The synthetic peptide T11F (TCRVDHRGLTF), with sequence identical to a fragment of the constant region of human IgM, and most of its alanine-substituted derivatives proved to possess a significant candidacidal activity in vitro. In this study, the therapeutic efficacy of T11F, D5A, the derivative most active in vitro, and F11A, characterized by a different conformation, was investigated in Galleria mellonella larvae infected with Candida albicans. A single injection of F11A and D5A derivatives, in contrast with T11F, led to a significant increase in survival of larvae injected with a lethal inoculum of C. albicans cells, in comparison with infected animals treated with saline. Peptide modulation of host immunity upon C. albicans infection w...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...
The synthetic peptide T11F (TCRVDHRGLTF), with sequence identical to a fragment of the constant regi...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Abstract Candida albicans, a ubiquitous opportunistic fungal pathogen, plays a pivotal role in human...
Mycoses still represent relevant opportunistic infections worldwide, although overshad-owed in recen...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...
The synthetic peptide T11F (TCRVDHRGLTF), with sequence identical to a fragment of the constant regi...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Abstract Candida albicans, a ubiquitous opportunistic fungal pathogen, plays a pivotal role in human...
Mycoses still represent relevant opportunistic infections worldwide, although overshad-owed in recen...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
It has been previously demonstrated that synthetic antibody-derived peptides could exert a significa...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
Synthetic peptides with sequences identical to fragments of the constant region of different classes...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...
The antibiofilm activity of a gH625 analogue was investigated to determine the in vitro inhibition a...