Evidence map›Paper›PMID 35314846›Full record

ArticleNature immunology2022

Loss of the intracellular enzyme QPCTL limits chemokine function and reshapes myeloid infiltration to augment tumor immunity.

Rosa Barreira da Silva, Ricardo M Leitao, Ximo Pechuan-Jorge, Scott Werneke, Jason Oeh, Vincent Javinal, Yingyun Wang, Wilson Phung, Christine Everett, Jim Nonomiya and 15 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  9. Development of DPP-4-resistant CXCL9-Fc and CXCL10-Fc chemokines for effective cancer immunotherapy.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Deciphering the role of CD47 in cancer immunotherapy.Journal of advanced research · 2024
    Review
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  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 3 institutions in 3 countries.

Rosa Barreira da SilvaGenentech Inc., South San Francisco, CA, USA. barreira.rosa@gene.com.ORCID http://orcid.org/0000-0002-2117-3280
Ricardo M LeitaoGenentech Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-0916-7945
Ximo Pechuan-JorgeGenentech Inc., South San Francisco, CA, USA.
Scott WernekeGenentech Inc., South San Francisco, CA, USA.
Jason OehGenentech Inc., South San Francisco, CA, USA.
Vincent JavinalGenentech Inc., South San Francisco, CA, USA.
Yingyun WangGenentech Inc., South San Francisco, CA, USA.
Wilson PhungGenentech Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-7793-3931
Christine EverettGenentech Inc., South San Francisco, CA, USA.
Jim NonomiyaGenentech Inc., South San Francisco, CA, USA.
David ArnottGenentech Inc., South San Francisco, CA, USA.
Cheng LuGenentech Inc., South San Francisco, CA, USA.
Yi-Chun HsiaoGenentech Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-4499-2999
James T KoerberGenentech Inc., South San Francisco, CA, USA.
Isidro HötzelGenentech Inc., South San Francisco, CA, USA.
James ZiaiGenentech Inc., South San Francisco, CA, USA.
Zora ModrusanGenentech Inc., South San Francisco, CA, USA.
Thomas H PillowGenentech Inc., South San Francisco, CA, USA.
Merone Roose-GirmaGenentech Inc., South San Francisco, CA, USA.
Jill M SchartnerGenentech Inc., South San Francisco, CA, USA.
Mark MerchantGenentech Inc., South San Francisco, CA, USA.
Sascha RutzGenentech Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-2431-0938
Céline EidenschenkGenentech Inc., South San Francisco, CA, USA.
Ira MellmanGenentech Inc., South San Francisco, CA, USA. mellman.ira@gene.com.ORCID http://orcid.org/0000-0002-6132-7299
Matthew L AlbertGenentech Inc., South San Francisco, CA, USA. matthew@hibio.com.ORCID http://orcid.org/0000-0001-7285-6973
Genesys (United States) · USGene Therapy Laboratory · FRSt. Matthew's University · KY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated macrophages are composed of distinct populations arising from monocytes or tissue macrophages, with a poorly understood link to disease pathogenesis. Here, we demonstrate that mouse monocyte migration was supported by glutaminyl-peptide cyclotransferase-like (QPCTL), an intracellular enzyme that mediates N-terminal modification of several substrates, including the monocyte chemoattractants CCL2 and CCL7, protecting them from proteolytic inactivation. Knockout of Qpctl disrupted monocyte homeostasis, attenuated tumor growth and reshaped myeloid cell infiltration, with loss of monocyte-derived populations with immunosuppressive and pro-angiogenic profiles. Antibody targeting of the receptor CSF1R, which more broadly eliminates tumor-associated macrophages, reversed tumor growth inhibition in Qpctl

Indexed as

AminoacyltransferasesCD8-Positive T-LymphocytesChemokinesNeoplasmsAnimalsImmunotherapyLeukemic InfiltrationMiceMice, KnockoutMonocytesAminoacyltransferasesChemokinesglutaminyl-peptide cyclotransferase

Identifiers

PMID35314846
OpenAlexW4220986500

What OpenQuestion holds

Textmetadata
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.