Evidence map›Paper›PMID 29912725›Full record

ArticleJournal of immunotherapy (Hagerstown, Md. : 1997)2018

Tumor Regression and Cure Depends on Sustained Th1 Responses.

Min Dai, Ingegerd Hellstrom, Yuen Y Yip, Hans Olov Sjögren, Karl Erik Hellstrom

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunotherapy (Hagerstown, Md. : 1997), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. AttenuatedFrontiers in immunology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. TInternational journal of molecular sciences · 2022
    Article
  10. Review
  11. Review
  12. Tumor-Specific CD4Frontiers in immunology · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
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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

5 authors at 2 institutions in 2 countries.

Min DaiDepartment of Pathology, University of Washington, Harborview Medical Center, Seattle, WA.
Ingegerd HellstromDepartment of Pathology, University of Washington, Harborview Medical Center, Seattle, WA.
Yuen Y YipDepartment of Pathology, University of Washington, Harborview Medical Center, Seattle, WA.
Hans Olov SjögrenThe Rausing Laboratory, Department of Neurosurgery, Lund University, Lund, Sweden.
Karl Erik HellstromDepartment of Pathology, University of Washington, Harborview Medical Center, Seattle, WA.
Harborview Medical Center · USLund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While immunomodulatory monoclonal antibodies (mAbs) have therapeutic efficacy against many tumors, few patients are cured. Attempting to improve their therapeutic efficacy we have applied the TC1 mouse lung carcinoma model and injected established subcutaneous tumors intratumorally with 3 weekly doses of various combinations of mAbs. Combinations of mAbs to CTLA4/PD1/CD137 (the 3 mAb combination) and to CTLA4/PD1/CD137/CD19 (the 4 mAb combination) were most efficacious to induce complete regression of both the injected tumor and an untreated tumor in the same mouse. Tumor cure was consistently associated with shifting a Th2 to a Th1 response in tumor-draining lymph nodes and spleen and it involved epitope specific and long-lived memory T cells as well as M1 macrophages. This shift and accompanying tumor rejection was harder to achieve as the treated tumors increased in size. Relapse of tumors which had initially regressed following treatment with immunomodulatory mAbs was associated with return of a Th2 microenvironment in tumors, tumor-draining lymph nodes and spleens rather than the emergence of immune-resistant tumor cells. While mAbs to CTLA4 plus PD-1 were therapeutically ineffective, combining the 2 of them with intraperitoneal cisplatin, 10 mg/kg, induced long-term complete tumor regression in most mice with small TC1 tumors and the therapeutic efficacy against larger tumors improved by administrating cisplatin together with the 3 or 4 mAb combination.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD19Antineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorCisplatinCTLA-4 AntigenDisease Models, AnimalFemaleLung NeoplasmsMice, Inbred C3HMice, Inbred C57BLNeoplasm Recurrence, LocalProgrammed Cell Death 1 ReceptorTh1 CellsAntibodies, MonoclonalAntigens, CD19Antineoplastic Agents, ImmunologicalCD19 antigen, mouseCisplatinCTLA-4 AntigenCtla4 protein, mousePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorTumor Necrosis Factor Receptor Superfamily, Member 9

Identifiers

PMID29912725
PMCPMC6133214
OpenAlexW2808486935

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.