Evidence map›Paper›PMID 39411786›Full record

ArticleGut microbes

Controlled infection with cryopreserved human hookworm induces CTLA-4 expression on Tregs and upregulates tryptophan metabolism.

Francesco Vacca, Thomas C Mules, Mali Camberis, Brittany Lavender, Sophia-Louise Noble, Alissa Cait, Kate Maclean, John Mamum, Bibek Yumnam, Tama Te Kawa and 5 more

Abstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

15 authors.

Francesco VaccaLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Thomas C MulesLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.ORCID 0000-0002-3943-9198
Mali CamberisLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Brittany LavenderLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Sophia-Louise NobleLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Alissa CaitLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Kate MacleanLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
John MamumLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Bibek YumnamLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Tama Te KawaLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Laura Ferrer-FontHugh Green Technology Centre, Malaghan Institute of Medical Research, Wellington, New Zealand.
Jeffry S TangLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Olivier GasserLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Graham Le GrosLe Gros Laboratory, Malaghan Institute of Medical Research, Wellington, New Zealand.
Stephen InnsDepartment of Medicine, University of Otago, Wellington, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infecting humans with controlled doses of helminths, such as human hookworm (termed hookworm therapy), is proposed to prevent or treat various intestinal and extraintestinal diseases. However, full-scale clinical trials examining hookworm therapy are limited by the inability to scale-up the production of hookworm larvae to infect sufficient numbers of patients. With the aim of overcoming this challenge, this study infected four healthy individuals with hookworm larvae that had been reanimated from cryopreserved eggs to examine their viability and immunogenicity. We demonstrate that reanimated cryopreserved hookworm larvae establish a viable hookworm infection and elicit a similar immune response to larvae cultured from fresh stool. Furthermore, a refined understanding of the therapeutic mechanisms of hookworm is imperative to determine which diseases to target with hookworm therapy. To investigate potential therapeutic mechanisms, this study assessed changes in the immune cells, microbiome, and plasma metabolome in the four healthy individuals infected with cryopreserved hookworm larvae and another nine individuals infected with larvae cultured from freshly obtained stool. We identified potential immunoregulatory mechanisms by which hookworm may provide a beneficial effect on its host, including increased expression of CTLA-4 on regulatory T cells (Tregs) and upregulation of tryptophan metabolism. Furthermore, we found that a participant's baseline microbiome predicted the severity of symptoms and intestinal inflammation experienced during a controlled hookworm infection. In summary, our findings demonstrate the feasibility of full-scale clinical trials examining hookworm therapy by minimizing the reliance on human donors and optimizing the culturing process, thereby enabling viable hookworm larvae to be mass-produced and enabling on-demand inoculation of patients. Furthermore, this study provides insights into the complex interactions between helminths and their host, which could inform the development of novel therapeutic strategies.

Indexed as

CryopreservationCTLA-4 AntigenHookworm InfectionsLarvaT-Lymphocytes, RegulatoryTryptophanAdultAncylostomatoideaAnimalsFecesFemaleHumansMaleUp-RegulationCTLA-4 AntigenCTLA4 protein, humanTryptophanclinical trialcontrolled infectioncryopreservationeosinophiliahelminthsHookwormimmune regulationmicrobiome

Identifiers

PMID39411786
PMCPMC11485773

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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.