Liposomes as immunological adjuvants in eliciting antibodies specific to the synthetic polypeptide poly(LTyr, LGlu)‐poly(DLAla)–poly(LLys) with high frequency of site‐associated idiotypic determinants
- 1 January 1981
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 11 (5), 398-404
- https://doi.org/10.1002/eji.1830110510
Abstract
The antibody response to the synthetic polypeptide, poly(LTyr, LGlu)-poly(DLAla)–poly(LLys), [(T, G)-A–L], injected entrapped in liposomes which served as adjuvant, has been analyzed. The liposomes used were composed of phosphatidylcholine, cholesterol, dicetylphosphate and DL α-tocopherol (molar ratios as 4:3:0.1:0.5) and therefore, were negatively charged. Since the (T, G)-A–L is also negatively charged, no free complexes were formed. The (T, G)-A–L was found to be entrapped inside the enclosed volume of the liposomes, and no (T, G)-A–L antigenic determinants could be detected on the liposomal membranes. Injection of high-responder C3H.SW (H-2b) mice with (T, G)-A–L-bearing liposomes demonstrated that the i.p. and the i.v. routes of immunization were efficient in eliciting (T, G)-A–L-specific antibodies, whereas the i.d. injection led to poor antibody responses. The latter route of immunization is the most effective when (T, G)-A–L is injected in complete Freund's adjuvant (CFA). When low doses (0.1 and 1 μg) of (T, G)-A–L were used for immunization, the liposomes were better adjuvants than CFA. The effectiveness of the liposomes as immunological adjuvants was also shown in their ability to induce high-potential, primed memory cells. The pattern of low (H-2k, a) and high (H-2b) responsiveness to (T, G)-A–L was retained following immunization with (T, G)-A–L entrapped in liposomes, as tested in two pairs of congenic strains. (T, G)-A–L-specific antibodies induced by injection with 1μ antigen entrapped in liposomes bear the (T, G)-A–L site-related idiotypic markers of C3H.SW (Igh-1a) mice in a significantly higher frequency than the homologous idiotypes, namely the antibodies elicited in this strain against (T, G)-A–L in CFA. Thus, liposomes may serve as adjuvants for the production of relatively restricted (T, G)-A–L-specific antibodies of high qualitiy.This publication has 28 references indexed in Scilit:
- Genetic regulation of delayed-type hypersensitivity responses to poly(LTyr,LGu)-poly(DLAla)--poly(LLys). I. Expression of the genetic defect at two phases of the immune process.The Journal of Experimental Medicine, 1980
- Vesicle Targeting: Timed Release and Specificity for Leukocytes in Mice by Subcutaneous InjectionScience, 1980
- In vitro and in vivo induction of effector T cells mediating DTH responses to a protein and a synthetic polypeptide antigenCellular Immunology, 1979
- Liposomes in Immunology: Impairment of the Adjuvant Effect of Liposomes by Incorporation of the Adjuvant Lysolecithin and the Role of MacrophagesImmunological Communications, 1979
- Mode of action of non-histone proteins in the stimulation of transcription from DNABiochemical and Biophysical Research Communications, 1976
- Varied effects of polyadenylic-polyuridylic acid on immune responsesBiochimie, 1976
- Distinctive adjuvanticity of synthetic analogs of mycobacterial water-soluble componentsCellular Immunology, 1976
- Immunogenicity of liposomal model membranes sensitized with mono(p-azobenzenearsonic acid)tyrosylphosphatidylethanolamine derivatives. Antibody formation and delayed hypersensitivity reactionBiochemistry, 1975
- Liposomes as immunological adjuvantsNature, 1974
- Antibody formation in response to liposomal model membranes sensitized with N-substituted phosphatidylethanolamine derivativesBiochemistry, 1974