Evidence map›Paper›PMID 37311583›Full record

ArticleLife science alliance2023

An immune-based tool platform for in vivo cell clearance.

Jieqiong Zhang, Tatsuya Tsukui, Xiumin Wu, Alyssa Brito, John Maxwell Trumble, Juan C Caraballo, Greg M Allen, José Zavala-Solorio, Chunlian Zhang, Jonathan Paw and 7 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 70% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

17 authors at 3 institutions in 1 country.

Jieqiong ZhangCalico Life Sciences LLC, South San Francisco, CA, USA zjq.thu@gmail.com.ORCID https://orcid.org/0009-0000-3642-0400
Tatsuya TsukuiDivision of Pulmonary, Critical Care, Allergy and Sleep, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.ORCID https://orcid.org/0000-0003-3100-6934
Xiumin WuCalico Life Sciences LLC, South San Francisco, CA, USA.
Alyssa BritoAbbVie Inc, Chicago IL, USA.
John Maxwell TrumbleAbbVie Inc, Chicago IL, USA.
Juan C CaraballoDivision of Pulmonary, Critical Care, Allergy and Sleep, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Greg M AllenDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
José Zavala-SolorioCalico Life Sciences LLC, South San Francisco, CA, USA.ORCID https://orcid.org/0000-0003-2025-2507
Chunlian ZhangCalico Life Sciences LLC, South San Francisco, CA, USA.
Jonathan PawCalico Life Sciences LLC, South San Francisco, CA, USA.
Wendell A LimDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID https://orcid.org/0000-0003-4052-8056
Jiefei GengAbbVie Inc, Chicago IL, USA.
Yuliya KutskovaAbbVie Inc, Chicago IL, USA.
Adam FreundCalico Life Sciences LLC, South San Francisco, CA, USA.
Ganesh KolumamCalico Life Sciences LLC, South San Francisco, CA, USA.
Dean SheppardDivision of Pulmonary, Critical Care, Allergy and Sleep, Department of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Robert L CohenCalico Life Sciences LLC, South San Francisco, CA, USA rlc@calicolabs.com.ORCID https://orcid.org/0009-0002-2355-1705
AbbVie (United States) · USUniversity of California, San Francisco · USSan Francisco Art Institute · US

Funding

Cellular and molecular delineation of pathologic fibroblasts in pulmonary fibrosisR00HL155786 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TSUKUI, TATSUYA · 2023 to 2025
$747k
Cellular and molecular delineation of pathologic fibroblasts in pulmonary fibrosisK99HL155786 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TSUKUI, TATSUYA · 2021 to 2022
$315k
NHLBI NIH HHS K99 HL155786NHLBI NIH HHS R00 HL155786
6 · The paper itself

Abstract

Immunological targeting of pathological cells has been successful in oncology and is expanding to other pathobiological contexts. Here, we present a flexible platform that allows labeling cells of interest with the surface-expressed model antigen ovalbumin (OVA), which can be eliminated via either antigen-specific T cells or newly developed OVA antibodies. We demonstrate that hepatocytes can be effectively targeted by either modality. In contrast, pro-fibrotic fibroblasts associated with pulmonary fibrosis are only eliminated by T cells in initial experiments, which reduced collagen deposition in a fibrosis model. This new experimental platform will facilitate development of immune-based approaches to clear potential pathological cell types in vivo.

Indexed as

AntibodiesPulmonary FibrosisFibroblastsHepatocytesHumansKineticsAntibodies

Identifiers

PMID37311583
PMCPMC10264967
OpenAlexW4380480369

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.