* cardiovascular instability that precludes initiation of hemofiltration. * irreversible brain damage based on available historical and clinical information. * presence of any solid organ transplant at any time. * patients with stem cell transplant in the previous 100 days or who have not engrafted. * acute or chronic use of circulatory support device such as extracorporeal membrane oxygenation (ecmo), left ventricular assist devices (lvads), right ventricular assist devices (rvads), biventricular assist devices (bivads). * metastatic malignancy which is actively being treated or may be treated with chemotherapy or radiation during the subsequent three-month period after study treatment. * chronic immunosuppression defined as use of any immunosuppressant medications (cyclophosphamide, azathioprine, methotrexate, rituximab, mycophenolate, cyclosporine); prednisone use is excepted. * patient is moribund or chronically debilitated for whom full supportive care is not indicated. * concurrent enrollment in another interventional clinical trial except trials of covid-19 convalescent plasma, anti-severe acute respiratory syndrome (sars)-cov2 monoclonal antibodies, or remdesivirtm. patients enrolled in observational studies (without the use of an investigative device or drug), are allowed to participate. any communication between the principal investigator (pi) of this protocol and the pi of any other clinical study will include the medical director of the sponsor; all such correspondence will be documented. * any reason the investigator deems exclusionary

* cardiovascular instability that precludes initiation of hemofiltration. * irreversible brain damage based on available historical and clinical information. * presence of any solid organ transplant at any time. * patients with stem cell transplant in the previous 100 days or who have not engrafted. * acute or chronic use of circulatory support device such as extracorporeal membrane oxygenation (ecmo), left ventricular assist devices (lvads), right ventricular assist devices (rvads), biventricular assist devices (bivads). * metastatic malignancy which is actively being treated or may be treated with chemotherapy or radiation during the subsequent three-month period after study treatment. * chronic immunosuppression defined as use of any immunosuppressant medications (cyclophosphamide, azathioprine, methotrexate, rituximab, mycophenolate, cyclosporine); prednisone use is excepted. * patient is moribund or chronically debilitated for whom full supportive care is not indicated. * concurrent enrollment in another interventional clinical trial except trials of covid-19 convalescent plasma, anti-severe acute respiratory syndrome (sars)-cov2 monoclonal antibodies, or remdesivirtm. patients enrolled in observational studies (without the use of an investigative device or drug), are allowed to participate. any communication between the principal investigator (pi) of this protocol and the pi of any other clinical study will include the medical director of the sponsor; all such correspondence will be documented. * any reason the investigator deems exclusionary

- cardiovascular instability that precludes initiation of hemofiltration. - irreversible brain damage based on available historical and clinical information. - presence of any solid organ transplant at any time. - patients with stem cell transplant in the previous 100 days or who have not engrafted. - acute or chronic use of circulatory support device such as extracorporeal membrane oxygenation (ecmo), left ventricular assist devices (lvads), right ventricular assist devices (rvads), biventricular assist devices (bivads). - metastatic malignancy which is actively being treated or may be treated with chemotherapy or radiation during the subsequent three-month period after study treatment. - chronic immunosuppression defined as use of any immunosuppressant medications (cyclophosphamide, azathioprine, methotrexate, rituximab, mycophenolate, cyclosporine); prednisone use is excepted. - patient is moribund or chronically debilitated for whom full supportive care is not indicated. - concurrent enrollment in another interventional clinical trial except trials of covid-19 convalescent plasma, anti-severe acute respiratory syndrome (sars)-cov2 monoclonal antibodies, or remdesivirtm. patients enrolled in observational studies (without the use of an investigative device or drug), are allowed to participate. any communication between the principal investigator (pi) of this protocol and the pi of any other clinical study will include the medical director of the sponsor; all such correspondence will be documented. - any reason the investigator deems exclusionary

- cardiovascular instability that precludes initiation of hemofiltration. - irreversible brain damage based on available historical and clinical information. - presence of any solid organ transplant at any time. - patients with stem cell transplant in the previous 100 days or who have not engrafted. - acute or chronic use of circulatory support device such as extracorporeal membrane oxygenation (ecmo), left ventricular assist devices (lvads), right ventricular assist devices (rvads), biventricular assist devices (bivads). - metastatic malignancy which is actively being treated or may be treated with chemotherapy or radiation during the subsequent three-month period after study treatment. - chronic immunosuppression defined as use of any immunosuppressant medications (cyclophosphamide, azathioprine, methotrexate, rituximab, mycophenolate, cyclosporine); prednisone use is excepted. - patient is moribund or chronically debilitated for whom full supportive care is not indicated. - concurrent enrollment in another interventional clinical trial except trials of covid-19 convalescent plasma, anti-severe acute respiratory syndrome (sars)-cov2 monoclonal antibodies, or remdesivirtm. patients enrolled in observational studies (without the use of an investigative device or drug), are allowed to participate. any communication between the principal investigator (pi) of this protocol and the pi of any other clinical study will include the medical director of the sponsor; all such correspondence will be documented. - any reason the investigator deems exclusionary