Document 0129 DOCN M9550129 TI Protection against tuberculosis by passive transfer with T-cell clones recognizing mycobacterial heat-shock protein 65. DT 9505 AU Silva CL; Silva MF; Pietro RC; Lowrie DB; Department of Parasitology, Microbiology and Immunology, School; of Medicine of Ribeirao Preto, University of Sao Paulo, Brazil. SO Immunology. 1994 Nov;83(3):341-6. Unique Identifier : AIDSLINE MED/95137660 AB We have previously shown that mice vaccinated by injection with J774 macrophage-like tumour cells that expressed Mycobacterium leprae heat-shock protein (hsp) 65 as a transgene had acquired a remarkably high degree of protection against subsequent challenge with virulent M. tuberculosis. We show here that antigen-specific T cells cloned from spleens of such vaccinated animals can transfer a high level of protection to non-vaccinated recipients. The most efficient cells were of T-cell receptor (TCR) alpha beta+ and CD4- CD8+ type and specifically lysed mycobacteria-infected macrophages. These findings are consistent with the importance for protective immunity of engaging the endogenous antigen-presenting pathway to bias the immune response towards a cytolytic action against a mycobacterial antigen that is expressed at the surface of infected macrophages. TCR gamma delta+ and TCR alpha beta+ cells interacted synergistically. DE Animal Antigen-Presenting Cells/IMMUNOLOGY Antigens, Bacterial/ADMINISTRATION & DOSAGE Chaperonins/*IMMUNOLOGY CD8-Positive T-Lymphocytes/IMMUNOLOGY Heat-Shock Proteins/*IMMUNOLOGY *Immunization, Passive Mice Mice, Inbred BALB C Mycobacterium leprae/*IMMUNOLOGY Receptors, Antigen, T-Cell, alpha-beta/IMMUNOLOGY Receptors, Antigen, T-Cell, gamma-delta/IMMUNOLOGY Support, Non-U.S. Gov't T-Lymphocytes/*IMMUNOLOGY Tuberculosis/*PREVENTION & CONTROL JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).