Outer membrane protein C (OMPC) epitope of Shigella flexneri 3a as a potential marker of primary immunodeficiencies (PID) and isolated anti-OmpC antibodies as a tool for immunoglobulin replacement therapy

The results demonstrate that the additional use of the cyclic/linear peptide-BSA conjugate offers a significant advantage over the use of the complete OmpC protein for immunological testing in PID diagnostics. Furthermore, specific anti-OmpC antibodies may be beneficial in the complementary therapy for patients with PIDS.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-11-19
DOI
https://doi.org/10.3389/fimmu.2025.1701211
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
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article

Outer membrane protein C (OMPC) epitope of Shigella flexneri 3a as a potential marker of primary immunodeficiencies (PID) and isolated anti-OmpC antibodies as a tool for immunoglobulin replacement therapy

Aleksandra Lewandowicz‐Uszyńska, Ewa Masłowska, Edyta Pawlak, Andrzej Gamian et al.
Frontiers in Immunology
Immunodeficiency and Autoimmune Disorders
article

Outer membrane protein C (OMPC) epitope of Shigella flexneri 3a as a potential marker of primary immunodeficiencies (PID) and isolated anti-OmpC antibodies as a tool for immunoglobulin replacement therapy

Aleksandra Lewandowicz‐Uszyńska, Ewa Masłowska, Edyta Pawlak, Andrzej Gamian, Piotr Naporowski, Danuta Witkowska, Jacek Rybka
article en

Abstract

The results demonstrate that the additional use of the cyclic/linear peptide-BSA conjugate offers a significant advantage over the use of the complete OmpC protein for immunological testing in PID diagnostics. Furthermore, specific anti-OmpC antibodies may be beneficial in the complementary therapy for patients with PIDS.

Frontiers in ImmunologyVol. 16
Wroclaw Medical University (PL), Łukasiewicz Research Network – PORT Polish Center for Technology Development (PL), Ludwik Hirszfeld Institute of Immunology and Experimental Therapy (PL)
Openalex Percentile: Top 62%
Immunodeficiency and Autoimmune Disorders
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