US2008166377A1PendingUtilityA1
Human Hookworm Vaccine
Est. expiryOct 25, 2026(~0.3 yrs left)· nominal 20-yr term from priority
Inventors:Peter HotezAlexander LoukasBin ZhanGaddam GoudJeffrey BethonyMaria Elena BottazziAaron Miles
A61K 2039/55505A61K 2039/55561A61P 33/00A61P 31/00A61K 39/0003A61K 2039/55572
55
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Claims
Abstract
A vaccine for human hookworm is provided. The vaccine comprises at least one L3 larval stage antigen (e.g. Na-ASP-2 or Na-SAA-2) and at least one adult stage human hookworm antigen (e.g. Na-APR-1, Na-CP-2, Na-CP-3, Na-CP-4, Na-CP-5, or Na-GST-1) and adjuvants.
Claims
exact text as granted — not AI-modified1 . A vaccine composition, comprising,
at least one larval-stage hookworm antigen; at least one adult-stage hookworm antigen; an aluminum-based adjuvant; and a second adjuvant.
2 . The vaccine composition of claim 1 , wherein said larval-stage hookworm antigen is selected from the group consisting of Na-ASP-2 and Na-SAA-2, or antigenic fragments thereof.
3 . The vaccine composition of claim 1 , wherein said adult-stage hookworm antigen is selected from the group consisting of Na-APR-1, Na-GST, Na-CP-2, Na-CP-3, Na-CP-4, Na-CP-5, or antigenic fragments thereof.
4 . The vaccine of claim 3 , wherein said Na-APR-1 is Pichia optimized Na-APR-1, or an antigenic fragment thereof.
5 . The vaccine composition of claim 1 , wherein said aluminum-based adjuvant is Alhydrogel®.
6 . The vaccine composition of claim 1 , wherein said second adjuvant is selected from the group consisting of: CpG and Synthetic lipid A.
7 . The vaccine composition of claim 1 , wherein said aluminum-based adjuvant and said second adjuvant are combined together.
8 . A method for vaccinating a patient in need thereof against hookworm infections, comprising the step of
administering to said patient a vaccine composition comprising,
at least one larval-stage hookworm antigen;
at least one adult-stage hookworm antigen;
an aluminum-based adjuvant; and
a second adjuvant.
9 . The method of claim 8 , wherein said larval-stage hookworm antigen is selected from the group consisting of Na-ASP-2 and Na-SAA-2, or antigenic fragments thereof.
10 . The method of claim 8 , wherein said adult-stage hookworm antigen is selected from the group consisting of Na-APR-1, Na-GST, Na-CP-2, Na-CP-3, Na-CP-4, Na-CP-5, or antigenic fragments thereof.
11 . The method of claim 10 , wherein said Na-APR-1 is Pichia optimized Na-APR-1, or an antigenic fragment thereof.
12 . The method of claim 8 , wherein said aluminum-based adjuvant is Alhydrogel®.
13 . The method of claim 8 , wherein said second adjuvant is selected from the group consisting of: CpG and Synthetic lipid A.
14 . The method of claim 8 , wherein said aluminum-based adjuvant and said second adjuvant are combined together.
15 . The method of claim 8 , further comprising the step of administering a deworming agent to said patient.
16 . A hookworm vaccine comprising
a hookworm larval stage antigen; an hookworm adult stage antigen; and one or more adjuvants.
17 . A method for vaccinating a patient in need thereof against hookworm infections, comprising the step of
administering to said patient a vaccine composition comprising,
a hookworm larval stage antigen;
an hookworm adult stage antigen; and
one or more adjuvants.Cited by (0)
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