IP Library Granted Patent US 10,570,194
Granted Patent B2
US 10,570,194 · App. 15/156,562 · Granted Feb 25, 2020

Method for treating infectious diseases using a composition comprising plasma-derived immunoglobulin M (IgM)

Inventors: Thomas Barnett (Chapel Hill, NC); David A. Ross (Cary, NC)
Assignee: GRIFOLS WORLDWIDE OPERATIONS LIMITED
C07K16/1282A61K31/407A61K38/14A61K38/1741A61K39/40C07K16/1214C07K16/1232C07K16/1271A61K2039/545C07K2317/76
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Quick Facts
Patent No.
US 10,570,194
App. No.
15/156,562
Granted
Feb 25, 2020
Kind
B2
Abstract

Compositions and methods of the present invention prevent, inhibit or reduce the toxic effects of proteins and toxins secreted from microbes. A method for neutralizing microbial protein products in a subject comprises administering a composition to the subject, said composition comprising plasma-derived IgM and optionally one or more excipients in a pharmaceutical carrier, wherein the composition is administered in an amount effective to neutralize the microbial protein products.

Claims (22)

1. A method for neutralizing secreted cytotoxic exotoxins during active microbial infections, the method comprising:

administering to a subject in need thereof an effective amount of a composition consisting of plasma-derived IgM, and, optionally one or more excipients in a diluent or vehicle, wherein the plasma-derived IgM is obtained from a waste stream of a standard blood fractionation process, wherein the plasma-derived IgM is effective to neutralize cytotoxic exotoxins secreted by microorganisms selected from the group consisting of Clostridium difficile and Clostridium tetani , and wherein the plasma-derived IgM comprises IgM antibody activity selected from the group consisting of anti- Clostridium difficile Toxin A activity, anti- Clostridium difficile Toxin B activity, anti- Clostridium tetani tetanus toxin activity, and combinations thereof.

2. The method according to claim 1 , wherein the plasma-derived IgM is administered to the subject in a dose of 75 mg to 1 g per kilogram of the subject.

3. The method according to claim 1 , wherein the plasma-derived IgM is administered to the subject in a dose of 75 mg to 600 mg per kilogram of the subject.

4. The method according to claim 1 , wherein the plasma-derived IgM is administered to the subject in a dose of 75 mg to 300 mg per kilogram of the subject.

5. The method according to claim 1 , wherein the plasma-derived IgM is administered daily, every other day, 3×/week, or once per week.

6. A method for treating a bacterial infection, the method comprising:

administering to a subject in need thereof an effective amount of a composition consisting of plasma-derived IgM, and, optionally one or more excipients in a diluent or vehicle, wherein the plasma-derived IgM is obtained from a waste stream of a standard blood fractionation process, wherein the plasma-derived IgM is effective to neutralize protein products secreted by microorganisms selected from the group consisting of Clostridium difficile and Clostridium tetani in the subject, wherein the protein products comprise exotoxins secreted by the one or more of Clostridium difficile or Clostridium tetani , and wherein the plasma-derived IgM comprises IgM antibody activity selected from the group consisting of anti- Clostridium difficile Toxin A activity, anti- Clostridium difficile Toxin B activity, anti- Clostridium tetani tetanus toxin activity, and combinations thereof.

7. The method of claim 1 , wherein the method consists essentially of the administering to the subject in need thereof the effective amount of the composition.

8. The method of claim 6 , wherein the plasma-derived IgM is administered at a dosage sufficient to neutralize the protein products secreted by the bacteria of the bacterial infection in the subject prior to death or lysis of the bacteria.

9. A method for neutralizing secreted cytotoxic exotoxins during active microbial infections, the method comprising:

administering to a subject in need thereof a therapeutically effective amount of a composition consisting essentially of:

a therapeutic molecule consisting of plasma-derived IgM, and,

optionally one or more excipients in a diluent or vehicle, wherein the plasma-derived IgM is obtained from a waste stream of a standard blood fractionation process, wherein the plasma-derived IgM is effective to neutralize cytotoxic exotoxins secreted by microorganisms selected from the group consisting of Clostridium difficile and Clostridium tetani , and wherein the plasma-derived IgM comprises IgM antibody activity selected from the group consisting of anti- Clostridium difficile Toxin A activity, anti- Clostridium difficile Toxin B activity, anti- Clostridium tetani tetanus toxin activity, and combinations thereof.

10. The method of claim 1 , wherein:

the cytotoxic exotoxins are secreted by the Clostridium difficile , and

the plasma-derived IgM is effective to neutralize the Clostridium difficile Toxin A and the Clostridium difficile Toxin B.

11. The method of claim 1 , wherein:

the cytotoxic exotoxins are secreted by the Clostridium tetani , and

the plasma-derived IgM is effective to neutralize the Clostridium tetani tetanus toxin.

12. The method of claim 9 , wherein the cytotoxic exotoxins are secreted by the Clostridium difficile.

13. The method of claim 9 , wherein the cytotoxic exotoxins are secreted by the Clostridium tetani.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2018
From: BARNETT, THOMAS; ROSS, DAVID A.
To: GRIFOLS WORLDWIDE OPERATIONS LIMITED
Reel/Frame 045144/0472 →
Continuity (2)
Provisional Application 62201910 · Aug 6, 2015
Related Publication 20170037115A1 · Feb 9, 2017