Evidence map›Paper›PMID 29454575›Full record

ReviewSeminars in immunology2018

Targeting complement-mediated immunoregulation for cancer immunotherapy.

Martin Kolev, Maciej M Markiewski

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

46 citing papers in PubMed, 65 citations in OpenAlex.

  1. Systemic and local dysregulation of the complement system in glioma: a comprehensive systematic review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. Liposomes in tumor treatment: a double-edged sword.Science China. Life sciences · 2026
    Review
  3. Article
  4. Review
  5. Inherited genetic risk factors in young-onset lung cancer.medRxiv : the preprint server for health sciences · 2026
    Article
  6. In vivo CAR engineering for immunotherapy.Nature reviews. Immunology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. gC1qR: A New Target for Cancer Immunotherapy.Frontiers in immunology · 2023
    Review
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Martin KolevComplement and Inflammation Research Section, DIR, NHLBI, NIH, Bethesda, MD, 20892, United States. Electronic address: martin.kolev@nih.gov.
Maciej M MarkiewskiDepartment of Immunotherapeutics and Biotechnology, School of Pharmacy, Texas Tech University Health Sciences Center, Abilene, TX, 79601, United States. Electronic address: maciej.markiewski@ttuhsc.edu.
National Institutes of Health · USTexas Tech University · US

Funding

Targeting the Premetastatic Niche by Antiangiogenic ImmunotherapyR01CA190209 · NCI · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI MARKIEWSKI, MACIEJ MICHAL · 2016 to 2020
$1.7M
Intramural NIH HHS Z99 HL999999NCI NIH HHS R01 CA190209
6 · The paper itself

Abstract

Complement was initially discovered as an assembly of plasma proteins "complementing" the cytolytic activity of antibodies. However, our current knowledge places this complex system of several plasma proteins, receptors, and regulators in the center of innate immunity as a bridge between the initial innate responses and adaptive immune reactions. Consequently, complement appears to be pivotal for elimination of pathogens, not only as an early response defense, but by directing the subsequent adaptive immune response. The discovery of functional intracellular complement and its roles in cellular metabolism opened novel avenues for research and potential therapeutic implications. The recent studies demonstrating immunoregulatory functions of complement in the tumor microenvironment and the premetastatic niche shifted the paradigm on our understanding of functions of the complement system in regulating immunity. Several complement proteins, through their interaction with cells in the tumor microenvironment and in metastasis-targeted organs, contribute to modulating tumor growth, antitumor immunity, angiogenesis, and therefore, the overall progression of malignancy and, perhaps, responsiveness of cancer to different therapies. Here, we focus on recent progress in our understanding of immunostimulatory vs. immunoregulatory functions of complement and potential applications of these findings to the design of novel therapies for cancer patients.

Indexed as

AnimalsComplement ActivationComplement System ProteinsCytotoxicity, ImmunologicHumansImmunity, InnateImmunomodulationImmunotherapyNeoplasmsTumor MicroenvironmentComplement System ProteinsCancerComplementImmune regulationPremetastatic nicheTumor microenvironment

Identifiers

PMID29454575
PMCPMC5984681
OpenAlexW2791274689

What OpenQuestion holds

Textmetadata
LicenceTDM
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.