Case Report: Relapse of SLE associated with EBV infection in a patient after CAR-T cell therapy: a clinical case
- 1Zunyi Medical University , , ,
- 2Department of Pediatric, Allergy Immune & Rheumatology, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University Guangdong Provincial Clinical Research Center for Child Health , ,
- 3Division of Immunology, Harvard Medical School , , ,
Abstract
We present the case of a 13-year-old boy with refractory systemic lupus erythematosus (SLE) who achieved drug-free remission after anti-CD19 CAR-T cell therapy, but subsequently experienced Epstein–Barr virus (EBV) reactivation on day 142 after CAR T-cell infusion and peak EBV load was 24,400 IU/mL with a severe drop in platelets to 8×10 ⁹ /L, which leading to relapse of SLE and manifestations of chronic active EBV disease (CAEBVD). The whole exogenous gene testing found X chromosome Xp22.33q28 region (chrX: 200855-155239820) a duplicate of about 155.04Mbp,which is associated with the development of Klinefelter syndrome (KS).The temporal association between EBV resurgence and SLE flare suggests that CAR-T-induced immunosuppression with some genetic background may permit EBV reactivation, which can be associated with the return of autoimmunity. This case highlights the need for vigilant monitoring for opportunistic infections and genetic background, particularly EBV, after CAR-T therapy for autoimmune diseases, as they may contribute to disease relapse.
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BibTeX
@article{zeng2026case,
title = {{Case Report: Relapse of SLE associated with EBV infection in a patient after CAR-T cell therapy: a clinical case}},
author = {Ping Zeng and Qi Ren and Xianfei Gao and Wei Xian and Pui Y. Lee and Feng Li and Caihong Xu and Mingqi Zhao and Wenhao Zhou},
journal = {Frontiers in immunology},
year = {2026},
month = sep,
doi = {10.3389/fimmu.2026.1956166},
url = {https://europepmc.org/article/PMC/PMC13661498},
note = {CC BY},
}
RIS
TY - JOUR
TI - Case Report: Relapse of SLE associated with EBV infection in a patient after CAR-T cell therapy: a clinical case
AU - Ping Zeng
AU - Qi Ren
AU - Xianfei Gao
AU - Wei Xian
AU - Pui Y. Lee
AU - Feng Li
AU - Caihong Xu
AU - Mingqi Zhao
AU - Wenhao Zhou
PY - 2026
DA - 2026/09/30
JO - Frontiers in immunology
DO - 10.3389/fimmu.2026.1956166
UR - https://europepmc.org/article/PMC/PMC13661498
AB - We present the case of a 13-year-old boy with refractory systemic lupus erythematosus (SLE) who achieved drug-free remission after anti-CD19 CAR-T cell therapy, but subsequently experienced Epstein–Barr virus (EBV) reactivation on day 142 after CAR T-cell infusion and peak EBV load was 24,400 IU/mL with a severe drop in platelets to 8×10 ⁹ /L, which leading to relapse of SLE and manifestations of chronic active EBV disease (CAEBVD). The whole exogenous gene testing found X chromosome Xp22.33q28 region (chrX: 200855-155239820) a duplicate of about 155.04Mbp,which is associated with the development of Klinefelter syndrome (KS).The temporal association between EBV resurgence and SLE flare suggests that CAR-T-induced immunosuppression with some genetic background may permit EBV reactivation, which can be associated with the return of autoimmunity. This case highlights the need for vigilant monitoring for opportunistic infections and genetic background, particularly EBV, after CAR-T therapy for autoimmune diseases, as they may contribute to disease relapse.
SN - 1664-3224
ER -