marotta, serena
(2017)
Novel anti-complement agents for PNH:from eculizumab to complement inhibition 2.0.
[Tesi di dottorato]
| Tipologia del documento: |
Tesi di dottorato
|
| Lingua: |
English |
| Titolo: |
Novel anti-complement agents for PNH:from eculizumab to complement inhibition 2.0 |
| Autori: |
| Autore | Email |
|---|
| marotta, serena | marotta.serena@gmail.com |
|
| Data: |
7 Dicembre 2017 |
| Numero di pagine: |
33 |
| Istituzione: |
Università degli Studi di Napoli Federico II |
| Dipartimento: |
dep13 |
| Dottorato: |
phd106 |
| Ciclo di dottorato: |
30 |
| Coordinatore del Corso di dottorato: |
| nome | email |
|---|
| Di Minno, Giovanni | giovanni.diminno@unina.it |
|
| Tutor: |
| nome | email |
|---|
| Risitano, Antonio | [non definito] |
|
| Data: |
7 Dicembre 2017 |
| Numero di pagine: |
33 |
| Parole chiave: |
pnh, anti-complement agents, eculizumab |
| Settori scientifico-disciplinari del MIUR: |
Area 06 - Scienze mediche > MED/15 - Malattie del sangue |
[error in script]
[error in script]
| Depositato il: |
21 Dic 2017 08:11 |
| Ultima modifica: |
10 Apr 2019 10:41 |
| URI: |
http://www.fedoa.unina.it/id/eprint/12066 |
Abstract
Therapeutic complement inhibition by eculizumab has revolutionized the treatment of paroxysmal nocturnal hemoglobinuria (PNH) with a major impact on its natural history. Nevertheless, emerging unmet clinical needs may benefit from the development of novel complement inhibitors. Novel strategies of complement inhibition exploit different agents targeting C5, as well as compound intercepting the complement cascade at the level of its key component C3, or even upstream at the level of component involved in complement alternative pathway initiation. Many of these agents are already in their clinical development; preliminary data together with a deep understanding of PNH biology may help to anticipate their possible clinical effect. Novel anti-C5 agents include monoclonal antibodies (even long-lasting) as well as other small molecules bioavailable by subcutaneous administration; an anti-C5 small interfering RNA has been developed too. All these anti-C5 agents seem to recapitulate safety and efficacy of current eculizumab treatment; their main improvement pertains to better patient compliance due to longer dosing interval and possible subcutaneous self-administration. The possibility of achieving a deeper C5 inhibition has been shown as well, but its actual clinical meaning remains to be elucidated. Upstream complement inhibitors include the anti-C3 small peptide compstatin (and its derivatives), and small inhibitors of complement factor D or complement factor B. This class of compound anticipates a possible efficacy in prevention of C3-mediated extravascular hemolysis, in addition to inhibition of intravascular hemolysis, possibly leading to improved hematological responses. The availability of all these compounds will result soon in a substantial improvement of PNH management.
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