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Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report
BACKGROUND: Although described by Hippocrates in 400 B.C., pemphigus disease still needs a safe therapeutical approach, given that the currently used therapies (i.e. corticosteroids and immunosuppressive drugs) often provoke collateral effects. Here we present preliminary data on the possible use of...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630706/ https://www.ncbi.nlm.nih.gov/pubmed/17062151 http://dx.doi.org/10.1186/1479-5876-4-43 |
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author | Angelini, Giovanni Bonamonte, Domenico Lucchese, Alberta Favia, Gianfranco Serpico, Rosario Mittelman, Abraham Simone, Simone Sinha, Animesh A Kanduc, Darja |
author_facet | Angelini, Giovanni Bonamonte, Domenico Lucchese, Alberta Favia, Gianfranco Serpico, Rosario Mittelman, Abraham Simone, Simone Sinha, Animesh A Kanduc, Darja |
author_sort | Angelini, Giovanni |
collection | PubMed |
description | BACKGROUND: Although described by Hippocrates in 400 B.C., pemphigus disease still needs a safe therapeutical approach, given that the currently used therapies (i.e. corticosteroids and immunosuppressive drugs) often provoke collateral effects. Here we present preliminary data on the possible use of a proteomics derived desmoglein peptide which appears promising in halting disease progression without adverse effects. METHODS: The low-similarity Dsg3(49–60)REWVKFAKPCRE peptide was topically applied for 1 wk onto a lesion in a patient with a late-stage Pemphigus vulgaris (PV) complicated by diabetes and cataract disease. The peptide was applied as an adjuvant in combination with the standard corticosteroid-based immunosuppressive treatment. RESULTS: After 1 wk, the treated PV eroded lesion appeared dimensionally reduced and with an increased rate of re-epithelization when compared to adjacent non-treated lesions. Short-term benefits were: decrease of anti-Dsg antibody titer and reduction of the corticosteroid dosage. Long-term benefits: after two years following the unique 1-wk topical treatment, the decrease of anti-Dsg antibody titer persists. The patient is still at the low cortisone dosage. Adverse effects: no adverse effect could be monitored. CONCLUSION: With the limits inherent to any preliminary study, this case report indicates that topical treatment with Dsg3(49–60)REWVKFAKPCRE peptide may represent a feasible first step in the search for a simple, effective and safe treatment of PV. |
format | Text |
id | pubmed-1630706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-16307062006-11-02 Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report Angelini, Giovanni Bonamonte, Domenico Lucchese, Alberta Favia, Gianfranco Serpico, Rosario Mittelman, Abraham Simone, Simone Sinha, Animesh A Kanduc, Darja J Transl Med Research BACKGROUND: Although described by Hippocrates in 400 B.C., pemphigus disease still needs a safe therapeutical approach, given that the currently used therapies (i.e. corticosteroids and immunosuppressive drugs) often provoke collateral effects. Here we present preliminary data on the possible use of a proteomics derived desmoglein peptide which appears promising in halting disease progression without adverse effects. METHODS: The low-similarity Dsg3(49–60)REWVKFAKPCRE peptide was topically applied for 1 wk onto a lesion in a patient with a late-stage Pemphigus vulgaris (PV) complicated by diabetes and cataract disease. The peptide was applied as an adjuvant in combination with the standard corticosteroid-based immunosuppressive treatment. RESULTS: After 1 wk, the treated PV eroded lesion appeared dimensionally reduced and with an increased rate of re-epithelization when compared to adjacent non-treated lesions. Short-term benefits were: decrease of anti-Dsg antibody titer and reduction of the corticosteroid dosage. Long-term benefits: after two years following the unique 1-wk topical treatment, the decrease of anti-Dsg antibody titer persists. The patient is still at the low cortisone dosage. Adverse effects: no adverse effect could be monitored. CONCLUSION: With the limits inherent to any preliminary study, this case report indicates that topical treatment with Dsg3(49–60)REWVKFAKPCRE peptide may represent a feasible first step in the search for a simple, effective and safe treatment of PV. BioMed Central 2006-10-24 /pmc/articles/PMC1630706/ /pubmed/17062151 http://dx.doi.org/10.1186/1479-5876-4-43 Text en Copyright © 2006 Angelini et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Angelini, Giovanni Bonamonte, Domenico Lucchese, Alberta Favia, Gianfranco Serpico, Rosario Mittelman, Abraham Simone, Simone Sinha, Animesh A Kanduc, Darja Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title | Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title_full | Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title_fullStr | Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title_full_unstemmed | Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title_short | Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
title_sort | preliminary data on pemphigus vulgaris treatment by a proteomics-defined peptide: a case report |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1630706/ https://www.ncbi.nlm.nih.gov/pubmed/17062151 http://dx.doi.org/10.1186/1479-5876-4-43 |
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