Tomás
Maira Litran
Profesor Titular
Brigham and Women's Hospital
Boston, Estados UnidosPublications en collaboration avec des chercheurs de Brigham and Women's Hospital (17)
2017
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Complexity of complement resistance factors expressed by acinetobacter baumannii needed for survival in human serum
Journal of Immunology, Vol. 199, Núm. 8, pp. 2803-2814
2014
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Alterations in the Staphylococcus epidermidis biofilm transcriptome following interaction with whole human blood
Pathogens and Disease, Vol. 70, Núm. 3, pp. 444-448
2013
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Antibody to a conserved antigenic target is protective against diverse prokaryotic and eukaryotic pathogens
Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, Núm. 24
2012
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Evaluation of the trimeric autotransporter ata as a vaccine candidate against Acinetobacter baumannii infections
Infection and Immunity, Vol. 80, Núm. 10, pp. 3381-3388
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Identification of Ata, a multifunctional trimeric autotransporter of Acinetobacter baumannii
Journal of Bacteriology, Vol. 194, Núm. 15, pp. 3950-3960
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Poly-n-acetyl-β-(1-6)-glucosamine is a target for protective immunity against acinetobacter baumannii infections
Infection and Immunity, Vol. 80, Núm. 2, pp. 651-656
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Synthesis and Evaluation of a Conjugate Vaccine Composed of Staphylococcus aureus Poly-N-Acetyl-Glucosamine and Clumping Factor A
PLoS ONE, Vol. 7, Núm. 9
2011
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Efficacy of a conjugate vaccine containing polymannuronic acid and flagellin against experimental Pseudomonas aeruginosa lung infection in mice
Infection and Immunity, Vol. 79, Núm. 8, pp. 3455-3464
2010
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Animal and human antibodies to distinct Staphylococcus aureus antigens mutually neutralize opsonic killing and protection in mice
Journal of Clinical Investigation, Vol. 120, Núm. 9, pp. 3220-3233
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Evaluation of flagella and flagellin of Pseudomonas aeruginosa as vaccines
Infection and Immunity, Vol. 78, Núm. 2, pp. 746-755
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Synthetic β-(1→6)-linked N-acetylated and nonacetylated oligoglucosamines used to produce conjugate vaccines for bacterial pathogens
Infection and Immunity, Vol. 78, Núm. 2, pp. 764-772
2008
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Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface
Microbiology, Vol. 154, Núm. 3, pp. 865-877
2007
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Molecular basis for preferential protective efficacy of antibodies directed to the poorly acetylated form of staphylococcal poly-N-acetyl-β-(1-6)- glucosamine
Infection and Immunity, Vol. 75, Núm. 7, pp. 3406-3413
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Protection against Escherichia coli infection by antibody to the Staphylococcus aureus poly-N-acetylglucosamine surface polysaccharide
Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 18, pp. 7528-7533
2005
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Comparative opsonic and protective activities of Staphylococcus aureus conjugate vaccines containing native or deacetylated staphylococcal poly-N-acetyl-β-(1-6)-glucosamine
Infection and Immunity, Vol. 73, Núm. 10, pp. 6752-6762
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Poly-N-acetylglucosamine production in Staphylococcus aureus is essential for virulence in murine models of systemic infection
Infection and Immunity, Vol. 73, Núm. 10, pp. 6868-6876