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Tandem repeats of T helper epitopes enhance immunogenicity of fusion proteins by promoting processing and presentation.

Artikel i vetenskaplig tidskrift
Författare Martin Kjerrulf
B Löwenadler
C Svanholm
Nils Y Lycke
Publicerad i Molecular immunology
Volym 34
Nummer/häfte 8-9
Sidor 599-608
ISSN 0161-5890
Publiceringsår 1997
Publicerad vid Institutionen för medicinsk mikrobiologi och immunologi
Sidor 599-608
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Animals, Antigen Presentation, immunology, Cell Separation, Dimerization, Epitope Mapping, Epitopes, T-Lymphocyte, chemistry, immunology, Female, Flow Cytometry, Male, Mice, Mice, Inbred BALB C, Receptors, Interleukin-2, chemistry, Recombinant Fusion Proteins, immunology, T-Lymphocytes, Helper-Inducer, immunology, Tumor Cells, Cultured
Ämneskategorier Biologiska vetenskaper, Medicinska grundvetenskaper

Sammanfattning

Empirical findings have shown that recombinant chimeric proteins may be made more immunogenic if T helper epitopes are incorporated as tandem repeats. In the present study we investigated the mechanisms responsible for the enhanced immunogenicity of fusion proteins composed of the heat-stable enterotoxin of enterotoxigenic E. coli (STa) linked to multiple copies of the ovalbumin323-339 T helper epitope (ova) and a connecting dimer of an Ig-binding region of Staphylococcus aureus protein A (ZZ), which were previously shown to stimulate strong anti-STa titres in mice. We used B cell and macrophage cell lines as APC and IL-2 production by ova-specific T cells as our read-out system. Fusion proteins containing four repeated T helper epitopes were found to be the most immunogenic and resulted in 50-fold higher IL-2 production than constructs with a single T helper epitope. Under limiting APC conditions the construct with four epitopes was the best inducer of IL-2, indicating that this construct was most effectively processed by the APC. Analysis of IL-2R alpha expression by flow cytometry confirmed that four copies gave the highest frequency of activated T cells in culture, indicating a direct correlation between ability to activate T cells and IL-2 production in culture. Also in vivo, the fusion protein with four epitopes exhibited the strongest T cell priming effect. Moreover, both in vitro and in vivo, the ZZ construct was found to serve as an efficient means for targeting of the fusion proteins to B cells, thereby allowing access to the Ig receptor uptake pathway for Ag. The present study provides direct evidence that fusion proteins can be constructed to optimize processing in the individual APC and enhance activation of clonal T cells.

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