Evidence map›Paper›PMID 26255628›Full record

ArticleOncotarget2015

Elevated Th22 as well as Th17 cells associated with therapeutic outcome and clinical stage are potential targets in patients with multiple myeloma.

Min Wang, Ping Chen, Yan Jia, Na He, Daqi Li, Chunyan Ji, Daoxin Ma

Abstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. T Cells Dysfunction in Multiple Myeloma.ImmunoTargets and therapy · 2025
    Review
  3. Article
  4. Bone Marrow Stromal Cells-Induced Drug Resistance in Multiple Myeloma.International journal of molecular sciences · 2020
    Review
  5. Review
  6. The Imbalance between Foxp3Journal of immunology research · 2018
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. 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.

Min WangDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.
Ping ChenDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.
Yan JiaDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.
Na HeDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.
Daqi LiDepartment of Hematology, Jinan Central Hospital, Affiliated to Shandong University, Jinan, China.
Chunyan JiDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.
Daoxin MaDepartment of Hematology, Qilu Hospital, Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T helper (Th) cell imbalance plays important roles in tumor development and their effects in Multiple myeloma (MM) remain unclear. In the present study, we investigated the levels and clinical significance of Th22, Th17 and Th1 cells in patients with MM. Th subsets were examined by flow cytometry. Plasma IL-22, IL-17A and IFN-γ concentrations were measured by ELISA. AHR and RORC mRNA expression was examined by RT-PCR. Here, we found that the frequency of Th22 cells was significantly elevated in peripheral blood (PB) and bone marrow (BM) of newly-diagnosed MM patients, and recovered in complete remission patients after chemotherapy. The circulating Th17 cells accompanied by IL-17A levels were also up-regulated in MM patients and decreased after remission. We also found that there was a significantly positive correlation between Th22 and Th17 cells in MM patients. Moreover, the frequencies of Th22 and Th17 cells were higher in stage III than in stage I+II of MM. Our data demonstrated that Th22 and Th17 cells might be important therapeutic targets in multiple myeloma and could facilitate the effect of antitumor immunotherapy.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCase-Control StudiesCD4 Lymphocyte CountChinaEnzyme-Linked Immunosorbent AssayFemaleHumansInterferon-gammaInterleukin-17Interleukin-22InterleukinsAHR protein, humanBasic Helix-Loop-Helix ProteinsBiomarkers, TumorIFNG protein, humanIL17A protein, humanInterferon-gammaInterleukin-17Interleukin-22InterleukinsNuclear Receptor Subfamily 1, Group F, Member 3Receptors, Aryl HydrocarbonRNA, MessengerRORC protein, humanmultiple myelomaPathology SectionTh1Th17Th22

Identifiers

PMID26255628
PMCPMC4627228

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Registered trials

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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.