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Raffaella Ghittoni

Researcher at University of Siena

Publications -  20
Citations -  1430

Raffaella Ghittoni is an academic researcher from University of Siena. The author has contributed to research in topics: Antigen & Cytotoxic T cell. The author has an hindex of 14, co-authored 20 publications receiving 1320 citations. Previous affiliations of Raffaella Ghittoni include International Agency for Research on Cancer & University of Arizona.

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The biological properties of E6 and E7 oncoproteins from human papillomaviruses

TL;DR: Most of the findings on the biological properties and molecular mechanisms of the oncoproteins E6 and E7 from mucosal and cutaneous HPV types are reviewed.
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IL-13 R130Q, a common variant associated with allergy and asthma, enhances effector mechanisms essential for human allergic inflammation.

TL;DR: The data indicate that natural variation in the coding region of IL13 may be an important genetic determinant of susceptibility to allergy, and suggests that increased allergic inflammation in carriers ofIL13+2044A depends on enhanced IL-13-mediated Th2 effector functions rather than increased Th2 differentiation.
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Anthrax toxins suppress T lymphocyte activation by disrupting antigen receptor signaling.

TL;DR: It is shown that LT and ET are potent suppressors of human T cell activation and proliferation triggered through the antigen receptor, which identifies a novel strategy of immune evasion by B. anthracis based on both effector subunits of the toxic complex and targeted to a key cellular component of adaptive immunity.
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Role of human papillomaviruses in carcinogenesis.

TL;DR: The demonstration that high-risk HPV types are the etiological agents of cervical cancer allowed the implementation in the clinical routine of novel screening strategies for cervical lesions, as well as the development of a very efficient prophylactic vaccine.
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Simvastatin inhibits T-cell activation by selectively impairing the function of Ras superfamily GTPases.

TL;DR: It is reported that simvastatin suppresses T‐cell activation and proliferation as the result of its capacity to inhibit HMG‐CoA reductase, and identifies Ras superfamily GTPases as strategic molecular targets in T‐ cell immunosuppression by statins.