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Status unknownNCT05452148IMPDHUpdated Jul 11, 2022

Specific Genotypes/Phenotypes of Pneumocystis Jirovecii in Solid Organ Transplant Recipients: Potential Involvement of Mycophenolic Acid

An observational study in Transplantation and Pulmonary Diseases, sponsored by University Hospital, Brest. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-07-11.

Sponsored by University Hospital, Brest · Observational

The sponsor has not verified this record recently (last verified Jul 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

To determine the presence of IMDPH mutants of Pneumocystis jirovecii in solid organ transplant recipient with prior exposition to mycophenolic acid.

Read the detailed description

Mycophenolic acid (MPA) targets inosine 5'-monophosphate dehydrogenase (IMPDH) of human lymphocytes. It is used as an immunosuppressant to prevent rejection in solid organ transplant (SOT) recipients who are otherwise at risk for Pneumocystis pneumonia (PCP). We recently hypothesized that MPA exerts selective pressure on Pneumocystis given the in vitro antifungal activity of this drug on other fungi. In a single center study, we identified a missense mutation G1020A in the impdh gene, corresponding to an amino acid change Ala261Thr in IMPDH protein, among Pneumocystis isolates from MPA-treated SOT recipients. Considering that the IMPDH of MPA-resistant Candida albicans isolates harbors Thr at the analogous position, this mutation was considered to be a marker of Pneumocystis strain selection related to MPA exposure.

The aim of this study is to strengthen these preliminary results with data from a large multicenter study.

The study will be conducted in 26 centers in France. About one hundred patients with PCP will be enrolled. Pneumocystis isolates from SOT recipients exposed to MPA and from control patients (non-SOT recipients, not exposed to MPA) will be examined.The analysis of the impdh gene was combined with a multilocus sequence typing (MLST) method (mtLSUrRNA, cytochrome b and superoxide dismutase genes) characterized by a high discriminatory power.

The expected results may show the presence of the G1020A mutation (Ala261Thr) in SOT recipients exposed to MPA and in none of the control patients not exposed to MPA. This mutation will be significantly associated with MPA exposure. It could also be associated with a specific multilocus genotype in SOT patients and none of the control patients.

The study will confirm that the G1020A mutation (Ala261Thr) represents the signature of MPA exposure. The results of the analysis of the impdh gene combined with the MLST will highlight the selection under MPA pressure of specific strains of Pneumocystis, which circulate in the population of SOT recipients.

02

Conditions studied

  • Transplantation
  • Pulmonary Diseases

Keywords

  • Pneumocystis jirovecii
  • IMPDH
  • Genetic variant
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In context

Pneumonia, Pneumocystis

107 studies on the registry are indexed under Pneumonia, Pneumocystis; 15 are open to participants now.

This study's planned enrollment of 100 is below the median of 220 across 32 observational studies indexed under Pneumonia, Pneumocystis.

Browse Pneumonia, Pneumocystis studies →

Lead sponsor

University Hospital, Brest is the lead sponsor of 594 studies on the registry; 135 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

organ transplant recipients vs. non transplant recipient

Inclusion criteria

  • >= 18 years old with PCP diagnoses, organ transplant recipient or not, acceptation to participate

Exclusion criteria

Exclusion Criteria:

  • \< 18 years old, no acceptation to participate
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Presence of Pneumocystis IMPDH gene mutant or not

    The main biological parameter which will be measured will be the positive or negative result for the detection of Pneumocystis IMPDH gene mutant

    Time frame: At patient enrollment

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 11, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05452148
Lead sponsor
University Hospital, Brest
Responsible party
Sponsor
First posted
Jul 11, 2022
Start date
Jul 25, 2022 (estimated)
Primary completion
Jul 25, 2023 (estimated)
Completion
Jul 25, 2023 (estimated)
Last update
Jul 11, 2022

Study contacts

Gilles nevez
Contact
gilles.nevez@chu-brest.fr
02 98 14 51 02
solene Le Gall
Contact
solene.legal@univ-brest.fr

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2022. You cannot join it, but the record below documents what was studied.

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