Risk Factors for Immune Recovery Uveitis in Patients with Cytomegalovirus Retinitis After Hematopoietic Stem Cell Transplantation

PURPOSE: To investigate the risk factors and clinical characteristics of immune recovery uveitis (IRU) in patients with cytomegalovirus (CMV) retinitis after hematopoietic stem cell transplantation (HSCT). METHODS: Clinical variables-including age, sex, type of hematologic disease, survival status, absolute neutrophil count, involved eye, visual acuity, number of intravitreal antiviral injections, recurrence of CMV retinitis, CMV titers in blood and aqueous humor, extent and location of retinal involvement, donor human leukocyte antigen matching, donor relationship, and systemic CMV treatment-were evaluated in patients with CMV retinitis following HSCT. RESULTS: = 0.027, respectively). CONCLUSION: Retinal involvement near the posterior pole, larger affected areas, and a shorter interval between HSCT and CMV retinitis diagnosis are significant risk factors for developing IRU in patients with CMV retinitis after HSCT. Careful monitoring for IRU remains essential even after resolution of CMV retinitis.

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Publication Details

Journal
Ocular Immunology and Inflammation
Published
2026-04-17
DOI
https://doi.org/10.1080/09273948.2026.2620452
Primary Topic
Cytomegalovirus and herpesvirus research
Type
article
Field-Weighted Citation Impact
0.00

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article

Risk Factors for Immune Recovery Uveitis in Patients with Cytomegalovirus Retinitis After Hematopoietic Stem Cell Transplantation

D Lee, Jae‐Joong Kim, Young Gun Park, Y M Park
Ocular Immunology and Inflammation
Cytomegalovirus and herpesvirus research
article

Risk Factors for Immune Recovery Uveitis in Patients with Cytomegalovirus Retinitis After Hematopoietic Stem Cell Transplantation

D Lee, Jae‐Joong Kim, Young Gun Park, Y M Park
article en

Abstract

PURPOSE: To investigate the risk factors and clinical characteristics of immune recovery uveitis (IRU) in patients with cytomegalovirus (CMV) retinitis after hematopoietic stem cell transplantation (HSCT). METHODS: Clinical variables-including age, sex, type of hematologic disease, survival status, absolute neutrophil count, involved eye, visual acuity, number of intravitreal antiviral injections, recurrence of CMV retinitis, CMV titers in blood and aqueous humor, extent and location of retinal involvement, donor human leukocyte antigen matching, donor relationship, and systemic CMV treatment-were evaluated in patients with CMV retinitis following HSCT. RESULTS: = 0.027, respectively). CONCLUSION: Retinal involvement near the posterior pole, larger affected areas, and a shorter interval between HSCT and CMV retinitis diagnosis are significant risk factors for developing IRU in patients with CMV retinitis after HSCT. Careful monitoring for IRU remains essential even after resolution of CMV retinitis.

Ocular Immunology and InflammationVol. 34(4)
Catholic University of Korea (KR)
National Research Foundation of Korea
Good health and well-being
Openalex Percentile: Top 25%
Cytomegalovirus and herpesvirus research
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