Context

Cytomegalovirus (CMV) infection is a frequent and potentially severe event in solid organ transplant (SOT) recipients.

Most of available treatment display adverse effects that limit their use. Therefore, in case of an infection, it is of primary importance to identify the patients at high risk of severe infection and/or disease, and who ill benefit the most from antiviral therapy.

As CMV infection is mainly controlled by cellular immunity, measuring specific anti-CMV T lymphocyte immunity could be an interesting tool for identifying these at-risk individuals. One of these tests is the QuantiFERON-CMV (QF-CMV) assay (QuiagenTM, Courtabœuf, France).

Aim of the study

The aim of the study is to determine the extent to which the QF-CMV can be use to identify, among SOT recipients with a CMV viremia, those that may not need antiviral therapy.

Methods

Participation to the study will be proposed to SOT recipients with an asymptomatic CMV infection with a blood viral load between 1,000 and 15,000 IU/mL.

The QF-CMV will be performed in included participants, and the result will be given or not to the clinician in charge (according to the attributed group through randomisation).

• In the group without result communication, the clinician in charge will determine whether a treatment is needed according to the guidelines and the local practices.
• in the group with result communication, the clinician in charge will be advised not to introduce antiviral therapy if the result is positive, and to determine whether a treatment is needed according to the guidelines and the local practices if the result is positive.

In the following weeks, the viral load will be monitored, along with creatininemia, cell blood count, and kalemia (to detect antiviral adverse effect).

The participants will be sampled:

• 5 to 12 days after QF-CMV sampling (V2) ;
• 7 to 14 days days after V2 (V3 - between D12 and D26) ;
• 7 to 14 days days after V3 (V4 - between D19 and D40) .

Endpoints

The primary endpoint is the rate of uncontrolled infection 5 to 12 days after QF-CMV sampling, defined as follows:

• Blood CMV viral load >10,000 IU/mL [4 log];
• And/or increase in blood viral load ≥0.5 log IU/mL with CV otherwise >5000 IU/mL;
• And/or the onset of CMV disease.

The secondary endpoint is the is the occurrence antiviral adverse effects (hematoxicity or nephrotoxicity).

Context.

Solid organ transplant (SOT) recipients are at high risk of opportunistic infections, particularly due to cytomegalovirus (CMV).

Regarding CMV infection after transplantation, two approaches are possible: either antiviral prophylaxis for several months, followed by monitoring of blood CMV viral load (or viremia), or immediate monitoring of viral load without prophylaxis.

In both cases, the detection of a CMV viral load raises a complex question: is antiviral treatment necessary? Indeed, not all viremia leads to CMV disease: some patients spontaneously control their viremia.

In order to limit unnecessary treatments, their toxicity and their cost, new tools are needed to identify people at high risk of developing a high viral load or CMV disease.

As CMV infection is mainly controlled by cellular immunity, measuring specific anti-CMV T lymphocyte immunity could be an interesting tool for identifying these at-risk individuals.

The QuantiFERON-CMV (QF-CMV) test (QuiagenTM, Courtabœuf, France) is an interferon-gamma (IFN-γ) release assay (IGRA), which measures the presence of anti-CMV T lymphocyte immunity. Results from previous retrospective studies suggest that in cases of CMV replication, it may be relevant to base the therapeutic attitude not only on the virological characteristics of this replication, but also on the existence of specific T lymphocyte immunity.

The aim of this study is therefore to prospectively assess the contribution of QF-CMV to therapeutic decisions in cases of intermediate CMV viral load (between 1,000 and 15,000 IU/mL).

Methods

SOT recipients with a detectable blood CMV viral load (CV1) between 1,000 and 15,000 IU/mL without symptoms (fever, organ damage) will be offered participation in the study within 48 hours of detection of this CMV viral load.

After inclusion, participants will be immediately sampled for QF-CMV.

They will be randomized (2:1) into 2 groups:

• An experimental group in which the result of the QF-CMV will be communicated to the doctor in charge;
• A control group in which the result is not reported to the doctor in charge.

In the experimental group, the recommended attitude will depend on the QF-CMV result:

• If positive, the physician in charge will be advised not to introduce antiviral treatment;
• If is negative or indeterminate, the physician in charge will be advised to proceed according to the standard of care. He/she will be free to introduce or not the antiviral molecule of his choice.

In the control group, the physician in charge will be advised to proceed according to the standard of care, based on current recommendations and local practices.

In both groups, as routinely done when a CMV viral load is detected in the blood, this parameter will be checked several times after the 1st detection (V0):

• 5 to 12 days after QF-CMV sampling (CV - V2 = D5 to D12) ;
• 7 to 14 days after CV2 (CV3 - V3 = D12 to D26) ;
• 7 to 14 days after CV3 (CV4 - V4 = D19 to D40). Similarly, blood cell count, kalemia and creatininemia were performed at baseline and then at V2, V3 and V4.

The primary endpoint is the rate of uncontrolled infection at 5 to 12 days after QF-CMV sampling (V2), defined as follows:

• Blood CMV viral load >10,000 IU/mL [4 log] ;
• And/or increase in blood viral load ≥0.5 log IU/mL with CV otherwise >5000 IU/mL ;
• And/or the onset of CMV disease.

Conversely, the blood CMV viral load will be considered controlled if its value at V2 does not exceed 10,000 IU/mL [4 log] and :

• It decreases (regardless of the magnitude of the decrease);
• Or increases, but by less than 0.5 log IU/mL ;
• or is stable. In the event of uncontrolled infection at V2, the physician in charge should manage the viral load in accordance with current recommendations and local practices (in most cases, antiviral treatment should be introduced if this has not already been done), and continue monitoring at V3 and V4. He will be free to introduce or not the antiviral molecule of his choice.

In the event of controlled infection at V2, the physician in charge will be advised not to initiate antiviral treatment if this has not already been done, and to continue monitoring at V3 and V4.

The secondary endpoint is the occurrence of an iatrogenic event (hematoxicity or nephrotoxicity) related to antivirals; parameters that may reflect such toxicity (blood cell count, kalemia, creatinin) will be collected at inclusion (V1) and then at the 3 times mentioned above (V2 to V4).

Inclusion Criteria:

• Age ≥ 18 years.

• Solid organ transplant recipient (heart, kidney, liver and lung)

• Detectable CMV viral load between 1,000 and 15,000 IU/mL (including 2 borderline values):

  • Asymptomatic (no fever or organ dysfunction) ;
  • Occurrence within 2 years of transplantation in the absence of primary post-transplant anti-CMV prophylaxis;
  • Or within 2 years of discontinuation of primary post-transplant anti-CMV prophylaxis if such prophylaxis was used.

• Having signed an informed consent form.

• Affiliated to a social security scheme.

Exclusion Criteria:

• Presence of anti-Herpesviridae treatment when CMV replication is detected ([val]aciclovir, [val]ganciclovir, foscarnet, cidofovir, letermovir, maribavir, anti-CMV immunoglobulins, cidofovir, brincidofovir).
• Pregnant or breast-feeding women.
• Persons under guardianship or trusteeship.
• Subjects under administrative or judicial supervision.
• Subject unable to be contacted in case of emergency.

Individual participant data that underlie the results reported in this article, after deidentification, will be available beginning 3 months and ending 5 years following article publication.

Researchers who provide a methodologically sound proposal.will be given access to these data. data requestors will need to sign a data access agreement.

Proposals should be directed to oepaulard@chu-grenoble.fr

beginning 3 months and ending 5 years following article publication.

beginning 3 months and ending 5 years following article publication.

Researchers who provide a methodologically sound proposal.will be given access to these data.