IP Library Granted Patent US 10,716,842
Granted Patent B2
US 10,716,842 · App. 16/260,554 · Granted Jul 21, 2020

Chlamydia antigens

Inventors: Guido Grandi (Siena, IT); Renata Maria Grifantini (Siena, IT); Oretta Finco (Siena, IT)
Assignee: GLAXOSMITHKLINE BIOLOGICALS SA
A61K39/118A61K39/3955A61P31/04C07K14/295C07K16/125G01N33/56927A61K2039/543A61K2039/545A61K2039/55544A61K2039/55561A61K2039/57G01N2333/295G01N2469/10
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Quick Facts
Patent No.
US 10,716,842
App. No.
16/260,554
Granted
Jul 21, 2020
Kind
B2
Abstract

The invention provides Chlamydia antigens for use in the treatment, prevention and/or diagnosis of Chlamydia infection. In particular, the invention provides antigens CT733, CTI 53, CT601, CT279, CT443, CT372, CT456, CT381, CT255, CT341, CT716, CT745, CT387, CT812, CT869, CT166, CT175, CT163, CT214, CT721, CT127, CT043, CT823 and/or CT600 from C. trachomatis for the treatment, prevention or diagnosis of Chlamydia infection.

Claims (18)

1. An immunogenic composition comprising an effective amount of a combination of isolated Chlamydia protein antigens, said combination comprising

(i) a CT823 antigen comprising the sequence of SEQ ID NO: 140, an antigen with at least 95% sequence identity to SEQ ID NO: 140, or an immunogenic fragment of SEQ ID NO: 140 that comprises the sequence of SEQ ID NO: 142;

(ii) a CT733 antigen comprising the sequence of SEQ ID NO: 2, an antigen with at least 95% sequence identity to SEQ ID NO: 2, or an immunogenic fragment of SEQ ID NO: 2 that comprises the sequence of SEQ ID NO: 64;

(iii) a CT043 antigen comprising the sequence of SEQ ID NO: 32, an antigen with at least 95% sequence identity to SEQ ID NO: 32, or an immunogenic fragment of SEQ ID NO: 32 that comprises the sequence of SEQ ID NO: 100; and

(iv) a CT456 antigen comprising the sequence of SEQ ID NO: 36, an antigen with at least 95% sequence identity to SEQ ID NO: 36, or an immunogenic fragment of SEQ ID NO: 36 that comprises the sequence of SEQ ID NO: 104.

2. The immunogenic composition of claim 1 , wherein

(i) the CT823 antigen has at least 95% sequence identity to SEQ ID NO: 140;

(ii) the CT733 antigen has at least 95% sequence identity to SEQ ID NO: 2;

(iii) the CT043 antigen has at least 95% sequence identity to SEQ ID NO: 32; and

(iv) the CT456 antigen has at least 95% sequence identity to SEQ ID NO: 36.

3. The immunogenic composition of claim 1 , wherein

(i) the CT823 antigen comprises the amino acid sequence SEQ ID NO: 142;

(ii) the CT733 antigen comprises the amino acid sequence SEQ ID NO: 64;

(iii) the CT043 antigen comprises the amino acid sequence SEQ ID NO: 100; and

(iv) the CT456 antigen comprises the amino acid sequence SEQ ID NO: 104.

4. The immunogenic composition of claim 1 , wherein the protein antigens are in purified or substantially purified form.

5. The immunogenic composition of claim 1 , wherein the protein antigens are present as individual separate polypeptides.

6. The immunogenic composition of claim 1 , wherein the protein antigens are present as hybrid polypeptides.

Continuity (6)
Division 15590570 · May 9, 2017
Division 14831535 · Aug 20, 2015
Continuation 14035750 · Sep 24, 2013
Continuation 13255002
Provisional Application 61157921 · Mar 6, 2009
Related Publication 20190282685A1 · Sep 19, 2019