Invasive fungal infections cause unacceptable mortality rates in neutropenic patients. Since survival of neutropenic patients with invasive fungal infections is linearly related to the patients' granulocyte counts, exogenous replacement of phagocytes is of great therapeutic potential for these infections. Although neutrophil transfusions have shown promising results, they fell out of favor in the early 1980s due to several technical difficulties. To address invasive fungal infections in neutropenic patients, we are developing a cell-based immunotherapy as an alternative to neutrophil transfusions. Our strategy is based on a human phagocytic cell-line, HL-60, which can be grown perpetually in vitro, but can then be activated to differentiate towards a mature neutrophil phenotype prior to infusion into an infected, myeloablated host. Activation of HL-60 cells into Activated Targeted Killer (ATAK) cells diminishes their replicative capacity and markedly increases the efficiency with which they kill Candida albicans, consistent with the cells'maturation towards mature granulocytes. Administration of ATAK cells substantively improves the survival of neutropenic mice infected with C. albicans or Aspergillus fumigatus. Therefore, ATAK cells are capable of recapitulating neutrophil host-defense functions in vitro and in vivo. We hypothesize that ATAK cells are effective at treating disseminated candidiasis because they circulate to infected tissues and there kill fungi by oxidative and/or non-oxidative mechanisms. We also hypothesize that insertion of an inducible suicide trap will enable rapid purging of the cells from a host when desired, thereby enhancing the safety of the strategy. We now seek to define the mechanisms by which ATAK cells kill fungi, to define the ability of an inducible suicide trap to purge the cells in vivo, and to define ATAK cell circulation, persistence, and efficacy in mice infected with a variety of fungal pathogens.
The specific aims of this proposal are to: 1) define the mechanisms of ATAK cell anti-fungal activity;2) transfect ATAK cells with a lentiviral construct containing a suicide trap and a reporter system for tracking cells;3) define the in vivo circulation, toxicities, and life-span of ATAK cells in neutropenic mice using clinical, laboratory, metabolomic, and histopathological evaluations in two species (mice and rabbit);and 4) define the breadth of protection of ATAK cells against three highly lethal mold infections: aspergillosis, mucormycosis, or fusariosis. Definition of the mechanism of protection and toxicities of ATAK cells will elucidate phagocytic host defense mechanisms against fungi in general, and is critical to future enhancement of ATAK efficacy. Furthermore, insertion of a suicide trap and luminescence marker will enable us to eliminate any residual ATAK cells when desired and to monitor the cells in real- time in vivo. We will also determine the breadth of efficacy of ATAK cells, and define long-term toxicity of the cells in the murine model using clinical, laboratory, metabolomic, and histopathological markers. Ultimately, the studies proposed will provide a foundation for a unique, cutting-edge strategy to recapitulate neutrophil functions in myeloablated hosts with invasive fungal infections.
Fungal infections are leading causes of death in cancer patients whose white blood cell counts are low from chemotherapy. For decades, physicians have tried to combat such infections by transfusing white blood cells. However, white cell transfusions have failed due to significant technical barriers. The current studies will enable development of a unique strategy to grow immature white blood cells in the test tube until such time as they are needed for an infected cancer patient. The cells are then treated with a combination of activating factors, which causes them to mature into Activated Targeted Killer (ATAK) cells. We propose to determine how ATAK cells kill pathogens and how the cells circulate through the body of an infected host. We also propose to insert a suicide trap into the cells so we can eliminate them when desired. Completion of the proposed studies will enable us to create a safe and effective strategy to overcome the barriers to white blood cell transfusions, revolutionizing the treatment of infections in cancer patients.
|Spellberg, Brad; Gilbert, David N (2014) The future of antibiotics and resistance: a tribute to a career of leadership by John Bartlett. Clin Infect Dis 59 Suppl 2:S71-5|
|Spellberg, Brad (2014) Antibiotic judo: working gently with prescriber psychology to overcome inappropriate use. JAMA Intern Med 174:432-3|
|Spellberg, Brad; Bonomo, Robert A (2014) The deadly impact of extreme drug resistance in Acinetobacter baumannii. Crit Care Med 42:1289-91|
|Lin, Lin; Tan, Brandon; Pantapalangkoor, Paul et al. (2013) Acinetobacter baumannii rOmpA vaccine dose alters immune polarization and immunodominant epitopes. Vaccine 31:313-8|
|Spellberg, Brad; Bartlett, John G; Gilbert, David N (2013) The future of antibiotics and resistance. N Engl J Med 368:299-302|
|Spellberg, Brad; Bonomo, Robert A (2013) "Airborne assault": a new dimension in Acinetobacter baumannii transmission*. Crit Care Med 41:2042-4|
|Montgomery, Christopher P; Daniels, Melvin D; Zhao, Fan et al. (2013) Local inflammation exacerbates the severity of Staphylococcus aureus skin infection. PLoS One 8:e69508|
|Luo, Guanpingshen; Lin, Lin; Ibrahim, Ashraf S et al. (2012) Active and passive immunization protects against lethal, extreme drug resistant-Acinetobacter baumannii infection. PLoS One 7:e29446|
|Lin, Lin; Ibrahim, Ashraf S; Baquir, Beverlie et al. (2012) Luminescent-activated transfected killer cells to monitor leukocyte trafficking during systemic bacterial and fungal infection. J Infect Dis 205:337-47|
|Spellberg, Brad; Talbot, George; Infectious Diseases Society of America et al. (2010) Recommended design features of future clinical trials of antibacterial agents for hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia. Clin Infect Dis 51 Suppl 1:S150-70|
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