Evidence map›Paper›PMID 30692527›Full record

ArticleNature communications2019

PD-1/PD-L1 checkpoint blockade harnesses monocyte-derived macrophages to combat cognitive impairment in a tauopathy mouse model.

Neta Rosenzweig, Raz Dvir-Szternfeld, Afroditi Tsitsou-Kampeli, Hadas Keren-Shaul, Hila Ben-Yehuda, Pierre Weill-Raynal, Liora Cahalon, Alex Kertser, Kuti Baruch, Ido Amit and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed, 2 pooled it
9.9field-weighted citation impact, top 2% 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

142 citing papers in PubMed, 2 syntheses or guidelines pooled it, 211 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. A phase 2A/B randomized trial of metabolic modulators intranasal insulin and empagliflozin for MCI and early AD.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Trial
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  18. Senescence of T cells and organ aging.Inflammation and regeneration · 2026
    Review
  19. Article
  20. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
    Review

82 more citing papers are in PubMed but not listed here.

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

12 authors at 1 institution in 1 country.

Neta RosenzweigDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Raz Dvir-SzternfeldDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Afroditi Tsitsou-KampeliDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Hadas Keren-ShaulDepartment of Immunology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Hila Ben-YehudaDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Pierre Weill-RaynalDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Liora CahalonDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Alex KertserDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Kuti BaruchDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Ido AmitDepartment of Immunology, Weizmann Institute of Science, Rehovot, 7610001, Israel.ORCID http://orcid.org/0000-0002-5880-2845
Assaf WeinerDepartment of Immunology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Michal SchwartzDepartment of Neurobiology, Weizmann Institute of Science, Rehovot, 7610001, Israel. Michal.Schwartz@weizmann.ac.il.
Weizmann Institute of Science · IL

Funding

European Research Council 232835
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a heterogeneous disorder with multiple etiologies. Harnessing the immune system by blocking the programmed cell death receptor (PD)-1 pathway in an amyloid beta mouse model was shown to evoke a sequence of immune responses that lead to disease modification. Here, blocking PD-L1, a PD-1 ligand, was found to have similar efficacy to that of PD-1 blocking in disease modification, in both animal models of AD and of tauopathy. Targeting PD-L1 in a tau-driven disease model resulted in increased immunomodulatory monocyte-derived macrophages within the brain parenchyma. Single cell RNA-seq revealed that the homing macrophages expressed unique scavenger molecules including macrophage scavenger receptor 1 (MSR1), which was shown here to be required for the effect of PD-L1 blockade in disease modification. Overall, our results demonstrate that immune checkpoint blockade targeting the PD-1/PD-L1 pathway leads to modification of common factors that go awry in AD and dementia, and thus can potentially provide an immunotherapy to help combat these diseases.

Indexed as

Alzheimer DiseaseAnimalsAntibodies, BlockingB7-H1 AntigenBrainCognitive DysfunctionDisease Models, AnimalHumansMacrophagesMice, Inbred BALB CMice, Inbred C57BLMice, Inbred StrainsMice, TransgenicProgrammed Cell Death 1 ReceptorTauopathiesAntibodies, BlockingB7-H1 AntigenCd274 protein, mouseProgrammed Cell Death 1 Receptor

Identifiers

PMID30692527
PMCPMC6349941
OpenAlexW2911778150

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.