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									<identifier>oai:www.peertechzpublications.org:10.17352/2640-7973.000023</identifier>
									<datestamp>2024-06-24</datestamp>
									<setSpec>PTZ.AOT:VOL9</setSpec>
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										<dc:title>
										Safe immunosuppression. New tool for personalized immunosuppressant treatment in renal transplantation. A case report
										</dc:title><dc:creator>Safe immunosuppression. New tool for personalized immunosuppressant treatment in renal transplantation. A case report</dc:creator><dc:description>&lt;p&gt;Background: The adjustment of immunosuppressive therapy after kidney transplantation (KT) to avoid graft rejection remains an important challenge for clinicians. It is difficult to achieve a good balance between under-immunosuppression (with an increased risk of graft rejection) and over-immunosuppression (with an increased risk of side effects) by only relying on the available information about immunosuppressive drugs (IMS).&lt;/p&gt;&lt;p&gt;Immunobiogram® (IMBG) is a novel in vitro diagnostic test that provides clinicians with information about the patient’s sensitivity to individual IMS.&lt;/p&gt;&lt;p&gt;Objective: To present a case report of a patient with renal transplant in the maintenance phase who presented several complications probably related to the immunosuppression during the follow-up, where the use of IMBG as complementary information helped clinicians to guide the therapeutical decision.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Methods: IMBG is a first-in-class in vitro immunoassay that involves the culture of the patient peripheral blood mononuclear cells (PBMCs) in a semi-solid 3D matrix, then submitted to immune stimulation. It reveals the capacity of an IMS over a gradient to inhibit the activation of immune cells. The read-out allows the building of a dose-response curve per IMS tested, which is mathematically analyzed by a software using the key curve parameters and finally to be translated into a sensitivity map to IMS.&lt;/p&gt;&lt;p&gt;Findings: We present a case report of a 72-year-old patient with a cadaveric donor kidney transplant receiving standard immunosuppressive treatment with mycophenolate, tacrolimus, and corticosteroids. The patient presented several episodes of infections during the follow-up (SARS-CoV2, Cytomegalovirus, spondylodisquitis by Staphylococcus aureus, and emphysematous cystitis) which were managed with different treatment adjustments such as de-escalation of mycophenolate and switching to mTOR. The information provided by the IMBG showed a lack of sensitivity to mTOR which allowed to confirm the final adjustment to a treatment with tacrolimus and corticosteroids, remaining the patient stable since then.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Discussion: Despite various adjustments to the immunosuppressive therapy during the follow-up, the patient continued experiencing adverse effects that could be related to an over-immunosuppression state. The IMBG provided pharmacodynamic information that complemented the clinical and pharmacokinetic data available, facilitating the individualization of the treatment.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Conclusion: The case highlights the potential of the IMBG as a complementary clinical tool for personalized treatment of kidney transplant patient management.&lt;/p&gt;</dc:description>
										<dc:publisher>Archives of Organ Transplantation - Peertechz Publications</dc:publisher>
										<dc:date>2024-06-24</dc:date>
										<dc:type>Case Report</dc:type>
										<dc:identifier>https://doi.org/10.17352/2640-7973.000023</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Safe immunosuppression. New tool for personalized immunosuppressant treatment in renal transplantation. A case report et al.</dc:rights>
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