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Pharmaceutical compositions comprising a stress protein complex and related molecules encoding or cells presenting such a complex are provided. The stress protein complex comprises an hsp110 or grp170 polypeptide complexed with an immunogenic polypeptide. The immunogenic polypeptide of the stress p

Pharmaceutical compositions comprising a stress protein complex and related molecules encoding or cells presenting such a complex are provided. The stress protein complex comprises an hsp110 or grp170 polypeptide complexed with an immunogenic polypeptide. The immunogenic polypeptide of the stress protein complex can be associated with a cancer or an infectious disease. The pharmaceutical compositions of the invention can be administered to a subject, thereby providing methods for inhibiting M. tuberculosis-infection, for inhibiting tumor growth, for inhibiting the development of a cancer, and for the treatment or prevention of infectious disease. The invention further provides a method for producing T cells directed against a tumor cell or a M. tuberculosis-infected cell, wherein a T cell is contacted with an APC that is modified to present an hsp110 or grp170 polypeptide and an immunogenic polypeptide associated with a tumor or with the M. tuberculosis-infected cell. Included in the invention are T cells produced by this method and a pharmaceutical composition comprising such T cells. The T cells can be contacted with a M. tuberculosis-infected cell in a method for killing a M. tuberculosis-infected cell, or with a tumor cell in a method for killing a tumor cell.

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What is claimed is: 1. A pharmaceutical composition comprising an isolated stress protein complex and a physiologically acceptable carrier, wherein the stress protein complex comprises an hsp110 polypeptide and an immunogenic polypeptide, and wherein the complex has been heated so as to enhance bin

What is claimed is: 1. A pharmaceutical composition comprising an isolated stress protein complex and a physiologically acceptable carrier, wherein the stress protein complex comprises an hsp110 polypeptide and an immunogenic polypeptide, and wherein the complex has been heated so as to enhance binding of the hsp110 polypeptide to the immunogenic polypeptide. 2. The pharmaceutical composition of claim 1, wherein the complex comprises a fusion protein. 3. The pharmaceutical composition of claim 1, wherein the complex is derived from a tumor. 4. The pharmaceutical composition of claim 1, wherein the complex is derived from a cell infected with an infectious agent. 5. The pharmaceutical composition of claim 1, wherein the stress protein complex further comprises a polypeptide selected from the group consisting of hsp70, hsp90, grp78 and grp94. 6. The pharmaceutical composition of claim 1, wherein the stress protein complex comprises hsp110 complexed with hsp70 and hsp25. 7. The pharmaceutical composition of claim 1, wherein the immunogenic polypeptide comprises a cancer antigen. 8. The pharmaceutical composition of claim 7, wherein the immunogenic polypeptide comprises a het-2/neu peptide. 9. The pharmaceutical composition of claim, wherein the her-2/neu peptide is derived from the intracellular domain of her-2/neu. 10. The pharmaceutical composition of claim 8, wherein the her-2/neu peptide is derived from the extracellular domain of her-2/neu. 11. The pharmaceutical composition of claim 8, wherein the her-2/neu peptide is derived from the extracellular domain of her-2/neu. 12. A pharmaceutical composition comprising an isolated stress protein complex and a physiologically acceptable carrier, wherein the stress protein complex comprises an hsp110 polypeptide and an immunogenic polypeptide, wherein the immunogenic polypeptide is a colon cancer antigen and wherein the complex has been heated so as to enhance binding of the hsp110 polypeptide to the immunogenic polypeptide. 13. The pharmaceutical composition of claim 1, further comprising an adjuvant. 14. A method for inhibiting tumor growth in a subject, comprising administering to the subject an effective amount of the pharmaceutical composition of claim 7 to elicit an anti-tumor immune response in the subject, and whereby inhibiting tumor growth in the subject. 15. A method of inhibiting tumor growth in a subject comprising administering to the subject an effective amount of a pharmaceutical composition comprising an isolated stress protein complex and a physiological acceptable carrier, wherein the stress protein complex comprises an hsp110 polypeptide and an immunogenic polypeptide that is a cancer antigen, and wherein the complex has been heated so as to enhance binding of the hsp110 polypeptide to the immunogenic polypeptide, and the administration of the pharmaceutical composition elicits an anti-tumor immune response in the subject, thereby inhibiting tumor growth in the subject. 16. The method of claim 15, wherein the complex of the pharmaceutical composition comprises a fusion protein. 17. The method of claim 15, wherein the complex of the pharmaceutical composition is derived from a tumor. 18. The method of claim 15, wherein the hsp110 of the pharmaceutical composition is complexed with hsp70 and hsp25. 19. The method of claim 15, wherein the immunogenic polypeptide of the pharmaceutical composition comprises a her-2/neu peptide. 20. The method of claim 19, wherein he her-2/neu peptide is derived from the intracellular domain of her-2/neu. 21. The method of claim 19, wherein the her-2/neu peptide derived from the extracellular domain of her-2/neu. 22. The method of claim 19, wherein the her-2/neu peptide is derived from the transmembrane region of her-2/neu. 23. The method of claim 15, wherein the cancer is colon cancer. 24. The method of claim 15, wherein the pharmaceutical composition further comprises an adjuvant. 25. The method of claim 14, wherein the complex of the pharmaceutical composition comprises a fusion protein. 26. The method of claim 14, wherein the complex of the pharmaceutical composition is derived from a tumor. 27. The method of claim 14, wherein the hsp110 of the pharmaceutical composition is complexed with hsp70 and hsp25. 28. The method of claim 14, wherein the immunogenic polypeptide of the pharmaceutical composition comprises a her-2/neu peptide. 29. The method of claim 28, wherein the her-2/neu peptide is derived from the intracellular domain of her-2/neu. 30. The method of claim 28, wherein the her-2/neu peptide is derived from the extracellular domain of her-2/neu. 31. The method of claim 28, wherein the her-2/neu peptide is derived from the transmembrane region of her-2/neu. 32. The method of claim 14, wherein the cancer antigen is a carbon cancer antigen. 33. The method of claim 14, wherein the pharmaceutical composition further comprises an adjuvant.