# Case Report: Telitacicept exposure in early pregnancy in a patient with SLE delivering an infant without any physical defect

**Authors:** Xiao-Shan Huang, Zhong-yu He, Shi-gang Wang, Qiang Xu, Chang-song Lin

PMC · DOI: 10.3389/fmed.2025.1737355 · Frontiers in Medicine · 2026-01-21

## TL;DR

A woman with lupus used telitacicept early in pregnancy and gave birth to a baby without physical defects, suggesting it may be safe.

## Contribution

Reports the first known case of telitacicept use during early pregnancy in an SLE patient with a healthy infant outcome.

## Key findings

- Telitacicept exposure in early pregnancy did not cause physical defects in the infant.
- The patient discontinued telitacicept upon pregnancy confirmation and used alternative medications safely.
- The infant was born at 32 weeks with no structural abnormalities.

## Abstract

Systemic lupus erythematosus (SLE) is a systemic autoimmune disorder characterized by inflammatory damage to multiple organs. Its incidence rate is relatively high among women of childbearing age. The use of biologics is not recommended during pregnancy in SLE patients; belimumab or rituximab may be considered selectively only during lactation. Telitacicept is a fusion protein composed of the extracellular domain of the transmembrane activator and CAML interactor (TACI)—a receptor for B-lymphocyte stimulator (BLyS)—and the Fc fragment of human IgG1. It was first approved in China in 2021 for the treatment of patients with active SLE. Currently, there is a lack of safety data on the use of telitacicept during pregnancy.

A 25-year-old woman with SLE was exposed to telitacicept during early pregnancy and delivered an infant without any physical defect. The patient was regularly receiving telitacicept injections. Her last dose was administered on 4 November 2024. Her last menstrual period was dated 7 November 2024, and telitacicept was discontinued upon pregnancy confirmation. During gestation, she was maintained on oral glucocorticoids, hydroxychloroquine, and tacrolimus. On 23 June 2025, at 32 weeks of gestation, she underwent a cesarean section due to “intrauterine growth restriction and preeclampsia” and delivered a male infant without any physical defects.

This case suggests that exposure to telitacicept in the early stage of pregnancy did not result in structural defects in this case.

## Linked entities

- **Chemicals:** hydroxychloroquine (PubChem CID 3652), tacrolimus (PubChem CID 445643)
- **Diseases:** intrauterine growth restriction (MONDO:0005030), preeclampsia (MONDO:0005081)

## Full-text entities

- **Genes:** TNFRSF13B (TNF receptor superfamily member 13B) [NCBI Gene 23495] {aka CD267, CVID, CVID2, IGAD2, RYZN, TACI}, TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}
- **Diseases:** preeclampsia (MESH:D011225), intrauterine growth restriction (MESH:D005317), SLE (MESH:D008180), inflammatory (MESH:D007249), autoimmune disorder (MESH:D001327)
- **Chemicals:** tacrolimus (MESH:D016559), belimumab (MESH:C511911), hydroxychloroquine (MESH:D006886), rituximab (MESH:D000069283)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868129/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868129/full.md

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Source: https://tomesphere.com/paper/PMC12868129