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Pediatr Blood Cancer ; 70(8): e30429, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37243390

ABSTRACT

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.


Subject(s)
Cytomegalovirus Retinitis , Hematopoietic Stem Cell Transplantation , Humans , Male , Infant , Cytomegalovirus Retinitis/therapy , Cytomegalovirus Retinitis/drug therapy , Antiviral Agents/therapeutic use , Hematopoietic Stem Cell Transplantation/adverse effects , Phosphoproteins , T-Lymphocytes
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