Evidence map›Paper›PMID 31318442›Full record

ArticleImmunology2019

Functionally significant metabolic differences between B and T lymphocyte lineages.

Jasneet Kaur Khalsa, Amanpreet Singh Chawla, Savit B Prabhu, Mukti Vats, Atika Dhar, Gagan Dev, Nabanita Das, Sandip Mukherjee, Shalini Tanwar, Hridesh Banerjee and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
  2. Altered B cell metabolic pathways characterize type 1 diabetes progression.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
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  16. Metabolic substrate utilization in stress-induced immune cells.Intensive care medicine experimental · 2020
    Review
  17. 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

15 authors at 4 institutions in 2 countries.

Jasneet Kaur KhalsaNational Institute of Immunology, New Delhi, India.
Amanpreet Singh ChawlaNational Institute of Immunology, New Delhi, India.
Savit B PrabhuWellcome Laboratory, Christian Medical College, Vellore, India.
Mukti VatsNational Institute of Immunology, New Delhi, India.
Atika DharNational Institute of Immunology, New Delhi, India.
Gagan DevNational Institute of Immunology, New Delhi, India.
Nabanita DasIndian Institute of Chemical Biology, Kolkata, India.
Sandip MukherjeeIndian Institute of Chemical Biology, Kolkata, India.
Shalini TanwarNational Institute of Immunology, New Delhi, India.
Hridesh BanerjeeNational Institute of Immunology, New Delhi, India.
Jeannine Marie DurdikDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, USA.
Vineeta BalNational Institute of Immunology, New Delhi, India.
Anna GeorgeNational Institute of Immunology, New Delhi, India.ORCID 0000-0001-9401-0944
Satyajit RathNational Institute of Immunology, New Delhi, India.ORCID 0000-0002-7343-1173
Gopalakrishnan Aneeshkumar ArimbasseriNational Institute of Immunology, New Delhi, India.
National Institute of Immunology · INIndian Institute of Chemical Biology · INChristian Medical College, Vellore · INUniversity of Arkansas at Fayetteville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of B and T lymphocytes leads to major remodelling of the metabolic landscape of the cells enabling their post-activation functions. However, naive B and T lymphocytes also show metabolic differences, and the genesis, nature and functional significance of these differences are not yet well understood. Here we show that resting B-cells appeared to have lower energy demands than resting T-cells as they consumed lower levels of glucose and fatty acids and produced less ATP. Resting B-cells are more dependent on OXPHOS, while T-cells show more dependence on aerobic glycolysis. However, despite an apparently higher energy demand, T lineage cells showed lower rates of protein synthesis than equivalent B lineage stages. These metabolic differences between the two lineages were established early during lineage differentiation, and were functionally significant. Higher levels of protein synthesis in B-cells were associated with increased synthesis of MHC class II molecules and other proteins associated with antigen internalization, transport and presentation. The combination of higher energy demand and lower protein synthesis in T-cells was consistent with their higher ATP-dependent motility. Our data provide an integrated perspective of the metabolic differences and their functional implications between the B and T lymphocyte lineages.

Indexed as

Oxidative PhosphorylationAdenosine TriphosphateAnimalsB-LymphocytesCell DifferentiationCell LineageFatty AcidsGene ExpressionGlucoseGlycolysisHistocompatibility Antigens Class IIImmunophenotypingLymphocyte ActivationMiceMice, Inbred C57BLMice, Inbred CBAAdenosine TriphosphateFatty AcidsGlucoseHistocompatibility Antigens Class IIB-cellsmetabolic differencesribo-seqRNA-seqT-cells

Identifiers

PMID31318442
PMCPMC6742768
OpenAlexW2963235463

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.