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Distinct EBV-Associated Phenotypes Due to a Novel Homozygous Missense Variant in CD27.

bioRxiv : the preprint server for biology 2026

Yang R, Turunbedu SK, Nandiwada S, Curry CV, Elghetany TM, Scull B, Geng J, Vargas-Hernandez A, Chinn IK, Ochoa S, Allen CE, Satter LF

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Biallelic deficiencies of CD27 and its ligand CD70 underlie selective susceptibility to Epstein-Barr virus (EBV) infection and its acute and chronic complications, underscoring their non-redundant rol

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APA Yang R, Turunbedu SK, et al. (2026). Distinct EBV-Associated Phenotypes Due to a Novel Homozygous Missense Variant in CD27.. bioRxiv : the preprint server for biology. https://doi.org/10.64898/2026.01.15.698722
MLA Yang R, et al.. "Distinct EBV-Associated Phenotypes Due to a Novel Homozygous Missense Variant in CD27.." bioRxiv : the preprint server for biology, 2026.
PMID 41607518

Abstract

Biallelic deficiencies of CD27 and its ligand CD70 underlie selective susceptibility to Epstein-Barr virus (EBV) infection and its acute and chronic complications, underscoring their non-redundant roles in anti-EBV immunity. To date, 16 pathogenic CD27 variants have been reported. Here, we describe three patients from two unrelated families, homozygous for a novel loss-of-function (LOF) CD27 variant, resulting in substitution of serine 70 with proline (S70P). All three patients presented with EBV viremia and lymphoproliferative disease, with variable immune dysregulation or recurrent otosinopulmonary infections. One patient developed EBV-associated Hodgkin lymphoma. Functional studies demonstrated that the S70P variant impaired surface expression of CD27 and abolished CD70 binding, rendering complete LOF. Together, S70P represents a novel pathogenic CD27 variant causing autosomal recessive (AR) CD27 deficiency, characterized by a unified susceptibility to EBV yet variable clinical manifestations, ranging from chronic viremia to malignancy.

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