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A 2\u2010day consortium of experts in infectious diseases, transplantation, vaccinology, and immunology was held with the objective to review evidence and create expert recommendations for clinicians when considering live viral vaccines post\u2010SOT. For consideration of VV and MMR post\u2010transplant, evidence exists only for kidney and liver transplant recipients. For MMR vaccine post\u2010SOT, consider vaccination during outbreak or travel to endemic risk areas. Patients who have received antiproliferative agents (eg. mycophenolate mofetil), T cell\u2013depleting agents, or rituximab; or have persistently elevated EBV viral loads, or are in a state of functional tolerance, should be vaccinated with caution and have a more in\u2010depth evaluation to define benefit of vaccination and net state of immune suppression prior to considering vaccination. MMR and\/or VV (not combined MMRV) is considered to be safe in patients who are clinically well, are greater than 1\u00a0year after liver or kidney transplant and 2\u00a0months after acute rejection episode, can be closely monitored, and meet specific criteria of \u201clow\u2010level\u201d immune suppression as defined in the document.<\/jats:p>","DOI":"10.1111\/petr.13571","type":"journal-article","created":{"date-parts":[[2019,9,9]],"date-time":"2019-09-09T08:16:45Z","timestamp":1568017005000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":105,"title":["Live vaccines after pediatric solid organ transplant: Proceedings of a consensus meeting, 2018"],"prefix":"10.1111","volume":"23","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0456-1860","authenticated-orcid":false,"given":"Sneha","family":"Suresh","sequence":"first","affiliation":[{"name":"Division of Infectious Disease and IHOPE, Department of Pediatrics, Stollery 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