# Рrospective multicenter study of treatment efficacy, safety, and quality of life in a large cohort of patients with inborn errors of immunity receiving subcutaneous immunoglobulin by the rapid push method

**Authors:** Asmik Avedova, Elena Deripapa, Yulia Rodina, Anna Mukhina, Elena Latysheva, Daria Yukhacheva, Vasily Burlakov, Nellie Kan, Daria Bogdanova, Anna Moiseeva, Natalia Kuzmenko, Zoya Nesterenko, Ekaterina Deordieva, Anna Ogneva, Victoria Bludova, Anna Roppelt, Daria Fomina, Natalia Zinovieva, Yulia Sevostyanova, Linara Kalmeteva, Dilara Prolygina, Lyudmila Barycheva, Olga Selezneva, Natalya Shakhova, Olga Laba, Elena Vlasova, Alla Gorenkova, Elena Timofeeva, Olga Trusova, Marina Guseva, Natalya Yudina, Evgeniya Grevtseva, Asya Ibisheva, Zema Bambaeva, Dina Mashkovskaya, Svetlana Isakova, Almazia Shakirova, Ekaterina Selina, Tatyana Shilova, Elena Zubova, Iman Khabaeva, Ekaterina Kitova, Anastasia Mandzhieva, Svetlana Starikova, Tatyana Pavlova, Elvira Tyulyakova, Pavel Levin, Nikolay Grachev, Anna Shcherbina

PMC · DOI: 10.3389/fimmu.2025.1598491 · Frontiers in Immunology · 2025-07-22

## TL;DR

A study found that subcutaneous immunoglobulin treatment is more effective and better tolerated than intravenous immunoglobulin in patients with immune disorders.

## Contribution

The study provides real-world evidence of SCIG efficacy and safety in a large, diverse cohort of IEI patients using the rapid push method.

## Key findings

- SCIG reduced infection rates significantly compared to IVIG.
- SCIG improved IgG levels and quality of life in patients.
- SCIG was preferred by 85.6% of patients after treatment.

## Abstract

Subcutaneous immunoglobulin (SCIG) preparations are widely used in patients with inborn errors of immunity (IEI), with proven efficacy and good tolerance. We assessed treatment efficacy, safety, and quality of life in a large cohort of IEI patients who switched from intravenous immunoglobulin (IVIG) to SCIG. Our observational study included 200 patients aged 1–65 years with IEI. SCIG Cutaquig (16.5%) was administered every 7–10 days for at least 12 months via the rapid push method. We assessed the rate of infection, immunoglobulin G (IgG) concentration, adverse events, and quality of life. A total of 8,787 SCIG doses were administered during the study. The rate of infections (per person/month) during SCIG treatment was 0.05, which was significantly lower compared to 0.19 during the IVIG period (p<0.001). The median trough IgG was 6.9 g/L on IVIG, compared to 9.0 g/L during the first six months, and 9.2 g/L during the next six months on SCIG. Systemic reactions occurred in 12.4% of the IVIG infusions and 1.9% of the SCIG infusions. The total scores on quality of life summary assessments of physical and mental health were higher on SCIG therapy compared with IVIG (p<0.001). At the end of the study, 85.6% of the patients chose to remain on SCIG. Our data suggest that SCIG infusion via the rapid push method is effective, well tolerated, and feasible in large groups of IEI patients, including those in large countries such as Russia.

## Linked entities

- **Diseases:** inborn errors of immunity (MONDO:0003778)

## Full-text entities

- **Genes:** STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 6772] {aka CANDF7, IMD31A, IMD31B, IMD31C, ISGF-3, STAT91}
- **Diseases:** immune thrombocytopenia (MESH:D016553), rash (MESH:D005076), seizures (MESH:D012640), hypertension (MESH:D006973), skin AEs (MESH:D002318), antibody deficiencies (MESH:D007153), DM (MESH:D009223), COVID-19 (MESH:D000086382), pain (MESH:D010146), genetic disorders (MESH:D030342), headache (MESH:D006261), contact dermatitis (MESH:D003877), Wiskott-Aldrich syndrome (MESH:D014923), dermatitis (MESH:D003872), asthenia (MESH:D001247), combined immunodeficiency (MESH:D053632), hematoma (MESH:D006406), malignancy (MESH:D009369), gain-of-function defect (MESH:D015430), Infection (MESH:D007239), thrombocytopenia (MESH:D013921), AEs (MESH:D064420), hyper-IgE syndrome (MESH:D007589), Netherton syndrome (MESH:D056770), lower back/leg pain (MESH:D017116), fever (MESH:D005334), Skin lesions (MESH:D012871), LRBA defect (MESH:D000013), atopic dermatitis (MESH:D003876), cutaneous hemorrhagic syndrome (MESH:D006470), IEI (MESH:D007154), vomiting (MESH:D014839)
- **Chemicals:** SCIG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12321879/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12321879/full.md

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Source: https://tomesphere.com/paper/PMC12321879