Method and composition for hyperthermally treating cells
A method and composition for hyperthermally treating tumor cells in a patient under conditions that affect tumor stem cells and tumor cells.
1. A method providing immunotherapy in combination with thermal therapy to a target site in a patient in need thereof, the method comprising
(i) providing thermotherapy by
administering to a patient a composition comprising a targeting agent and/or antitumor-antibody-labeled nanoparticle wherein the nanoparticle forms a targeting agent and/or antibody labeled nanoparticle-cell complex at a tumor site,
exposing the patient to an energy source wherein the nanoparticles respond by expanding thus generating an acoustic signal,
measuring the acoustic signal and relating the measured signal to a temperature of the nanoparticle-cell complex, and
controlling the temperature of the nanoparticle-cell complex from about 39° C. to about 58° C. based on the acoustic signal to hyperthermally damage or kill cells in the tumor; and
(ii) providing immunotherapy by at least one of
providing to the patient an immunotherapy agent associated with the nanoparticles,
providing to the patient an immunotherapy agent not associated with the nanoparticles,
providing a therapeutic concentration of autologous leukocytes to the patient; the immunotherapy to enhance a patient's immune response.
2. The method of claim 1 where thermotherapy is performed in the absence of a contrast agent.
3. The method of claim 1 where thermotherapy is performed substantially simultaneously with immune therapy.
4. The method of claim 1 where thermotherapy is performed prior to immune therapy.
5. The method of claim 1 where thermotherapy is performed subsequent to immune therapy.
6. The method of claim 1 where the immunotherapy reduces at least one effect of immunosuppression, and where the thermotherapy supplements chemotherapy and/or radiation therapy.
7. The method of claim 1 further comprising evaluating at least one marker to assess a therapy effect.
8. The method of claim 1 where the nanoparticle is associated with a member of specific binding pair.
9. The method of claim 8 where the specific binding pair is selected from the group consisting of streptavidin-biotin, cellular receptor-agonist or antagonist, enzyme-substrate, antibody-antigen, and combinations thereof.
10. The method of claim 1 where the nanoparticle is associated with a virus.
11. The method of claim 10 where the virus is selected from the group consisting of a modified virus, a tumoricidal virus, an adenovirus, and combinations thereof.