Evidence map›Paper›PMID 27358028›Full record

ReviewClinical science (London, England : 1979)2016

The end of the road for the tryptophan depletion concept in pregnancy and infection.

Abdulla A-B Badawy, Aryan M A Namboodiri, John R Moffett

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.6field-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

49 citing papers in PubMed, 88 citations in OpenAlex.

  1. Tryptophan's Journey Through Pregnancy: The Role of Serotonin.International journal of tryptophan research : IJTR · 2026
    Review
  2. Indoleamine 2,3-Dioxygenase Regulates Placental Trophoblast Cell Invasion.International journal of molecular sciences · 2025
    Article
  3. Review
  4. Article
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  6. Review
  7. Bridging the divide: unveiling mutual immunological pathways of cancer and pregnancy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. The Function of the Kynurenine Pathway in the Placenta: A Novel Pharmacotherapeutic Target?International journal of environmental research and public health · 2021
    Review
  17. Review
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Abdulla A-B BadawySchool of Health Sciences, Cardiff Metropolitan University, Western Avenue, Cardiff CF5 2YB, Wales, U.K. ABadawy@cardiffmet.ac.uk.
Aryan M A NamboodiriDepartments of Anatomy, Physiology and Genetics and Neuroscience Program, Uniformed Services University of the Health Sciences, Bethesda, MD, U.S.A.
John R MoffettDepartments of Anatomy, Physiology and Genetics and Neuroscience Program, Uniformed Services University of the Health Sciences, Bethesda, MD, U.S.A.
Uniformed Services University of the Health Sciences · USCardiff Metropolitan University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We hypothesize that: (1) L-tryptophan (Trp) is greatly utilized and not depleted in pregnancy; (2) fetal tolerance is achieved in part through immunosuppressive kynurenine (Kyn) metabolites produced by the flux of plasma free (non-albumin-bound) Trp down the Kyn pathway; (3) the role of indoleamine 2,3-dioxygenase (IDO) in infection is not related to limitation of an essential amino acid, but is rather associated with stress responses and the production of Kyn metabolites that regulate the activities of antigen presenting cells and T-cells, as well as increased NAD(+) synthesis in IDO-expressing cells; (4) Trp depletion is not a host defence mechanism, but is a consequence of Trp utilization. We recommend that future studies in normal and abnormal pregnancies and in patients with infections or cancer should include measurements of plasma free Trp, determinants of Trp binding (albumin and non-esterified fatty acids), total Trp, determinants of activities of the Trp-degrading enzymes Trp 2,3-dioxygenase (TDO) (cortisol) and IDO (cytokines) and levels of Kyn metabolites. We also hypothesize that abnormal pregnancies and failure to combat infections or cancer may be associated with excessive Trp metabolism that can lead to pathological immunosuppression by excessive production of Kyn metabolites. Mounting evidence from many laboratories indicates that Trp metabolites are key regulators of immune cell behaviour, whereas Trp depletion is an indicator of extensive utilization of this key amino acid.

Indexed as

Immune ToleranceAntigen-Presenting CellsCommunicable DiseasesFemaleFetusHumansIndoleamine-Pyrrole 2,3,-DioxygenaseKynurenineNADOxidative StressPregnancyPregnancy ComplicationsProtein BindingT-LymphocytesTryptophanTryptophan OxygenaseIndoleamine-Pyrrole 2,3,-DioxygenaseKynurenineNADTryptophanTryptophan Oxygenaseimmunosuppressionkynurenine metabolitesplasma free tryptophantryptophan utilization concept

Identifiers

PMID27358028
PMCPMC4926258
OpenAlexW2467541392

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.