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Tailoring cytomegalovirus prophylaxis based on T cell immunity panel assessment in kidney transplant patients at high risk of cytomegalovirus.
Servais, Abigail M; McMullen, John S; Bowen, Riley; Kleiboeker, Steven B; Ulloa, Isabelle; Duncan, Kara; Miles, Clifford D.
Afiliación
  • Servais AM; Department of Pharmaceutical and Nutrition Care, Nebraska Medical Center Omaha, Omaha, Nebraska, USA.
  • McMullen JS; Department of Pharmaceutical and Nutrition Care, Nebraska Medical Center Omaha, Omaha, Nebraska, USA.
  • Bowen R; University of Nebraska Medical Center College of Pharmacy, Nebraska Medical Center Omaha, Omaha, Nebraska, USA.
  • Kleiboeker SB; Eurofins Viracor, Lenexa, Kansas, USA.
  • Ulloa I; Eurofins Viracor, Lenexa, Kansas, USA.
  • Duncan K; Eurofins Viracor, Lenexa, Kansas, USA.
  • Miles CD; Department of Internal Medicine, Division of Nephrology, Nebraska Medical Center, Omaha, Nebraska, USA.
Transpl Infect Dis ; : e14291, 2024 May 06.
Article en En | MEDLINE | ID: mdl-38708965
ABSTRACT

BACKGROUND:

Valganciclovir prophylaxis against cytomegalovirus (CMV) is recommended for solid organ transplant recipients, but is associated with drawbacks, including expense and leukopenia. Our center adopted a strategy of serial assessment with a CMV-specific T cell immunity panel (CMV-TCIP) and cessation of valganciclovir prophylaxis upon demonstration of adequate CD4+ responses in kidney transplant patients at high risk of CMV disease.

METHODS:

We retrospectively reviewed adult recipients of a kidney or pancreas transplant between August 2019 and July 2021 undergoing serial CMV-TCIP monitoring. Included patients were considered high risk for CMV, defined by donor positive (D+)/recipient negative (R-) CMV IgG serostatus, or recipient positive (R+) patients who received induction with a lymphocyte-depleting agent. Prophylaxis was discontinued after a patient's first CMV-specific CD4+ T cell value of ≥0.20%. Risk of clinically significant CMV infection (csCMVi) in those who underwent early discontinuation of CMV prophylaxis and predictors of CMV T cell immunity were analyzed.

RESULTS:

Of 54 included patients, 22 stopped prophylaxis early due to CMV-specific CD4+ T cell immunity at a median of 4.7 (IQR 3.8-5.4) months after transplant. No instances of csCMVi were observed in the 22 patients who had prophylaxis discontinued early, of whom 19/22 were CMV R+ and 3/22 were CMV D+/R-. Donor/recipient CMV serostatus was predictive of immunity (p <.001).

CONCLUSION:

Early discontinuation of valganciclovir prophylaxis in patients with CMV CD4+ T cellular immunity appears safe and potentially beneficial in this preliminary series, especially in R+ patients. Further study is warranted, given that truncated prophylaxis may yield patient-level benefits.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos