Evidence map›Paper›PMID 42866400›Full record

ArticleFASEB bioAdvances2026

The Proteome of Plasma Extracellular Vesicles in Latent and Active Tuberculosis Reveals Phase-Specific Composition and Immunometabolic Insights.

Eliud S-Peregrino, Jessica Castañeda-Casimiro, Luis Vallejo-Castillo, Mishelle Soria-Fragoso, Gloria M Ortega-Díaz, Karen I Mondragón-Lara, Alfonso Méndez-Tenorio, Rommel Chacón-Salinas, Blanca E García-Pérez, Jeanet Serafín-López and 4 more

Abstract read
In one paragraph

Article in FASEB bioAdvances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Eliud S-PeregrinoInstituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB), Posgrado en Inmunología Mexico City Mexico.ORCID https://orcid.org/0000-0001-6281-3590
Jessica Castañeda-CasimiroInstituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB), Posgrado en Inmunología Mexico City Mexico.ORCID https://orcid.org/0009-0002-5639-3467
Luis Vallejo-CastilloDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0002-9532-3472
Mishelle Soria-FragosoDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0009-0008-1620-3124
Gloria M Ortega-DíazInstituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB), Posgrado en Inmunología Mexico City Mexico.ORCID https://orcid.org/0009-0004-2670-8303
Karen I Mondragón-LaraDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0009-0003-6534-6846
Alfonso Méndez-TenorioDepartamento de Bioquímica Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0003-1871-4311
Rommel Chacón-SalinasDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0002-4500-0253
Blanca E García-PérezDepartamento de Microbiología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0001-6610-5559
Jeanet Serafín-LópezDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0003-2736-2688
Carlos Wong-BaezaDepartamento de Bioquímica Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0002-6262-8106
Víctor Hugo Rosales-GarcíaCentro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Laboratorios Nacionales de Servicios Experimentales (LANSE) Mexico City Mexico.ORCID https://orcid.org/0000-0002-5204-7789
Alejandro Hernández-SolisUniversidad Nacional Autónoma de México (UNAM), Facultad de Medicina Mexico City Mexico.ORCID https://orcid.org/0000-0002-9314-3515
Isabel Wong-BaezaDepartamento de Inmunología Instituto Politécnico Nacional (IPN), Escuela Nacional de Ciencias Biológicas (ENCB) Mexico City Mexico.ORCID https://orcid.org/0000-0002-2516-0081

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) is an infectious disease that affects millions of people worldwide. Extracellular vesicles (EVs) are mediators of intercellular communication that participate in the immunopathogenesis of TB. Here, we characterized plasma EVs from healthy individuals and from individuals with latent (LTB) or active TB (ATB). We found increased total protein concentrations in EVs from LTB and ATB individuals compared to healthy controls, without significant differences in EV concentrations, but reduced exosome abundance in LTB. Proteomic and bioinformatic analysis showed that LTB EVs were enriched in proteins associated with the regulation of inflammation, tissue remodeling, and lipid metabolism, including TGFβ and apolipoproteins (APO) A1 and E. In contrast, ATB EVs were enriched in mycobacterial antigens and host proteins associated with acute inflammation, including serum amyloid A1 and A2 (SAA1/A2) and the calgranulin complex proteins S100A8 and S100A9. These host proteins were central and/or cohesive nodes in the protein-protein interaction networks of these EVs. Dot blot analysis confirmed the increased levels of these EV proteins in a second group of individuals with LTB or ATB. The EV levels of mycobacterial antigens correlated positively with the EV levels of SAA1/A2 and S100A8/A9, but negatively with their levels of TGFβ and APOA1. Principal component analysis and hierarchical clustering suggested that the simultaneous analysis of mycobacterial antigens and these EV proteins could discriminate between healthy, LTB, and ATB individuals. Our findings confirm that plasma EVs provide insights into the host immunometabolic response to TB and may be a source of clinically useful biomarkers.

Indexed as

apolipoproteinsextracellular vesiclesinflammationproteometuberculosis

Identifiers

PMID42866400
PMCPMC13656203

What OpenQuestion holds

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Registered trials

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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.