| Title: |
COMPOSITIONS AND METHODS FOR DETECTION, PREVENTION, AND TREATMENT OF ANTHRAX AND OTHER INFECTIOUS DISEASES |
| Document Number: |
20090280513 |
| Publication Date: |
November 12, 2009 |
| Appl. No: |
10/809831 |
| Application Filed: |
March 26, 2004 |
| Abstract: |
Compositions and methods for the detection, prevention, or treatment of anthrax or other infectious diseases. In one aspect, the present invention provides methods of immunizing humans or animals against Bacillus anthracis or other capsulated pathogens. The methods include administering a capsular polypeptide of a pathogen of interest and a CD40 agonist to a human or animal. The capsular polypeptide or the CD40 agonist is administered in such an amount or frequency that an immunoprotective response can be elicited in the human or animal against the pathogen of interest. In another aspect, the present invention provides methods of using passive immunization with anti-capsular polypeptide antibodies to prevent or treat infections caused by Bacillus anthracis or other pathogens. In yet another aspect, the present invention provides methods useful for diagnosis of anthrax by detection of capsular polypeptide in serum or other biological samples. |
| Inventors: |
Kozel, Thomas R. (Reno, NV, US); Murphy, William J. (Reno, NV, US); Brandt, Suzanne (Reno, NV, US); Thorkildson, Peter (Reno, NV, US); Percival, Ann (Reno, NV, US); Blazar, Bruce R. (Golden Valley, MN, US); Lovchik, Julie A. (Albuquerque, NM, US); Lyons, C. Rick (Albuquerque, NM, US) |
| Claim: |
1-14. (canceled) |
| Claim: |
15. A method for detecting bacterial infection by a polyglutamic acid-(PGA-) producing pathogen in a subject comprising: detecting a level of soluble PGA in a biological sample from a subject, wherein the subject is a member of a vertebrate species; and comparing the level of soluble PGA to a reference value of soluble PGA representative of vertebrate species members uninfected by the PGA-producing pathogen; wherein the level of soluble PGA indicates that the subject has been infected by a PGA-producing pathogen if the level of soluble PGA is greater than the reference value. |
| Claim: |
16. The method according to claim 15, wherein the level of soluble PGA is detected by an immunoassay. |
| Claim: |
17. The method according to claim 16, wherein the immunoassay is a competitive assay. |
| Claim: |
18. The method according to claim 16, wherein the immunoassay is in a direct format. |
| Claim: |
19. The method according to claim 15, wherein the vertebrate species is human, and the biological sample is a blood sample. |
| Claim: |
20-39. (canceled) |
| Claim: |
40. A method for detecting infection by a PGA-producing bacterium in a subject comprising: contacting a biological sample prepared from a subject with an anti-PGA antibody, wherein the subject is a member of a vertebrate species; measuring a level of soluble PGA in said biological sample; and comparing the level of soluble PGA to a reference value of soluble PGA representative of vertebrate species members uninfected by the PGA-producing bacterium; wherein the level of soluble PGA indicates that the subject has been infected by a PGA-producing bacterium if the level of soluble PGA exceeds the reference value. |
| Claim: |
41. The method of claim 40, wherein said biological sample is a body fluid sample. |
| Claim: |
42. The method of claim 41, wherein said body fluid sample is a blood sample. |
| Claim: |
43. The method of claim 41, wherein said vertebrate species is mammalian. |
| Claim: |
44. The method of claim 41, wherein said vertebrate species is human. |
| Claim: |
45. The method of claim 44, wherein the level of soluble PGA is detected by an immunoassay. |
| Claim: |
46. The method of claim 45, wherein said immunoassay is selected from the group consisting of an ELISA, an RIA, a lateral flow assay, a particle agglutination assay, a sandwich assay, and a protein chip assay. |
| Claim: |
47. The method of claim 45, wherein said immunoassay is an antigen capture immunoassay. |
| Claim: |
48. The method of claim 45, wherein said immunoassay is a non-competitive assay. |
| Claim: |
49. The method according to claim 45, wherein said immunoassay is in a direct assay format. |
| Claim: |
50. (canceled) |
| Claim: |
51. A method for evaluating progression of infection by a PGA-producing bacterium in a vertebrate of interest, said method comprising: contacting a biological sample prepared from said vertebrate with an anti-PGA antibody; measuring a level of soluble PGA in said biological sample; and comparing the level of soluble PGA with a reference value, wherein the reference value comprises a level of soluble PGA in a biological sample obtained from said vertebrate at another time; wherein comparing the level of soluble PGA in said biological sample to the reference value is indicative of the progression of said infection. |
| Claim: |
52. The method of claim 51, wherein said biological sample is a body fluid sample. |
| Claim: |
53. The method of claim 52, wherein said body fluid sample is a blood sample. |
| Claim: |
54. The method of claim 52, wherein said vertebrate is a mammal. |
| Claim: |
55. The method of claim 52, wherein said vertebrate is a human. |
| Claim: |
56. The method of claim 55, wherein the level of soluble PGA is detected by an immunoassay. |
| Claim: |
57. The method of claim 56, wherein said immunoassay is selected from the group consisting of an ELISA, an RIA, a lateral flow assay, a particle agglutination assay, a sandwich assay, and a protein chip assay. |
| Claim: |
58. The method of claim 56, wherein said immunoassay is an antigen capture immunoassay. |
| Claim: |
59. The method of claim 56, wherein said immunoassay is a non-competitive assay. |
| Claim: |
60. The method of claim 45, wherein said immunoassay is in a direct format. |
| Claim: |
61. (canceled) |
| Current U.S. Class: |
435/794 |
| Current International Class: |
01; 40 |
| Accession Number: |
edspap.20090280513 |
| Database: |
USPTO Patent Applications |
