Yeast-based immunotherapy against Clostridium difficile infection

Patent metadata

Field	Value
Publication number	US-12384833-B2
Application number	US-202217955537-A
Country	US
Kind code	B2
Filing date	Sep 29, 2022
Priority date	Oct 13, 2015
Publication date	Aug 12, 2025
Grant date	Aug 12, 2025

Abstract

Antibody-based binding agents derived from human and camelid immunoglobulins are described, as well as strains of yeast engineered to secrete the binding agents, and methods of treating and preventing Clostridium difficile infections using the engineered strains of yeast. These binding agents recognize and bind with specificity to Clostridium difficile toxin A and/or toxin B and in some cases exhibit toxin neutralizing activity. The binding agents include camelid V H H peptide monomers, linked groups of V H H peptide monomers, V H H peptide monomers joined to antibody Fc domains, and V H H peptide monomers joined to IgG antibodies.

First claim

The invention claimed is:

1. A method of treating a Clostridum difficile ( C. difficile ) infection in a subject, comprising administering an effective amount of an engineered strain of Saccharomyces boulardii yeast to the subject, wherein the engineered strain of Saccharomyces boulardii yeast produces a tetra-specific, tetrameric ABAB binding agent comprising: (i) a first, a second, a third, and a fourth linked V H H peptide monomer each independently having binding specificity for an epitope of C. difficile toxin A (TcdA) or C. difficile toxin B (TcdB), and (ii) an amino acid sequence of SEQ ID NO: 109 or an amino acid sequence that is at least 95% identical to SEQ ID NO: 109.

2. The method of claim 1 , wherein two of the monomers have binding specificity for epitopes of TcdA and two of the monomers have binding specificity for epitopes of TcdB.

3. The method of claim 1 , wherein the monomers independently have binding specificity for an epitope in the glucosyltransferase domain, cysteine protease domain, translocation domain, or receptor binding domain of TcdA or TcdB.

4. The method of claim 1 , wherein the first V H H peptide monomer comprises an amino acid sequence of SEQ ID NO: 7, the second V H H peptide monomer comprises an amino acid sequence of SEQ ID NO: 1, the third V H H peptide monomer comprises an amino acid sequence of SEQ ID NO: 5, and the fourth V H H peptide monomer comprises an amino acid sequence of SEQ ID NO: 3.

5. The method of claim 1 , wherein the ABAB binding agent comprises an amino acid sequence of SEQ ID NO 19.

6. The method of claim 1 , wherein the ABAB binding agent further comprises an N-terminal secretion signal selected from SEQ ID NO:99 and SEQ ID NO: 103.

7. The method of claim 1 , wherein the ABAB binding agent comprises an amino acid sequence of SEQ ID NO: 107.

8. The method of claim 1 , wherein the ABAB binding agent comprises the amino acid sequence of SEQ ID NO: 109.

9. The method of claim 1 , wherein the engineered strain of Saccharomyces boulardii yeast is administered in an amount between 10 μg/kg and 100 mg/kg per body weight of the subject.

10. The method of claim 1 , wherein the engineered strain of Saccharomyces boulardii yeast is administered to the subject orally, nasally or rectally.

11. The method of claim 1 , wherein the engineered strain of Saccharomyces boulardii yeast is in a pharmaceutical formulation comprising a pharmaceutically acceptable carrier or diluent.

12. The method of claim 1 further comprising administering an antibiotic to the subject.

Assignees

• Feng Hanping
• Galen James Eugene
• Chen Kevin
• Zhu Yixuan
• Univ Maryland

Inventors

• Feng Hanping
• Galen James Eugene
• Chen Kevin
• Zhu Yixuan

Classifications

• G01N33/56961

  Plant cells or fungi · CPC title

• C12N1/18

  Baker's yeast; Brewer's yeast · CPC title

• C07K2317/94

  Stability, e.g. half-life, pH, temperature or enzyme-resistance · CPC title

• C07K2317/52

  Constant or Fc region; Isotype · CPC title

• C07K2317/21

  from primates, e.g. man · CPC title