Американское общество гирудотерапии

Peptide-based immunotherapy of experimental autoimmune encephalomyelitis without anaphylaxis

Research article published in European journal of immunology (2007)

Последнее обновление: June 18, 2026Рецензент: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Preclinical (animal)Безопасность и инфекционный контрольКлинические исследованияLeech MD et al. · European journal of immunology, 2007

Abstract

Administration of peptide antigens in tolerogenic form holds promise as a specific treatment for autoimmune and allergic disorders. However, experiments in rodent autoimmune models have highlighted the risk of anaphylaxis in response to systemic peptide application once the aberrant immune response is underway. Thus, mice with clinical signs of experimental autoimmune encephalomyelitis (EAE) or diabetes have been reported to suffer fatal anaphylaxis upon administration of native autoantigenic peptides. Clearly, this might represent a significant barrier to the use of synthetic peptides in the treatment of ongoing human autoimmune conditions. Here we describe the development of an altered peptide ligand (APL) engineered to prevent anaphylaxis (no antibody binding) whilst retaining the ability to silence pathogenic myelin-reactive T lymphocytes. Administration of the APL to mice with an ongoing anti-myelin immune response did not cause anaphylaxis, but led to complete protection from the subsequent induction of EAE and, when given during ongoing EAE, led to a rapid remission of clinical signs. The approach of removing antibody recognition whilst maintaining the desired functional effect (in this case T cell tolerance) may be of value in other situations in which there is a risk of triggering anaphylaxis with peptide-based drugs.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleResearch Support, Non-U.S. Gov't
Indexed MeSH termsAnaphylaxisAnimalsAutoantibodiesAutoantigensBinding SitesDesensitization, ImmunologicDrug Evaluation, PreclinicalEncephalomyelitis, Autoimmune, ExperimentalEpitopes, T-LymphocyteFemaleGlycoproteinsImmune Tolerance

Резюме

Administration of peptide antigens in tolerogenic form holds promise as a specific treatment for autoimmune and allergic disorders.

Почему это важно для гирудотерапии

This study describes an engineered altered peptide ligand (APL) designed to silence pathogenic myelin-reactive T lymphocytes without triggering antibody-mediated anaphylaxis, tested in mouse models of experimental autoimmune encephalomyelitis (EAE). The APL retained T cell tolerance induction while preventing the fatal anaphylaxis seen with native autoantigenic peptides, achieving complete protection from EAE induction and rapid remission of ongoing disease. There is no defensible leech or hirudotherapy link in this abstract; it contains no mention of thrombin, coagulation, leeches, or leech-derived substances. The research concerns peptide-based immunotherapy for autoimmune disease, which falls outside ASH's domain of hirudotherapy and the leech secretome.

Цитирование

Peptide-based immunotherapy of experimental autoimmune encephalomyelitis without anaphylaxis

Leech MD et al. · European journal of immunology, 2007

Связанный клинический контекст

Узнайте, как это исследование связано с клинической практикой

Добавлено в библиотеку ASH: May 27, 2026 · Последнее обновление сайта: June 18, 2026

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