Evidence map›Paper›PMID 33431697›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Natural cystatin C fragments inhibit GPR15-mediated HIV and SIV infection without interfering with GPR15L signaling.

Manuel Hayn, Andrea Blötz, Armando Rodríguez, Solange Vidal, Nico Preising, Ludger Ständker, Sebastian Wiese, Christina M Stürzel, Mirja Harms, Rüdiger Gross and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. GPR15-guided CD8Nature · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Endogenous Peptide Inhibitors of HIV Entry.Advances in experimental medicine and biology · 2022
    Article
  13. The Role of GPR15 Function in Blood and Vasculature.International journal of molecular sciences · 2021
    Review
  14. Review
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

20 authors at 5 institutions in 3 countries.

Manuel HaynInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0001-5908-3099
Andrea BlötzInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
Armando RodríguezCore Facility Functional Peptidomics, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0001-5921-3770
Solange VidalNovartis Institutes for Biomedical Research, 4056 Basel, Switzerland.ORCID 0000-0003-0289-9569
Nico PreisingCore Facility Functional Peptidomics, Ulm University Medical Center, 89081 Ulm, Germany.
Ludger StändkerCore Facility Functional Peptidomics, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0002-8436-4260
Sebastian WieseCore Unit Mass Spectrometry and Proteomics, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0001-5697-2608
Christina M StürzelInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
Mirja HarmsInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
Rüdiger GrossInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0003-0355-7915
Christoph JungInstitute of Electrochemistry, Ulm University, 89081 Ulm, Germany.ORCID 0000-0002-1422-4991
Miriam KieneInfection Biology Unit, German Primate Center-Leibniz Institute for Primate Research, 37077 Göttingen, Germany.
Timo JacobInstitute of Electrochemistry, Ulm University, 89081 Ulm, Germany.ORCID 0000-0001-7777-2306
Stefan PöhlmannInfection Biology Unit, German Primate Center-Leibniz Institute for Primate Research, 37077 Göttingen, Germany.ORCID 0000-0001-6086-9136
Wolf-Georg ForssmannPHARIS Biotec GmbH, 30625 Hannover, Germany.
Jan MünchInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0001-7316-7141
Konstantin M J SparrerInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.ORCID 0000-0002-8682-1779
Klaus SeuwenNovartis Institutes for Biomedical Research, 4056 Basel, Switzerland.ORCID 0000-0002-6847-6676
Beatrice H HahnDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6076; bhahn@pennmedicine.upenn.edu frank.kirchhoff@uni-ulm.de.ORCID 0000-0002-9400-9887
Frank KirchhoffInstitute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany; bhahn@pennmedicine.upenn.edu frank.kirchhoff@uni-ulm.de.ORCID 0000-0002-7052-2360
Universität Ulm · DEGerman Primate Center · DENovartis (Switzerland) · CHPharis Biotec (Germany) · DEUniversity of Pennsylvania · US

Funding

First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
Natural SIV Reservoirs and Human Zoonotic RiskR01AI050529 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HAHN, BEATRICE H · 2001 to 2022
$6.1M
Restriction of HIV-1 transmission by type 1 interferonsR01AI114266 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HAHN, BEATRICE H · 2014 to 2018
$3.2M
NIAID NIH HHS R01 AI050529NIAID NIH HHS R01 AI114266NIAID NIH HHS UM1 AI126620
6 · The paper itself

Abstract

GPR15 is a G protein-coupled receptor (GPCR) proposed to play a role in mucosal immunity that also serves as a major entry cofactor for HIV-2 and simian immunodeficiency virus (SIV). To discover novel endogenous GPR15 ligands, we screened a hemofiltrate (HF)-derived peptide library for inhibitors of GPR15-mediated SIV infection. Our approach identified a C-terminal fragment of cystatin C (CysC95-146) that specifically inhibits GPR15-dependent HIV-1, HIV-2, and SIV infection. In contrast, GPR15L, the chemokine ligand of GPR15, failed to inhibit virus infection. We found that cystatin C fragments preventing GPR15-mediated viral entry do not interfere with GPR15L signaling and are generated by proteases activated at sites of inflammation. The antiretroviral activity of CysC95-146 was confirmed in primary CD4

Indexed as

AnimalsCystatin CHIV-1HIV InfectionsHumansReceptors, G-Protein-CoupledReceptors, PeptideReceptors, VirusSignal TransductionSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusT-LymphocytesVirus InternalizationCystatin CGPR15 protein, humanReceptors, G-Protein-CoupledReceptors, PeptideReceptors, Viruschemokinescystatin CGPR15G protein-coupled receptorsimmunodeficiency viruses

Identifiers

PMID33431697
PMCPMC7826402
OpenAlexW3118420879

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.