Abstract
Omalizumab, a humanized monoclonal antibody that
binds the CH3 domain near the binding site for the high
affinity type-I IgE Fc receptors of human IgE, can neutralize free IgE and inhibit the IgE allergic pathway [1].
The current indications for treatment with omalizumab are limited to severe persistent allergic asthma
and chronic spontaneous urticaria (CSU) when it is not
controlled by conventional anti-H1 treatment at the maximum dosage.
In recent years, several studies [1] have shown that
omalizumab is effective in a large number of IgE-mediated and non-IgE-mediated disorders, indicating that
omalizumab treatment acts on many levels and not only
on immunoglobulins
Lingua originale | English |
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pagine (da-a) | 921-923 |
Numero di pagine | 3 |
Rivista | Postepy Dermatologii I Alergologii |
Volume | 38 |
DOI | |
Stato di pubblicazione | Pubblicato - 2021 |
Keywords
- latex
- omalizumab