Evidence map›Paper›PMID 33198297›Full record

ReviewInternational journal of molecular sciences2020

Tfh Cells in Health and Immunity: Potential Targets for Systems Biology Approaches to Vaccination.

Hannah Law, Vanessa Venturi, Anthony Kelleher, C Mee Ling Munier

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Predicting SARS-CoV-2-specific CD4Clinical and experimental medicine · 2025
    Article
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  6. Host Immune Responses toTropical medicine and infectious disease · 2023
    Review
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  9. Review
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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

4 authors at 1 institution in 1 country.

Hannah LawThe Kirby Institute, UNSW Sydney, Sydney 2052, Australia.
Vanessa VenturiThe Kirby Institute, UNSW Sydney, Sydney 2052, Australia.ORCID 0000-0003-3340-2367
Anthony KelleherThe Kirby Institute, UNSW Sydney, Sydney 2052, Australia.
C Mee Ling MunierThe Kirby Institute, UNSW Sydney, Sydney 2052, Australia.ORCID 0000-0002-6419-142X
UNSW Sydney · AU

Funding

Australian National Health and Medical Research Council 1067590Australian National Health and Medical Research Council 1149990UNSW RTP Scholarship RSAP1000
6 · The paper itself

Abstract

T follicular helper (Tfh) cells are a specialised subset of CD4+ T cells that play a significant role in the adaptive immune response, providing critical help to B cells within the germinal centres (GC) of secondary lymphoid organs. The B cell receptors of GC B cells undergo multiple rounds of somatic hypermutation and affinity maturation within the GC response, a process dependent on cognate interactions with Tfh cells. B cells that receive sufficient help from Tfh cells form antibody-producing long-lived plasma and memory B cells that provide the basis of decades of effective and efficient protection and are considered the gold standard in correlates of protection post-vaccination. However, the T cell response to vaccination has been understudied, and over the last 10 years, exponential improvements in the technological underpinnings of sampling techniques, experimental and analytical tools have allowed multidisciplinary characterisation of the role of T cells and the immune system as a whole. Of particular interest to the field of vaccinology are GCs and Tfh cells, representing a unique target for improving immunisation strategies. Here, we discuss recent insights into the unique journey of Tfh cells from thymus to lymph node during differentiation and their role in the production of high-quality antibody responses as well as their journey back to the periphery as a population of memory cells. Further, we explore their function in health and disease and the power of next-generation sequencing techniques to uncover their potential as modulators of vaccine-induced immunity.

Indexed as

Systems BiologyVaccinesAnimalsBiomarkersB-LymphocytesCD4-Positive T-LymphocytesCell DifferentiationGerminal CenterHumansImmune SystemLymph NodesReceptors, Antigen, T-CellRNA-SeqRNA, Small CytoplasmicSignal TransductionT Follicular Helper CellsBiomarkersReceptors, Antigen, T-CellRNA, Small CytoplasmicVaccinesgerminal centre (GC)lymph node (LN)scRNA-seqsystems biologyT cell receptor (TCR)T follicular helper cells (Tfh)

Identifiers

PMID33198297
PMCPMC7696930
OpenAlexW3105503938

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.