Document 0559 DOCN M9610559 TI Induction of a CD8+ cytotoxic T lymphocyte response to soluble antigen given together with a novel muramyl dipeptide adjuvant, N-acetyl-D-glucosaminyl-(beta 1-4)-N-acetylmuramyl-L-alanyl-D-isoglutamine (GMDP). DT 9601 AU Hornung RL; Longo DL; Gowda VL; Kwak LW; Biological Carcinogenesis & Development Program, Program; Resources, Inc./DynCorp, Frederick, MD, USA. SO Ther Immunol. 1995 Feb;2(1):7-14. Unique Identifier : AIDSLINE MED/96002631 AB We have investigated the ability of the novel muramyl dipeptide, GMDP, to act as an adjuvant for the induction of ovalbumin (OVA)-specific, CD8+ cytotoxic T lymphocyte (CTL) responses. C57Bl/6 mice were twice immunized s.c. with 50 micrograms OVA emulsified with a squalane, L121 pluronic containing Tween-80 vehicle either with (STP-GMDP) or without (STP) GMDP. Splenic precursor CD8+ CTL activity against E.G7-OVA, but not against EL-4 parental targets was detected in STP-GMDP immunized mice after 5 days of in vitro re-stimulation with irradiated E.G7-OVA cells, while mice immunized with OVA in STP alone or OVA alone failed to demonstrate CTL activity. OVA emulsified in a microfluidized STP vehicle formulation without GMDP also elicited the E.G7-OVA precursor CTL. The ability of GMDP to induce a class I-restricted, CD8+ CTL response to a soluble protein antigen may have implications for the development of useful vaccines against viral pathogens or tumours against which CTL responses are desirable. DE Acetylmuramyl-Alanyl-Isoglutamine/*ANALOGS & DERIVATIVES/ ADMINISTRATION & DOSAGE Adjuvants, Immunologic/*ADMINISTRATION & DOSAGE Animal Antigens/*ADMINISTRATION & DOSAGE *Cytotoxicity, Immunologic CD8-Positive T-Lymphocytes/*IMMUNOLOGY Female Immunization In Vitro Mice Mice, Inbred C57BL Ovalbumin/IMMUNOLOGY Solubility Tumor Cells, Cultured JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).