Evidence map›Paper›PMID 33751597›Full record

ReviewImmunological reviews2021

Classical CD4 T cells as the cornerstone of antimycobacterial immunity.

Jeffrey Morgan, Kaylin Muskat, Rashmi Tippalagama, Alessandro Sette, Julie Burel, Cecilia S Lindestam Arlehamn

Abstract readReview
In one paragraph

Review in Immunological reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

  1. Article
  2. Construction of RecombinantPathogens (Basel, Switzerland) · 2026
    Article
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  7. Review
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  12. Article
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  14. Article
  15. Article
  16. Article
  17. Polyfunctionality of CD4Frontiers in immunology · 2025
    Article
  18. Article
  19. Article
  20. Article
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.

Jeffrey MorganCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.
Kaylin MuskatCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.
Rashmi TippalagamaCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.
Alessandro SetteCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.
Julie BurelCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.
Cecilia S Lindestam ArlehamnCenter for Infectious Disease, La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID 0000-0001-7302-8002

Funding

Large Scale T Cell Epitope Discovery: Proteome-wide characterization of T cell epitopes from Mycobacterium tuberculosis in vaccination and active infection75N93019C00067 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI PETERS, BJOERN · 2019 to 2023
$4.5M
NIAID NIH HHS 75N93019C00067
6 · The paper itself

Abstract

Tuberculosis is a significant health problem without an effective vaccine to combat it. A thorough understanding of the immune response and correlates of protection is needed to develop a more efficient vaccine. The immune response against Mycobacterium tuberculosis (Mtb) is complex and involves all aspects of the immune system, however, the optimal protective, non-pathogenic T cell response against Mtb is still elusive. This review will focus on discussing CD4 T cell immunity against mycobacteria and its importance in Mtb infection with a primary focus on human studies. We will in particular discuss the large heterogeneity of immune cell subsets that have been revealed by recent immunological investigations at an unprecedented level of detail. These studies have identified specific classical CD4 T cell subsets important for immune responses against Mtb in various states of infection. We further discuss the functional attributes that have been linked to the various subsets such as upregulation of activation markers and cytokine production. Another important topic to be considered is the antigenic targets of Mtb-specific immune responses, and how antigen reactivity is influenced by both disease state and environmental exposure(s). These are key points for both vaccines and immune diagnostics development. Ultimately, these factors are holistically considered in the definition and investigations of what are the correlates on protection and resolution of disease.

Indexed as

Mycobacterium tuberculosisTuberculosisAntigens, BacterialCD4-Positive T-LymphocytesHumansImmunityT-Lymphocyte SubsetsAntigens, BacterialCD4 T cellsMtb-specific T cellsmycobacteriaTB

Identifiers

PMID33751597
PMCPMC8252593

What OpenQuestion holds

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LicenceCC BY-NC
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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.