Human-derived bacteria that induce proliferation or accumulation of regulatory T cells
Provided herein are methods of treating graft-versus-host disease in a subject by administering pharmaceutical compositions containing bacterial strains of the Clostridia class. Also described herein are exemplary human-derived bacteria belonging to the Clostridia class, combinations of which have been shown to induce accumulation of regulatory T cells (Treg cells) in the colon and suppress immune functions, and are therefore useful for mitigating pathological immune responses. Pharmaceutical compositions containing these and/or related bacteria can be used to prevent and treat immune-mediated diseases such as graft-versus-host disease.
1. A method of treating graft versus host disease in a subject, the method comprising administering a pharmaceutical composition comprising a purified bacterial mixture comprising two or more bacteria comprising 16S rDNA sequences of at least 95% homology to SEQ ID NO:22, 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:40, SEQ ID NO:41, or SEQ ID NO:42 to the subject in an amount sufficient to treat the graft versus host disease.
2. The method of claim 1 , wherein the graft versus host disease is graft versus host disease following bone marrow transplant.
3. The method of claim 1 , wherein the purified bacterial mixture comprises at least 3, at least 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, or at least 11 bacterial strains.
4. The method of claim 1 , wherein the purified bacterial mixture comprises two or more bacterial strains comprising 16S rDNA sequence of at least 95% homology to SEQ ID NO:22, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:34, or SEQ ID NO:40.
5. The method of claim 1 , wherein the bacterial strains are human-derived bacteria.
6. The method of claim 1 , wherein the bacterial strains are isolated from a chloroform-treated fecal sample or a heat-treated fecal sample.
7. The method of claim 1 , wherein at least a portion of the bacterial strains are in spore-form.
8. The method of claim 1 , wherein the pharmaceutical composition is formulated for oral administration.
9. The method of claim 1 , wherein the pharmaceutical composition is lyophilized.
10. The method of claim 1 , wherein the pharmaceutical composition comprises one or more enteric polymers.