IP Library Granted Patent US 8,518,415
Granted Patent B2
US 8,518,415 · App. 13/321,399 · Granted Aug 27, 2013

Engineered type IV pilin of

Inventor: Michael Donnenberg (Baltimore, MD)
Assignee: University of Maryland, Baltimore
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Quick Facts
Patent No.
US 8,518,415
App. No.
13/321,399
Granted
Aug 27, 2013
Kind
B2
Abstract

The present invention relates to engineered Clostridium difficile type IV pilin (tfp) genes, type IV pilin proteins which can serve as a diagnostic marker for identification of patients infected with C. difficile , and vaccines comprising type IV pilin proteins, antigenic fragments and variants thereof for therapeutic interventions.

Claims (48)

1. A method of inducing an immune response against Clostridium difficile , comprising administering to a subject in need thereof an immunologically-effective amount of a composition comprising an isolated Clostridium difficile type IV pilin or an antigenic fragment or variant thereof, wherein the variant is recognized by an antibody that binds the C. difficile type IV pilin.

2. The method of claim 1 , wherein a combination of C. difficile type IV pilins or antigenic fragments or variants thereof are administered.

3. The method of claim 1 , wherein an antigenic fragment is administered from a type IV pilin selected from the group consisting of:

a. SEQ ID NO:2;

b. SEQ ID NO:6;

c. SEQ ID NO:10;

d. SEQ ID NO:14;

e. SEQ ID NO:18;

f. SEQ ID NO:22;

g. SEQ ID NO:26;

h. SEQ ID NO:30;

i. SEQ ID NO:34;

j. SEQ ID NO:38; and

k. SEQ ID NO:42.

4. The method of claim 1 , wherein the antigenic fragment comprises a peptide selected from the group consisting of:

a. amino acids 35-173 of SEQ ID NO:2;

b. amino acids 35-173 of SEQ ID NO:6;

c. amino acids 35-173 of SEQ ID NO:10;

d. amino acids 35-171 of SEQ ID NO:14;

e. amino acids 35-170 of SEQ ID NO:18;

f. amino acids 34-119 of SEQ ID NO:22;

g. amino acids 31-116 of SEQ ID NO:26;

h. amino acids 32-164 of SEQ ID NO:30;

i. amino acids 32-164 of SEQ ID NO:34;

j. amino acids 32-162 of SEQ ID NO:38; and

k. amino acids 36-272 of SEQ ID NO:42.

5. The method of claim 4 , wherein the antigenic fragment is recombinantly produced.

6. The method of claim 5 , wherein the antigenic fragment is produced in E. coli.

7. The method of claim 6 , wherein the antigenic fragment is encoded by a nucleic acid sequence optimized to increase expression in E. coli comprising an affinity tag sequence and enzymatic cleavage sequence to facilitate purification.

8. The method of claim 7 , wherein the nucleic acid sequence is selected from the group consisting of:

a. SEQ ID NO:3;

b. SEQ ID NO:7;

c. SEQ ID NO:11;

d. SEQ ID NO:15;

e. SEQ ID NO:19;

f. SEQ ID NO:23;

g. SEQ ID NO:27;

h. SEQ ID NO:31;

i. SEQ ID NO:35;

j. SEQ ID NO:39; and

k. SEQ ID NO:43.

9. The method of claim 2 , wherein the combination comprises an antigenic fragment of SEQ ID NO:2.

10. The method of claim 9 , wherein the combination further comprises an antigenic fragment of a type IV pilin selected from the group consisting of:

a. SEQ ID NO:6;

b. SEQ ID NO:10;

c. SEQ ID NO:14;

d. SEQ ID NO:18; and

e. combinations thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2011
From: DONNENBERG, MICHAEL
To: UNIVERSITY OF MARYLAND, BALTIMORE
Reel/Frame 027417/0843 →
CONFIRMATORY LICENSE Recorded Dec 9, 2011
From: THE UNIVERSITY OF MARYLAND, BALTIMORE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027358/0591 →
Continuity (2)
Provisional Application 61179747 · May 20, 2009
Related Publication 20120064105A1 · Mar 15, 2012