Evidence mapPaperPMID 41741422Full record

ReviewCell death & disease2026

Modulation of immune cells and metabolic reprogramming in efferocytosis.

Karen Cristina Oliveira, Caroline Maria Marcos, Letícia de Aquino Penteado, Naiara Naiana Dejani, Pedro M Moraes-Vieira, Alexandra I Medeiros

Abstract readReview
In one paragraph

Review in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

6 authors.

Karen Cristina OliveiraDepartment of Biological Sciences, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil.
Caroline Maria MarcosLaboratory of Biology, Control and Surveillance of Insect Vectors, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
Letícia de Aquino PenteadoDepartment of Biological Sciences, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil.
Naiara Naiana DejaniDepartment of Biomedical Sciences, Federal University of Paraíba (UFPB), João Pessoa, Brazil.
Pedro M Moraes-VieiraDepartment of Genetics, Microbiology and Immunology, and Experimental Medicine Research Cluster (EMRC), State University of Campinas (UNICAMP), Institute of Biology, Campinas, Brazil.
Alexandra I MedeirosDepartment of Biological Sciences, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara, São Paulo, Brazil. alexandra.medeiros@unesp.br.ORCID http://orcid.org/0000-0001-6048-3647

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Brazilian Federal Agency for the Support and Evaluation of Graduate Education) Finance Code 001Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 21/02506-5
6 · The paper itself

Abstract

Under physiological conditions, cell apoptosis is a silent death process during tissue renewal and remodeling. The phagocytosis of apoptotic cells, known as efferocytosis, is a key process performed primarily by macrophages and dendritic cells, as well as by non-professional phagocytes, such as epithelial cells and fibroblasts. This process, which involves the removal of apoptotic cells, is not just a routine task. It plays a significant role in producing anti-inflammatory mediators that are instrumental in maintaining tissue homeostasis. However, during infection, pathogens can induce different patterns of cell death, including apoptosis. Efferocytosis of infected apoptotic cells is a crucial part of the host defense mechanism. It aids in bacterial clearance, activates the effector functions of phagocytes, and directs the activation of CD4+T lymphocytes. The different stages of the efferocytosis process are not just a sequence of events, but a complex interplay that can interfere with the microenvironment by releasing soluble mediators ("find-me signals") as a rich source of nutrients for phagocytes during the digestion process ("digest-me"), such as amino acids, nucleotides, lipids, and carbohydrates. In recent years, several studies have contributed to unraveling the impact of the different stages of the efferocytosis process on regulating metabolic pathways that support the continuous phagocytosis of apoptotic cells, the activation profile, and the effector functions of phagocytes. In this review, we discuss the impact of efferocytosis on immune cells during homeostasis and infectious diseases, and in the metabolic reprogramming on phagocyte activation. We also explore the role of efferocytosis during the clearance of apoptotic cells in different pathologies.

Indexed as

EfferocytosisPhagocytosisAnimalsApoptosisHumansMacrophagesMetabolic ReprogrammingPhagocytes

Identifiers

PMID41741422
PMCPMC12988870

What Socratic holds

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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.