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Comparison of the frequency of viral infections in patients with inborn errors of immunity receiving immunoglobulin by different routes

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Köse, Hülya
Özkan, Gözde
Şimşek, Abdurrahman
Karali, Yasin
Sağlık, İmran
Ağca, Harun
Kılıç, Sara Şebnem

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Springer

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Immunoglobulin replacement therapy (IRT) is the primary treatment for immunocompromised patients and can be administered via intravenous, subcutaneous, or facilitated subcutaneous routes. In this study, our objective was to compare the incidence of viral infections among patients receiving IRT via different administration routes during the winter season. Fifty-eight patients with primary immunodeficiency (PID) receiving immunoglobulin replacement therapy (IRT) were enrolled in the study. Patients were monitored for their immunoglobulin (Ig) levels, nasal swabs were studied with PCR monthly, and any viral infections were documented. The study included 58 patients with PID, with 33 males (56.8%) and 25 females (43.1%). The median age of the patients was 17 years (IQR, 28.5), and the median age at diagnosis was 11.5 years (IQR, 25.5). The most common IRT route was IVIG, used by 55.1% (n = 32) of patients, followed by cSCIG 27.5% (n = 16), and facilitated subcutaneous immunoglobulin (fSCIG) 17% (n = 10) of patients. The overall frequency of viral infections was 3.79%, distributed among IRT routes as follows: IVIG (n = 32, 4.2%), cSCIG (n = 16, 2.5%), and fSCIG (n = 10, 4.4%). The infection rate in the cSCIG route was significantly lower than in the IVIG and fSCIG routes (p < 0.05). The most common viral agents were adenovirus (21.8%), influenza A (16.4%), and human rhinovirus/enterovirus (16.4%). Conclusion: In a 3-month evaluation of patients, the infection rate was lower in the cSCIG route compared to the other IRT routes. cSCIG is a safe and viable treatment option that can effectively improve the quality of life for immunocompromised patients.

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Neonatal fc-receptor, Intravenous immunoglobulin, Subcutaneous immunoglobulin, Gamma-globulin, Immunodeficiency, Efficacy, Therapy, Pid, Cvid, Ivig, Cscig, Fscig, Virus, Infection, Science & Technology, Life Sciences & Biomedicine, Pediatrics

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