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.
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Authors | Raul Montiel-Esparza, Suzanne M Michalak, Anthony Huy Dinh Le, Christopher Or, Quan Dong Nguyen, Ruby Khoury, Michael S Grimley, Alice Bertaina, Edna Klinger, Ami J Shah, Edward H Wood |
Journal | Pediatric blood & cancer
(Pediatr Blood Cancer)
Vol. 70
Issue 8
Pg. e30429
(Aug 2023)
ISSN: 1545-5017 [Electronic] United States |
PMID | 37243390
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2023 Wiley Periodicals LLC. |
Chemical References |
- Antiviral Agents
- Phosphoproteins
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Topics |
- Humans
- Male
- Infant
- Cytomegalovirus Retinitis
(therapy, drug therapy)
- Antiviral Agents
(therapeutic use)
- Hematopoietic Stem Cell Transplantation
(adverse effects)
- Phosphoproteins
- T-Lymphocytes
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