Evidence map›Paper›PMID 40365939›Full record

ArticleJournal of proteome research2025

Dynamic Changes in Lymphocyte Subsets and Inflammation-Immune-Related Proteins in Patients with Thyroid Papillary Carcinoma before and after Radioactive Iodine Therapy.

Junyu Zhang, Lulu Shi, Zhilin Zhang, Wanshu Peng, Peifen Chen, Jiaxin Cao, Jing Liu, Jin Zhang, Keyi Lu, Zhifang Wu and 2 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2025. 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
–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

2 citing papers in PubMed.

  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

12 authors.

Junyu ZhangDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Lulu ShiDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Zhilin ZhangDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Wanshu PengDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Peifen ChenDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Jiaxin CaoDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Jing LiuDepartment of Thyroid Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Jin ZhangDepartment of Thyroid Surgery, First Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Keyi LuDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Zhifang WuDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.
Haiyan LiuDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.ORCID 0000-0002-4961-4252
Sijin LiDepartment of Nuclear Medicine, First Hospital of Shanxi Medical University, Taiyuan 030001, China.ORCID 0000-0002-2010-3459

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radioactive iodine therapy (RAIT) is one of the main treatment methods for patients with papillary thyroid carcinoma (PTC). Peripheral blood samples were collected from 29 PTC patients who underwent total thyroidectomy 1-2 days before RAIT (RAIT-0), 30 days after (RAIT-30), and 90 days after (RAIT-90). Flow cytometry was used to detect the absolute counts of peripheral blood lymphocyte subpopulations, and the Proximity Extension Assay (PEA) was used for targeted proteome quantification. We found that after RAIT, peripheral blood lymphocyte subpopulations and the abundance of inflammation-related proteins in PTC patients changed and did not return to pretreatment levels for a long time. The immune pathway "Cytokine-cytokine receptor interaction" related to cytokine signaling may be activated. In addition, there were two types of protein trends that were similar to the lymphocyte count trends. The five proteins with the greatest degree of trend change were MCP-1, TRAIL, TGF-alpha, Flt3L, and IL15. In RAIT-30 vs RAIT-0, B cells were significantly negatively correlated with protein Flt3L, and Th17 cells were significantly positively correlated with protein CRTAM. MCP-1, TRAIL, IL15, Flt3L, TGF-alpha, and CRTAM may be potential marker proteins for immune recovery in PTC patients after RAIT.

Indexed as

Iodine RadioisotopesLymphocyte SubsetsThyroid NeoplasmsAdultAgedCarcinoma, PapillaryCytokinesFemaleHumansInflammationMaleMiddle AgedThyroid Cancer, PapillaryThyroidectomyCytokinesIodine Radioisotopeslymphocyte subgroupspapillaryproximity extension assayradioactive iodine therapythyroid cancer

Identifiers

PMID40365939
PMCPMC12151066

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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.