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Pediatr Blood Cancer ; 70(8): e30429, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37243390

RESUMEN

Cytomegalovirus retinitis (CMVR) following hematopoietic stem cell transplantation (HCT) for a primary immunodeficiency is a rare but highly morbid condition with potential irreversible consequences despite optimal antiviral pharmacotherapy. Viral-specific T cells (VSTs) pose a promising and safe approach eradicating intractable viral disease. We describe the case of a 21-month-old male with Wiskott-Aldrich syndrome (WAS) and CMVR post HCT with sustained long-term virologic and clinical response after CMV-specific T-cell therapy. This case highlights the need to consider VST as an adjunct upfront strategy in refractory CMVR and for routine ophthalmologic screening and surveillance in high-risk patients post HCT.


Asunto(s)
Retinitis por Citomegalovirus , Trasplante de Células Madre Hematopoyéticas , Humanos , Masculino , Lactante , Retinitis por Citomegalovirus/terapia , Retinitis por Citomegalovirus/tratamiento farmacológico , Antivirales/uso terapéutico , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Fosfoproteínas , Linfocitos T
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