Evidence map›Paper›PMID 40181978›Full record

ArticleFrontiers in immunology2025

Targeting CCRL2 enhances therapeutic outcomes in a tuberculosis mouse model.

Tianyin Wang, Darla Quijada, Taha Ahmedna, Jennie Ruelas Castillo, Nour Sabiha Naji, J David Peske, Petros C Karakousis, Suman Paul, Theodoros Karantanos, Styliani Karanika

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Tianyin Wang *Division of Infectious Diseases, Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, United States.
Darla Quijada *Division of Infectious Diseases, Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, United States.
Taha AhmednaLudwig Center and Lustgarten Laboratory, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Jennie Ruelas CastilloDivision of Infectious Diseases, Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, United States.
Nour Sabiha NajiDivision of Hematologic Malignancies, Department of Medical Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
J David PeskeDivision of Hematopathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Petros C KarakousisDivision of Infectious Diseases, Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, United States.
Suman PaulLudwig Center and Lustgarten Laboratory, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Theodoros Karantanos *Division of Hematologic Malignancies, Department of Medical Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Styliani Karanika *Division of Infectious Diseases, Department of Medicine, The Johns Hopkins Hospital, Baltimore, MD, United States.

Funding

Vaccine Response and Immunotherapeutics SWGP30AI094189 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Anna Palmer Durbin · 2012 to 2026
$67.0M
Pharmacology and Pharmacometrics CoreP30AI168436 · NIAID · JOHNS HOPKINS UNIVERSITY · PI MAUNANK SHAH · 2022 to 2026
$6.1M
Therapeutic vaccination to augment stringent response-specific T-cell immunity to MTB persistersR01AI148710 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KARAKOUSIS, PETROS C, MARKHAM, RICHARD B. · 2020 to 2024
$3.8M
TCR Targeting Antibodies for the Treatment of T cell CancersK08CA270403 · NCI · JOHNS HOPKINS UNIVERSITY · PI Suman Paul · 2022 to 2026
$1.1M
Mentoring in Immunometabolic Dysregulation in TB and TB/HIVK24AI143447 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KARAKOUSIS, PETROS C · 2019 to 2024
$956k
CCRL2 as a Regulator of Growth and Novel Target in Myelodysplastic SyndromeK08HL168777 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Theodoros Karantanos · 2023 to 2026
$687k
Mechanisms of a therapeutic DNA vaccine targeting Mycobacterium tuberculosis persistersK08AI174959 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Styliani Karanika · 2024 to 2026
$603k
NCI NIH HHS K08 CA270403NHLBI NIH HHS K08 HL168777NIAID NIH HHS K08 AI174959NIAID NIH HHS K24 AI143447NIAID NIH HHS P30 AI094189NIAID NIH HHS P30 AI168436NIAID NIH HHS R01 AI148710
6 · The paper itself

Abstract

Tuberculosis (TB) remains among the leading infectious causes of death. Due to the limited number of antimicrobials in the TB drug discovery pipeline, interest has developed in host-directed approaches to improve TB treatment outcomes. C-C motif chemokine-like receptor 2 (CCRL2) is a unique seven-transmembrane domain receptor that is upregulated by inflammatory signals and mediates leucocyte migration. However, little is known about its role in TB infection. Here, we show that

Indexed as

Antitubercular AgentsImmunoconjugatesMycobacterium tuberculosisReceptors, CCRTuberculosisAnimalsDendritic CellsDisease Models, AnimalFemaleLungMacrophages, AlveolarMiceMice, Inbred C57BLNeutrophilsAntitubercular AgentsImmunoconjugatesReceptors, CCRadjunctive therapeutic treatmentalveolar macrophagesantibody-drug conjugateCCRL2dendritic cellsneutrophilsTB

Identifiers

PMID40181978
PMCPMC11965133

What Socratic 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 Socratic graph.