Literature DB >> 26680375

Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients.

Ajit P Limaye1, Corinna La Rosa, Jeff Longmate, Don J Diamond.   

Abstract

BACKGROUND: Immune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk.
METHODS: Plasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT: 13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation.
RESULTS: IL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity.
CONCLUSIONS: The exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.

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Year:  2016        PMID: 26680375      PMCID: PMC4685744          DOI: 10.1097/TP.0000000000000816

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  36 in total

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2.  Effects of the intensity of immunosuppressive therapy on outcome of treatment for CMV disease in organ transplant recipients.

Authors:  A Asberg; A G Jardine; A A Bignamini; H Rollag; M D Pescovitz; C C Gahlemann; A Humar; A Hartmann
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4.  PD-1 expression and IL-2 loss of cytomegalovirus- specific T cells correlates with viremia and reversible functional anergy.

Authors:  U Sester; D Presser; J Dirks; B C Gärtner; H Köhler; M Sester
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5.  A prospective longitudinal analysis of cytomegalovirus (CMV)-specific CD4+ and CD8+ T cells in kidney allograft recipients at risk of CMV infection.

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Review 9.  Management of cytomegalovirus infection and disease in liver transplant recipients.

Authors:  Jackrapong Bruminhent; Raymund R Razonable
Journal:  World J Hepatol       Date:  2014-06-27

10.  Dysregulated cytokine responses during cytomegalovirus infection in renal transplant recipients.

Authors:  Mahmoud Sadeghi; Volker Daniel; Cord Naujokat; Paul Schnitzler; Jan Schmidt; Arianeb Mehrabi; Martin Zeier; Gerhard Opelz
Journal:  Transplantation       Date:  2008-07-27       Impact factor: 4.939

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Journal:  Med Microbiol Immunol       Date:  2019-03-25       Impact factor: 3.402

2.  The human cytomegalovirus glycoprotein pUL11 acts via CD45 to induce T cell IL-10 secretion.

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Journal:  PLoS Pathog       Date:  2017-06-19       Impact factor: 6.823

Review 3.  Human Cytomegalovirus Interleukin 10 Homologs: Facing the Immune System.

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Journal:  Front Cell Infect Microbiol       Date:  2020-06-09       Impact factor: 5.293

4.  Cytokine Profiles in Children After Pediatric Kidney Transplantation With Acute Cellular Compared to Chronic Antibody-mediated Rejection and Stable Patients: A Pilot Study.

Authors:  Nadja Borsum; Murielle Verboom; Thurid Ahlenstiel-Grunow; Lars Pape
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