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Fragmentation of SIV-gag Vaccine Induces Broader T Cell Responses

Overview of attention for article published in PLOS ONE, October 2012
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Title
Fragmentation of SIV-gag Vaccine Induces Broader T Cell Responses
Published in
PLOS ONE, October 2012
DOI 10.1371/journal.pone.0048038
Pubmed ID
Authors

Adel Benlahrech, Andrea Meiser, Shanthi Herath, Timos Papagatsias, Takis Athanasopoulos, Fucheng Li, Steve Self, Veronique Bachy, Catherine Hervouet, Karen Logan, Linda Klavinskis, George Dickson, Steven Patterson

Abstract

High mutation rates of human immunodeficiency virus (HIV) allows escape from T cell recognition preventing development of effective T cell vaccines. Vaccines that induce diverse T cell immune responses would help overcome this problem. Using SIV gag as a model vaccine, we investigated two approaches to increase the breadth of the CD8 T cell response. Namely, fusion of vaccine genes to ubiquitin to target the proteasome and increase levels of MHC class I peptide complexes and gene fragmentation to overcome competition between epitopes for presentation and recognition.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 6%
Portugal 1 6%
Unknown 14 88%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 31%
Student > Ph. D. Student 3 19%
Librarian 2 13%
Lecturer 1 6%
Student > Master 1 6%
Other 1 6%
Unknown 3 19%
Readers by discipline Count As %
Immunology and Microbiology 4 25%
Medicine and Dentistry 2 13%
Agricultural and Biological Sciences 2 13%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Biochemistry, Genetics and Molecular Biology 1 6%
Other 2 13%
Unknown 4 25%