Amyloid conjugate and uses and methods thereof
Abstract
A composition includes aluminum hydroxide gel and a conjugate of at least one CysA13(33-40) peptide linked to the keyhole limpet hemocyanin (KLH). Maleimidobutyric acid Nhydroxysuccinimide ester (SM) serves as cross-linking agent. The composition can produce an effective and specific immune response against Aβ40. The antibodies produced are specific for Aβ40 without significantly binding to Aβ42. The composition can increase the response against Aβ40 compared with the response produced by other conjugates that include CysAβ(33-40) peptide and KLH, and are bound or conjugated by other crosslinking agents.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A composition comprising aluminum hydroxide gel and a conjugate of at least one CysAβ(33-40) peptide (SEQ ID NO: 1) linked to the keyhole limpet hemocyanin (KLH), wherein the crosslinking agent connecting each CysAβ(33-40) peptide to the keyhole limpet hemocyanin (KLH) of the conjugate is the maleimidobutyric acid Nhydroxysuccinimide ester (SM), wherein at least 45 CysAβ(33-40) peptides (SEQ ID NO: 1) is linked to each keyhole limpet hemocyanin (KLH).
2 . A pharmaceutical composition comprising i) a conjugate comprising at least one CysAβ(33-40) peptide (SEQ ID NO: 1) linked to keyhole limpet hemocyanin (KLH) via a crosslinking agent, and ii) an aluminum hydroxide gel, wherein the crosslinking agent connecting each CysAβ(33-40) peptide to the keyhole limpet hemocyanin (KLH) of the conjugate is maleimidobutyric acid N-hydroxysuccinimide ester (SM), and wherein a pH of the composition ranges from 5.8 to 7.0.
3 . The pharmaceutical composition according to claim 2 , wherein the pH of the composition ranges from 6.2 to 7.0.
4 . The pharmaceutical composition according to claim 2 , wherein the pH of the composition ranges from 5.8 to 6.2.
5 . The pharmaceutical composition according to claim 2 , wherein the concentration of the at least one CysAβ(33-40) peptide (SEQ ID NO: 1) is at least 100 μg.
6 . The pharmaceutical composition according to claim 2 , wherein the concentration of the at least one CysAβ(33-40) peptide (SEQ ID NO: 1) is at least 150 μg.
7 . The pharmaceutical composition according to claim 2 , wherein the concentration of the at least one CysAβ(33-40) peptide (SEQ ID NO: 1) is from 150 μg to 400 μg.
8 . The pharmaceutical composition according to claim 2 , wherein the concentration of the at least one CysAβ(33-40) peptide (SEQ ID NO: 1) is from 160 μg to 240 μg.
9 . A glass ampule comprising the pharmaceutical composition of claim 2 .Join the waitlist — get patent alerts
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