For research use only
| Cat No. | ABC-TC4361 |
| Product Type | Diseased Human Peripheral Blood Mononuclear Cells |
| Cell Type | Mononuclear Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Clostridioides difficile |
| Storage | Liquid Nitrogen |
Human Clostridioides Difficile PBMCs regulate CDI via Th1/Th17 responses and cytokine storm activity,influencing infection severity and immune homeostasis.
Human Clostridioides difficile infection (CDI) peripheral blood mononuclear cells (PBMCs) are isolated from peripheral blood of patients with clinically confirmed C. difficile-associated diarrhea (CDAD) or colitis, providing critical insights into the host immune response to this nosocomial pathogen. These human-derived PBMCs contain immune cell populations—including Th17 cells, regulatory T cells, and activated monocytes—that exhibit dysregulated mucosal immunity, characterized by exhausted T-cell phenotypes (PD-1⁺/LAG-3⁺) and impaired Th17/IL-17 responses, which correlate with disease severity and recurrence. The cells exhibit typical mononuclear morphology with intact surface markers and maintain robust functional responses to bacterial antigens, reflecting the complex interplay between gut microbiota disruption, antibiotic exposure, and systemic immunity in CDAD pathogenesis. These PBMCs are particularly valuable for studying toxin-mediated immune modulation and vaccine development against this increasingly antibiotic-resistant pathogen.
| Product Code | Human C. difficile Peripheral Blood Mononuclear Cells, hCDiff-PBMC, PBMCs from C. difficile Patients |
| Species | Human |
| Cat.No | ABC-TC4361 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Mononuclear Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Peripheral Blood |
| Disease | Clostridioides difficile |
| Storage | Liquid Nitrogen |
| Product Type | Diseased Human Peripheral Blood Mononuclear Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
These CDI PBMCs enable researchers to investigate toxin-specific T cell responses, evaluate novel vaccine candidates targeting TcdA/TcdB, and study biomarkers of disease severity. Scientists utilize these cells to characterize mucosal IgA memory B cell responses, examine monocyte activation patterns, and develop immunotherapies for recurrent CDAD. The PBMCs also support research into fecal microbiota transplantation (FMT) immune modulation and preclinical testing of anti-toxin biologics.
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