myoung Soo KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8975-8381
Yu Seun KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-5105-1567
Kyu Ha HuhThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-1364-6989
Beom Seok KimThe Research Institute for Transplantation, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-5732-2583
Yonsei University · KR

Funding

Korea Health Industry Development Institute HI18C0629Korean Society for Transplantation 161028Yonsei University College of Medicine 6-2018-0106
6 · The paper itself

Abstract

purposeIn organ transplantation, the need for immune modulation rather than immune suppression has been emphasized. In this study, we investigated whether combinatorial treatments of with thalidomide (TM) and dexamethasone (DX) might be new approaches to induce systemic immunomodulation on T cells and other immune cells that regulate the expression of co-inhibitory molecules. MATERIALS AND

methodsNaïve splenic T cells from C57BL/6 mice were sort-purified and cultured in vitro for CD4

resultsCTLA-4 expressions in effector T cells in vivo and in Tregs in vivo/vitro significantly increased upon TM/DX combinatorial treatment. Corresponding to increased CTLA-4 expression in T cells, the expression of ligand molecules for CTLA-4 significantly increased in splenic dendritic cells in TM/DX-treated groups. In addition, MLR results demonstrated that splenocytes isolated from TM/DX-treated mice significantly suppressed the proliferation of T cells isolated from other strains.

conclusionBased on these results, we suggest that TM/DX combinatorial treatments might be efficient immunomodulatory methods for regulating T cell immunity.

Indexed as

AnimalsCell DifferentiationCell ProliferationCTLA-4 AntigenDendritic CellsDexamethasoneFlow CytometryImmunomodulationLymphocyte ActivationLymphocyte Culture Test, MixedMaleMiceMice, Inbred C57BLProgrammed Cell Death 1 ReceptorSpleenThalidomideCTLA-4 AntigenDexamethasonePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorThalidomideCTLA-4 antigendendritic cellsdexamethasoneImmunomodulationthalidomideT-lymphocytes

Identifiers

PMID33527793
PMCPMC7859687
OpenAlexW3129028022

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.