Evidence map›Paper›PMID 36555775›Full record

ReviewInternational journal of molecular sciences2022

LAIR1, an ITIM-Containing Receptor Involved in Immune Disorders and in Hematological Neoplasms.

François Van Laethem, Lucie Donaty, Emmanuelle Tchernonog, Vanessa Lacheretz-Szablewski, Jennifer Russello, Delphine Buthiau, Marion Almeras, Jérôme Moreaux, Caroline Bret

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

François Van LaethemDepartment of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.
Lucie DonatyDepartment of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.
Emmanuelle TchernonogDepartment of Clinical Hematology, CHU Montpellier, 34295 Montpellier, France.
Vanessa Lacheretz-SzablewskiDepartment of Biopathology, CHU Montpellier, 34295 Montpellier, France.
Jennifer RusselloDepartment of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.
Delphine ButhiauCH Béziers, 34500 Béziers, France.
Marion AlmerasCH Béziers, 34500 Béziers, France.
Jérôme MoreauxDepartment of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.ORCID 0000-0002-5717-3207
Caroline BretDepartment of Biological Hematology, CHU Montpellier, 34295 Montpellier, France.
Centre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier de Béziers · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

Agence Nationale de la Recherche ANR-18-CE15-0010-01 PLASMADIFF-3DFrench National Cancer Institute PLBIO18-362PIT-MMFrench National Cancer Institute PLBIO19-098 INCA_13832 FATidique
6 · The paper itself

Abstract

Leukocyte-associated immunoglobulin (Ig)-like receptor 1 (LAIR1, CD305) belongs to the family of immune-inhibitory receptors and is widely expressed on hematopoietic mature cells, particularly on immune cells. Four different types of ligands of LAIR1 have been described, including collagens, suggesting a potential immune-regulatory function on the extracellular matrix. By modulating cytokine secretion and cellular functions, LAIR1 displays distinct patterns of expression among NK cell and T/B lymphocyte subsets during their differentiation and cellular activation and plays a major negative immunoregulatory role. Beyond its implications in physiology, the activity of LAIR1 can be inappropriately involved in various autoimmune or inflammatory disorders and has been implicated in cancer physiopathology, including hematological neoplasms. Its action as an inhibitory receptor can result in the dysregulation of immune cellular responses and in immune escape within the tumor microenvironment. Furthermore, when expressed by tumor cells, LAIR1 can modulate their proliferation or invasion properties, with contradictory pro- or anti-tumoral effects depending on tumor type. In this review, we will focus on its role in normal physiological conditions, as well as during pathological situations, including hematological malignancies. We will also discuss potential therapeutic strategies targeting LAIR1 for the treatment of various autoimmune diseases and cancer settings.

Indexed as

Hematologic NeoplasmsImmune System DiseasesNeoplasmsGene ExpressionHumansT-Lymphocyte SubsetsTumor Microenvironmentautoimmunitycollagenhematological neoplasmsimmunoregulatoryinflammationinhibitory receptorLAIR1

Identifiers

PMID36555775
PMCPMC9788452
OpenAlexW4312211211

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.