Composition for inducing proliferation or accumulation of regulatory T cells
US-9415079-B2 · Aug 16, 2016 · US
US10624933B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10624933-B2 |
| Application number | US-201916427899-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 31, 2019 |
| Priority date | Dec 1, 2011 |
| Publication date | Apr 21, 2020 |
| Grant date | Apr 21, 2020 |
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Species of human-derived bacteria belonging to the Clostridia class have been shown to induce accumulation of regulatory T cells (Treg cells) in the colon and suppress immune functions. Pharmaceutical compositions containing these bacteria can be used to prevent and treat immune-mediated diseases such as autoimmune diseases.
Opening claim text (preview).
What is claimed is: 1. A method of treating an autoimmune disease in a subject, the method comprising administering a pharmaceutical composition comprising a purified bacterial mixture consisting of bacteria comprising 16S rDNA sequences of at least 95% homology to SEQ ID NO: 19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:30, SEQ ID NO:31, SEQ ID NO:32, SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:39; SEQ ID NO:40, SEQ ID NO:41, and SEQ ID NO:42 to the subject in an amount sufficient to treat the autoimmune disease. 2. The method of claim 1 , wherein the autoimmune disease is organ transplant rejection, inflammatory bowel disease (IBD), ulcerative colitis, pouchitis, Crohn's disease, sprue, rheumatoid arthritis, Type 1 diabetes, graft versus host disease, or multiple sclerosis. 3. The method of claim 2 , wherein the autoimmune disease is inflammatory bowel disease (IBD), ulcerative colitis, pouchitis, or Crohn's disease. 4. The method of claim 1 , wherein the bacteria are human-derived bacteria. 5. The method of claim 1 , wherein the bacteria are isolated from a chloroform-treated fecal sample. 6. The method of claim 1 , wherein the bacteria are isolated from a heat-treated fecal sample. 7. The method of claim 1 , wherein at least a portion of the bacteria are in spore-form. 8. The method of claim 1 , further comprising a pharmaceutically acceptable excipient. 9. The method of claim 1 , wherein the pharmaceutical composition is formulated for oral administration. 10. The method of claim 1 , wherein the pharmaceutical composition comprises one or more enteric polymers.
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