US2011027810A1PendingUtilityA1
Chimeric recombinant antigens of toxoplasma gondii
Est. expiryMar 8, 2025(expired)· nominal 20-yr term from priority
A61P 33/02A61P 29/00A61P 15/06A61K 38/00A61K 2039/53C07K 14/45A61K 39/002C07K 16/00
35
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Claims
Abstract
The invention described herein relates to a method for combining antigen fragments of Toxoplasma gondii proteins, in the form of chimeric fusion products, and their use as diagnostic and immunogenic agents.
Claims
exact text as granted — not AI-modified1 - 31 . (canceled)
32 . A chimeric recombinant antigen containing a fusion of at least three different antigenic fragments of Toxoplasma gondii polypeptides, wherein said antigenic fragments are B-cell epitopes which bind to Toxoplasma gondii -specific antibodies and wherein the three different antigenic regions have an amino acid sequence selected from the group consisting of: SEQ ID NO: 2, SEQ ID NO: 4, SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, SEQ ID NO: 12, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41 and SEQ ID NO: 42.
33 . The chimeric antigen of claim 32 , wherein the Toxoplasma gondii specific antibodies are extracted from sera of subjects who have been infected by Toxoplasma gondii.
34 . The chimeric antigen of claim 32 , wherein the at least three different antigenic regions are linked by a covalent bond or by a peptide linker.
35 . A nucleotide sequence coding for the chimeric recombinant antigen of claim 32 .
36 . The nucleotide sequence according to claim 35 , comprising at least three different nucleotide sequences selected from the group consisting of: SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9 AND SEQ ID NO:11.
37 . The nucleotide sequence according to claim 35 , comprising the nucleotide sequence of SEQ ID NO:27.
38 . The nucleotide sequence according to claim 35 , comprising the nucleotide sequence of SEQ ID NO:29.
39 . The nucleotide sequence according to claim 35 , comprising the nucleotide sequence of SEQ ID NO:31.
40 . A nucleotide sequence that hybridizes under stringent hybridization conditions with a nucleotide sequence coding for the chimeric recombinant antigen of claim 32 .
41 . The chimeric recombinant antigen encoded by the nucleotide sequence of claim 40 .
42 . The nucleotide sequence of claim 35 , which is a DNA sequence.
43 . A vector comprising the DNA sequence of claim 42 .
44 . A host cell transformed with the vector of claim 43 .
45 . The chimeric recombinant antigen according to claim 32 , obtained by a process comprising
culturing a host cell transformed with a vector comprising a nucleotide sequence that codes for the chimeric recombinant antigen of claim 32 or that hybridizes under stringent hybridization conditions with a complement of a nucleotide sequence coding for the chimeric recombinant antigen of claim 32 , and isolating the chimeric recombinant antigen from the cultured host cells.
46 . A method for diagnosing a Toxoplasma gondii infection in a subject, the method comprising:
contacting a chimeric recombinant antigen according to claim 32 with a body component of the subject for a time and under condition to allow the chimeric antigen to form an antigen/antibody immune complex; and detecting the antigen/antibody immune complex comprising the chimeric antigen.
47 . The method according to claim 46 , wherein the Toxoplasma gondii infection is a congenital toxoplasmosis and the subject is an infant.
48 . The method according to claim 46 , wherein the detecting of the antigen/antibody immune complex is indicative of a time of infection.
49 . A kit for diagnosis of a Toxoplasma gondii infection, containing at least one chimeric recombinant antigen according to claim 32 .
50 . The kit of claim 49 , wherein the kit is for the diagnosis of an acute and/or chronic Toxoplasma gondii infection.Join the waitlist — get patent alerts
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