Evidence map›Paper›PMID 27467705›Full record

ArticlePLoS pathogens2016

CD4+ T Cells Recognizing PE/PPE Antigens Directly or via Cross Reactivity Are Protective against Pulmonary Mycobacterium tuberculosis Infection.

Fadel Sayes, Alexandre Pawlik, Wafa Frigui, Matthias I Gröschel, Samuel Crommelynck, Catherine Fayolle, Felipe Cia, Gregory J Bancroft, Daria Bottai, Claude Leclerc and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. A proteome-wide atlas of humoral immunity toFrontiers in immunology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. The PE/PPE family proteins ofFrontiers in immunology · 2025
    Review
  7. Article
  8. Frontiers in immunology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Evolutionary genomic and bacteria GWAS analysis ofApplied and environmental microbiology · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

12 authors at 4 institutions in 3 countries.

Fadel SayesInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Alexandre PawlikInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Wafa FriguiInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Matthias I GröschelInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Samuel CrommelynckInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Catherine FayolleInstitut Pasteur, Unité de Régulation Immunitaire et Vaccinologie, Paris, France.
Felipe CiaLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Gregory J BancroftLondon School of Hygiene and Tropical Medicine, London, United Kingdom.
Daria BottaiUniversity of Pisa, Ricerca Traslazionale e delle Nuove Tecnologie in Medicina e Chirurgia, Pisa, Italy.
Claude LeclercInstitut Pasteur, Unité de Régulation Immunitaire et Vaccinologie, Paris, France.
Roland BroschInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Laleh MajlessiInstitut Pasteur, Unité de Pathogénomique Mycobactérienne Intégrée, Paris, France.
Institut Pasteur · FRLondon School of Hygiene & Tropical Medicine · GBInserm · FRUniversity of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb), possesses at least three type VII secretion systems, ESX-1, -3 and -5 that are actively involved in pathogenesis and host-pathogen interaction. We recently showed that an attenuated Mtb vaccine candidate (Mtb Δppe25-pe19), which lacks the characteristic ESX-5-associated pe/ppe genes, but harbors all other components of the ESX-5 system, induces CD4+ T-cell immune responses against non-esx-5-associated PE/PPE protein homologs. These T cells strongly cross-recognize the missing esx-5-associated PE/PPE proteins. Here, we characterized the fine composition of the functional cross-reactive Th1 effector subsets specific to the shared PE/PPE epitopes in mice immunized with the Mtb Δppe25-pe19 vaccine candidate. We provide evidence that the Mtb Δppe25-pe19 strain, despite its significant attenuation, is comparable to the WT Mtb strain with regard to: (i) its antigenic repertoire related to the different ESX systems, (ii) the induced Th1 effector subset composition, (iii) the differentiation status of the Th1 cells induced, and (iv) its particular features at stimulating the innate immune response. Indeed, we found significant contribution of PE/PPE-specific Th1 effector cells in the protective immunity against pulmonary Mtb infection. These results offer detailed insights into the immune mechanisms underlying the remarkable protective efficacy of the live attenuated Mtb Δppe25-pe19 vaccine candidate, as well as the specific potential of PE/PPE proteins as protective immunogens.

Indexed as

AnimalsAntigens, BacterialBacterial ProteinsCD4-Positive T-LymphocytesCross ReactionsDisease Models, AnimalFemaleFlow CytometryMiceMice, Inbred C57BLMycobacterium tuberculosisTh1 CellsTuberculosis, PulmonaryTuberculosis VaccinesAntigens, BacterialBacterial ProteinsPPE2 protein, Mycobacterium tuberculosisTuberculosis Vaccines

Identifiers

PMID27467705
PMCPMC4965174
OpenAlexW2476497360

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.